首页 > 最新文献

Anemia最新文献

英文 中文
Correlations between Iron Load and CD4 in Adult Transfusion-Dependent Beta Thalassemia. 成人输血依赖型β地中海贫血症患者铁负荷与 CD4 之间的相关性。
IF 2.9 Q3 HEMATOLOGY Pub Date : 2021-06-17 eCollection Date: 2021-01-01 DOI: 10.1155/2021/5549503
Tubagus Djumhana Atmakusuma, Ralph Girson, Sukamto Koesnoe

Background: Thalassemia is a hereditary disease, and severe anemia is the main phenotype of major thalassemia. Furthermore, the most important method in the management of this disease is red blood cell transfusion. Regular transfusions administered 1 or 2 times every month improve prognosis and survival. However, there is higher risk of infections and iron overload, especially in transfusion-dependent thalassemia (TDT). Infections are the second leading cause of death in adult TDT, after heart failure. Higher risk of infection is also influenced by multiple blood transfusions which causes alteration in immune response due to alloimmunization, transfusion-related infections, and iron overload. Meanwhile, iron overload in TDT alters both innate and specific immune responses. Furthermore, previous studies have shown the correlation between ferritin with CD4, but this has not been carried out in Indonesia. Therefore, this study aims to determine the correlations between iron overload (serum ferritin and transferrin saturation) and specific immune cells (CD4).

Methods: This is a cross-sectional study, and a total number of 64 subjects were examined consecutively. Chest X-ray and blood sera were obtained. The total number of subjects was 64. The seromarkers HBsAg, anti-HCV, and anti-HIV were tested using the ELISA method. Serum ferritin and transferrin saturation was tested using ECLIA, and lymphocyte subsets were analyzed using flowcytometry. Meanwhile, the correlation between variables was determined using Spearman's test.

Results: The results showed that 4.9% subjects were HBsAg positive, 10.7% were anti-HCV positive, and none were anti-HIV positive. There were 4 subjects with lung tuberculosis based on the 41 chest X-ray. Meanwhile, there was a weak negative and insignificant correlation between serum ferritin with CD4 (p=0.75; r = -0.04) and a weak positive and insignificant correlation between transferrin saturation with CD4 (p=0.133; r= 0.19).

Conclusion: There were no correlations between iron overload (ferritin) and cellular immunity (CD4) in adult transfusion-dependent thalassemia.

背景:地中海贫血是一种遗传性疾病,严重贫血是重型地中海贫血的主要表现型。此外,治疗这种疾病最重要的方法是输注红细胞。每月定期输血 1 至 2 次可改善预后和存活率。然而,感染和铁超载的风险较高,尤其是输血依赖型地中海贫血(TDT)患者。感染是成人地中海贫血患者的第二大死因,仅次于心力衰竭。感染风险较高还受到多次输血的影响,因为多次输血会导致同种免疫、输血相关感染和铁超载等免疫反应的改变。同时,TDT 中的铁超载会改变先天性免疫反应和特异性免疫反应。此外,以往的研究显示铁蛋白与 CD4 之间存在相关性,但这一研究尚未在印度尼西亚开展。因此,本研究旨在确定铁超载(血清铁蛋白和转铁蛋白饱和度)与特异性免疫细胞(CD4)之间的相关性:方法:这是一项横断面研究,共有 64 名受试者接受了连续检查。方法:这是一项横断面研究,共对 64 名受试者进行了连续检查,并采集了胸部 X 光片和血清。受试者总数为 64 人。采用 ELISA 方法检测血清标志物 HBsAg、抗-HCV 和抗-HIV。使用 ECLIA 检测血清铁蛋白和转铁蛋白饱和度,使用流式细胞仪分析淋巴细胞亚群。同时,使用斯皮尔曼检验确定变量之间的相关性:结果显示,4.9%的受试者为 HBsAg 阳性,10.7%为抗-HCV 阳性,无抗-HIV 阳性。根据 41 张胸部 X 光片,有 4 名受试者患有肺结核。同时,血清铁蛋白与 CD4 呈微弱负相关,不显著(p=0.75;r=-0.04),转铁蛋白饱和度与 CD4 呈微弱正相关,不显著(p=0.133;r=0.19):结论:在成人输血依赖型地中海贫血症患者中,铁过载(铁蛋白)与细胞免疫(CD4)之间没有相关性。
{"title":"Correlations between Iron Load and CD4 in Adult Transfusion-Dependent Beta Thalassemia.","authors":"Tubagus Djumhana Atmakusuma, Ralph Girson, Sukamto Koesnoe","doi":"10.1155/2021/5549503","DOIUrl":"10.1155/2021/5549503","url":null,"abstract":"<p><strong>Background: </strong>Thalassemia is a hereditary disease, and severe anemia is the main phenotype of major thalassemia. Furthermore, the most important method in the management of this disease is red blood cell transfusion. Regular transfusions administered 1 or 2 times every month improve prognosis and survival. However, there is higher risk of infections and iron overload, especially in transfusion-dependent thalassemia (TDT). Infections are the second leading cause of death in adult TDT, after heart failure. Higher risk of infection is also influenced by multiple blood transfusions which causes alteration in immune response due to alloimmunization, transfusion-related infections, and iron overload. Meanwhile, iron overload in TDT alters both innate and specific immune responses. Furthermore, previous studies have shown the correlation between ferritin with CD4, but this has not been carried out in Indonesia. Therefore, this study aims to determine the correlations between iron overload (serum ferritin and transferrin saturation) and specific immune cells (CD4).</p><p><strong>Methods: </strong>This is a cross-sectional study, and a total number of 64 subjects were examined consecutively. Chest X-ray and blood sera were obtained. The total number of subjects was 64. The seromarkers HBsAg, anti-HCV, and anti-HIV were tested using the ELISA method. Serum ferritin and transferrin saturation was tested using ECLIA, and lymphocyte subsets were analyzed using flowcytometry. Meanwhile, the correlation between variables was determined using Spearman's test.</p><p><strong>Results: </strong>The results showed that 4.9% subjects were HBsAg positive, 10.7% were anti-HCV positive, and none were anti-HIV positive. There were 4 subjects with lung tuberculosis based on the 41 chest X-ray. Meanwhile, there was a weak negative and insignificant correlation between serum ferritin with CD4 (<i>p</i>=0.75; <i>r</i> = -0.04) and a weak positive and insignificant correlation between transferrin saturation with CD4 (<i>p</i>=0.133; <i>r</i> <i>=</i> 0.19).</p><p><strong>Conclusion: </strong>There were no correlations between iron overload (ferritin) and cellular immunity (CD4) in adult transfusion-dependent thalassemia.</p>","PeriodicalId":46055,"journal":{"name":"Anemia","volume":"2021 ","pages":"5549503"},"PeriodicalIF":2.9,"publicationDate":"2021-06-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8233081/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39166361","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Human Acquired Aplastic Anemia Patients' Bone-Marrow-Derived Mesenchymal Stem Cells Are Not Influenced by Hematopoietic Compartment and Maintain Stemness and Immune Properties. 人获得性再生障碍性贫血患者骨髓间充质干细胞不受造血区室影响并保持干性和免疫特性
IF 2.9 Q3 HEMATOLOGY Pub Date : 2021-04-29 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6678067
Vandana Sharma, Sonali Rawat, Suchi Gupta, Sweta Tamta, Rinkey Sharma, Tulika Seth, Sujata Mohanty

Methods: In the current study, we investigated the morphological differences, proliferation capacity, population doubling time (PDT), surface marker profiling, trilineage differentiation potential, and immunosuppressive ability of BM Mesenchymal Stem Cells (BM-MSCs) from untreated aAA patients and in the same number of age- and gender-matched controls.

Results: We observed similar morphology, proliferation capacity, phenotype, trilineage differentiation potential, and immunomodulatory properties of BM-MSCs in aAA patients and control subjects.

Conclusion: Our results confirm that the basic and immunosuppressive properties of BM-MSCs from aAA patients do not differ from normal BM-MSCs. Our data suggest that BM-MSCs from aAA patients might not be involved in disease pathogenesis. However, owing to a smaller number of samples, it is not conclusive, and future studies with more exhaustive investigation at transcriptome level are warranted.

方法:在目前的研究中,我们研究了未经治疗的aAA患者和相同数量的年龄和性别匹配的对照组的BM间充质干细胞(BM- mscs)的形态学差异、增殖能力、群体倍增时间(PDT)、表面标记谱、三岁分化潜力和免疫抑制能力。结果:我们观察到aAA患者和对照组BM-MSCs的形态、增殖能力、表型、三期分化潜力和免疫调节特性相似。结论:我们的研究结果证实,aAA患者的骨髓间充质干细胞的基本特性和免疫抑制特性与正常骨髓间充质干细胞没有区别。我们的数据表明来自aAA患者的BM-MSCs可能与疾病的发病机制无关。然而,由于样本数量较少,这并不是决定性的,未来的研究需要在转录组水平上进行更详尽的调查。
{"title":"Human Acquired Aplastic Anemia Patients' Bone-Marrow-Derived Mesenchymal Stem Cells Are Not Influenced by Hematopoietic Compartment and Maintain Stemness and Immune Properties.","authors":"Vandana Sharma,&nbsp;Sonali Rawat,&nbsp;Suchi Gupta,&nbsp;Sweta Tamta,&nbsp;Rinkey Sharma,&nbsp;Tulika Seth,&nbsp;Sujata Mohanty","doi":"10.1155/2021/6678067","DOIUrl":"https://doi.org/10.1155/2021/6678067","url":null,"abstract":"<p><strong>Methods: </strong>In the current study, we investigated the morphological differences, proliferation capacity, population doubling time (PDT), surface marker profiling, trilineage differentiation potential, and immunosuppressive ability of BM Mesenchymal Stem Cells (BM-MSCs) from untreated aAA patients and in the same number of age- and gender-matched controls.</p><p><strong>Results: </strong>We observed similar morphology, proliferation capacity, phenotype, trilineage differentiation potential, and immunomodulatory properties of BM-MSCs in aAA patients and control subjects.</p><p><strong>Conclusion: </strong>Our results confirm that the basic and immunosuppressive properties of BM-MSCs from aAA patients do not differ from normal BM-MSCs. Our data suggest that BM-MSCs from aAA patients might not be involved in disease pathogenesis. However, owing to a smaller number of samples, it is not conclusive, and future studies with more exhaustive investigation at transcriptome level are warranted.</p>","PeriodicalId":46055,"journal":{"name":"Anemia","volume":"2021 ","pages":"6678067"},"PeriodicalIF":2.9,"publicationDate":"2021-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8105116/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38998738","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Iron Overload in Transfusion-Dependent Indonesian Thalassemic Patients. 输血依赖性印尼地中海贫血患者的铁超载。
IF 2.9 Q3 HEMATOLOGY Pub Date : 2021-04-15 eCollection Date: 2021-01-01 DOI: 10.1155/2021/5581831
Pandji Irani Fianza, Anita Rahmawati, Sri Hudaya Widihastha, Shofura Afifah, Mohammad Ghozali, Andre Indrajaya, Dilli Marayuzan Akbar Pratama, Dimmy Prasetya, Teddy Arnold Sihite, Mas Rizky A A Syamsunarno, Djatnika Setiabudi, Suthat Fucharoen, Ramdan Panigoro

Thalassemia is a genetic disease caused by disruption of globin chain synthesis leading to severe anemia and thus regular blood transfusion is necessary. However, there have been known transfusions-related consequences, including iron overload and multi-organ damage. The aims of this study were to evaluate liver and cardiac function in youth and adult transfusion-dependent Indonesian thalassemic patients and to assess its correlation with serum ferritin levels, as well as T2 magnetic resonance imaging (MRI). Transfusion-dependent thalassemic (TDT) outpatients (n = 66; mean age, 21.5 ± 7.2 years) were carried out for the complete assessment consisting of blood test including liver enzyme and serum ferritin, followed by electrocardiography (ECG) and echocardiography. Subjects were also divided by serum ferritin levels into three groups: < 2500 ng/mL, 2500-5000 ng/mL, and >5000 ng/mL. Additionally, subgroup analysis in patients with T2 MRI assessment was conducted. In terms of age of first blood transfusion, subjects with ferritin >5000 ng/mL were the youngest among others. The alanine aminotransferase (ALT) levels in group with serum ferritin >5000 ng/mL were significantly higher than those of the group with serum ferritin <2500 ng/mL. Additionally, youth and adult TDT patients whose serum ferritin >5000 ng/mL had significantly lower tricuspid annular plane systolic excursion (TAPSE) when compared with those who had serum ferritin <2500 ng/mL. Similarly, TAPSE in patients with moderate cardiac siderosis based on cardiac T2 MRI was significantly lower than those without cardiac siderosis. There was significant, but only moderate correlation between serum ferritin and cardiac T2 MRI. Based on these findings, it is important to routinely monitor iron accumulation-related complications, including liver and cardiac damage in youth and adult TDT patients.

地中海贫血是一种遗传性疾病,由珠蛋白链合成中断导致严重贫血,因此需要定期输血。然而,已知输血相关的后果,包括铁超载和多器官损伤。本研究的目的是评估青年和成人输血依赖型印尼地中海贫血患者的肝功能和心功能,并评估其与血清铁蛋白水平以及T2 *磁共振成像(MRI)的相关性。输血依赖型地中海贫血(TDT)门诊患者(n = 66;平均年龄21.5±7.2岁)进行全面评估,包括血液检查包括肝酶和血清铁蛋白,然后进行心电图和超声心动图检查。根据血清铁蛋白水平将受试者分为< 2500 ng/mL、2500-5000 ng/mL和>5000 ng/mL三组。此外,对T2 * MRI评估患者进行亚组分析。从首次输血年龄来看,铁蛋白>5000 ng/mL的受试者年龄最小。血清铁蛋白≥5000ng /mL组丙氨酸转氨酶(ALT)水平显著高于血清铁蛋白≥5000ng /mL组,三尖瓣环形平面收缩位移(TAPSE)显著低于血清铁蛋白* MRI显著低于无心脏铁素体沉积组。血清铁蛋白与心脏T2 * MRI之间有显著但仅中等程度的相关性。基于这些发现,常规监测铁积累相关并发症,包括青年和成人TDT患者的肝脏和心脏损伤是很重要的。
{"title":"Iron Overload in Transfusion-Dependent Indonesian Thalassemic Patients.","authors":"Pandji Irani Fianza,&nbsp;Anita Rahmawati,&nbsp;Sri Hudaya Widihastha,&nbsp;Shofura Afifah,&nbsp;Mohammad Ghozali,&nbsp;Andre Indrajaya,&nbsp;Dilli Marayuzan Akbar Pratama,&nbsp;Dimmy Prasetya,&nbsp;Teddy Arnold Sihite,&nbsp;Mas Rizky A A Syamsunarno,&nbsp;Djatnika Setiabudi,&nbsp;Suthat Fucharoen,&nbsp;Ramdan Panigoro","doi":"10.1155/2021/5581831","DOIUrl":"https://doi.org/10.1155/2021/5581831","url":null,"abstract":"<p><p>Thalassemia is a genetic disease caused by disruption of globin chain synthesis leading to severe anemia and thus regular blood transfusion is necessary. However, there have been known transfusions-related consequences, including iron overload and multi-organ damage. The aims of this study were to evaluate liver and cardiac function in youth and adult transfusion-dependent Indonesian thalassemic patients and to assess its correlation with serum ferritin levels, as well as T2 <sup><i>∗</i></sup> magnetic resonance imaging (MRI). Transfusion-dependent thalassemic (TDT) outpatients (<i>n</i> = 66; mean age, 21.5 ± 7.2 years) were carried out for the complete assessment consisting of blood test including liver enzyme and serum ferritin, followed by electrocardiography (ECG) and echocardiography. Subjects were also divided by serum ferritin levels into three groups: < 2500 ng/mL, 2500-5000 ng/mL, and >5000 ng/mL. Additionally, subgroup analysis in patients with T2<sup>∗</sup> MRI assessment was conducted. In terms of age of first blood transfusion, subjects with ferritin >5000 ng/mL were the youngest among others. The alanine aminotransferase (ALT) levels in group with serum ferritin >5000 ng/mL were significantly higher than those of the group with serum ferritin <2500 ng/mL. Additionally, youth and adult TDT patients whose serum ferritin >5000 ng/mL had significantly lower tricuspid annular plane systolic excursion (TAPSE) when compared with those who had serum ferritin <2500 ng/mL. Similarly, TAPSE in patients with moderate cardiac siderosis based on cardiac T2<sup>∗</sup> MRI was significantly lower than those without cardiac siderosis. There was significant, but only moderate correlation between serum ferritin and cardiac T2<sup>∗</sup> MRI. Based on these findings, it is important to routinely monitor iron accumulation-related complications, including liver and cardiac damage in youth and adult TDT patients.</p>","PeriodicalId":46055,"journal":{"name":"Anemia","volume":"2021 ","pages":"5581831"},"PeriodicalIF":2.9,"publicationDate":"2021-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8062201/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38963998","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Microcytic and Malarial Anaemia Prevalence in Urban Children ≤15 Years in the Mount Cameroon Area: A Cross-Sectional Study on Risk Factors. 喀麦隆山地区≤15岁城市儿童小细胞和疟疾贫血患病率:危险因素的横断面研究
IF 2.9 Q3 HEMATOLOGY Pub Date : 2021-04-08 eCollection Date: 2021-01-01 DOI: 10.1155/2021/5712309
Sharon Odmia Sama, Seraphine Njuontsop Chiamo, Germain Sotoing Taiwe, Gwendolyne Elobe Njume, Irene Ule Ngole Sumbele

Background: Anaemia, a common nutritional deficiency, is a public health problem in the Mount Cameroon area. This study determined the prevalence and possible risk factors of microcytic and malarial anaemia in children less than ≤15 years residing in the Buea and Limbe municipalities in the Mount Cameroon area.

Methods: A total of 566 children were clinically examined in a cross-sectional study from December 2018 to August 2019 for anaemia and malaria parasites. Blood samples collected were used in evaluating full blood count with the aid of an automated haemoanalyser, and malaria parasite was confirmed by microscopy. Anaemia was defined based on WHO standards while microcytic anaemia and malarial anaemia were defined as microcytosis + anaemia and malaria + anaemia, respectively. Factors that showed significance in the bivariate analysis were entered into a multinomial logistic regression to determine risk factors for microcytic and malarial anaemia.

Results: The overall prevalence for anaemia, microcytosis, microcytic anaemia, and malarial anaemia was, respectively, 68.7%, 48.9%, 36.9%, and 19.6% with microcytic anaemia representing 53.7% of all anaemic cases. Risk factors for microcytic anaemia included child age of 1-5 years (P=0.007), forest ethnicity (P=0.019), parents being farmers (P=0.038) or jobless (P=0.009), and having moderate malaria parasitaemia (P=0.048) while those for malarial anaemia were child age of 6-10 years (P=0.008), parents' age of 26-35 years (P=0.049), parents being jobless (P=0.023), and consuming plantains 3-4 times (P=0.024) a week.

Conclusion: Microcytic anaemia is getting to be a severe public health concern while malarial anaemia is a mild public health issue in children residing in urban areas of Mount Cameroon. Parents' occupation was directly linked to all anaemia forms; hence, any intervention to curb anaemia should consider aspects that will raise the socioeconomic status of the population.

背景:贫血是一种常见的营养缺乏症,是喀麦隆山地区的一个公共卫生问题。本研究确定了喀麦隆山地区布埃亚市和林贝市居住的≤15岁儿童中小细胞贫血和疟疾贫血的患病率和可能的危险因素。方法:2018年12月至2019年8月,对566名儿童进行贫血和疟疾寄生虫的横断面临床检查。收集的血液样本在自动血液分析仪的帮助下用于评估全血细胞计数,并通过显微镜确认疟疾寄生虫。贫血根据世卫组织标准定义,小细胞贫血和疟疾贫血分别定义为小细胞血症+贫血和疟疾+贫血。在双变量分析中显示有意义的因素被输入到多项逻辑回归中,以确定小细胞贫血和疟疾贫血的危险因素。结果:贫血、小细胞贫血、小细胞贫血和疟疾的总患病率分别为68.7%、48.9%、36.9%和19.6%,其中小细胞贫血占所有贫血病例的53.7%。小细胞贫血的危险因素为儿童年龄1 ~ 5岁(P=0.007)、森林民族(P=0.019)、父母为农民(P=0.038)或无业(P=0.009)、中度疟疾寄生虫病(P=0.048);疟疾贫血的危险因素为儿童年龄6 ~ 10岁(P=0.008)、父母年龄26 ~ 35岁(P=0.049)、父母无业(P=0.023)、每周食用大蕉3 ~ 4次(P=0.024)。结论:小细胞贫血正在成为一个严重的公共卫生问题,而疟疾贫血在居住在喀麦隆山城市地区的儿童中是一个轻微的公共卫生问题。父母的职业与所有贫血形式直接相关;因此,任何遏制贫血的干预措施都应考虑提高人口社会经济地位的方面。
{"title":"Microcytic and Malarial Anaemia Prevalence in Urban Children ≤15 Years in the Mount Cameroon Area: A Cross-Sectional Study on Risk Factors.","authors":"Sharon Odmia Sama, Seraphine Njuontsop Chiamo, Germain Sotoing Taiwe, Gwendolyne Elobe Njume, Irene Ule Ngole Sumbele","doi":"10.1155/2021/5712309","DOIUrl":"10.1155/2021/5712309","url":null,"abstract":"<p><strong>Background: </strong>Anaemia, a common nutritional deficiency, is a public health problem in the Mount Cameroon area. This study determined the prevalence and possible risk factors of microcytic and malarial anaemia in children less than ≤15 years residing in the Buea and Limbe municipalities in the Mount Cameroon area.</p><p><strong>Methods: </strong>A total of 566 children were clinically examined in a cross-sectional study from December 2018 to August 2019 for anaemia and malaria parasites. Blood samples collected were used in evaluating full blood count with the aid of an automated haemoanalyser, and malaria parasite was confirmed by microscopy. Anaemia was defined based on WHO standards while microcytic anaemia and malarial anaemia were defined as microcytosis + anaemia and malaria + anaemia, respectively. Factors that showed significance in the bivariate analysis were entered into a multinomial logistic regression to determine risk factors for microcytic and malarial anaemia.</p><p><strong>Results: </strong>The overall prevalence for anaemia, microcytosis, microcytic anaemia, and malarial anaemia was, respectively, 68.7%, 48.9%, 36.9%, and 19.6% with microcytic anaemia representing 53.7% of all anaemic cases. Risk factors for microcytic anaemia included child age of 1-5 years (<i>P</i>=0.007), forest ethnicity (<i>P</i>=0.019), parents being farmers (<i>P</i>=0.038) or jobless (<i>P</i>=0.009), and having moderate malaria parasitaemia (<i>P</i>=0.048) while those for malarial anaemia were child age of 6-10 years (<i>P</i>=0.008), parents' age of 26-35 years (<i>P</i>=0.049), parents being jobless (<i>P</i>=0.023), and consuming plantains 3-4 times (<i>P</i>=0.024) a week.</p><p><strong>Conclusion: </strong>Microcytic anaemia is getting to be a severe public health concern while malarial anaemia is a mild public health issue in children residing in urban areas of Mount Cameroon. Parents' occupation was directly linked to all anaemia forms; hence, any intervention to curb anaemia should consider aspects that will raise the socioeconomic status of the population.</p>","PeriodicalId":46055,"journal":{"name":"Anemia","volume":"2021 ","pages":"5712309"},"PeriodicalIF":2.9,"publicationDate":"2021-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8049821/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38933195","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Anemia and Contributing Factors in Severely Malnourished Infants and Children Aged between 0 and 59 Months Admitted to the Treatment Centers of the Amhara Region, Ethiopia: A Multicenter Chart Review Study. 埃塞俄比亚阿姆哈拉地区治疗中心收治的 0 至 59 个月严重营养不良婴幼儿的贫血症及其诱因:多中心病历回顾研究》。
IF 2.9 Q3 HEMATOLOGY Pub Date : 2021-03-27 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6636043
Wubet Worku Takele, Adhanom Gebreegziabher Baraki, Haileab Fekadu Wolde, Hanna Demelash Desyibelew, Behailu Tariku Derseh, Abel Fekadu Dadi, Eskedar Getie Mekonnen, Temesgen Yihunie Akalu

Background: Anemia among severely malnourished children is a double burden that could make the treatment outcome of severe acute malnutrition (SAM) more unfavorable. The burden and the factors are, however, uncovered among children in the Amhara region. Therefore, the study was aimed at determining the prevalence of anemia and identifying contributing factors in severely malnourished children aged between 0 and 59 months admitted to the treatment centers of the Amhara region referral hospitals.

Methods: A facility-based cross-sectional study was conducted that included 1,301 infants and children, who developed SAM and were admitted to the three referral hospitals of the Amhara region. Data were extracted using a data extraction checklist. The binary logistic regression analysis was employed to show an association between the dependent and independent variables. Multicollinearity was assessed using the variance inflation factor (VIF) and no problem was detected (overall VIF = 1.67). The presence of association was declared based on the p-value (≤0.05), and the adjusted odds ratio with its respective 95% confidence interval was used to report the direction, as well as the strength of association.

Results: About 41.43% (95% CI: 38.78%-44.13%) of severely malnourished infants and children have developed anemia, of which around half (47%) of them were under six months old. Rural residence (AOR = 1.56; 95% CI: 1.14-2.12) and HIV infection (AOR = 2.00; 95% CI: 1.04-3.86) were significantly associated with higher odds of anemia. Furthermore, being exclusively breastfed (AOR = 0.57; 95% CI 0.39-0.83) remarkably reduced the likelihood of anemia.

Conclusions: This data confirms that anemia among severely malnourished infants and children is a public health problem in the Amhara region. Infants younger than six months were at a higher risk of anemia. Being a rural resident and contracting HIV infection have elevated the occurrence of anemia, whereas being exclusively breastfed decreased the risk. Therefore, the study gives an insight to policymakers and planners to strengthen the existing exclusive breastfeeding practice. Strategies being practiced to prevent HIV transmission and early detection, as well as treatment, should also be strengthened. Furthermore, mothers/caretakers of infants and children residing in the rural areas deserve special attention through delivering nutrition education.

背景:严重营养不良儿童贫血是一种双重负担,可能会使严重急性营养不良(SAM)的治疗结果更加不利。然而,在阿姆哈拉地区的儿童中,这种负担和因素尚未被发现。因此,本研究旨在确定阿姆哈拉地区转诊医院治疗中心收治的 0 至 59 个月严重营养不良儿童的贫血患病率,并找出导致贫血的因素:研究对象包括阿姆哈拉地区三家转诊医院收治的 1,301 名患严重营养不良症的婴幼儿。研究人员使用数据提取清单提取数据。采用二元逻辑回归分析来显示因变量和自变量之间的关联。使用方差膨胀因子(VIF)对多重共线性进行了评估,没有发现问题(总体 VIF = 1.67)。根据 p 值(≤0.05)宣布是否存在关联,并使用调整后的几率及其各自的 95% 置信区间来报告关联的方向和强度:约 41.43%(95% CI:38.78%-44.13%)的严重营养不良婴幼儿出现贫血,其中约一半(47%)的婴幼儿年龄在 6 个月以下。农村居民(AOR = 1.56;95% CI:1.14-2.12)和艾滋病病毒感染(AOR = 2.00;95% CI:1.04-3.86)与较高的贫血几率明显相关。此外,纯母乳喂养(AOR = 0.57;95% CI 0.39-0.83)明显降低了贫血的可能性:这些数据证实,严重营养不良的婴幼儿贫血是阿姆哈拉地区的一个公共卫生问题。六个月以下的婴儿患贫血的风险更高。农村居民和艾滋病毒感染会增加贫血的发生率,而纯母乳喂养则会降低贫血的风险。因此,这项研究为政策制定者和规划者加强现有的纯母乳喂养做法提供了启示。同时,还应加强预防艾滋病毒传播、早期发现和治疗的策略。此外,通过提供营养教育,居住在农村地区的婴幼儿母亲/看护人应得到特别关注。
{"title":"Anemia and Contributing Factors in Severely Malnourished Infants and Children Aged between 0 and 59 Months Admitted to the Treatment Centers of the Amhara Region, Ethiopia: A Multicenter Chart Review Study.","authors":"Wubet Worku Takele, Adhanom Gebreegziabher Baraki, Haileab Fekadu Wolde, Hanna Demelash Desyibelew, Behailu Tariku Derseh, Abel Fekadu Dadi, Eskedar Getie Mekonnen, Temesgen Yihunie Akalu","doi":"10.1155/2021/6636043","DOIUrl":"10.1155/2021/6636043","url":null,"abstract":"<p><strong>Background: </strong>Anemia among severely malnourished children is a double burden that could make the treatment outcome of severe acute malnutrition (SAM) more unfavorable. The burden and the factors are, however, uncovered among children in the Amhara region. Therefore, the study was aimed at determining the prevalence of anemia and identifying contributing factors in severely malnourished children aged between 0 and 59 months admitted to the treatment centers of the Amhara region referral hospitals.</p><p><strong>Methods: </strong>A facility-based cross-sectional study was conducted that included 1,301 infants and children, who developed SAM and were admitted to the three referral hospitals of the Amhara region. Data were extracted using a data extraction checklist. The binary logistic regression analysis was employed to show an association between the dependent and independent variables. Multicollinearity was assessed using the variance inflation factor (VIF) and no problem was detected (overall VIF = 1.67). The presence of association was declared based on the <i>p</i>-value (≤0.05), and the adjusted odds ratio with its respective 95% confidence interval was used to report the direction, as well as the strength of association.</p><p><strong>Results: </strong>About 41.43% (95% CI: 38.78%-44.13%) of severely malnourished infants and children have developed anemia, of which around half (47%) of them were under six months old. Rural residence (AOR = 1.56; 95% CI: 1.14-2.12) and HIV infection (AOR = 2.00; 95% CI: 1.04-3.86) were significantly associated with higher odds of anemia. Furthermore, being exclusively breastfed (AOR = 0.57; 95% CI 0.39-0.83) remarkably reduced the likelihood of anemia.</p><p><strong>Conclusions: </strong>This data confirms that anemia among severely malnourished infants and children is a public health problem in the Amhara region. Infants younger than six months were at a higher risk of anemia. Being a rural resident and contracting HIV infection have elevated the occurrence of anemia, whereas being exclusively breastfed decreased the risk. Therefore, the study gives an insight to policymakers and planners to strengthen the existing exclusive breastfeeding practice. Strategies being practiced to prevent HIV transmission and early detection, as well as treatment, should also be strengthened. Furthermore, mothers/caretakers of infants and children residing in the rural areas deserve special attention through delivering nutrition education.</p>","PeriodicalId":46055,"journal":{"name":"Anemia","volume":"2021 ","pages":"6636043"},"PeriodicalIF":2.9,"publicationDate":"2021-03-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8019621/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25592035","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Anaemia in the Hospitalized Elderly in Tanzania: Prevalence, Severity, and Micronutrient Deficiency Status. 坦桑尼亚住院老年人贫血症:坦桑尼亚住院老人中的贫血症:患病率、严重程度和微量营养素缺乏状况》(Prevalence, Severity, and Micronutrient Deficiency Status.
IF 2.9 Q3 HEMATOLOGY Pub Date : 2021-02-26 eCollection Date: 2021-01-01 DOI: 10.1155/2021/9523836
Clara Chamba, Ahlam Nasser, William F Mawalla, Upendo Masamu, Neema Budodi Lubuva, Erius Tebuka, Pius Magesa

Introduction: Anaemia is a common problem in sub-Saharan Africa. While most literature has focused on children, women of childbearing age, and pregnant women, data for the elderly population are relatively scarce. Anaemia exhorts negative consequences to functional ability of elderly patients, both physically and cognitively. The purpose of this study was to determine the prevalence of anaemia, severity, and micronutrient deficiency status in the elderly hospitalized patients in Tanzania.

Methods: A total of 156 hospitalized adults aged 60 years and above were enrolled in this study. A structured questionnaire was used to capture sociodemographic and clinical characteristics. Blood samples were collected, and a complete blood count, serum cobalamin, serum ferritin, and serum folate levels were measured to assess anaemia and micronutrient deficiency status in all participants who had anaemia.

Results: The prevalence of anaemia was 79.5% (124/156) with severe anaemia in 33.9% (42/124) of participants, moderate anaemia in 42.7% (53/124) of participants, and 23.4% (29/124) of all participants had mild anaemia. Micronutrient deficiency was found in 14.5% (18/124) of all participants with anaemia. Combined deficiency (either iron and vitamin B12 deficiency or iron and folate deficiency) was the most common micronutrient deficiency anaemia with a frequency of 33.3% (6/18), followed by isolated iron and folate deficiencies at equal frequency of 27.8% (5/18) and vitamin B12 deficiency at 11.1% (2/18).

Conclusion: The prevalence of anaemia in the hospitalized elderly population is high warranting public health attention and mostly present in moderate and severe forms. Micro-nutrient deficiency anaemia is common in this age group and is mostly due to combined micronutrient deficiency.

导言:贫血是撒哈拉以南非洲地区的一个常见问题。虽然大多数文献都侧重于儿童、育龄妇女和孕妇,但有关老年人口的数据却相对较少。贫血会对老年患者的身体和认知能力造成负面影响。本研究旨在确定坦桑尼亚住院老年患者的贫血患病率、严重程度和微量营养素缺乏状况:本研究共招募了 156 名 60 岁及以上的住院成年人。采用结构化问卷调查社会人口学和临床特征。研究人员采集了血液样本,并测量了全血细胞计数、血清钴胺素、血清铁蛋白和血清叶酸水平,以评估所有贫血患者的贫血和微量营养素缺乏状况:贫血患病率为 79.5%(124/156),其中 33.9%(42/124)为重度贫血,42.7%(53/124)为中度贫血,23.4%(29/124)为轻度贫血。在所有患有贫血症的参与者中,14.5%(18/124)的人患有微量营养素缺乏症。综合缺乏症(铁和维生素 B12 缺乏症或铁和叶酸缺乏症)是最常见的微量营养素缺乏性贫血,发生率为 33.3%(6/18),其次是单独的铁和叶酸缺乏症,发生率为 27.8%(5/18),维生素 B12 缺乏症发生率为 11.1%(2/18):结论:住院老年人群中贫血症的发病率很高,应引起公共卫生方面的重视,且多为中度和重度贫血。微量营养素缺乏性贫血在这一年龄组中很常见,主要是由于综合微量营养素缺乏所致。
{"title":"Anaemia in the Hospitalized Elderly in Tanzania: Prevalence, Severity, and Micronutrient Deficiency Status.","authors":"Clara Chamba, Ahlam Nasser, William F Mawalla, Upendo Masamu, Neema Budodi Lubuva, Erius Tebuka, Pius Magesa","doi":"10.1155/2021/9523836","DOIUrl":"10.1155/2021/9523836","url":null,"abstract":"<p><strong>Introduction: </strong>Anaemia is a common problem in sub-Saharan Africa. While most literature has focused on children, women of childbearing age, and pregnant women, data for the elderly population are relatively scarce. Anaemia exhorts negative consequences to functional ability of elderly patients, both physically and cognitively. The purpose of this study was to determine the prevalence of anaemia, severity, and micronutrient deficiency status in the elderly hospitalized patients in Tanzania.</p><p><strong>Methods: </strong>A total of 156 hospitalized adults aged 60 years and above were enrolled in this study. A structured questionnaire was used to capture sociodemographic and clinical characteristics. Blood samples were collected, and a complete blood count, serum cobalamin, serum ferritin, and serum folate levels were measured to assess anaemia and micronutrient deficiency status in all participants who had anaemia.</p><p><strong>Results: </strong>The prevalence of anaemia was 79.5% (124/156) with severe anaemia in 33.9% (42/124) of participants, moderate anaemia in 42.7% (53/124) of participants, and 23.4% (29/124) of all participants had mild anaemia. Micronutrient deficiency was found in 14.5% (18/124) of all participants with anaemia. Combined deficiency (either iron and vitamin B12 deficiency or iron and folate deficiency) was the most common micronutrient deficiency anaemia with a frequency of 33.3% (6/18), followed by isolated iron and folate deficiencies at equal frequency of 27.8% (5/18) and vitamin B12 deficiency at 11.1% (2/18).</p><p><strong>Conclusion: </strong>The prevalence of anaemia in the hospitalized elderly population is high warranting public health attention and mostly present in moderate and severe forms. Micro-nutrient deficiency anaemia is common in this age group and is mostly due to combined micronutrient deficiency.</p>","PeriodicalId":46055,"journal":{"name":"Anemia","volume":"2021 ","pages":"9523836"},"PeriodicalIF":2.9,"publicationDate":"2021-02-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7935608/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25485500","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Establishment of Hematological Reference Values among Healthy Adults in Bamenda, North West Region of Cameroon. 喀麦隆西北部巴门达地区健康成人血液学参考值的建立
IF 2.9 Q3 HEMATOLOGY Pub Date : 2021-02-24 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6690926
Nfor Omarine Nlinwe, Yunika Larissa Kumenyuy, Che Precious Funwi

The use of the reference range of values of a laboratory test is highly significant in diagnostic accuracy. However, race and ethnic variations may affect the safe use of reference ranges from a different setting/population. Because the establishment of reference ranges for the Cameroonian population will possibly improve the quality of health care, this study was designed to establish hematological reference ranges among healthy adults in Bamenda, North West region of Cameroon. This was a cross-sectional study carried out within the period of five months from February 2020 to June 2020, at the Bamenda Regional Hospital. A total of 350 (139 females and 211 males) study participants who met the inclusion criteria were included in the study. The Urit 3300 autoanalyzer (Urit Medical Electronic (Group) Co., Ltd, Guilin, China) was used to analyze the hematological parameters. The general health questionnaire for donors, for verification of reference range study and laboratory tests, was used for data collection. Descriptive statistics were used to calculate reference ranges, means, and medians at 95% confidence intervals. Maximum and minimum reference ranges were computed at 97.5th and 2.5th percentiles. The nonparametric test (Mann-Whitney test) was used to determine the significance of the difference in hematological values between the male and female groups. Three (MID%, LYM#, and MID#) out of the 19 hematological parameters were verified, while sixteen (WBC, LYM%, GRAN%, GRAN#, RBC, HGB, HCT%, MCV, MCH, MCHC, RDW_CV, RDW_SD, PLT, MPV, PDW, and PCT%) were established. The currently used reference intervals do not represent the population of the North West region. Therefore, other regional hospitals in Cameroon should establish reference intervals applicable to their respective regions.

使用实验室测试值的参考范围对诊断准确性非常重要。然而,种族和民族差异可能会影响来自不同环境/人群的参考范围的安全使用。由于建立喀麦隆人口参考范围可能会提高卫生保健质量,本研究旨在建立喀麦隆西北部巴门达地区健康成年人的血液学参考范围。这是一项横断面研究,于2020年2月至2020年6月的五个月内在巴门达地区医院进行。共有350名(139名女性和211名男性)符合纳入标准的研究参与者被纳入研究。使用中国桂林优利特医疗电子(集团)有限公司的Urit 3300自动分析仪分析血液学参数。数据收集使用了捐助者一般健康调查表,以核实参考范围研究和实验室测试。描述性统计用于计算95%置信区间的参考范围、平均值和中位数。最大和最小参考范围分别在97.5和2.5个百分位计算。采用非参数检验(Mann-Whitney检验)确定男女两组血液学指标差异的显著性。对19项血液学参数中的3项(MID%、LYM#、MID#)进行了验证,同时建立了16项(WBC、LYM%、GRAN%、GRAN#、RBC、HGB、HCT%、MCV、MCH、MCHC、RDW_CV、RDW_SD、PLT、MPV、PDW、PCT%)。目前使用的参考区间不能代表西北地区的人口。因此,喀麦隆其他地区医院应建立适用于各自地区的参考区间。
{"title":"Establishment of Hematological Reference Values among Healthy Adults in Bamenda, North West Region of Cameroon.","authors":"Nfor Omarine Nlinwe,&nbsp;Yunika Larissa Kumenyuy,&nbsp;Che Precious Funwi","doi":"10.1155/2021/6690926","DOIUrl":"https://doi.org/10.1155/2021/6690926","url":null,"abstract":"<p><p>The use of the reference range of values of a laboratory test is highly significant in diagnostic accuracy. However, race and ethnic variations may affect the safe use of reference ranges from a different setting/population. Because the establishment of reference ranges for the Cameroonian population will possibly improve the quality of health care, this study was designed to establish hematological reference ranges among healthy adults in Bamenda, North West region of Cameroon. This was a cross-sectional study carried out within the period of five months from February 2020 to June 2020, at the Bamenda Regional Hospital. A total of 350 (139 females and 211 males) study participants who met the inclusion criteria were included in the study. The Urit 3300 autoanalyzer (Urit Medical Electronic (Group) Co., Ltd, Guilin, China) was used to analyze the hematological parameters. The general health questionnaire for donors, for verification of reference range study and laboratory tests, was used for data collection. Descriptive statistics were used to calculate reference ranges, means, and medians at 95% confidence intervals. Maximum and minimum reference ranges were computed at 97.5th and 2.5th percentiles. The nonparametric test (Mann-Whitney test) was used to determine the significance of the difference in hematological values between the male and female groups. Three (MID%, LYM#, and MID#) out of the 19 hematological parameters were verified, while sixteen (WBC, LYM%, GRAN%, GRAN#, RBC, HGB, HCT%, MCV, MCH, MCHC, RDW_CV, RDW_SD, PLT, MPV, PDW, and PCT%) were established. The currently used reference intervals do not represent the population of the North West region. Therefore, other regional hospitals in Cameroon should establish reference intervals applicable to their respective regions.</p>","PeriodicalId":46055,"journal":{"name":"Anemia","volume":"2021 ","pages":"6690926"},"PeriodicalIF":2.9,"publicationDate":"2021-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7932772/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25467088","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
Factors Associated with Anemia among Pregnant Women of Underprivileged Ethnic Groups Attending Antenatal Care at Provincial Level Hospital of Province 2, Nepal. 尼泊尔第二省省级医院接受产前护理的贫困民族孕妇贫血的相关因素
IF 2.9 Q3 HEMATOLOGY Pub Date : 2021-02-12 eCollection Date: 2021-01-01 DOI: 10.1155/2021/8847472
Umesh Kumar Yadav, Prabesh Ghimire, Archana Amatya, Ashish Lamichhane

Background: This study aims at determining the factors associated with anemia among pregnant women of underprivileged ethnic groups attending antenatal care at the provincial level hospital of Province 2.

Methods: A hospital-based cross-sectional study was carried out in Janakpur Provincial Hospital of Province 2, Southern Nepal. 287 pregnant women from underprivileged ethnic groups attending antenatal care were selected and interviewed. Face-to-face interviews using a structured questionnaire were undertaken. Anemia status was assessed based on hemoglobin levels determined at the hospital's laboratory. Bivariate and multiple logistic regression analyses were used to identify the factors associated with anemia. Analyses were performed using IBM SPSS version 23 software.

Results: The overall anemia prevalence in the study population was 66.9% (95% CI, 61.1-72.3). The women from most underprivileged ethnic groups (Terai Dalit, Terai Janajati, and Muslims) were twice more likely to be anemic than Madhesi women. Similarly, women having education lower than secondary level were about 3 times more likely to be anemic compared to those with secondary level or higher education. Women who had not completed four antenatal visits were twice more likely to be anemic than those completing all four visits. The odds of anemia were three times higher among pregnant women who had not taken deworming medication compared to their counterparts. Furthermore, women with inadequate dietary diversity were four times more likely to be anemic compared to women having adequate dietary diversity.

Conclusions: The prevalence of anemia is a severe public health problem among pregnant women of underprivileged ethnic groups in Province 2. Being Dalit, Janajati, and Muslim, having lower education, less frequent antenatal visits, not receiving deworming medication, and having inadequate dietary diversity are found to be the significant factors. The present study highlights the need of improving the frequency of antenatal visits and coverage of deworming program in ethnic populations. Furthermore, promoting a dietary diversity at the household level would help lower the prevalence of anemia. The study findings also imply that the nutrition interventions to control anemia must target and reach pregnant women from the most-marginalized ethnic groups and those with lower education.

背景:本研究旨在了解在第二省省级医院接受产前护理的贫困民族孕妇贫血的相关因素。方法:在尼泊尔南部第二省贾纳克布尔省立医院进行了一项以医院为基础的横断面研究,选取287名参加产前保健的贫困民族孕妇进行访谈。采用结构化问卷进行面对面访谈。根据医院实验室测定的血红蛋白水平评估贫血状况。使用双变量和多元逻辑回归分析来确定与贫血相关的因素。采用IBM SPSS version 23软件进行分析。结果:研究人群的总体贫血患病率为66.9% (95% CI, 61.1-72.3)。来自最贫困民族(特赖达利特、特赖贾纳贾提和穆斯林)的妇女患贫血的可能性是马德西人妇女的两倍。同样,受教育程度低于中等的妇女患贫血的可能性是受过中等或高等教育的妇女的3倍左右。未完成四次产前检查的妇女患贫血的可能性是完成四次产前检查的妇女的两倍。未服用驱虫药物的孕妇患贫血的几率是未服用驱虫药物的孕妇的三倍。此外,饮食多样性不足的妇女患贫血的可能性是饮食多样性充足的妇女的四倍。结论:二省贫困民族孕妇贫血的流行是一个严重的公共卫生问题。达利特、Janajati和穆斯林、受教育程度较低、产前检查频率较低、未接受驱虫药物治疗以及饮食多样性不足被认为是重要因素。本研究强调需要提高产前检查的频率和驱虫计划在少数民族人口的覆盖率。此外,在家庭层面促进饮食多样性将有助于降低贫血的患病率。研究结果还表明,控制贫血的营养干预措施必须针对和覆盖最边缘化的少数民族和受教育程度较低的孕妇。
{"title":"Factors Associated with Anemia among Pregnant Women of Underprivileged Ethnic Groups Attending Antenatal Care at Provincial Level Hospital of Province 2, Nepal.","authors":"Umesh Kumar Yadav,&nbsp;Prabesh Ghimire,&nbsp;Archana Amatya,&nbsp;Ashish Lamichhane","doi":"10.1155/2021/8847472","DOIUrl":"https://doi.org/10.1155/2021/8847472","url":null,"abstract":"<p><strong>Background: </strong>This study aims at determining the factors associated with anemia among pregnant women of underprivileged ethnic groups attending antenatal care at the provincial level hospital of Province 2.</p><p><strong>Methods: </strong>A hospital-based cross-sectional study was carried out in Janakpur Provincial Hospital of Province 2, Southern Nepal. 287 pregnant women from underprivileged ethnic groups attending antenatal care were selected and interviewed. Face-to-face interviews using a structured questionnaire were undertaken. Anemia status was assessed based on hemoglobin levels determined at the hospital's laboratory. Bivariate and multiple logistic regression analyses were used to identify the factors associated with anemia. Analyses were performed using IBM SPSS version 23 software.</p><p><strong>Results: </strong>The overall anemia prevalence in the study population was 66.9% (95% CI, 61.1-72.3). The women from most underprivileged ethnic groups (Terai Dalit, Terai Janajati, and Muslims) were twice more likely to be anemic than Madhesi women. Similarly, women having education lower than secondary level were about 3 times more likely to be anemic compared to those with secondary level or higher education. Women who had not completed four antenatal visits were twice more likely to be anemic than those completing all four visits. The odds of anemia were three times higher among pregnant women who had not taken deworming medication compared to their counterparts. Furthermore, women with inadequate dietary diversity were four times more likely to be anemic compared to women having adequate dietary diversity.</p><p><strong>Conclusions: </strong>The prevalence of anemia is a severe public health problem among pregnant women of underprivileged ethnic groups in Province 2. Being Dalit, Janajati, and Muslim, having lower education, less frequent antenatal visits, not receiving deworming medication, and having inadequate dietary diversity are found to be the significant factors. The present study highlights the need of improving the frequency of antenatal visits and coverage of deworming program in ethnic populations. Furthermore, promoting a dietary diversity at the household level would help lower the prevalence of anemia. The study findings also imply that the nutrition interventions to control anemia must target and reach pregnant women from the most-marginalized ethnic groups and those with lower education.</p>","PeriodicalId":46055,"journal":{"name":"Anemia","volume":"2021 ","pages":"8847472"},"PeriodicalIF":2.9,"publicationDate":"2021-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7896867/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25403309","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 15
Prevalence of Anaemia and Its Associated Factors among Type 2 Diabetes Mellitus Patients in University of Gondar Comprehensive Specialized Hospital. 贡达尔大学综合专科医院2型糖尿病患者贫血患病率及相关因素分析
IF 2.9 Q3 HEMATOLOGY Pub Date : 2021-02-10 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6627979
Sewnet Adem Kebede, Biruk Shalmeno Tusa, Adisu Birhanu Weldesenbet

Background: Anaemia is one of the commonest blood disorders seen in patients with diabetes. In Ethiopia, chronic illnesses are tremendously raising with their complications. But very little research has been conducted, particularly on anaemia among diabetes mellitus (DM) patients. Therefore, this study aimed at assessing the prevalence of anaemia and associated factors among type 2 diabetes mellitus patients in Northwest Ethiopia.

Methods: A cross-sectional study design was employed at University of Gondar Comprehensive Specialized Hospital from March 1 to April 15, 2019, among 372 type 2 diabetes mellitus patients (T2DM). Multivariable logistic regression analysis was fitted, and the corresponding adjusted odds ratio (AOR) and 95% CI were used to identify factors associated with anaemia. Level of significance was declared at the p value less than 0.05.

Results: The study revealed 8.06% (95% CI: 5.68-11.31%) of the participants were anaemic. Being male (AOR = 2.74, CI: 1.02, 7.38), combined type of treatment (AOR = 8.38, CI: 1.66, 42.25), having diabetes-related microvascular complications (AOR = 3.24, CI: 1.14, 9.26), and hypertension (AOR = 0.01, CI: 0.002, 0.06) were the significant factors associated with anaemia.

Conclusions: The finding of the current study revealed low prevalence of anaemia among T2DM patients. Sex, type of treatment, diabetes-related microvascular complications, and hypertension were factors associated with anaemia. Assessment of haemoglobin levels among T2DM patients may help to prevent ensuing microvascular complications. Incorporate anaemia screening into the routine assessment of diabetic complication particularly for those who are hypertensive and took combined treatment to allow early appreciation and treatment of anaemia and later improve the overall care of patients with diabetes.

背景:贫血是糖尿病患者最常见的血液疾病之一。在埃塞俄比亚,慢性病及其并发症正在急剧增加。但是很少有研究进行,特别是对糖尿病(DM)患者的贫血。因此,本研究旨在评估埃塞俄比亚西北部2型糖尿病患者的贫血患病率及其相关因素。方法:采用横断面研究设计,于2019年3月1日至4月15日在贡达尔大学综合专科医院对372例2型糖尿病(T2DM)患者进行研究。拟合多变量logistic回归分析,采用相应的调整优势比(AOR)和95% CI确定与贫血相关的因素。p值小于0.05为显著性水平。结果:研究显示8.06% (95% CI: 5.68-11.31%)的参与者贫血。男性(AOR = 2.74, CI: 1.02, 7.38)、联合治疗(AOR = 8.38, CI: 1.66, 42.25)、糖尿病相关微血管并发症(AOR = 3.24, CI: 1.14, 9.26)和高血压(AOR = 0.01, CI: 0.002, 0.06)是与贫血相关的显著因素。结论:目前的研究结果显示,2型糖尿病患者中贫血的患病率较低。性别、治疗方式、糖尿病相关微血管并发症和高血压是与贫血相关的因素。评估2型糖尿病患者的血红蛋白水平可能有助于预防随后的微血管并发症。将贫血筛查纳入糖尿病并发症的常规评估,特别是对高血压患者和接受联合治疗的患者,以便早期发现和治疗贫血,并在以后改善糖尿病患者的整体护理。
{"title":"Prevalence of Anaemia and Its Associated Factors among Type 2 Diabetes Mellitus Patients in University of Gondar Comprehensive Specialized Hospital.","authors":"Sewnet Adem Kebede,&nbsp;Biruk Shalmeno Tusa,&nbsp;Adisu Birhanu Weldesenbet","doi":"10.1155/2021/6627979","DOIUrl":"https://doi.org/10.1155/2021/6627979","url":null,"abstract":"<p><strong>Background: </strong>Anaemia is one of the commonest blood disorders seen in patients with diabetes. In Ethiopia, chronic illnesses are tremendously raising with their complications. But very little research has been conducted, particularly on anaemia among diabetes mellitus (DM) patients. Therefore, this study aimed at assessing the prevalence of anaemia and associated factors among type 2 diabetes mellitus patients in Northwest Ethiopia.</p><p><strong>Methods: </strong>A cross-sectional study design was employed at University of Gondar Comprehensive Specialized Hospital from March 1 to April 15, 2019, among 372 type 2 diabetes mellitus patients (T2DM). Multivariable logistic regression analysis was fitted, and the corresponding adjusted odds ratio (AOR) and 95% CI were used to identify factors associated with anaemia. Level of significance was declared at the <i>p</i> value less than 0.05.</p><p><strong>Results: </strong>The study revealed 8.06% (95% CI: 5.68-11.31%) of the participants were anaemic. Being male (AOR = 2.74, CI: 1.02, 7.38), combined type of treatment (AOR = 8.38, CI: 1.66, 42.25), having diabetes-related microvascular complications (AOR = 3.24, CI: 1.14, 9.26), and hypertension (AOR = 0.01, CI: 0.002, 0.06) were the significant factors associated with anaemia.</p><p><strong>Conclusions: </strong>The finding of the current study revealed low prevalence of anaemia among T2DM patients. Sex, type of treatment, diabetes-related microvascular complications, and hypertension were factors associated with anaemia. Assessment of haemoglobin levels among T2DM patients may help to prevent ensuing microvascular complications. Incorporate anaemia screening into the routine assessment of diabetic complication particularly for those who are hypertensive and took combined treatment to allow early appreciation and treatment of anaemia and later improve the overall care of patients with diabetes.</p>","PeriodicalId":46055,"journal":{"name":"Anemia","volume":"2021 ","pages":"6627979"},"PeriodicalIF":2.9,"publicationDate":"2021-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7889375/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25402853","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
Genotype-Phenotype Correlation of G6PD Mutations among Central Thai Children with G6PD Deficiency. 泰国中部G6PD缺乏症儿童G6PD突变的基因型-表型相关性
IF 2.9 Q3 HEMATOLOGY Pub Date : 2021-02-09 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6680925
Boonchai Boonyawat, Tim Phetthong, Nithipun Suksumek, Chanchai Traivaree
Background Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common X-linked inherited erythroenzymopathy in Thailand. The clinical and hematological manifestations of G6PD deficiency are variable. Objective This study aimed to characterize the genotype-phenotype correlation of G6PD mutations in Thai pediatric patients who were followed-up in Phramongkutklao Hospital, a tertiary center in central Thailand. Material and Method. A total of 102 children including 73 males (71.6%) and 29 females (28.4%) were included in our study. Mutation analysis was performed by direct DNA sequencing of all coding exons of the G6PD gene. Ninety-one patients (89.2%) were presented with neonatal hyperbilirubinemia and 11 patients (10.8%) were presented with acute hemolytic anemia beyond the neonatal period. Results Molecular analysis of the G6PD gene in 102 G6PD-deficient Thai children identified 12 different mutations. G6PD Viangchan (871G > A) and G6PD Canton (1376G > T) were the first (46.2%) and the second (15.4%) most common identified mutations among both male and female G6PD-deficient individuals, respectively. All affected males were hemizygous for G6PD mutations and had an average G6PD level of 16.7 ± 11.5 (3–76) IU/ml.RBC. Majority of female patients (27 in 29, 93.1%) were heterozygous for G6PD mutations and had an average G6PD level of 133.6 ± 43.4 (9–195) IU/ml.RBC. Two female patients (6.9%) were either homozygous or compound heterozygous for the mutations and had G6PD level in the affected male range (35 and 10 IU/ml.RBC). Only 1 in 27 heterozygous females (3.7%) had G6PD level in the affected male range (9 IU/ml.RBC) which is possibly explained by nonrandom X-chromosome inactivation. The correlation of genotypes, G6PD levels, and clinical phenotypes was not demonstrated in our study in which all of the included G6PD-deficient patients were presented with neonatal hyperbilirubinemia and acute hemolytic anemia, since the genotype-phenotype correlation is normally demonstrated in chronic nonspherocytic hemolytic anemia (CNSHA) G6PD-deficient individuals. Conclusion This study characterizes the molecular heterogeneity of G6PD variants causing G6PD deficiency in Thai children. Our study demonstrated the efficiency of direct DNA sequencing which can identify 12 missense mutations in Thai children.
背景:葡萄糖-6-磷酸脱氢酶(G6PD)缺乏症是泰国最常见的x连锁遗传性红酶病。G6PD缺乏症的临床和血液学表现多种多样。目的:本研究旨在描述泰国中部三级医院Phramongkutklao医院随访的泰国儿科患者G6PD突变的基因型-表型相关性。材料和方法。本研究共纳入102例儿童,其中男性73例(71.6%),女性29例(28.4%)。突变分析通过G6PD基因所有编码外显子的直接DNA测序进行。91例(89.2%)出现新生儿高胆红素血症,11例(10.8%)出现新生儿期后急性溶血性贫血。结果:对102名G6PD缺陷泰国儿童的G6PD基因进行分子分析,鉴定出12种不同的突变。G6PD Viangchan (871G > A)和G6PD Canton (1376G > T)分别是男性和女性G6PD缺陷个体中最常见的突变(46.2%)和第二常见突变(15.4%)。所有受影响的男性G6PD突变为半合子,平均G6PD水平为16.7±11.5 (3-76)IU/ml。大多数女性患者(29例中27例,93.1%)G6PD突变为杂合子,平均G6PD水平为133.6±43.4 (9-195)IU/ml。2名女性患者(6.9%)突变为纯合子或复合杂合子,G6PD水平在男性范围内(35和10 IU/ml.RBC)。27例杂合子女性中仅有1例(3.7%)G6PD水平在男性(9 IU/ml.RBC)范围内,这可能与非随机x染色体失活有关。基因型、G6PD水平和临床表型之间的相关性在我们的研究中没有得到证实。在我们的研究中,所有纳入的G6PD缺陷患者都出现了新生儿高胆红素血症和急性溶血性贫血,因为基因型-表型相关性通常在慢性非球型溶血性贫血(CNSHA) G6PD缺陷个体中得到证实。结论:本研究揭示了导致泰国儿童G6PD缺乏症的G6PD变异的分子异质性。我们的研究证明了直接DNA测序的效率,可以在泰国儿童中识别出12种错义突变。
{"title":"Genotype-Phenotype Correlation of G6PD Mutations among Central Thai Children with G6PD Deficiency.","authors":"Boonchai Boonyawat,&nbsp;Tim Phetthong,&nbsp;Nithipun Suksumek,&nbsp;Chanchai Traivaree","doi":"10.1155/2021/6680925","DOIUrl":"https://doi.org/10.1155/2021/6680925","url":null,"abstract":"Background Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common X-linked inherited erythroenzymopathy in Thailand. The clinical and hematological manifestations of G6PD deficiency are variable. Objective This study aimed to characterize the genotype-phenotype correlation of G6PD mutations in Thai pediatric patients who were followed-up in Phramongkutklao Hospital, a tertiary center in central Thailand. Material and Method. A total of 102 children including 73 males (71.6%) and 29 females (28.4%) were included in our study. Mutation analysis was performed by direct DNA sequencing of all coding exons of the G6PD gene. Ninety-one patients (89.2%) were presented with neonatal hyperbilirubinemia and 11 patients (10.8%) were presented with acute hemolytic anemia beyond the neonatal period. Results Molecular analysis of the G6PD gene in 102 G6PD-deficient Thai children identified 12 different mutations. G6PD Viangchan (871G > A) and G6PD Canton (1376G > T) were the first (46.2%) and the second (15.4%) most common identified mutations among both male and female G6PD-deficient individuals, respectively. All affected males were hemizygous for G6PD mutations and had an average G6PD level of 16.7 ± 11.5 (3–76) IU/ml.RBC. Majority of female patients (27 in 29, 93.1%) were heterozygous for G6PD mutations and had an average G6PD level of 133.6 ± 43.4 (9–195) IU/ml.RBC. Two female patients (6.9%) were either homozygous or compound heterozygous for the mutations and had G6PD level in the affected male range (35 and 10 IU/ml.RBC). Only 1 in 27 heterozygous females (3.7%) had G6PD level in the affected male range (9 IU/ml.RBC) which is possibly explained by nonrandom X-chromosome inactivation. The correlation of genotypes, G6PD levels, and clinical phenotypes was not demonstrated in our study in which all of the included G6PD-deficient patients were presented with neonatal hyperbilirubinemia and acute hemolytic anemia, since the genotype-phenotype correlation is normally demonstrated in chronic nonspherocytic hemolytic anemia (CNSHA) G6PD-deficient individuals. Conclusion This study characterizes the molecular heterogeneity of G6PD variants causing G6PD deficiency in Thai children. Our study demonstrated the efficiency of direct DNA sequencing which can identify 12 missense mutations in Thai children.","PeriodicalId":46055,"journal":{"name":"Anemia","volume":"2021 ","pages":"6680925"},"PeriodicalIF":2.9,"publicationDate":"2021-02-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7886513/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25403308","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
期刊
Anemia
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1