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Factors Associated with Growth Retardation in Children Suffering from Sickle Cell Anemia: First Report from Central Africa. 镰状细胞性贫血儿童生长迟缓的相关因素:来自中非的第一份报告。
IF 2.9 Q3 HEMATOLOGY Pub Date : 2017-01-01 Epub Date: 2017-01-30 DOI: 10.1155/2017/7916348
Aimé Lukusa Kazadi, René Makuala Ngiyulu, Jean Lambert Gini-Ehungu, Jean Marie Mbuyi-Muamba, Michel Ntetani Aloni

Background. The aim of this study was to investigate and determine the risk factors associated with poor growth among SCA children. Methods. A cross-sectional study was conducted in Kinshasa, the capital's country. The nutritional status was assessed using the Z scores of the anthropometric indices. Results. We gathered data on the 256 patients, 138 females (53.9%), who entered the study. The mean age at presentation was 8.4 ± 4.9 years of age. Underweight, stunting, and wasting were found, respectively, in 47.7%, 10.5%, and 50.3% of SCA children. A history of hand-foot syndrome, more than 3 blood transfusions, being less than 12 months of age when receiving the first transfusion, more than two severe sickle crises per year, a medical history of severe infections, and the presence of hepatomegaly were associated with poor growth. When comparing sickle cell patients under 12 years of age (n = 159) to a group of 296 age-matched children with normal Hb-AA, a significantly higher proportion of subjects with stunting and underweight were found among SCA. Conclusion. Nutritional status encountered in Congolese sickle cell children has been described for the first time in this study. A high prevalence of poor growth in SCA children was found in our study.

背景。本研究的目的是调查和确定与SCA儿童生长不良相关的危险因素。方法。在首都金沙萨进行了一项横断面研究。采用人体测量指数Z值评价营养状况。结果。我们收集了256例患者的数据,其中138例为女性(53.9%)。平均发病年龄8.4±4.9岁。体重不足、发育迟缓和消瘦分别在47.7%、10.5%和50.3%的SCA儿童中被发现。手足综合征病史、3次以上输血、第一次输血时小于12个月、每年2次以上严重镰状危重症、严重感染病史和肝肿大的存在与生长不良相关。当将12岁以下的镰状细胞患者(n = 159)与296名Hb-AA正常的年龄匹配儿童进行比较时,SCA中发育迟缓和体重不足的比例明显更高。结论。本研究首次描述了刚果镰状细胞儿童的营养状况。在我们的研究中发现,SCA儿童生长不良的患病率很高。
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引用次数: 25
Prevalence, Severity, and Determinant Factors of Anemia among Pregnant Women in South Sudanese Refugees, Pugnido, Western Ethiopia 埃塞俄比亚西部普格尼多南苏丹难民孕妇贫血的患病率、严重程度和决定因素
IF 2.9 Q3 HEMATOLOGY Pub Date : 2016-12-12 DOI: 10.1155/2016/9817358
Aklilu Alemayehu, Lealem Gedefaw, T. Yemane, Yaregal Asres
Background. Anemia is one of the major health problems among refugee pregnant women in the world. Anemia among pregnant women is multifactorial and results in detrimental consequences on the mothers and infants. The aim of this study was to determine the prevalence, severity, and determinants of anemia among pregnant women in South Sudanese refugees, Pugnido western, Ethiopia. Methods. A facility-based cross-sectional study was conducted in Pugnido Administration Refugee and Returnee Affairs Health Center from April 15 to June 30, 2015. Demographic and related data were collected using questionnaire based interview. Complete blood count was done using CELL-DYN 1800 (Abbott USA). Blood smear and fecal specimen were examined for hemoparasite and intestinal parasite, respectively. Bivariate and multivariate logistic regression analyses were done using SPSS-Version 20.0. Results. The overall prevalence of anemia was 36.1%, from whom 2.3% had severe anemia. Being in third trimester, eating meat at most once a week, drinking tea immediately after meal at least once a day, having mid-upper arm circumference below 21 centimeters, and intestinal parasitic infection were identified as independent factors of anemia. Conclusion. More than one-third of pregnant women had anemia in this study. Intervention based strategies on identified determinant factors will be very important to combat anemia among the group.
背景。贫血是世界上难民孕妇的主要健康问题之一。孕妇贫血是多因素的,对母亲和婴儿造成有害后果。本研究的目的是确定埃塞俄比亚普格尼多西部南苏丹难民孕妇贫血的患病率、严重程度和决定因素。方法。本研究于2015年4月15日至6月30日在普格尼多行政难民和返回者事务卫生中心进行了一项基于设施的横断面研究。采用问卷调查法收集人口学及相关数据。全血细胞计数使用CELL-DYN 1800 (Abbott USA)。血液涂片和粪便标本分别检测血液寄生虫和肠道寄生虫。采用SPSS-Version 20.0进行双变量和多变量logistic回归分析。结果。总体贫血患病率为36.1%,其中2.3%为重度贫血。妊娠晚期、每周最多吃一次肉、每天至少一次饭后立即喝茶、上臂中围小于21厘米、肠道寄生虫感染是贫血的独立因素。结论。在这项研究中,超过三分之一的孕妇患有贫血。基于确定的决定因素的干预策略对于在群体中对抗贫血非常重要。
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引用次数: 33
Malaria, Moderate to Severe Anaemia, and Malarial Anaemia in Children at Presentation to Hospital in the Mount Cameroon Area: A Cross-Sectional Study 喀麦隆山地区送医儿童的疟疾、中度至重度贫血和疟疾贫血:一项横断面研究
IF 2.9 Q3 HEMATOLOGY Pub Date : 2016-11-08 DOI: 10.1155/2016/5725634
I. Sumbele, Sharon Odmia Sama, H. Kimbi, G. S. Taiwé
Background. Malaria remains a major killer of children in Sub-Saharan Africa, while anaemia is a public health problem with significant morbidity and mortality. Examining the factors associated with moderate to severe anaemia (MdSA) and malarial anaemia as well as the haematological characteristics is essential. Methodology. Children (1–14 years) at presentation at the Regional Hospital Annex-Buea were examined clinically and blood samples were collected for malaria parasite detection and full blood count evaluation. Results. Plasmodium falciparum, anaemia, and malarial anaemia occurred in 33.8%, 62.0%, and 23.6% of the 216 children, respectively. Anaemia prevalence was significantly higher in malaria parasite positive children and those with fever than their respective counterparts. MdSA and moderate to severe malarial anaemia (MdSMA) were detected in 38.0% and 15.3% of the participants, respectively. The prevalence of MdSA was significantly higher in children whose household head had no formal education, resided in the lowland, or was febrile, while MdSMA was significantly higher in febrile children only. Children with MdSMA had significantly lower mean white blood cell, lymphocyte, and platelet counts while the mean granulocyte count was significantly higher. Conclusion. Being febrile was the only predictor of both MdSA and MdSMA. More haematological insult occurred in children with MdSMA compared to MdSA.
背景。疟疾仍然是撒哈拉以南非洲儿童的主要杀手,而贫血是一个发病率和死亡率很高的公共卫生问题。检查与中度至重度贫血(MdSA)和疟疾贫血相关的因素以及血液学特征是必不可少的。方法。在附件布埃亚地区医院就诊的儿童(1-14岁)接受了临床检查,并收集了血液样本,用于疟疾寄生虫检测和全血细胞计数评估。结果。恶性疟原虫、贫血和疟疾的发生率分别为33.8%、62.0%和23.6%。疟疾寄生虫阳性儿童和发烧儿童的贫血患病率明显高于相应的儿童。MdSA和中度至重度疟疾贫血(MdSMA)分别在38.0%和15.3%的参与者中检测到。家庭户主未受过正规教育、居住在低地或有发热症状的儿童MdSA患病率显著高于家庭户主,而只有发热儿童MdSMA患病率显著高于家庭户主。MdSMA患儿的平均白细胞、淋巴细胞和血小板计数显著降低,而平均粒细胞计数显著升高。结论。发热是MdSA和MdSMA的唯一预测因子。与MdSA相比,MdSMA儿童的血液学损伤发生率更高。
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引用次数: 49
Erythropoiesis in Malaria Infections and Factors Modifying the Erythropoietic Response 疟疾感染中的红细胞生成和改变红细胞生成反应的因素
IF 2.9 Q3 HEMATOLOGY Pub Date : 2016-02-29 DOI: 10.1155/2016/9310905
V. Pathak, K. Ghosh
Anemia is the primary clinical manifestation of malarial infections and is responsible for the substantial rate of morbidity. The pathophysiology discussed till now catalogued several causes for malarial anemia among which ineffective erythropoiesis being remarkable one occurs silently in the bone marrow. A systematic literature search was performed and summarized information on erythropoietic response upon malaria infection and the factors responsible for the same. This review summarizes the clinical and experimental studies on patients, mouse models, and in vitro cell cultures reporting erythropoietic changes upon malaria infection as well as factors accountable for the same. Inadequate erythropoietic response during malaria infection may be the collective effect of various mediators generated by host immune response as well as parasite metabolites. The interplay between various modulators causing the pathophysiology needs to be explored further. Globin gene expression profiling upon malaria infection should also be looked into as abnormal production of globin chains could be a possible contributor to ineffective erythropoiesis.
贫血是疟疾感染的主要临床表现,也是疟疾发病率居高不下的原因。迄今为止讨论的病理生理学列出了疟疾性贫血的几种原因,其中红细胞生成无效是显著的,骨髓中静默发生。我们进行了系统的文献检索,总结了疟疾感染后红细胞生成反应及其相关因素的信息。本文综述了疟疾感染后红细胞生成变化的临床和实验研究、小鼠模型和体外细胞培养及其相关因素。疟疾感染期间红细胞生成反应不足可能是宿主免疫反应和寄生虫代谢物产生的各种介质的共同作用。引起病理生理的各种调节因子之间的相互作用有待进一步探讨。疟疾感染时的珠蛋白基因表达谱也应加以研究,因为珠蛋白链的异常产生可能是导致红细胞生成无效的一个可能因素。
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引用次数: 37
Prevalence of Anemia and Its Associated Factors among Pregnant Women Attending Antenatal Care in Health Institutions of Arba Minch Town, Gamo Gofa Zone, Ethiopia: A Cross-Sectional Study 埃塞俄比亚Gamo Gofa区Arba Minch镇卫生机构产前保健孕妇贫血患病率及其相关因素:一项横断面研究
IF 2.9 Q3 HEMATOLOGY Pub Date : 2016-02-22 DOI: 10.1155/2016/1073192
A. Bekele, M. Tilahun, Aleme Mekuria
Background. Anemia during pregnancy is a major cause of morbidity and mortality of pregnant women in developing countries and has both maternal and fetal consequences. Despite its known serious effect on health, there is very little research based evidence on this vital public health problem in Gamo Gofa zone in general and in Arba Minch town of Southern Ethiopia in particular. Therefore, this study aims to assess the prevalence and factors associated with anemia among pregnant women attending antenatal care in health institutions of Arba Minch town, Gamo Gofa zone, Southern Ethiopia. Method. Institution-based, cross-sectional study was conducted from February 16 to April 8, 2015, among 332 pregnant women who attended antenatal care at government health institutions of Arba Minch town. Interviewer-administered questionnaire supplemented by laboratory tests was used to obtain the data. Bivariate and multivariate logistic regressions were used to identify predictors of anemia. Result. The prevalence of anemia among antenatal care attendant pregnant women of Arba Minch town was 32.8%. Low average monthly income of the family (AOR = 4.0; 95% CI: 5.62–11.01), having birth interval less than two years (AOR = 3.1; 95% CI: 6.01, 10.23), iron supplementation (AOR = 2.31; 95% CI: 7.21, 9.31), and family size >2 (AOR = 2.8; 95% CI: 1.17, 6.81) were found to be independent predictors of anemia in pregnancy. Conclusion. Anemia is found to be a moderate public health problem in the study area. Low average monthly income, birth interval less than two years, iron supplementation, and large family size were found to be risk factors for anemia in pregnancy. Awareness creation towards birth spacing, nutritional counselling on consumption of iron-rich foods, and iron supplementation are recommended to prevent anemia among pregnant women with special emphasis on those having low income and large family size.
背景。妊娠期贫血是发展中国家孕妇发病和死亡的一个主要原因,对孕产妇和胎儿都有影响。尽管已知其对健康的严重影响,但在整个加莫戈法区,特别是在埃塞俄比亚南部的阿尔巴明奇镇,关于这一重大公共卫生问题的研究证据很少。因此,本研究旨在评估在埃塞俄比亚南部加莫戈法区阿尔巴明奇镇卫生机构接受产前保健的孕妇中贫血的患病率及其相关因素。方法。本研究于2015年2月16日至4月8日对在Arba Minch镇政府卫生机构接受产前保健的332名孕妇进行了基于机构的横断面研究。采用访谈者管理的问卷,辅以实验室测试来获取数据。使用双变量和多变量logistic回归来确定贫血的预测因子。结果。Arba Minch镇产前护理孕妇贫血患病率为32.8%。家庭平均月收入低(AOR = 4.0);95% CI: 5.62-11.01),生育间隔小于2年(AOR = 3.1;95% CI: 6.01, 10.23),补铁(AOR = 2.31;95% CI: 7.21, 9.31)和家庭规模(AOR = 2.8;95% CI: 1.17, 6.81)是妊娠期贫血的独立预测因子。结论。在研究地区,贫血被认为是一个中度的公共卫生问题。平均月收入低、生育间隔少于两年、补铁和家庭人口多是妊娠期贫血的危险因素。建议提高对生育间隔的认识,就食用富含铁的食物提供营养咨询,并补充铁,以预防孕妇贫血,特别强调低收入和大家庭的孕妇。
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引用次数: 94
Antianemic Treatment of Cancer Patients in German Routine Practice: Data from a Prospective Cohort Study—The Tumor Anemia Registry 德国常规实践中癌症患者的抗贫血治疗:来自肿瘤贫血登记的前瞻性队列研究的数据
IF 2.9 Q3 HEMATOLOGY Pub Date : 2016-02-04 DOI: 10.1155/2016/8057650
T. Steinmetz, J. Schröder, M. Plath, H. Link, M. Vogt, M. Frank, N. Marschner
The aim of this prospective cohort study was to assess current antianemic treatment of cancer patients in German routine practice, including diagnostics, treatments, and quality of life (QoL). 88 study sites recruited 1018 patients at the start of antianemic treatment with hemoglobin (Hb) levels <11 g/dL (females) or <12 g/dL (males). Patients were followed up for 12 weeks. 63% of the patients had inoperable solid tumors, 22% operable solid tumors, and 15% hematological malignancies. Over 85% received chemotherapy. Median age was 67 years; 48% were male. Red blood cell transfusions (RBCTx) were given to 59% of all patients and to 55% of the patients with Hb ≥8 g/dL on day 1 of the observation period (day 1 treatment). Erythropoiesis-stimulating agents (ESAs) were the second most frequently applied day 1 treatment (20%), followed by intravenous (IV) iron (15%) and ESA + IV iron (6%). Only about a third of patients were tested for blood serum iron parameters at the start of treatment. Overall, more than half of the patients had long-term responses to antianemic therapy. Our data suggest that in routine practice diagnostics for treatable causes of anemia are underused. A high proportion of cancer patients receive RBCTx. It should be discussed whether thorough diagnostics and earlier intervention could decrease the need for RBCTx. This trial is registered with NCT01795690.
这项前瞻性队列研究的目的是评估目前德国常规实践中癌症患者的抗贫血治疗,包括诊断、治疗和生活质量(QoL)。88个研究地点招募了1018名抗贫血治疗开始时血红蛋白(Hb)水平<11 g/dL(女性)或<12 g/dL(男性)的患者。随访12周。不可手术的实体瘤占63%,可手术的实体瘤占22%,血液系统恶性肿瘤占15%。超过85%的患者接受了化疗。中位年龄67岁;48%是男性。在观察期第1天(治疗第1天),59%的患者和55%的Hb≥8 g/dL的患者接受红细胞输注(RBCTx)。促红细胞生成剂(ESA)是第1天最常用的治疗方法(20%),其次是静脉(IV)铁(15%)和ESA + IV铁(6%)。只有大约三分之一的患者在治疗开始时进行了血清铁参数检测。总的来说,超过一半的患者对抗贫血治疗有长期反应。我们的数据表明,在常规实践中,对可治疗的贫血病因的诊断未得到充分利用。接受RBCTx治疗的癌症患者比例很高。应该讨论彻底诊断和早期干预是否可以减少RBCTx的需求。本试验注册号为NCT01795690。
{"title":"Antianemic Treatment of Cancer Patients in German Routine Practice: Data from a Prospective Cohort Study—The Tumor Anemia Registry","authors":"T. Steinmetz, J. Schröder, M. Plath, H. Link, M. Vogt, M. Frank, N. Marschner","doi":"10.1155/2016/8057650","DOIUrl":"https://doi.org/10.1155/2016/8057650","url":null,"abstract":"The aim of this prospective cohort study was to assess current antianemic treatment of cancer patients in German routine practice, including diagnostics, treatments, and quality of life (QoL). 88 study sites recruited 1018 patients at the start of antianemic treatment with hemoglobin (Hb) levels <11 g/dL (females) or <12 g/dL (males). Patients were followed up for 12 weeks. 63% of the patients had inoperable solid tumors, 22% operable solid tumors, and 15% hematological malignancies. Over 85% received chemotherapy. Median age was 67 years; 48% were male. Red blood cell transfusions (RBCTx) were given to 59% of all patients and to 55% of the patients with Hb ≥8 g/dL on day 1 of the observation period (day 1 treatment). Erythropoiesis-stimulating agents (ESAs) were the second most frequently applied day 1 treatment (20%), followed by intravenous (IV) iron (15%) and ESA + IV iron (6%). Only about a third of patients were tested for blood serum iron parameters at the start of treatment. Overall, more than half of the patients had long-term responses to antianemic therapy. Our data suggest that in routine practice diagnostics for treatable causes of anemia are underused. A high proportion of cancer patients receive RBCTx. It should be discussed whether thorough diagnostics and earlier intervention could decrease the need for RBCTx. This trial is registered with NCT01795690.","PeriodicalId":46055,"journal":{"name":"Anemia","volume":"2016 1","pages":""},"PeriodicalIF":2.9,"publicationDate":"2016-02-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2016/8057650","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"64547205","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 8
Sickle-Cell Disease Healthcare Cost in Africa: Experience of the Congo 非洲镰状细胞病的医疗费用:刚果的经验
IF 2.9 Q3 HEMATOLOGY Pub Date : 2016-02-02 DOI: 10.1155/2016/2046535
L. Ngolet, M. Moyen Engoba, I. Kocko, A. Elira Dokékias, J. Mombouli, G. Moyen
Background. Lack of medical coverage in Africa leads to inappropriate care that has an impact on the mortality rate. In this study, we aimed to evaluate the cost of severe acute sickle-cell related complications in Brazzaville. Methods. A retrospective study was conducted in 2014 in the Paediatric Intensive Care Unit. It concerned 94 homozygote sickle-cell children that developed severe acute sickle-cell disease related complications (average age 69 months). For each patient, we calculated the cost of care complication. Results. The household income was estimated as low (
背景。非洲缺乏医疗覆盖,导致护理不当,对死亡率产生影响。在这项研究中,我们旨在评估布拉柴维尔严重急性镰状细胞相关并发症的成本。方法。2014年在儿科重症监护室进行了一项回顾性研究。它涉及94名发生严重急性镰状细胞病相关并发症的纯合子镰状细胞儿童(平均年龄69个月)。对于每位患者,我们计算了护理并发症的成本。结果。27.7%的家庭收入估计较低(< 9万里亚尔/< 158.40美元)。镰状细胞相关急性并发症的住院总中位费用为65,460澳币/ 115.21美元。费用随严重急性并发症的发生因素而波动(p = 0.041)。细菌感染引起的并发症较高(从66,765 XAF / 117.50美元到135,271.50 XAF / 238.07美元),与疟疾相关的并发症较低(从28,305/49.82 XAF到64,891.63 XAF / 114.21美元)。死亡率为17%,与病例管理费用相关(p = 0.006)。结论。在刚果,儿童镰状细胞病严重急性并发症的病例管理费用很高。
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引用次数: 14
Magnitude of Anemia and Hematological Predictors among Children under 12 Years in Odisha, India. 印度奥迪沙 12 岁以下儿童贫血症的严重程度和血液学预测因素。
IF 2.9 Q3 HEMATOLOGY Pub Date : 2016-01-01 Epub Date: 2016-04-04 DOI: 10.1155/2016/1729147
Shuchismita Behera, Gandham Bulliyya

Background. Anemia is a wide spread public health problem in India which affects children. The present study evaluates the prevalence of anemia and status of various hematological parameters among children of Khurda district, Odisha. Method. A total of 313 children aged 0-12 years were enrolled for the study which included preschool (0-5 years) and school aged (6-12 years) groups. Hematological indicators were measured by standard procedures, which include red blood cell (RBC) indicators, white blood cell (WBC) indicators, and plasma ferritin. Results. Mean hemoglobin (Hb) of the study population was 10.43 ± 3.33 g/dL and prevalence of anemia was 62%. In this population, boys had a lower mean Hb value than that of the girls. All grades of anemia were higher among school age children than preschool children. Mean plasma ferritin was found to be higher in school age boys than their counterpart girls. The mean level of WBC count was found to be higher among preschool age boys than among the school age boys (p = 0.025). Conclusion. The prevalence of anemia was higher with concomitant acute infection among study population, which is a matter of concern. Since the hematological parameters are interrelated with each other as well as with the age and gender, relevant intervention strategy and constant monitoring are needed while providing public health nutrition programs to eradicate anemia.

背景。贫血是印度广泛存在的公共卫生问题,对儿童的影响很大。本研究评估了奥迪沙邦库尔达地区儿童的贫血患病率和各种血液学参数的状况。研究方法研究共招募了 313 名 0-12 岁的儿童,包括学龄前(0-5 岁)和学龄期(6-12 岁)儿童。采用标准程序测量血液指标,包括红细胞(RBC)指标、白细胞(WBC)指标和血浆铁蛋白。结果显示研究人群的平均血红蛋白(Hb)为 10.43 ± 3.33 g/dL,贫血发生率为 62%。男孩的平均血红蛋白值低于女孩。学龄儿童的各等级贫血率均高于学龄前儿童。学龄男孩的平均血浆铁蛋白高于女孩。学龄前男孩的白细胞计数平均水平高于学龄前男孩(p = 0.025)。结论在研究人群中,伴随急性感染的贫血发生率较高,这是一个值得关注的问题。由于血液学参数与年龄和性别相互关联,因此在提供公共卫生营养计划以消除贫血的同时,还需要相关的干预策略和持续监测。
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引用次数: 0
Absolute Reticulocyte Count and Reticulocyte Hemoglobin Content as Predictors of Early Response to Exclusive Oral Iron in Children with Iron Deficiency Anemia. 绝对网织红细胞计数和网织红细胞血红蛋白含量作为缺铁性贫血儿童口服铁治疗早期反应的预测指标。
IF 2.9 Q3 HEMATOLOGY Pub Date : 2016-01-01 Epub Date: 2016-03-22 DOI: 10.1155/2016/7345835
Emilia Parodi, Maria Teresa Giraudo, Fulvio Ricceri, Maria Luigia Aurucci, Raffaela Mazzone, Ugo Ramenghi
We report data regarding kinetic of response to oral iron in 34 iron deficiency anemia children. Twenty-four/34 patients (70.5%) reached reference value of hemoglobin (Hb) concentration for age and sex at day + 30 from the beginning of treatment (complete early responders (CERs)), and 4/34 (12%) reached an Hb concentration at least 50% higher than the original (partial early responders (PERs)). CHr at T1 (within 7 days from the beginning of treatment) was significantly different in the different groups (22.95 in CERs versus 18.41 in other patients; p = 0.001; 22.42 in early responders versus 18.07 in NERs; p = 0.001). Relative increase of CHr from T0 to T1 resulted significantly higher in CERs than in other patients (0.21 versus 0.11, p = 0.042) and in early responders than in NERs (0.22 versus 0.004, p = 0.006). Multivariate logistic models revealed a higher probability of being a complete early responder due to relative increase of ARC from T0 to T1 [OR (95% CI) = 44.95 (1.54–1311.98)] and to CHr at T1 [OR (95% CI) =3.18 (1.24–8.17)]. Our preliminary data confirm CHr as early and accurate predictor of hematological response to oral iron.
我们报告了34例缺铁性贫血儿童口服铁反应动力学的数据。24 /34例患者(70.5%)在治疗开始后第30天达到年龄和性别血红蛋白(Hb)浓度参考值(完全早期反应者(CERs)), 4/34例(12%)的Hb浓度比原始(部分早期反应者(PERs))至少高出50%。不同组T1时(治疗开始后7天内)的CHr有显著差异(CERs组22.95,其他组18.41;P = 0.001;早期响应者为22.42,晚期响应者为18.07;P = 0.001)。从T0到T1的CHr相对升高导致cer患者显著高于其他患者(0.21比0.11,p = 0.042),早期应答者显著高于ner患者(0.22比0.004,p = 0.006)。多变量logistic模型显示,由于ARC从T0到T1的相对增加[OR (95% CI) = 44.95(1.54-1311.98)]和T1时的CHr [OR (95% CI) =3.18(1.24-8.17)],成为完全早期应答者的可能性更高。我们的初步数据证实CHr是口服铁的血液学反应的早期和准确的预测因子。
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引用次数: 22
Evaluation of Serum Leptin Levels and Growth in Patients with β-Thalassaemia Major. β-地中海贫血患者血清瘦素水平和生长的评价。
IF 2.9 Q3 HEMATOLOGY Pub Date : 2016-01-01 Epub Date: 2016-03-21 DOI: 10.1155/2016/8454286
Lamia Mustafa Al-Naama, Meaad Kadum Hassan, Muhannad Maki Abdul Karim

Background. Iron deposition in the body can damage the endocrine glands of patients with β-thalassaemia major (β-TM). Leptin plays a key role in the regulation of appetite, body fat mass, and endocrine function. Objectives. This study aimed to evaluate the relationship between serum leptin and growth and pubertal development in patients with β-TM, as well as whether serum leptin can predict growth retardation and delayed puberty in these patients. Methods. Fifty β-TM patients (aged 8-20 years) and 75 age-matched healthy controls were recruited. Anthropometric data and sexual maturity ratings were assessed. Serum leptin was measured by ELISA. Results. Serum leptin levels were significantly lower in patients with β-TM than in healthy individuals (P < 0.001). Leptin levels were also significantly reduced in female patients with short stature (P < 0.002) and in patients who displayed delayed puberty (P = 0.032) compared to those with normal stature who had reached puberty. The sensitivity of leptin for predicting short stature and delayed puberty among patients was 84.6% and 92.3%, respectively. Conclusion. Low serum leptin is sensitive to predict short stature and significant in β-TM females only. This link could thus be used as a guide for further therapeutic or hormonal modulation.

背景。β-地中海贫血(β-TM)患者体内的铁沉积会损害内分泌腺体。瘦素在调节食欲、体脂量和内分泌功能方面起着关键作用。目标。本研究旨在探讨血清瘦素与β-TM患者生长发育和青春期发育的关系,以及血清瘦素是否可以预测这些患者的生长发育迟缓和青春期延迟。方法。招募了50例β-TM患者(8-20岁)和75名年龄匹配的健康对照。评估了人体测量数据和性成熟评分。ELISA法测定血清瘦素水平。结果。β-TM患者血清瘦素水平明显低于健康人群(P < 0.001)。身材矮小的女性患者(P < 0.002)和青春期延迟的女性患者(P = 0.032)的瘦素水平也明显低于已经进入青春期的正常身材患者。瘦素预测患者身材矮小和青春期延迟的敏感性分别为84.6%和92.3%。结论。低血清瘦素仅在β-TM女性中对身材矮小敏感。因此,这种联系可以作为进一步治疗或激素调节的指导。
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引用次数: 9
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Anemia
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