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Potential linkages between Alzheimer's disease and major depression 阿尔茨海默病与严重抑郁症之间的潜在联系
Pub Date : 2023-01-01 DOI: 10.4103/mj.mj_65_22
F. Raudino
Alzheimer's disease (AD) and major depression (MD) are frequent diseases with a significant impact on the quality of life, and epidemiological studies show a correlation between early depressive episodes and AD. Although apparently different, they nonetheless maintain significant similarities, such as the common genetic substrate, involvement of similar structures, and a number of common pathogenetic hypotheses. This in-depth literature review aims at highlighting possible linkages between the two diseases: A chronic inflammatory process that selectively alters the blood–brain barrier in certain regions can be hypothesized.
阿尔茨海默病(AD)和重度抑郁症(MD)是对生活质量有重大影响的常见疾病,流行病学研究表明早期抑郁发作与AD之间存在相关性。尽管明显不同,但它们仍然保持着显著的相似性,如共同的遗传基础、相似结构的参与、,以及一些常见的病因假说。这篇深入的文献综述旨在强调这两种疾病之间的可能联系:可以假设这是一种选择性改变某些区域血脑屏障的慢性炎症过程。
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引用次数: 0
Effect of celecoxib alone or in combination of sitagliptin in monoiodoacetate rat model of osteoarthritis 塞来昔布单用或联用西格列汀对单碘乙酸骨关节炎大鼠模型的影响
Pub Date : 2023-01-01 DOI: 10.4103/mj.mj_51_22
Rabab Al-Uqabi, A. Al-Gareeb, Ali K. Al-buhadily
Background: Osteoarthritis (OA) is considered an attractive research issue; as it is the most common musculoskeletal progressive condition with no cure yet. Aims: To evaluate effect of celecoxib alone or in combination of sitagliptin in monoiodo acetate rat model of OA. Methods: A total of 40 Sprague-Dawley male rats were divided into 4 groups, negative control (n=10), positive control group (OA induced by monoiodoacetate (MIA)) (n=10), celecoxib 50mg/kg (n=10), and celecoxib 50mg/kg plus sitagliptin 20mg/kg group (n=10). Serum levels of inflammatory biomarkers and serum CTX-II were assessed for all groups. Data were analyzed statistically by SPSS version 28.00. Results: group treated with celecoxib showed a significant reduction in the inflammatory biomarkers and CTX-II serum levels compared with the OA group (P<0.01). A significant reduction in CTX-II level in combination treated group relative to celecoxib treated group. Conclusion: Celecoxib imparted anti-inflammatory and cartilage protective effect in OA induced rat model. Sitagliptin combination with celecoxib added an extra cartilage protective effect by reducing cartilage degradation evident by lowering CTX-II serum levels.
背景:骨关节炎(OA)被认为是一个有吸引力的研究问题;因为它是最常见的肌肉骨骼进行性疾病,目前尚未治愈。目的:评价塞来昔布单独或联合西他列汀对单碘乙酸大鼠OA模型的影响。方法:将40只Sprague-Dawley雄性大鼠分为4组,阴性对照组(n=10)、阳性对照组(单碘乙酸盐诱导OA)(n=10,塞来昔布50mg/kg组(n=1 0)和塞来昔布50 mg/kg加西他列汀20mg/kg组(n=2 0)。对所有组的炎症生物标志物和血清CTX-II的血清水平进行评估。数据采用SPSS 28.00进行统计分析。结果:与OA组相比,塞来昔布治疗组的炎症生物标志物和CTX-II血清水平显著降低(P<0.01)。与塞来昔布处理组相比,联合治疗组的CTX-II水平显著降低。结论:塞来昔布具有抗炎和软骨保护作用。西格列汀与塞来昔布联合使用可通过降低CTX-II血清水平来减少软骨降解,从而增加额外的软骨保护作用。
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引用次数: 0
Evaluation of protective effect of metformin in rats with experimental osteoarthritis 二甲双胍对实验性骨关节炎大鼠保护作用的评价
Pub Date : 2023-01-01 DOI: 10.4103/mj.mj_43_22
Ali K. Al-buhadily, Rabab Al-Uqabi, A. Al-Gareeb
Objective: The objective of this study is to evaluate metformin proposed protective effect against the development of osteoarthritis (OA) in rats. Materials and Methods: A total of 40 male Sprague–Dawley rats were included, divided into four groups: negative control (n = 10), positive control (OA induced by monoiodoacetate [MIA]) (n = 10), metformin 200mg/kg group (n = 10) preinduction of OA, and metformin 200 mg/kg group (n = 10) postinduction of OA. Serum C-telopeptide type II collagen (CTX-II), inflammatory biomarkers were evaluated for each group. For data analysis, SPSS version 26.00 was used. Results: Metformin-treated groups showed a significant reduction in inflammatory biomarkers and CTX-II serum levels compared with OA group (P < 0.05). Pretreatment with 200 mg/kg metformin imparted extra cartilage protective effect and further decreased inflammatory cytokines compared to posttreated (P < 0.05). Conclusion: Metformin produced a beneficial protective effect in experimental OA in rats. It attenuates the inflammatory reactions progression by preventing the release of pro-inflammatory cytokines in rats with experimental OA. Furthermore, metformin reduced cartilage degradation evidenced by lowering CTX-II serum levels experimental OA in rats.
目的:评价二甲双胍对大鼠骨关节炎(OA)的保护作用。材料与方法:选取雄性Sprague-Dawley大鼠40只,分为阴性对照组(n = 10)、阳性对照组(单碘乙酸[MIA]诱导OA) (n = 10)、OA诱导前二甲双胍200mg/kg组(n = 10)、OA诱导后二甲双胍200mg/kg组(n = 10)。评估各组血清c -末端肽II型胶原蛋白(CTX-II)、炎症生物标志物。数据分析采用SPSS 26.00版本。结果:与OA组相比,二甲双胍治疗组炎症生物标志物和血清CTX-II水平显著降低(P < 0.05)。200 mg/kg二甲双胍预处理能增加软骨保护作用,并进一步降低炎症因子(P < 0.05)。结论:二甲双胍对实验性OA大鼠有良好的保护作用。它通过阻止实验性OA大鼠的促炎细胞因子的释放来减轻炎症反应的进展。此外,二甲双胍通过降低实验性OA大鼠血清CTX-II水平来减少软骨退化。
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引用次数: 0
A pilot study on hypogonadism in male leprosy patients in rural tertiary care hospital in central India 印度中部农村三级护理医院男性麻风病患者性腺功能减退的初步研究
Pub Date : 2023-01-01 DOI: 10.4103/mj.mj_35_23
Pratiksha Sonkusale, S. Kar, A. Deshmukh, Subhor Nandwani, Sangeeta Galui, Aditya Ambulkar
Background: Leprosy is a chronic granulomatous infectious disease caused by Mycobacterium leprae. Besides the skin and peripheral nerves, it also involves many internal organs. Testicular involvement is mainly seen in leprosy. Hypogonadism in males with leprosy can occur due the involvement of testis. Aim: The aim was to evaluate the gonadal function impairment in males with leprosy and to analyze the relation of follicle-stimulating hormone (FSH), luteinizing hormone (LH), and testosterone to the activity, duration, and disease classification in Central India. Patients and Methods: This was a prospective observational pilot study. We evaluated 30 patients of leprosy. They were subjected to careful history taking, dermatological and genital examination, assessment of FSH, LH, and testosterone levels, and slit skin smear for acid-fast bacilli. Diagnosis of leprosy was confirmed histopathologically. The collected data were encoded and entered electronically in a computer excel worksheet 2010 version. The statistical analysis was performed using SPSS version 17.0 for Windows. Pearson correlation coefficient was used to establish relationship between different variables. P ≤ 0.05 was considered statistically significant. Results: A positive correlation was found between FSH and LH hormones which was highly significant, whereas there was a negative correlation between testosterone and FSH and LH levels. There was a positive correlation between age, duration of disease, and reaction in leprosy with those of FSH and LH levels. There was a positive correlation between disease activity bacillary index (BI) and FSH, LH and a negative correlation between BI and testosterone. Conclusion: It is recommended that lepromatous leprosy patients should be routinely screened for hypogonadism using FSH, LH, and testosterone levels.
背景:麻风是由麻风分枝杆菌引起的一种慢性肉芽肿性传染病。除了皮肤和周围神经外,它还涉及许多内脏器官。累及睾丸主要见于麻风病。男性麻风病患者的性腺功能减退可因睾丸受累而发生。目的:评价印度中部地区男性麻风患者的性腺功能损害,分析促卵泡激素(FSH)、黄体生成素(LH)和睾酮与麻风活动、病程和疾病分类的关系。患者和方法:这是一项前瞻性观察性初步研究。我们评估了30名麻风病患者。他们接受了详细的病史记录、皮肤和生殖器检查、FSH、LH和睾酮水平的评估以及抗酸杆菌的切开皮肤涂片检查。麻风病的诊断经病理组织学证实。收集到的数据被编码并以电子方式输入到计算机excel工作表2010版本中。采用SPSS 17.0 for Windows进行统计分析。采用Pearson相关系数建立不同变量之间的关系。P≤0.05认为有统计学意义。结果:FSH与LH呈显著正相关,而睾酮与FSH、LH呈显著负相关。年龄、病程、麻风病反应与FSH、LH水平呈正相关。疾病活动性杆菌指数(BI)与FSH、LH呈正相关,与睾酮呈负相关。结论:建议对麻风性麻风患者进行FSH、LH和睾酮水平的常规筛查,以检查其性腺功能减退。
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引用次数: 0
Caudal septal deviation surgical techniques 尾间隔偏曲手术技术
Pub Date : 2023-01-01 DOI: 10.4103/mj.mj_8_23
Nasir Hassen
Background: Caudal septal repair is hard to confront in otolaryngology and plastic surgeon, due to cartilage memory. It causes nasal obstruction or esthetical problems to the nasal base and columella. Although different modalities have been described for the treatment of this abnormality, these techniques not only improve the function but also preserve or improve the appearance of the nose. Objective: The objective was to discuss the different surgical conservative procedures that can be used to treat alterations of the caudal septum and change the position of the cartilage in the midline and find which is the best. Patients and Methods: A descriptive study was conducted on 40 patients who aged 20–40 years, had attended the Otolaryngology Outpatient Clinic in Al Karama Teaching Hospital, Baghdad, Iraq, between October 2016 and March 2020, and with a history of obstructed nose; conservative nasal septal surgery was done for them depending on the severity. Results: Regarding the result of the type of surgery, the patients were satisfied with their esthetic and functional perfection; patients with preoperative nasal obstruction reported improved breathing. In scoring technique with (NOSE) score pre and postoparative results were 58.21 and 22.66, in reshaping technique were 60.66 and 17.21 as a pre and postoparative results and in batten graft the results were 62.34 and 20.26 as a pre and postoparative results alternatively. Reshaping and batten graft techniques are better results than the scoring technique. Conclusion: The study outcomes that the approaches for improvement of caudal septal deviation are safe and effective. The approach of surgery will depend on the severity of the deviation.
背景:由于软骨记忆的原因,尾部间隔修复在耳鼻喉科和整形外科医生中很难解决。它会导致鼻阻塞或鼻基底和鼻小柱的美观问题。尽管已经描述了治疗这种异常的不同方式,但这些技术不仅改善了功能,还保留或改善了鼻子的外观。目的:探讨可用于治疗尾中隔改变和改变中线软骨位置的不同手术保守程序,并找出最佳方案。患者和方法:对40名年龄在20-40岁之间的患者进行了描述性研究,这些患者在2016年10月至2020年3月期间曾在伊拉克巴格达Al Karama教学医院的耳鼻咽喉门诊就诊,并有鼻阻塞史;根据严重程度,对其进行保守性鼻中隔手术。结果:就手术类型而言,患者对其美学和功能的完美感到满意;术前鼻塞患者报告呼吸改善。在评分技术和(NOSE)评分的前后结果分别为58.21和22.66,在整形技术的前后结果为60.66和17.21,在板条移植的前后结果交替为62.34和20.26。整形和板条移植技术比评分技术效果更好。结论:研究结果表明,改进尾侧间隔偏斜的方法是安全有效的。手术方法将取决于偏差的严重程度。
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引用次数: 0
Correlation of NF-kB serum level with the expression pattern of microrna-221 in a sample of hcv-exposed Iraqi patients 伊拉克hcv暴露患者血清NF-kB水平与microrna-221表达模式的相关性
Pub Date : 2023-01-01 DOI: 10.4103/mj.mj_20_22
Shaima’a R. Al-Salihy, R. Al-Shawk, Safaa A. Al-Waysi, M. Rasheed
Background: Hepatitis C virus (HCV) has the ability to change cellular messenger RNA transcription and translation by stimulating the synthesis of cellular microRNAs (miRNAs) that impair immune response and facilitate viral reproduction. One of the most important members of the immune response against HCV is nuclear factor-kappa B (NF-κB), which is regulated by cellular miRNAs. Aims: we aimed to investigate the correlation of NF-κB serum level with circulatory miRNA-221 (miR-221) fold change in HCV-exposed individuals. Materials and Methods: Serum level of NF-κB in 88 samples (22 patients with persistent HCV infection, 22 individuals with spontaneous HCV virus clearance, 22 individuals treated with direct-acting antivirals (DAAs) drugs, and 22 uninfected apparently healthy blood donors as control) was measured by enzyme-linked immunosorbent assay. Reverse transcriptase–polymerase chain reaction was used to quantify the expression fold of circulatory miR-221. Results: The results showed that there was a significant decrease in the mean level of NF-κB at P < 0.000 among HCV-exposed patients (2.0058 ng/ml) as compared to the control group (2.9841 ng/ml). The mean fold change of miR-221 was significantly upregulated about six more times among HCV-exposed patients (mean = 6.3545) compared to the control group (mean = 1.1864). Furthermore, the mean ± standard deviation of miR-221 fold change in patients with persistent HCV infection was significantly higher compared to patients cured after DAA therapy (P = 0.048), there was a weak negative correlation (r = −0.246, P = 0.021) between NF-κB serum level and miR-221 folding level. Conclusion: HCV infection disrupts NF-κB activation, resulting in dysregulation of miR-221 that persists long after the virus has been cleared. Thus, quantification of serum NF-κB and miR-221in HCV-exposed patients could be used as noninvasive prognostic marker during long-term follow-up. Furthermore, a miRNAs profile analysis can help distinguish HCV-exposed from healthy individuals.
背景:丙型肝炎病毒(HCV)能够通过刺激细胞微小RNA(miRNA)的合成来改变细胞信使RNA的转录和翻译,从而损害免疫反应并促进病毒繁殖。抗HCV免疫反应中最重要的成员之一是核因子κB(NF-κB),它受到细胞miRNA的调节。目的:我们旨在研究HCV暴露个体血清NF-κB水平与循环miRNA-221(miR-221)倍数变化的相关性。材料和方法:采用酶联免疫吸附法测定88例样本(22例持续性丙型肝炎病毒感染者、22例自发性丙型肝炎病毒清除者、22名直接作用抗病毒药物治疗者和22名未感染的明显健康献血者作为对照)的血清NF-κB水平。逆转录聚合酶链式反应用于定量循环miR-221的表达倍数。结果:与对照组(2.9841 ng/ml)相比,暴露于HCV的患者(2.0058 ng/ml)在P<0.000时NF-κB的平均水平显著降低。与对照组(平均值=1.1864)相比,暴露于HCV的患者中miR-221的平均倍数变化显著上调了约6倍(平均值=6.3545)。此外,持续性HCV感染患者的miR-221倍数变化的平均±标准差显著高于DAA治疗后治愈的患者(P=0.048),血清NF-κB水平与miR-221折叠水平呈弱负相关(r=-0.246,P=0.021)。结论:HCV感染破坏了NF-κB的激活,导致miR-221的失调,这种失调在病毒清除后很长一段时间仍存在。因此,HCV暴露患者血清NF-κB和miR-221的定量可作为长期随访中的无创预后标志物。此外,miRNA图谱分析可以帮助区分暴露于HCV的健康个体。
{"title":"Correlation of NF-kB serum level with the expression pattern of microrna-221 in a sample of hcv-exposed Iraqi patients","authors":"Shaima’a R. Al-Salihy, R. Al-Shawk, Safaa A. Al-Waysi, M. Rasheed","doi":"10.4103/mj.mj_20_22","DOIUrl":"https://doi.org/10.4103/mj.mj_20_22","url":null,"abstract":"Background: Hepatitis C virus (HCV) has the ability to change cellular messenger RNA transcription and translation by stimulating the synthesis of cellular microRNAs (miRNAs) that impair immune response and facilitate viral reproduction. One of the most important members of the immune response against HCV is nuclear factor-kappa B (NF-κB), which is regulated by cellular miRNAs. Aims: we aimed to investigate the correlation of NF-κB serum level with circulatory miRNA-221 (miR-221) fold change in HCV-exposed individuals. Materials and Methods: Serum level of NF-κB in 88 samples (22 patients with persistent HCV infection, 22 individuals with spontaneous HCV virus clearance, 22 individuals treated with direct-acting antivirals (DAAs) drugs, and 22 uninfected apparently healthy blood donors as control) was measured by enzyme-linked immunosorbent assay. Reverse transcriptase–polymerase chain reaction was used to quantify the expression fold of circulatory miR-221. Results: The results showed that there was a significant decrease in the mean level of NF-κB at P < 0.000 among HCV-exposed patients (2.0058 ng/ml) as compared to the control group (2.9841 ng/ml). The mean fold change of miR-221 was significantly upregulated about six more times among HCV-exposed patients (mean = 6.3545) compared to the control group (mean = 1.1864). Furthermore, the mean ± standard deviation of miR-221 fold change in patients with persistent HCV infection was significantly higher compared to patients cured after DAA therapy (P = 0.048), there was a weak negative correlation (r = −0.246, P = 0.021) between NF-κB serum level and miR-221 folding level. Conclusion: HCV infection disrupts NF-κB activation, resulting in dysregulation of miR-221 that persists long after the virus has been cleared. Thus, quantification of serum NF-κB and miR-221in HCV-exposed patients could be used as noninvasive prognostic marker during long-term follow-up. Furthermore, a miRNAs profile analysis can help distinguish HCV-exposed from healthy individuals.","PeriodicalId":33069,"journal":{"name":"mjl@ lmstnSry@ lTby@","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47134819","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: 0
Vagal nerve stimulation for refractory epilepsy: Eight years of experience on 183 Iraqi patients 迷走神经刺激治疗难治性癫痫:183例伊拉克患者的8年经验
Pub Date : 2023-01-01 DOI: 10.4103/mj.mj_14_22
Mohamed Al Tamimi, AhmedA Salam Al Atraqchi, Ahmed Tahseen, Hayder Qatran
Background: Vagus nerve stimulation has been broadly known as one of treatment lines for refractory epilepsy, especially in poor applicants for resection surgeries or in whom resection has failed. Its use for different seizure-types control is increasing. Aims: We aimed to assess the efficacy of Vagal nerve stimulation (VNS) therapy outcome predictive aspects utilizing subgroup analysis. Materials and Methods: From 2008 until 2016, 183/190 refractory epilepsy cases with specific inclusion criteria were selected. All underwent pre- and postimplantation assessment of response utilizing Engel criteria and Chalfont seizure severity scoring system for 2 years. Descriptive and statistical data analysis was accomplished for the data of age at epilepsy start and VNS insertion, seizures nature, device stimulation parameters, and peri-surgical antiepileptic medicines. Results: At 12 months follow-up period (29.5%), patients were assigned to a Class I and II outcome (representing very good seizure outcome) especially among patients with G. T. C seizure. 38.8% had a “worthwhile” improvement and consigned as Class III outcome mostly among P. S. G patients. The response was better at 24 months' follow-up period. Patients <10 years of age with pre surgery mean duration of epilepsy of 10 (+5) years and mean age at onset of epilepsy of 7 (+5) years showed better response. Mean seizure frequency reduction was 69.8% (+18). Conclusions: Stimulation parameters needed was lower for class I and II with significant reduction of required anti-epileptic drugs (AED). Our study may help to provide response predictive characteristics.
背景:迷走神经刺激已被广泛认为是难治性癫痫的治疗方法之一,尤其是在切除手术申请不佳或切除失败的患者中。它在不同癫痫发作类型控制中的应用正在增加。目的:我们旨在利用亚组分析评估迷走神经刺激(VNS)治疗结果预测方面的疗效。材料和方法:从2008年到2016年,选择183/190例具有特定纳入标准的难治性癫痫病例。所有患者均采用Engel标准和Chalfont癫痫发作严重程度评分系统进行了2年的植入前和植入后反应评估。对癫痫发作开始和VNS插入时的年龄、癫痫发作性质、装置刺激参数和围手术期抗癫痫药物的数据进行了描述性和统计数据分析。结果:在12个月的随访期(29.5%),患者被分为I级和II级结果(代表非常好的癫痫发作结果),尤其是在G.T.C癫痫患者中。38.8%的患者有“值得”的改善,并被列为III级结果,主要发生在P.S.G患者中。在24个月的随访期间,反应更好。年龄<10岁的患者,术前平均癫痫持续时间为10(+5)年,癫痫发作时平均年龄为7(+5)岁,表现出更好的反应。癫痫发作频率平均降低69.8%(+18)。结论:I级和II级所需的刺激参数较低,所需抗癫痫药物(AED)显著减少。我们的研究可能有助于提供反应预测特征。
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引用次数: 0
Cardiovascular health in turner syndrome: Manifestations, endocrine, and metabolic risk factors with a look at clinical practice 特纳综合征的心血管健康:临床实践中的表现、内分泌和代谢危险因素
Pub Date : 2022-07-01 DOI: 10.4103/mj.mj_13_22
W. Abdullah, Abdulameer Jawad al-Gburi, Saba Younis Al-Obaidi
Turner syndrome (TS) is the most frequent female chromosomal abnormality, with a higher overall mortality rate than the general population; cardiovascular events are a significant risk factor. Cardiovascular manifestations in TS include congenital heart diseases, in addition to acquired heart diseases such as acute aortic dissection, stroke, myocardial infarction, and hypertension. Growth hormone-insulin growth factor 1 axis abnormality, estrogen hormone deficiency, liability for diabetes mellitus, and dyslipidemia all are endocrine risk factors affecting cardiovascular health in TS. Heart anatomical defects should be closely monitored for progression and associated complications throughout the patient's lifetime by a skilled cardiologist.
特纳综合征(TS)是最常见的女性染色体异常,其总死亡率高于一般人群;心血管事件是一个重要的危险因素。TS的心血管表现除获得性心脏病如急性主动脉夹层、脑卒中、心肌梗死、高血压外,还包括先天性心脏病。生长激素-胰岛素生长因子1轴异常、雌激素激素缺乏、糖尿病易感性和血脂异常都是影响TS患者心血管健康的内分泌危险因素。在患者的一生中,应由熟练的心脏病专家密切监测心脏解剖缺陷的进展和相关并发症。
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引用次数: 0
C-reactive protein in elderly and pregnant COVID-19 cases: A new role for an old marker 老年人和孕妇新冠肺炎病例中的C反应蛋白:一种旧标志物的新作用
Pub Date : 2022-07-01 DOI: 10.4103/mj.mj_54_22
E. Ali, D. Salman, Wassan Nori
The clinical characteristics and prognosis of high-risk groups, including elderly and pregnant women, may vary according to the overall susceptibility of novel coronavirus. For that, numerous researchers worldwide have concentrated their efforts on finding a trustworthy biomarker that can determine the severity, prognosis, and survival of those affected. C-reactive protein (CRP), an inflammatory biomarker that showed higher levels in coronavirus 2019 (COVID-19) cases, underlay inflammation degree and was used to gauge the severity of COVID-19. In this review, we discuss whether CRP might have other uses in COVID-19 cases besides predicting the severity and the clinical outcomes among vulnerable risk groups. Doctors must analyze CRP levels along with the period of illness to identify those liable for rapid progress and be able to categorize case severity to guide the clinical decision to improve prognosis.
高危人群(包括老年人和孕妇)的临床特征和预后可能因整体易感性而异。为此,世界各地的许多研究人员都集中精力寻找一种可信赖的生物标志物,以确定患者的严重程度、预后和生存率。c反应蛋白(CRP)是一种炎症生物标志物,在2019冠状病毒(COVID-19)病例中显示出较高的水平,是炎症程度的基础,并用于衡量COVID-19的严重程度。在这篇综述中,我们讨论CRP是否可能在COVID-19病例中有其他用途,除了预测易感危险人群的严重程度和临床结局。医生必须根据病程分析CRP水平,以确定病情快速发展的原因,并能够对病例严重程度进行分类,以指导临床决策,改善预后。
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引用次数: 2
Siblings with dyschromatosis universalis hereditaria a rare case report 同胞遗传性普遍性色素沉着病一例罕见病例报告
Pub Date : 2022-07-01 DOI: 10.4103/mj.mj_9_22
P. Kumari, Sonia Jain, Pratiksha Sonkusale, A. Deshmukh
Dyschromatoses are a group of genodermatosis characterized by the presence of both hyperpigmented and hypopigmented macules of variable shapes and sizes. Here, we report siblings presented with asymptomatic progressive mottled pigmentation of reticulate pattern over the trunk and limbs since 6 years of their age without any systemic or other cutaneous illness. They were born to nonconsanguineous parents following an uneventful pregnancy. Their paternal grandfather had a similar appearance. Histological examination was consistent with dyschromatosis universalis hereditaria (DUH). Based on the clinical and histological findings, a diagnosis of DUH was made. We report this case of rare genodermatosis in siblings affected by the same disease.
色素沉着病是一组遗传性皮肤病,其特征是存在不同形状和大小的色素沉着过度和色素沉着不足的黄斑。在这里,我们报告了兄弟姐妹从6岁起,在躯干和四肢出现无症状的进行性网状斑点色素沉着,没有任何系统性或其他皮肤疾病。他们的父母在平静的怀孕后不爱流血。他们的祖父也有相似的外貌。组织学检查与遗传性普遍性色素沉着病(DUH)一致。根据临床和组织学表现,诊断为DUH。我们报告了一例罕见的遗传性皮肤病的兄弟姐妹受相同疾病的影响。
{"title":"Siblings with dyschromatosis universalis hereditaria a rare case report","authors":"P. Kumari, Sonia Jain, Pratiksha Sonkusale, A. Deshmukh","doi":"10.4103/mj.mj_9_22","DOIUrl":"https://doi.org/10.4103/mj.mj_9_22","url":null,"abstract":"Dyschromatoses are a group of genodermatosis characterized by the presence of both hyperpigmented and hypopigmented macules of variable shapes and sizes. Here, we report siblings presented with asymptomatic progressive mottled pigmentation of reticulate pattern over the trunk and limbs since 6 years of their age without any systemic or other cutaneous illness. They were born to nonconsanguineous parents following an uneventful pregnancy. Their paternal grandfather had a similar appearance. Histological examination was consistent with dyschromatosis universalis hereditaria (DUH). Based on the clinical and histological findings, a diagnosis of DUH was made. We report this case of rare genodermatosis in siblings affected by the same disease.","PeriodicalId":33069,"journal":{"name":"mjl@ lmstnSry@ lTby@","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49181291","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: 0
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