微细胞性缺血性贫血患者的血红蛋白变异:印度研究的综述
Kaustubh Kharche1, Arvind Bhake1
1Department of Pathology, Jawaharlal Nehru Medical College, Datta Meghe Institute of Higher Education and Research, Wardha, IND.
Cureus
|June 2, 2023
概括
微细胞缺血性贫血通常源于血红蛋白病变. 贝塔血症特征是印度最常见的病因,需要高性能液体染色学 (HPLC) 诊断耐火病例.
科学领域:
- 血液学 血液学 血液学
- 遗传学 是一个遗传学.
- 公共卫生 公共卫生
背景情况:
- 微细胞低染色性贫血与溶血成分是常见的临床发现.
- 血球蛋白病变及其变体是这种类型贫血的重要病因因素.
- 印度人口呈现出高患病率和高血红蛋白病变的多样性,区域差异很大.
研究的目的:
- 系统地审查和评估微细胞缺血性贫血的潜在原因,重点关注血红蛋白病变.
- 为了比较印度各个地区不同血红蛋白病的患病率.
- 为了识别与微细胞低染色贫血相关的最常见的血红蛋白病.
主要方法:
- 按照系统审查和元分析 (PRISMA) 准则的首选报告项目进行了系统审查.
- 关键词被用于谷歌的高级搜索,以确定相关的研究.
- 从选定的文章中分析了数据,以确定血红蛋白病变的类型和频率.
主要成果:
- 贝塔血症特征 (βTT) 被确定为最频繁报告的血红蛋白病.
- 其他异常的血红蛋白变体,虽然不太常见,也被记录在审查的文献中.
- 观察到特定血红蛋白病变的流行率的区域差异.
结论:
- 贝塔血症特征是印度人口中微细胞低染色贫血的主要原因.
- 对标准治疗不耐药的微细胞性缺血性贫血患者应检查潜在的血红蛋白病变.
- 推使用高性能液体染色学 (HPLC) 来确定血红蛋白病变和异常血红蛋白变异的确诊.
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