Ahmed Sagir G, Ibrahim Umma A
Department of Hematology, Aminu Kano Teaching Hospital, Kano State, Nigeria.
Department of Pediatrics, Aminu Kano Teaching Hospital, Kano State, Nigeria.
Oman Med J. 2021 May 31;36(3):e261. doi: 10.5001/omj.2021.102. eCollection 2021 May.
Apart from hemoglobin-S (HbS), there are other Hb variants (non-S sickling Hb variants) that cause sickle cell disease. However, the profiles of these non-S sickling Hb variants have neither been collated nor harmonized. A literature search revealed 14 non-S sickling Hb variants (HbC-Harlem, HbC-Ziguinchor, HbS-Travis, HbS-Antilles, HbS-Providence, HbS-Oman, HbS-Cameroon, HbS-South End, Hb Jamaica Plain, HbC-Ndjamena, HbS-Clichy, HbS-San Martin, HbS-Wake, and HbS-São Paulo). Generally, the non-S sickling Hb variants are double mutants with the HbS mutation (GAG>GTG: βGlu6Val) and additional β-chain mutations. Consequently, non-S sickling Hb variants give positive solubility and sickling tests, but they differ from HbS with respect to stability, oxygen affinity, and electro-chromatographic characteristics. Similarities and discrepancies between HbS and non-S sickling Hb variants create diagnostic pitfalls that can only be resolved by elaborate electro-chromatographic and/or genetic tests. It is therefore imperative that tropical hematologists should have a thorough understanding of these atypical sickling Hb variants. Collated and harmonized appraisal of the non-S sickling Hb variants have not been previously undertaken. Hence, this paper aims to provide a comprehensive but concise historical, genetic, comparative, diagnostic, and clinical overview of non-S sickling Hb variants. The elaborate techniques often required for precise diagnosis of non-S sickling Hb variants are regrettably not readily available in low resource tropical countries, which paradoxically carry the heaviest burden of sickling disorders. We strongly recommend that tropical countries should upgrade their diagnostic laboratory facilities to avoid misdiagnosis of these atypical Hb mutants.
除了血红蛋白 - S(HbS)之外,还有其他导致镰状细胞病的血红蛋白变体(非 S 型镰状血红蛋白变体)。然而,这些非 S 型镰状血红蛋白变体的特征既未被整理也未得到统一。文献检索发现了 14 种非 S 型镰状血红蛋白变体(HbC - 哈莱姆、HbC - 齐金乔尔、HbS - 特拉维斯、HbS - 安的列斯、HbS - 普罗维登斯、HbS - 阿曼、HbS - 喀麦隆、HbS - 南端、Hb 牙买加平原、HbC - 恩贾梅纳、HbS - 克利希、HbS - 圣马丁、HbS - 韦克和 HbS - 圣保罗)。一般来说,非 S 型镰状血红蛋白变体是与 HbS 突变(GAG>GTG:β 链谷氨酸 6 缬氨酸)以及额外的 β 链突变构成的双突变体。因此,非 S 型镰状血红蛋白变体的溶解度和镰变试验呈阳性,但它们在稳定性、氧亲和力和电色谱特征方面与 HbS 不同。HbS 和非 S 型镰状血红蛋白变体之间的异同造成了诊断陷阱,只有通过精细的电色谱和/或基因检测才能解决。因此,热带地区的血液学家必须全面了解这些非典型的镰状血红蛋白变体。此前尚未对非 S 型镰状血红蛋白变体进行整理和统一评估。因此,本文旨在提供关于非 S 型镰状血红蛋白变体全面但简洁的历史、遗传、比较、诊断和临床概述。遗憾的是,在资源匮乏的热带国家,通常需要用于精确诊断非 S 型镰状血红蛋白变体的精细技术并不容易获得,而这些国家却反常地承担着镰状细胞病最重的负担。我们强烈建议热带国家升级其诊断实验室设施,以避免对这些非典型血红蛋白突变体的误诊。