印度拉贾斯坦邦计划区部落镰状细胞血红蛋白、β-地中海贫血和G-6-PD缺乏症基因的简要回顾:关注部落健康

S. L. Choubisa, Anurag Choubisa
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引用次数: 1

摘要

拉贾斯坦邦位于印度西北部,是印度最大的邦,共有33个区。通过合并8个部落主导地区,即班斯瓦拉、奇图尔加尔、登格尔普尔、巴利、普拉塔普加尔、拉贾斯坦邦、西罗希和乌代普尔,政府创建了一个名为“计划区”的特殊地区,其中70%以上的人是部落。这个地区大多是落后和不发达的,疟疾也是高度流行的。在这一地区,Bhil、Damor、Meena、Garasiya、Kathudia和sahara是最主要的内婚部落。除了该地区的几种传染性和非传染性疾病外,某些红细胞遗传性疾病、镰状细胞血红蛋白(Hb-S)、β-地中海贫血和G-6-PD缺乏症(Gd)也使部落的健康状况恶化,并造成他们的发病率和死亡率。这些红细胞遗传性疾病的基因在部落人群中更为普遍和广泛分布。这些血液遗传疾病在部落中的最高患病率分别为31.14%、9.00%和22.00%。由于该部落地区的地下水含有大量氟化物(F),饮用它会使已经具有镰状细胞和β-地中海贫血基因纯合状态的部落人民过早死亡的风险很高。在本通讯中,除了对部落健康的关注外,还对预定地区不同部落族群中镰状细胞血红蛋白、β-地中海贫血和G-6-PD缺乏症基因的状况、这些血液遗传性疾病与疟疾的相关性、F中毒对患有红细胞遗传性疾病的部落受试者的影响以及这些红细胞遗传性疾病在部落人群中的预防和控制进行了严格审查。本综述的结果对印度拉贾斯坦邦规划地区部落这些血液遗传性疾病的预防和控制规划的制定和实施具有重要意义和优势。此外,本文还指出了研究空白,以供进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Brief Review of Sickle-Cell Haemoglobin, β-Thalassaemia and G-6-PD Deficiency Genes among Tribals of Scheduled Area of Rajasthan, India: Focus on Tribal Health
Rajasthan, situated at the north-western part of India is the biggest state in the country of India and has total of 33 districts. By merging eight tribal dominating districts namely, Banswara, Chittourgarh, Dungarpur, Pali, Pratapgarh, Rajasamand, Sirohi, and Udaipur of these, the government has created a special area called the ‘schedule area” in which >70% of the people are tribal. This area is mostly backward and underdeveloped where malaria is also hyperendemic. In this area, Bhil, Damor, Meena, Garasiya, Kathudia and Sahariya are the most dominating and major endogamous tribes. Besides the several communicable and non-communicable diseases in this area, certain erythrocyte genetic disorders, Sickle-Cell Haemoglobin (Hb-S), β-thalassaemia and G-6-PD deficiency (Gd) are also deteriorating the tribal health and causing morbidity and mortality in them. Genes of these red cell genetic disorders are more prevalent and widely distributed among tribal people. The maximum prevalence of these blood genetic disorders in tribes was found as 31.14%, 9.00% and 22.00%, respectively. Since the groundwater of this tribal area contains a high amount of Fluoride (F), drinking it poses a high risk of premature death of tribal people who already have homozygous state of sickle-cell and β-thalassaemic genes. In present communication, besides the focus on tribal health, the status of genes of sickle-cell haemoglobin, β-thalassaemia and G-6-PD deficiency in different tribal ethnic groups of scheduled area, the correlation of these blood genetic disorders with malaria, impact of F intoxication in tribal subjects possessing red cell genetic disorders and the prevention and control of these erythrocyte genetic disorders in tribal people have been critically reviewed. The results of this review are significant and advantageous in making and execution of prevention and control programme of these blood genetic disorders in tribals of scheduled area of Rajasthan, India. Moreover, in this review, research gaps are also highlighted for further research work.
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