Banjoko Alabi W, Ng'uni Tiza, Naidoo Nitalia, Ramsuran Veron, Hyrien Olivier, Ndhlovu Zaza M
Africa Health Research Institute (AHRI), Nelson R. Mandela School of Medicine, Durban, South Africa.
Department of Statistics, University of Ilorin, Kwara state, Nigeria.
bioRxiv. 2024 Sep 8:2024.09.04.611164. doi: 10.1101/2024.09.04.611164.
Africa remains significantly underrepresented in high-resolution Human Leukocyte Antigen (HLA) data, despite being one of the most genetically diverse regions in the world. This critical gap in genetic information poses a substantial barrier to HLA-based research on the continent. In this study, Class I HLA data from Eastern and Southern African populations were analysed to assess genetic diversity across the region. We examined allele and haplotype frequency distributions, deviations from Hardy-Weinberg Equilibrium (HWE), linkage disequilibrium (LD), and conducted neutrality tests of homozygosity across various populations. Additionally, the African HLA data were compared to those of Caucasian and African American populations using the Jaccard index and multidimensional scaling (MDS) methods. The study revealed that South African populations exhibited 50.4% more genetic diversity within the Class I HLA region compared to other African populations. Zambia showed an estimated 36.5% genetic diversity, with Kenya, Rwanda and Uganda showing 35.7%, 34.2%, and 31.1%, respectively. Furthermore, an analysis of in-country diversity among different tribes indicated an average Class I HLA diversity of 25.7% in Kenya, 17% in Rwanda, 2.8% in South Africa, 13.6% in Uganda, and 6.5% in Zambia. The study also highlighted the genetic distinctness of Caucasian and African American populations compared to African populations. Notably, the differential frequencies of disease-promoting and disease-preventing HLA alleles across these populations emphasize the urgent need to generate high-quality HLA data for all regions of Africa and its major ethnic groups. Such efforts will be crucial in enhancing healthcare outcomes across the continent.
尽管非洲是世界上遗传多样性最丰富的地区之一,但在高分辨率人类白细胞抗原(HLA)数据方面,非洲的代表性仍然严重不足。这一遗传信息的关键差距对非洲大陆基于HLA的研究构成了重大障碍。在本研究中,对来自东非和南非人群的I类HLA数据进行了分析,以评估该地区的遗传多样性。我们研究了等位基因和单倍型频率分布、偏离哈迪-温伯格平衡(HWE)的情况、连锁不平衡(LD),并对不同人群进行了纯合性中性测试。此外,使用杰卡德指数和多维标度(MDS)方法将非洲HLA数据与白种人和非裔美国人的数据进行了比较。研究表明,与其他非洲人群相比,南非人群在I类HLA区域内的遗传多样性高出50.4%。赞比亚的遗传多样性估计为36.5%,肯尼亚、卢旺达和乌干达分别为35.7%、34.2%和31.1%。此外,对不同部落的国内多样性分析表明,肯尼亚I类HLA的平均多样性为25.7%,卢旺达为17%,南非为2.8%,乌干达为13.6%,赞比亚为6.5%。该研究还强调了白种人和非裔美国人与非洲人群相比的遗传独特性。值得注意的是,这些人群中促进疾病和预防疾病的HLA等位基因频率的差异强调了为非洲所有地区及其主要族群生成高质量HLA数据的迫切需求。这些努力对于改善整个非洲大陆的医疗保健结果至关重要。