Red blood cell antigen genotype analysis for 9087 Asian, Asian American, and Native American blood donors

血清学 基因型 抗原 ABO血型系统 等位基因频率 等位基因 太平洋岛民 单核苷酸多态性 SNP公司 生物 免疫学 民族 医学 遗传学 抗体 人口 基因 环境卫生 社会学 人类学
作者
Meghan Delaney,Samantha Harris,Askale Haile,Jill M. Johnsen,Gayle Teramura,Karen Nelson
出处
期刊:Transfusion [Wiley]
卷期号:55 (10): 2369-2375 被引量:46
标识
DOI:10.1111/trf.13163
摘要

BACKGROUND There has yet to be a comprehensive analysis of blood group antigen prevalence in Asian Americans and Native Americans. There may be ethnic differences in blood group frequencies that would result in clinically important mismatches through transfusion. STUDY DESIGN AND METHODS Blood donors who self‐identified as Asian or Native American were tested using a single‐nucleotide polymorphism (SNP) DNA array (HEA BeadChip kit, Bioarray Solutions Ltd) that predicts expression of 38 human erythrocyte antigens (HEAs) and by serology for ABO, D, C, M, N, Jk a , and Jk b . The prevalence of blood group antigens was compared to published European prevalence. Discrepancies between SNP‐predicted and serology‐detected antigens were tallied. RESULTS A total of 9087 blood donors were tested from nine Asian and Native American heritages. The predicted prevalence of selected antigens in the RHCE, JK, FY, MNS, LU, CO, and DO blood group systems were variable between Asian populations, but overall not significantly different than Europeans. Compared to European frequencies, Kell blood group allele frequencies were significantly different in the Chinese, Native American, Hawaiian/Pacific Islander, South Asian, and Southeast Asian heritage blood donors; Diego antigens Di a and Di b were different in donors of Native American and South Asian ancestries (p < 0.05). Of the donors tested, 4.5% showed a SNP‐serology discrepancy that segregated within specific ethnic groups. CONCLUSION This study provides HEA allele frequency and antigen prevalence data in a cohort of Asian and Native Americans donors. Several ethnic groups exhibited differences in HEA frequencies compared to Europeans. Genotype‐serotype discrepancies were detected in all systems studied.
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