Tandeter Howard, Glick Karina, Moser Asher
a Department of Family Medicine and Siaal Research Center for Family Medicine and Primary Care , Ben-Gurion University of the Negev , Beer-Sheva , Israel.
b Department of Internal Medicine C , Ha'emek Medical Center , Afula , Israel.
Eur J Gen Pract. 2016 Dec;22(4):213-218. doi: 10.1080/13814788.2016.1206071. Epub 2016 Jul 27.
Due to trends of population movements, Israeli family physicians are treating increasing numbers of African immigrants from Ethiopia. These immigrants were found to have complete blood counts (CBC) that are different from other ethnic groups, with a higher prevalence of eosinophilia and neutropenia.
To evaluate haematological findings in an attempt to define whether they behave as familial (genetic) or environmental.
Retrospective chart review of 300 patients from a primary care clinic: 100 individuals of Ethiopian heritage born in Ethiopia (EE); 100 individuals of Ethiopian heritage born in Israel, whose parents were born in Ethiopia (EI), and a control group of 100 patients who were not of Ethiopian heritage (C).
Absolute eosinophilia (greater than 500/dl) was found in 13% of the EE study group significantly higher than the two other groups (P < 0.05), with no difference between EI and C. neutropenia (defined as less than 1500/dl) was found in 32% of EE group, 20% of EI, and 1% of C (P < 0.01).
On the one hand, findings point to a marked environmental influence on the eosinophilic response (most probably due to intestinal parasites present in immigrants from Ethiopia). On the other hand, a familial-genetic nature is probably the reason for the higher prevalence of neutropenia in this population, although some environmental influence may play a role. The knowledge of these findings may be useful for physicians treating people migrating from Africa.
由于人口流动趋势,以色列家庭医生正在诊治越来越多来自埃塞俄比亚的非洲移民。这些移民的全血细胞计数(CBC)与其他种族群体不同,嗜酸性粒细胞增多症和中性粒细胞减少症的患病率更高。
评估血液学检查结果,以确定其表现为家族性(遗传性)还是环境性。
对一家初级保健诊所的300名患者进行回顾性病历审查:100名出生在埃塞俄比亚的有埃塞俄比亚血统的个体(EE);100名出生在以色列、父母出生在埃塞俄比亚的有埃塞俄比亚血统的个体(EI),以及100名非埃塞俄比亚血统的患者作为对照组(C)。
在EE研究组中,13%的患者出现绝对嗜酸性粒细胞增多(大于500/dl),显著高于其他两组(P<0.05),EI组和C组之间无差异。在EE组中,32%的患者出现中性粒细胞减少(定义为小于1500/dl),EI组为20%,C组为1%(P<0.01)。
一方面,研究结果表明环境对嗜酸性粒细胞反应有显著影响(很可能是由于来自埃塞俄比亚的移民体内存在肠道寄生虫)。另一方面,家族遗传性质可能是该人群中性粒细胞减少症患病率较高的原因,尽管一些环境影响可能也起作用。了解这些研究结果可能对治疗从非洲移民来的人有帮助。