Miller J Z, Grim C E, Conneally P M, Weinberger M H
Hypertension. 1979 Sep-Oct;1(5):493-7. doi: 10.1161/01.hyp.1.5.493.
Persons participating in a 5-day diagnostic protocol were routinely typed for ABO, Rh, MNS, Kell, Kidd, Duffy, P, Haptoglobin, phosphoglucomutase-1 (PGM-1), and acid phosphatase (AcP). The study population was composed of 164 normotensive whites, 34 normotensive blacks, 161 whites and 43 blacks with essential hypertension, and 52 whites with secondary forms of hypertension (18 atherosclerotic renovascular hypertensives, 17 patients with fibromuscular disease, and 17 patients with primary aldosteronism). There were no significant differences in phenotype frequencies in ABO, Rh, Kidd, Kell, Duffy, P, Haptoglobin, PGM-1 or AcP in any of the comparisons. However, there was a significantly different distribution of MNS phenotypes in comparisons of essential and atherosclerotic renovascular hypertensives with normotensive controls. Essential hypertensives had a lower frequency of the S gene and a higher frequency of s in whites (X2 = 12.21, p less than 0.005). Atherosclerotic renovascular hypertensives differed from the normotensive population in the frequencies of both MN (X 2 = 4.34, p less than 0.05) and Ss (X2 = 4.21, p less than 0.05). The finding of disease-blood group associations supports the hypothesis that there may be significant physiological differences between individuals of different blood types.
参与为期5天诊断方案的人员常规进行ABO、Rh、MNS、凯尔(Kell)、基德(Kidd)、达菲(Duffy)、P、触珠蛋白、磷酸葡萄糖变位酶-1(PGM-1)和酸性磷酸酶(AcP)分型。研究人群包括164名血压正常的白人、34名血压正常的黑人、161名白人及43名黑人原发性高血压患者,以及52名患有继发性高血压的白人(18名动脉粥样硬化性肾血管性高血压患者、17名纤维肌性疾病患者和17名原发性醛固酮增多症患者)。在任何比较中,ABO、Rh、基德、凯尔、达菲、P、触珠蛋白、PGM-1或AcP的表型频率均无显著差异。然而,在原发性高血压患者和动脉粥样硬化性肾血管性高血压患者与血压正常对照组的比较中,MNS表型的分布存在显著差异。原发性高血压患者中,白人的S基因频率较低,s频率较高(X2 = 12.21,p小于0.005)。动脉粥样硬化性肾血管性高血压患者在MN(X2 = 4.34,p小于0.05)和Ss(X2 = 4.21,p小于0.05)频率方面与血压正常人群不同。疾病与血型关联的发现支持了不同血型个体之间可能存在显著生理差异这一假说。