J. Delanghe et al., MN BLOOD-GROUP, A GENETIC-MARKER FOR ESSENTIAL ARTERIAL-HYPERTENSION IN YOUNG-ADULTS, European heart journal, 16(9), 1995, pp. 1269-1276
The MN blood group has been linked with blood pressure levels and sodi
um-lithium counter-transport in red blood cells of normotensives. The
aim of the study was to compared the distribution of MN phenotypes acc
ording to age at diagnosis of essential hypertension and to investigat
e the relationship between MN phenotypes, severity of complications an
d therapeutic needs. MN blood group polymorphism was studied in 386 Ca
ucasians with established essential arterial hypertension, treated for
at least one year. In 285 healthy normotensive blood donors, blood pr
essure was measured and MN blood group was typed. MN blood group were
typed with polyclonal antisera and confirmed with monoclonal antisera.
MN blood group phenotype frequencies in hypertensives were 0.207 (MM)
, 0.601 (MN), and 0.192 (NN), which differs (P<0.000002) from the dist
ribution in the controls: 0.270 (MM), 0.540 (MN) and 0.189 (NN). The r
elative MN phenotype frequency was strongly over-represented (P<0.05).
Age at detection of hypertension was significantly lower for MN patie
nts (P<0.0005). With increasing age of detection, the relative frequen
cy of MN phenotype gradually decreases from 0.73 in those detected bef
ore age 40 to 0.50 for patients detected after age 60. This observatio
n holds true for both male and female hypertensives. Furthermore, hype
rtensives with an MM blood group had a lower (P<0.05) prevalence of ce
rebrovascular accidents. In controls, blood pressure was comparable fo
r the three MN phenotypes. The present study suggests that the MN phen
otype is a genetic factor associated with early detection of essential
hypertension.