The CAG Repeat Polymorphism in the AR Gene Affects High Density Lipoprotein Cholesterol and Arterial Vasoreactivity
Genomic effects of T are exerted via the AR. The length of the polymorphic CAG repeat sequence in the AR gene is inversely correlated with the transcriptional regulation of target genes by T. In 110 healthy men (20–50 yr), we investigated the interactions among this polymorphism, serum levels of sex...
Gespeichert in:
Veröffentlicht in: | The journal of clinical endocrinology and metabolism 2001-10, Vol.86 (10), p.4867-4873 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Genomic effects of T are exerted via the AR. The length of the
polymorphic CAG repeat sequence in the AR gene is inversely correlated
with the transcriptional regulation of target genes by T. In 110
healthy men (20–50 yr), we investigated the interactions among this
polymorphism, serum levels of sex hormones, cardiovascular risk
factors, and flow-mediated and nitrate-induced vasodilatation of the
brachial artery. The number of CAG repeat had no significant
correlations with serum concentrations of total or free T. Stepwise
multiple regression analysis revealed positive correlations of the
number of CAG repeat with serum levels of high density lipoprotein
cholesterol (partial r = 0.44; P < 0.001) and
flow-mediated vasodilatation (partial r = 0.37;
P < 0.001). The association of CAG repeat with
high density lipoprotein (HDL) cholesterol was independent of body fat
content and serum levels of free T, which both had significant negative
correlations with HDL cholesterol. The association of CAG repeat with
flow-mediated vasodilatation was independent of cigarette smoking and
serum levels of free T and low density lipoprotein cholesterol, which
also were correlated with flow-mediated vasodilatation. We conclude
that a low number of CAG repeat in the AR gene implies a greater chance
for low levels of HDL cholesterol and reduced endothelial response to
ischemia, which are both important risk factors for coronary heart
disease. |
---|---|
ISSN: | 0021-972X 1945-7197 |
DOI: | 10.1210/jcem.86.10.7889 |