Key result
TGF-beta-1 polymorphisms were not associated with microalbuminuria, whereas the ACE D/D genotype was associated with a higher frequency of microalbuminuria in essential hypertensive men.
Why the study?
Is there an association between TGF-beta-1 polymorphic variants and microalbuminuria in never-treated, uncomplicated essential hypertensive men?
Cross-Sectional (n=222)
Is there an association between TGF-beta-1 polymorphic variants and microalbuminuria in never-treated, uncomplicated essential hypertensive men?
TGF-beta-1 polymorphisms are not associated with microalbuminuria in uncomplicated essential hypertensive men, unlike the ACE D/I polymorphism.
TGF-β1 variants may associate with microalbuminuria in hypertension; hypothesis-generating, needs replication before clinical consideration.
BACKGROUND: Polymorphisms within the gene for transforming growth factor (TGF)-beta-1, a pro-fibrogenic cytokine pathophysiologically involved in hypertension and hypertensive target damage, might modulate the biological activity of the encoded protein. Through that mechanism, they might contribute to microalbuminuria, a marker of subclinical renal damage and a correlate of systemic inflammation and endothelial dysfunction in hypertension, a possibility never before tested. For this reason, we assessed the association of four TGF-beta-1 polymorphic variants (C-509T, Leu(10)-->Pro, Arg(25)-->Pro, Thr(263)-->Ile) with albuminuria in uncomplicated essential hypertensive men, using (circulating active + acid-activatable latent) TGF-beta-1 levels as an indirect index of their in vivo biological activity. Because of the close pathophysiological link of TGF-beta-1 with the renin-angiotensin system, we also tested the behaviour of the angiotensin converting enzyme (ACE) deletion/insertion (D/I) polymorphism. METHODS: Albuminuria (three overnight collections), office and 24-h BP, left ventricular mass index (LVMI), BMI, renal function, glucose, lipids, plasma TGF-beta-1 (n = 162, ELISA) were measured in 222 genetically unrelated, never-treated, uncomplicated Caucasian hypertensive men. ACE D/I polymorphisms were analysed by the polymerase chain reaction technique or a 5' nuclease assay with further restriction analysis when required. RESULTS: Urine albumin levels or microalbuminuria (albuminuria > or =15 microg/min) did not differ by TGF-beta-1 genotypes, but both parameters were more frequent in ACE D/D homozygotes. Plasma TGF-beta-1 was similar across genetic backgrounds and was unrelated to albuminuria. Cardiovascular, renal, metabolic parameters were homogeneously distributed across genotypes. CONCLUSIONS: In contrast to its link with the ACE D/I genotype, microalbuminuria was independent of TGF-beta-1 polymorphism in this group of never-treated, uncomplicated essential hypertensive men.
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Dell'Omo et al. (2009) conducted a cross-sectional in Essential hypertension (n=222). TGF-beta-1 and ACE D/I polymorphisms vs. Different genotypes was evaluated on Albuminuria or microalbuminuria. TGF-beta-1 polymorphisms were not associated with microalbuminuria, whereas the ACE D/D genotype was associated with a higher frequency of microalbuminuria in essential hypertensive men.
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