AI Article Synopsis

  • The study analyzed the T29C TGFβ1 gene polymorphism in 198 hypertensive patients with left ventricular hypertrophy (LVH) and 235 without it.
  • Hypertensives with the TC or CC genotypes showed significantly higher levels of microalbuminuria, TGFβ1, procollagen type III, and left ventricular mass compared to those with the TT genotype.
  • Findings suggest that the T29C TGFβ1 gene polymorphism may help identify hypertensive patients with LVH who have more severe hypertension.

Article Abstract

The distribution of the T29C TGFβ1 gene polymorphism was analyzed in 198 hypertensives with left ventricular hypertrophy (LVH) and in 235 hypertensives without LVH. Circulating TGFβ1 levels, procollagen type III levels, microalbuminuria, and left ventricular geometry and function were evaluated in all the hypertensives with LVH subgrouped according to T29C TGFβ1 gene polymorphism. Circulating TGFβ1 was evaluated by ELISA technique, procollagen type III by a specific radioimmunoassay, microalbuminuria by radioimmunoassay, and left ventricular geometry and function by echocardiography. All groups were comparable for gender, age, and sex. Regarding T29C TGFβ1 gene polymorphism, prevalence of TC or CC genotypes was significantly (P < .05) higher in hypertensives with LVH than hypertensives without LVH TC and CC LVH hypertensives were characterized by a higher prevalence of subjects with microalbuminuria (P < .05 TC and CC versus TT), by increased levels of TGFβ1, procollagen type III, urinary albumin excretion, LVM, LVM/h(2.7), and lower values of left ventricular ejection fraction (P < .05 TC and CC versus TT). Our data suggest that T29C TGFβ1 gene polymorphism was associated with clinical characteristics adequate to recognize a subset of LVH hypertensives with a higher severity of hypertension.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2958444PMC
http://dx.doi.org/10.4061/2010/647147DOI Listing

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