PMID- 8901839 OWN - NLM STAT- MEDLINE DCOM- 19961206 LR - 20220419 IS - 0194-911X (Print) IS - 0194-911X (Linking) VI - 28 IP - 5 DP - 1996 Nov TI - Polymorphisms of the transforming growth factor-beta 1 gene in relation to myocardial infarction and blood pressure. The Etude Cas-Temoin de l'Infarctus du Myocarde (ECTIM) Study. PG - 881-7 AB - Transforming growth factor-beta 1 (TGF-beta 1) plays an important role in the modulation of cellular growth and differentiation and the production and degradation of the extracellular matrix. A number of experimental results suggest that TGF-beta 1 may be involved in cardiovascular physiopathology. In the present study, we assessed whether the TGF-beta 1 gene is a candidate gene for coronary heart disease or hypertension. We screened the coding region and 2181 bp upstream of the TGF-beta gene for polymorphisms and identified seven polymorphisms: 3 in the upstream region of the gene at positions -988, -800, and -509 from the first transcribed nucleotide; 1 in a nontranslated region at position +72; 2 in the signal peptide sequence Leu10-->Pro, Arg25-->Pro; and 1 in the region of the gene coding for the precursor part of the protein not present in the active form, Thr263-->Ile. We analyzed these TGF-beta 1 polymorphisms in 563 patients with myocardial infarction and 629 control subjects from four regions in Northern Ireland and France. The Pro25 allele was more frequent in patients than in control subjects in Belfast (P < .01) and Strasbourg (P < .05). The TGF-beta 1 polymorphisms were not associated with the degree of angiographically assessed coronary artery disease in patients. The presence of a Pro25 allele was associated with a lower systolic pressure in the four control groups (P < .002), and a history of hypertension was significantly less frequent in homozygotes or heterozygotes for Pro25 than in hormozygotes for Arg25 (odds ratio, 0.43, 95% confidence interval, 0.19 to 0.92; P < .03). Since the Pro25 allele was associated with an increased risk of myocardial infarction and a reduced risk of hypertension, we favor a cautious interpretation of these apparently inconsistent results. Other studies will need to verify whether these associations are real. FAU - Cambien, F AU - Cambien F AD - INSERM SC7, Paris, France. cambien@infobiogen.fr FAU - Ricard, S AU - Ricard S FAU - Troesch, A AU - Troesch A FAU - Mallet, C AU - Mallet C FAU - Generenaz, L AU - Generenaz L FAU - Evans, A AU - Evans A FAU - Arveiler, D AU - Arveiler D FAU - Luc, G AU - Luc G FAU - Ruidavets, J B AU - Ruidavets JB FAU - Poirier, O AU - Poirier O LA - eng PT - Clinical Trial PT - Controlled Clinical Trial PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - Hypertension JT - Hypertension (Dallas, Tex. : 1979) JID - 7906255 RN - 0 (Transforming Growth Factor beta) SB - IM CIN - Hypertension. 1996 Nov;28(5):880. PMID: 8901838 MH - Adult MH - Alleles MH - Blood Pressure/genetics MH - Genotype MH - Humans MH - Hypertension/*genetics MH - Male MH - Middle Aged MH - Myocardial Infarction/*genetics MH - Polymorphism, Genetic MH - Transforming Growth Factor beta/*genetics EDAT- 1996/11/01 00:00 MHDA- 1996/11/01 00:01 CRDT- 1996/11/01 00:00 PHST- 1996/11/01 00:00 [pubmed] PHST- 1996/11/01 00:01 [medline] PHST- 1996/11/01 00:00 [entrez] AID - 10.1161/01.hyp.28.5.881 [doi] PST - ppublish SO - Hypertension. 1996 Nov;28(5):881-7. doi: 10.1161/01.hyp.28.5.881.