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The fat mass and obesity-associated (FTO) gene variant rs9939609 predicts long-term incidence of cardiovascular disease and related death independent of the traditional risk factors.

Identifieur interne : 000052 ( PubMed/Checkpoint ); précédent : 000051; suivant : 000053

The fat mass and obesity-associated (FTO) gene variant rs9939609 predicts long-term incidence of cardiovascular disease and related death independent of the traditional risk factors.

Auteurs : Meiju Ij L [Finlande] ; Justiina Ronkainen [Finlande] ; Tuija Huusko [Finlande] ; Elina Malo [Finlande] ; Eeva-Riitta Savolainen [Finlande] ; Markku J. Savolainen [Finlande] ; Tuire Salonurmi [Finlande] ; Risto Bloigu [Finlande] ; Y Antero Kes Niemi [Finlande] ; Olavi Ukkola [Finlande]

Source :

RBID : pubmed:26555680

Abstract

The impact of the rs9939609 FTO variant on cardiovascular events was investigated in the 19-year follow-up of subjects recruited to the OPERA study.

DOI: 10.3109/07853890.2015.1091088
PubMed: 26555680


Affiliations:


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pubmed:26555680

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<div type="abstract" xml:lang="en">The impact of the rs9939609 FTO variant on cardiovascular events was investigated in the 19-year follow-up of subjects recruited to the OPERA study.</div>
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<ArticleTitle>The fat mass and obesity-associated (FTO) gene variant rs9939609 predicts long-term incidence of cardiovascular disease and related death independent of the traditional risk factors.</ArticleTitle>
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<AbstractText Label="OBJECTIVE AND METHODS" NlmCategory="OBJECTIVE">The impact of the rs9939609 FTO variant on cardiovascular events was investigated in the 19-year follow-up of subjects recruited to the OPERA study.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">A total of 212 cardiovascular disease (CVD) and 152 coronary heart disease (CHD) events or deaths occurred during follow-up. The logistic regression analysis revealed that among the AA genotype the incidence of CHD (OR 1.905; 95% CI 1.250-2.903, p = 0.001) and CVD (OR 1.849; 1.265-2.702, p = 0.003) events or death was significantly higher when adjusted for age, sex, and study group. After further adjustment with BMI, smoking status, systolic blood pressure, and low-density lipoprotein cholesterol, the higher incidence of CHD and CVD events or death among subjects with the AA genotype remained significant (OR 1.895; p = 0.002 and p = 0.004, respectively). In Cox regression analysis, the AA genotype displayed a higher rate of CVD and CHD death when the model was adjusted for sex, age, and study group (p = 0.006 and p = 0.046). FTO rs9939609 AA genotype improved the C-index of the final predictive model from 0.709 to 0.715. In reclassification analyses, the integrated discrimination index was significant 0.011 (p = 0.010).</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">The AA genotype of FTO rs9939609 seems to be associated with a higher risk of CVD, and this phenomenon seems to be independent of the traditional risk factors for atherosclerosis.</AbstractText>
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HfdIndexSelect -h $EXPLOR_AREA/Data/PubMed/Checkpoint/RBID.i   -Sk "pubmed:26555680" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/PubMed/Checkpoint/biblio.hfd   \
       | NlmPubMed2Wicri -a OperaV1 

Wicri

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Data generation: Thu Apr 14 14:59:05 2016. Site generation: Thu Oct 8 06:48:41 2020