3.8 Article

Pro12Ala Polymorphism of the PPARγ2 Gene Interacts With a Mediterranean Diet to Prevent Telomere Shortening in the PREDIMED-NAVARRA Randomized Trial

Journal

CIRCULATION-CARDIOVASCULAR GENETICS
Volume 8, Issue 1, Pages 91-U171

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/CIRCGENETICS.114.000635

Keywords

diet; genetic polymorphism; nutrigenomics; telomere

Funding

  1. Linea Especial, Nutricion, Obesidad y Salud of the University of Navarra [LE/97]
  2. Spanish Government [FIS-ISCIII: PI051579, PI050976, PI070240, PI081943, PI1002293, PI13/01090]
  3. Spanish Government, Instituto de Salud Carlos III [RTIC RD 06/0045]
  4. CIBER Fisiopatologia de la Obesidad y Nutricion [CNIC/06, SAF-2010-20367]
  5. Government of Navarra [PI41/2005, PI79/2006, PI36/2008, PI54/2009]
  6. FPU fellowship from the Spanish Ministry

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Background-The gene variant Pro/Ala (rs1801282) in the PPAR gamma 2 has been associated with lower cardiovascular risk and greater benefit from lifestyle interventions. This polymorphism also seems to be associated with longer lifespan, but no information on telomere length (TL) is available. Our aim was to study the association between the Ala allele and changes in TL in high cardiovascular risk subjects and the potential interaction with a Mediterranean dietary pattern. Methods and Results-A total of 521 subjects (55-80 years) participating in the Prevencion con Dieta Mediterranea randomized trial were genotyped. Changes in TL, measured by quantitative real-time polymerase chain reaction (PCR), were assessed over 5 years of a nutritional intervention, which promoted adherence to the Mediterranean diet (MeDiet). Interestingly, Ala carriers showed lower telomere shortening after 5 years compared with the Pro/Pro genotype (P=0.031). This association was modulated by MeDiet because those Ala carriers who reported better conformity to the MeDiet exhibited increased TL (P<0.001). Moreover, a reduction in carbohydrate intake (<= 9.5 g/d) resulted in increased TL among Ala carriers. Notably, an apparent gene-diet interaction was found through the observed changes in the MUFA+PUFA/carbohydrates ratio: as this ratio increased, TL lengthening was detected to a greater extent in the Ala carriers compared with the Pro/Pro subjects (P for interaction <0.001). Conclusions-The Pro12Ala polymorphism is associated with TL homeostasis after 5 years follow-up in subjects at high cardiovascular risk. In addition, a higher adherence to the MeDiet pattern strengthens the prevention of telomere shortening among Ala carriers.

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