Background Peroxisome proliferator activated receptor gamma (PPARG) belongs to the nuclear receptor superfamily functioning as transcription factors to regulate cellular differentiation, development and metabolism. Moreover, it has been implicated in the
Maria García-Ricobaraza +8 more
doaj +1 more source
Association of the PPARγ2 Pro12Ala polymorphism with increased risk of cardiovascular diseases
This meta-analysis investigated the correlation between the PPARγ2 Pro12Ala polymorphism and cardiovascular disease (CVD). Electronic database and manual searches were conducted to retrieve studies published relevant to the PPARγ2 Pro12Ala polymorphism and CVD.
Y, Li, J, Zhu, J Q, Ding
openaire +2 more sources
The Peroxisome Poliferator–Activated Receptor-γ2 Pro12Ala Variant [PDF]
Recent studies have identified a common proline-to-alanine substitution (Pro12Ala) in the peroxisome proliferator–activated receptor-γ2 (PPAR-γ2), a nuclear receptor that regulates adipocyte differentiation and possibly insulin sensitivity. The Pro12Ala variant has been associated in some studies with diabetes-related traits and/or protection against ...
Julie A. Douglas +13 more
openaire +1 more source
The Frequency of Pro12Ala Genotypes of the PPARγ Gene in Diabetic and Non-Diabetic Patients with Polycystic Ovary Syndrome Referred to Imam Reza and Ghaem Hospitals, Mashhad, 2021 [PDF]
Introduction: The Pro12Ala polymorphism of the PPARγ gene affects insulin sensitivity, but its distribution in Iranian patients with polycystic ovary syndrome (PCOS) based on diabetic status has been less investigated.
Nafiseh Saghafi +2 more
doaj +1 more source
The Association of PPARγ Pro12Ala and C161T Polymorphisms with Polycystic Ovary Syndrome and Their Influence on Lipid and Lipoprotein Profiles [PDF]
Background The aim of present study was to clarify the role of the peroxisome proliferator-activated receptor (PPAR) γ Pro12Ala and C161T polymorphisms in the pathogenesis of polycystic ovary syndrome (PCOS) and their influence on lipid and ...
Zohreh Rahimi +5 more
doaj +1 more source
Abstract Obstructive sleep apnea is associated with an increased risk of hypertension, diabetes and dyslipidaemia. Both obstructive sleep apnea and its comorbidities are at least partly heritable, suggesting a common genetic background. Our aim was to analyse the heritability of the relationship between obstructive sleep apnea and its comorbidities ...
Martina Meszaros +10 more
wiley +1 more source
Does Pro12Ala Polymorphism Enhance the Physiological Role of PPARγ2?
Obesity and type 2 diabetes mellitus (T2D) are two major public health problems that have motivated the scientific community to investigate the high contribution of genetic factors to these disorders.
A. C. Pereira +3 more
doaj +1 more source
The PPARG Pro12Ala Polymorphism and 20-year Cognitive Decline [PDF]
Previous reports suggest race/ethnic and sex heterogeneity in the association between the Pro12Ala polymorphism of the peroxisome proliferator-activated receptor gamma (PPARG) gene and cognitive decline. Tests of verbal memory, processing speed, and verbal fluency and a composite global Z-score were used to assess cognitive performance longitudinally ...
Nancy A, West +5 more
openaire +2 more sources
Investigation of the association of Pro12Ala polymorphism in the PPARG gene with the occurence of obesity and metabolic syndrome in postmenopausal women [PDF]
Introduction: During menopause, the prevalence of metabolic disorders in women increases significantly. Postmenopausal women have increased waist circumference, high blood pressure, hypertriglyceridemia, hyperglycemia and low HDL cholesterol, which leads
Pucar Aleksandra +3 more
doaj +1 more source
Diabetic retinopathy (DR) is a condition that develops after long‐lasting and poorly handled diabetes and is presently the main reason for blindness among elderly and youth. Peroxisome proliferator‐activated receptors (PPARs) are nuclear receptors that are involved in carbohydrate and fatty‐acid metabolism and have also been associated with DR.
Špela Tajnšek +4 more
wiley +1 more source

