2001
DOI: 10.1007/s001250100647
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Mutations of the peroxisome proliferator-activated receptor γ (PPARγ) gene in a Japanese population : the Pro12Ala mutation in PPARγ2 is associated with lower concentrations of serum total and non-HDL cholesterol

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Cited by 15 publications
(13 citation statements)
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“…The most important findings were that Pro12Ala polymorphism in its homozygous and heterozygous forms may itself increase the area of sdLDL4-7 independent of potential confounding factors such as age, sex, BMI, habitual exercise, alcohol intake, and lipid concentration. The present finding that subjects with the X/Ala genotype had a lipid atherogenic profile is consistent with some previous results [8,9] but not all [3][4][5][6]. It has been proposed that the PPARγ2 gene is one of the mediators of gene-environmental interactions.…”
Section: Discussionsupporting
confidence: 95%
See 1 more Smart Citation
“…The most important findings were that Pro12Ala polymorphism in its homozygous and heterozygous forms may itself increase the area of sdLDL4-7 independent of potential confounding factors such as age, sex, BMI, habitual exercise, alcohol intake, and lipid concentration. The present finding that subjects with the X/Ala genotype had a lipid atherogenic profile is consistent with some previous results [8,9] but not all [3][4][5][6]. It has been proposed that the PPARγ2 gene is one of the mediators of gene-environmental interactions.…”
Section: Discussionsupporting
confidence: 95%
“…However, studies on the association between the Pro12Ala polymorphism and lipid profiles have been controversial. Several studies have shown the effect of Pro12Ala polymorphism on lower lipid and lipoprotein levels [3][4][5][6], but others have yielded inconsistent results [7][8][9].…”
Section: Introductionmentioning
confidence: 99%
“…The results displayed that the sensitivity decreased to 63.9% and the 1-specificity increased from 16.3% to 23.9% (data not shown). Accordingly, PPARg gene owns potential capacity for the predisposition to hyperuricemia due to its association with xanthine oxidase/reductase activity (Cheung et al, 2007), obesity (Chen et al, 2009a), glucose (Ylonen et al, 2008;Ruchat et al, 2010), blood pressure (Halabi et al, 2008), and lipid (Iwata et al, 2001;Ylonen et al, 2008;Johansson et al, 2009) homeostasis. We supposed that PPARg gene may play a foundational role in hyperuricemia etiology rather than metabolic abnormality, dietary protein intake, and obesity, which were downstream of the physiological pathway regulated by PPARg gene.…”
Section: Lee Et Al Discussionmentioning
confidence: 99%
“…The PPARg gene is associated with xanthine oxidase/ reductase activity (Cheung et al, 2007), glucose (Ylonen et al, 2008;Ruchat et al, 2010), blood pressure (Halabi et al, 2008), and lipid metabolism (Iwata et al, 2001;Ylonen et al, 2008;Johansson et al, 2009). We also have previously reported that polymorphisms of the PPARg gene were strongly associated with obesity in Han Chinese (Chen et al, 2009a).…”
Section: Introductionmentioning
confidence: 89%
“…Ala12 allele is inversely associated with blood TAG concentrations in one report [54] while it has also been found to be associated with a trend of an increase in TAG and hyperlipidemia in another [152]. This variant has also been shown to be associated with lower levels of serum total and nonhigh-density lipoprotein (non-HDL)-cholesterol in a general population [153], lower low-density lipoprotein (LDL)-cholesterol in T2D patients [154], or higher levels of serum HDL-cholesterol in family-based or population-based studies [155, 156]. however, several studies also show an association of Ala12 allele with higher concentration of low-density lipoprotein (LDL)-cholesterol [68, 157] and lower HDL-cholesterol [70].…”
Section: Effect On Other Components Of Metabolic Syndromementioning
confidence: 99%