2008
DOI: 10.1016/j.ymgme.2008.06.011
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LPIN1 genetic variation is associated with rosiglitazone response in type 2 diabetic patients

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Cited by 28 publications
(15 citation statements)
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“…It is significant that LPIN1 genotype is associated with several individual features of the metabolic syndrome, as well as with an overall "metabolic syndrome factor score" (61), and may reflect the roles that lipin-1 has in several tissues that influence metabolic homeostasis. Furthermore, a specific LPIN1 polymorphism is associated with the response of type 2 diabetics to thiazolidinedione treatment (63).…”
Section: Genetic Variation In Lipin Genes and Human Diseasementioning
confidence: 99%
“…It is significant that LPIN1 genotype is associated with several individual features of the metabolic syndrome, as well as with an overall "metabolic syndrome factor score" (61), and may reflect the roles that lipin-1 has in several tissues that influence metabolic homeostasis. Furthermore, a specific LPIN1 polymorphism is associated with the response of type 2 diabetics to thiazolidinedione treatment (63).…”
Section: Genetic Variation In Lipin Genes and Human Diseasementioning
confidence: 99%
“…Among these are insulin and/or glucose levels (17,34,35), resting metabolic rate (34), and systolic blood pressure (36,37). LPIN1 polymorphisms that are associated with response of type 2 diabetic patients to rosiglitazone have also been reported (36).…”
Section: Lipin-1 Gene Mutations and Polymorphisms Associated With Dismentioning
confidence: 99%
“…Among these are insulin and/or glucose levels (17,34,35), resting metabolic rate (34), and systolic blood pressure (36,37). LPIN1 polymorphisms that are associated with response of type 2 diabetic patients to rosiglitazone have also been reported (36). One particularly notable LPIN1 polymorphism causes an amino acid substitution within the C-LIP domain and is associated with statin-induced myopathy (33), an unfortunate side effect experienced by some of individuals who take statin drugs to treat hypercholesterolemia [reviewed in (38)].…”
Section: Lipin-1 Gene Mutations and Polymorphisms Associated With Dismentioning
confidence: 99%
“…188 In humans, overexpression of PLIN 2 decreases gene expression of several PPARa target genes and facilitates intramyocellular lipid. 148 In pigs, PLIN2 gene expression was associated with IM deposition.…”
mentioning
confidence: 99%