The effects of the Pro12Ala polymorphism of the peroxisome proliferator-activated receptor-?2 gene on insulin sensitivity and insulin metabolism interact with size at birth
The effects of the Pro12Ala polymorphism of the peroxisome proliferator-activated receptor-?2 gene on insulin sensitivity and insulin metabolism interact with size at birth
Type 2 diabetes is known to be associated with a small body size at birth. Body size at birth is an indicator of the intrauterine environment. There is also a well-established association between the peroxisome proliferator-activated receptor (PPAR)-?2 gene and type 2 diabetes. We therefore assessed whether the effects of the Pro12Ala polymorphism of the PPAR-?2 gene on insulin sensitivity and insulin concentrations in adult life are modified by size at birth. We found that the effects of the Pro12Pro and Pro12Ala polymorphisms of the PPAR-?2 gene in elderly people depended on their body size at birth. The well-known association between small body size at birth and insulin resistance was seen only in individuals with the high-risk Pro12Pro allele. In those who had low birth weight, the Pro12Pro polymorphism of the PPAR-?2 gene was associated with increased insulin resistance (P < 0.002) and elevated insulin concentrations (P < 0.003). These interactions between the effects of the Pro12Ala polymorphisms of the PPAR-?2 gene on adult traits and the effects of birth weight link two previously unknown associations together within the context of type 2 diabetes. We suggest that these findings reflect gene-environment interaction.
2321-2324
Eriksson, Johan G.
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Lindi, Virpi
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Uusitupa, Matti
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Forsen, Tom J.
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Laakso, Markku
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Osmond, Clive
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Barker, David J. P.
84efdf7a-7c52-45fc-aa16-9647f3743c27
2002
Eriksson, Johan G.
eb96b1c5-af07-4a52-8a73-7541451d32cd
Lindi, Virpi
3866552e-b953-47fe-9345-e3b88d5a290f
Uusitupa, Matti
7e87195e-7dfc-4887-91dc-146463d5f17e
Forsen, Tom J.
55342e20-c4a5-40e5-ad81-2a64c1e0f333
Laakso, Markku
081d2484-2485-4783-9d51-5fe0a8db6715
Osmond, Clive
2677bf85-494f-4a78-adf8-580e1b8acb81
Barker, David J. P.
84efdf7a-7c52-45fc-aa16-9647f3743c27
Eriksson, Johan G., Lindi, Virpi, Uusitupa, Matti, Forsen, Tom J., Laakso, Markku, Osmond, Clive and Barker, David J. P.
(2002)
The effects of the Pro12Ala polymorphism of the peroxisome proliferator-activated receptor-?2 gene on insulin sensitivity and insulin metabolism interact with size at birth.
Diabetes, 51 (7), .
Abstract
Type 2 diabetes is known to be associated with a small body size at birth. Body size at birth is an indicator of the intrauterine environment. There is also a well-established association between the peroxisome proliferator-activated receptor (PPAR)-?2 gene and type 2 diabetes. We therefore assessed whether the effects of the Pro12Ala polymorphism of the PPAR-?2 gene on insulin sensitivity and insulin concentrations in adult life are modified by size at birth. We found that the effects of the Pro12Pro and Pro12Ala polymorphisms of the PPAR-?2 gene in elderly people depended on their body size at birth. The well-known association between small body size at birth and insulin resistance was seen only in individuals with the high-risk Pro12Pro allele. In those who had low birth weight, the Pro12Pro polymorphism of the PPAR-?2 gene was associated with increased insulin resistance (P < 0.002) and elevated insulin concentrations (P < 0.003). These interactions between the effects of the Pro12Ala polymorphisms of the PPAR-?2 gene on adult traits and the effects of birth weight link two previously unknown associations together within the context of type 2 diabetes. We suggest that these findings reflect gene-environment interaction.
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Published date: 2002
Additional Information:
Brief Genetics Report
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Local EPrints ID: 25469
URI: http://eprints.soton.ac.uk/id/eprint/25469
ISSN: 0012-1797
PURE UUID: 659abb2e-0556-442e-84fb-2d3ee66f1960
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Date deposited: 12 Apr 2006
Last modified: 23 Jul 2022 01:39
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Author:
Johan G. Eriksson
Author:
Virpi Lindi
Author:
Matti Uusitupa
Author:
Tom J. Forsen
Author:
Markku Laakso
Author:
David J. P. Barker
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