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Exposure to the Chinese Famine in Early Life and the Risk of Metabolic Syndrome in Adulthood

OBJECTIVE: To examine whether exposure to the Chinese famine during fetal life and early childhood is associated with the risks of metabolic syndrome and whether this association is modified by later life environment. RESEARCH DESIGN AND METHODS: We used data of 7,874 adults born between 1954 and 19...

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Autores principales: Li, Yanping, Jaddoe, Vincent W., Qi, Lu, He, Yuna, Wang, Dong, Lai, Jianqiang, Zhang, Jian, Fu, Ping, Yang, Xiaoguang, Hu, Frank B.
Formato: Texto
Lenguaje:English
Publicado: American Diabetes Association 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3064015/
https://www.ncbi.nlm.nih.gov/pubmed/21310886
http://dx.doi.org/10.2337/dc10-2039
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author Li, Yanping
Jaddoe, Vincent W.
Qi, Lu
He, Yuna
Wang, Dong
Lai, Jianqiang
Zhang, Jian
Fu, Ping
Yang, Xiaoguang
Hu, Frank B.
author_facet Li, Yanping
Jaddoe, Vincent W.
Qi, Lu
He, Yuna
Wang, Dong
Lai, Jianqiang
Zhang, Jian
Fu, Ping
Yang, Xiaoguang
Hu, Frank B.
author_sort Li, Yanping
collection PubMed
description OBJECTIVE: To examine whether exposure to the Chinese famine during fetal life and early childhood is associated with the risks of metabolic syndrome and whether this association is modified by later life environment. RESEARCH DESIGN AND METHODS: We used data of 7,874 adults born between 1954 and 1964 from the 2002 China National Nutrition and Health Survey. Famine exposure groups were defined as nonexposed; fetal exposed; and early childhood, midchildhood, or late childhood exposed. Excess death rate was used to determine the severity of the famine. The ATP III criteria were used for the definition of metabolic syndrome (three or more of the following variables: elevated fasting triglyceride levels, lower HDL cholesterol levels, elevated fasting glucose levels, higher waist circumference, high blood pressure). RESULTS: In severely affected famine areas, adults who were exposed to the famine during fetal life had a higher risk of metabolic syndrome, as compared with nonexposed subjects (odds ratio 3.13 [95% CI 1.24–7.89, P = 0.016]). Similar associations were observed among adults who were exposed to the famine during early childhood, but not for adults exposed to the famine during mid- or late childhood. Participants who were born in severely affected famine areas and had Western dietary habits in adulthood or were overweight in adulthood had a particularly high risk of metabolic syndrome in later life. CONCLUSIONS: Exposure to the Chinese famine during fetal life or infancy is associated with an increased risk of metabolic syndrome in adulthood. These associations are stronger among subjects with a Western dietary pattern or who were overweight in adulthood.
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spelling pubmed-30640152012-04-01 Exposure to the Chinese Famine in Early Life and the Risk of Metabolic Syndrome in Adulthood Li, Yanping Jaddoe, Vincent W. Qi, Lu He, Yuna Wang, Dong Lai, Jianqiang Zhang, Jian Fu, Ping Yang, Xiaoguang Hu, Frank B. Diabetes Care Original Research OBJECTIVE: To examine whether exposure to the Chinese famine during fetal life and early childhood is associated with the risks of metabolic syndrome and whether this association is modified by later life environment. RESEARCH DESIGN AND METHODS: We used data of 7,874 adults born between 1954 and 1964 from the 2002 China National Nutrition and Health Survey. Famine exposure groups were defined as nonexposed; fetal exposed; and early childhood, midchildhood, or late childhood exposed. Excess death rate was used to determine the severity of the famine. The ATP III criteria were used for the definition of metabolic syndrome (three or more of the following variables: elevated fasting triglyceride levels, lower HDL cholesterol levels, elevated fasting glucose levels, higher waist circumference, high blood pressure). RESULTS: In severely affected famine areas, adults who were exposed to the famine during fetal life had a higher risk of metabolic syndrome, as compared with nonexposed subjects (odds ratio 3.13 [95% CI 1.24–7.89, P = 0.016]). Similar associations were observed among adults who were exposed to the famine during early childhood, but not for adults exposed to the famine during mid- or late childhood. Participants who were born in severely affected famine areas and had Western dietary habits in adulthood or were overweight in adulthood had a particularly high risk of metabolic syndrome in later life. CONCLUSIONS: Exposure to the Chinese famine during fetal life or infancy is associated with an increased risk of metabolic syndrome in adulthood. These associations are stronger among subjects with a Western dietary pattern or who were overweight in adulthood. American Diabetes Association 2011-04 2011-03-21 /pmc/articles/PMC3064015/ /pubmed/21310886 http://dx.doi.org/10.2337/dc10-2039 Text en © 2011 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.
spellingShingle Original Research
Li, Yanping
Jaddoe, Vincent W.
Qi, Lu
He, Yuna
Wang, Dong
Lai, Jianqiang
Zhang, Jian
Fu, Ping
Yang, Xiaoguang
Hu, Frank B.
Exposure to the Chinese Famine in Early Life and the Risk of Metabolic Syndrome in Adulthood
title Exposure to the Chinese Famine in Early Life and the Risk of Metabolic Syndrome in Adulthood
title_full Exposure to the Chinese Famine in Early Life and the Risk of Metabolic Syndrome in Adulthood
title_fullStr Exposure to the Chinese Famine in Early Life and the Risk of Metabolic Syndrome in Adulthood
title_full_unstemmed Exposure to the Chinese Famine in Early Life and the Risk of Metabolic Syndrome in Adulthood
title_short Exposure to the Chinese Famine in Early Life and the Risk of Metabolic Syndrome in Adulthood
title_sort exposure to the chinese famine in early life and the risk of metabolic syndrome in adulthood
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3064015/
https://www.ncbi.nlm.nih.gov/pubmed/21310886
http://dx.doi.org/10.2337/dc10-2039
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