Association between early life famine exposure and risk of metabolic syndrome in later life

Background Previous studies reported that famine exposure had an effect on metabolic syndrome (MetS). However, there is an inadequacy of study regarding the association between famine exposure, adulthood general obesity, and the risk of MetS. Methods A total of 8883 subjects aged ≥40 years from Jiad...

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Published inJournal of diabetes Vol. 14; no. 10; pp. 685 - 694
Main Authors Zhang, Yi, Qi, Hongyan, Hu, Chunyan, Wang, Shuangyuan, Zhu, Yuanyue, Lin, Hong, Lin, Lin, Zhang, Jie, Wang, Tiange, Zhao, Zhiyun, Li, Mian, Xu, Yu, Xu, Min, Bi, Yufang, Wang, Weiqing, Chen, Yuhong, Lu, Jieli, Ning, Guang
Format Journal Article
LanguageEnglish
Published Melbourne Wiley Publishing Asia Pty Ltd 01.10.2022
John Wiley & Sons, Inc
Subjects
Online AccessGet full text
ISSN1753-0393
1753-0407
1753-0407
DOI10.1111/1753-0407.13319

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Abstract Background Previous studies reported that famine exposure had an effect on metabolic syndrome (MetS). However, there is an inadequacy of study regarding the association between famine exposure, adulthood general obesity, and the risk of MetS. Methods A total of 8883 subjects aged ≥40 years from Jiading community in Shanghai were included. We defined famine exposure subgroups as nonexposed (1963–1974), fetal exposed (1959–1962), childhood exposed (1949–1958), and adolescence exposed (1941–1948). MetS was defined based on the National Cholesterol Education Program Adult Treatment Panel III (NCEP‐ATP III) criteria. Results Compared with the nonexposed group, the risks of MetS were increased in the fetal‐, childhood‐, and adolescence‐exposed groups with odds ratios (OR) and 95% confidence intervals (CI) of 1.48 (1.23–1.78), 1.89 (1.63–2.20), and 2.34 (1.99–2.74), respectively. After adjusting for sex, age, smoking status, drinking status, education, body mass index (BMI), and physical activity, the increased risk of MetS related to the fetal‐exposed and childhood‐exposed groups with OR and 95% CI of 1.42 (1.04–1.94) and 1.50 (1.02–2.21), respectively, were observed only in women. Famine exposure was significantly associated with MetS among individuals with a BMI < 23 kg/m2 (p for interaction between BMI categories and famine exposure = 0.0002 in the whole cohort), while there existed a gender difference (p = 0.0023 in females, p = 0.4484 in males). When evaluating the joint effects of the combination of famine exposure in early life and general obesity in adulthood on MetS, we observed the highest estimate in participants with both adulthood general obesity and fetal famine exposure (OR 17.52; 95% CI, 10.07–30.48) compared with those without famine exposure nor adulthood obesity. Conclusions Obesity in adulthood significantly further aggravated the risk of MetS in individuals who experienced early life undernutrition, especially in females. 摘要 背景 以前的研究报道了饥荒暴露对代谢综合征(MetS)有影响。然而, 关于饥荒暴露、成年期肥胖和 MetS 风险之间的关系则较少研究。 方法 纳入上海市嘉定社区年龄 >40岁的8883名受试者。我们将饥荒暴露亚组定义为未暴露(1963‐1974)、胎儿暴露(1959‐1962)、儿童暴露(1949‐1958)和青春期暴露(1941‐1948)。 MetS根据 NCEP‐ATP III标准定义。 结果 与未暴露组相比, 胎儿、儿童和青春期暴露组的 MetS 风险增加, OR 和 95% CI 分别为 1.48 (1.23‐1.78)、1.89 (1.632.20) 和 2.34 (1.99‐ 2.74)。在校正性别、年龄、吸烟状况、饮酒状况、教育程度、体重指数(BMI)和体力活动后, 女性中观察到胎儿暴露组和儿童暴露组发生 MetS 的风险增加, OR 和 95%CI 分别为 1.42( 1.04‐1.94) 和 1.50 (1.02‐2.21)。在 BMI<23 kg/m2 的个体中, 饥荒暴露与 MetS 显着相关(整个队列中 BMI 类别与饥荒暴露之间的交互作用 P = 0.0002), 但存在性别差异(女性 P=0.0023, 男性P=0.4484)。在评估生命早期饥荒暴露和成年期肥胖对 MetS 的联合影响时, 我们观察到与没有饥荒暴露或成年肥胖的人相比, 成年肥胖和胎儿饥荒暴露的参与者有最高估计值(OR, 95%CI:17.52, 10.07‐ 30.48)。 结论 成年期肥胖显著加剧了早年营养不良个体(尤其是女性)发生 MetS 的风险。 Highlights In a community‐dwelling Chinese population, famine exposure in early life, especially during the fetal and childhood stages, has an association with an increased risk of metabolic syndrome (MetS) in later life, but the above findings only applied to females, not males. Compared to nonexposed and nonobese participants, those with both fetal famine exposure and adulthood general obesity had a higher risk of MetS of more than 17‐folds. The coexistence of malnutrition in early life and adulthood overweight/obesity had an association with a higher risk of MetS.
AbstractList BackgroundPrevious studies reported that famine exposure had an effect on metabolic syndrome (MetS). However, there is an inadequacy of study regarding the association between famine exposure, adulthood general obesity, and the risk of MetS.MethodsA total of 8883 subjects aged ≥40 years from Jiading community in Shanghai were included. We defined famine exposure subgroups as nonexposed (1963–1974), fetal exposed (1959–1962), childhood exposed (1949–1958), and adolescence exposed (1941–1948). MetS was defined based on the National Cholesterol Education Program Adult Treatment Panel III (NCEP‐ATP III) criteria.ResultsCompared with the nonexposed group, the risks of MetS were increased in the fetal‐, childhood‐, and adolescence‐exposed groups with odds ratios (OR) and 95% confidence intervals (CI) of 1.48 (1.23–1.78), 1.89 (1.63–2.20), and 2.34 (1.99–2.74), respectively. After adjusting for sex, age, smoking status, drinking status, education, body mass index (BMI), and physical activity, the increased risk of MetS related to the fetal‐exposed and childhood‐exposed groups with OR and 95% CI of 1.42 (1.04–1.94) and 1.50 (1.02–2.21), respectively, were observed only in women. Famine exposure was significantly associated with MetS among individuals with a BMI < 23 kg/m2 (p for interaction between BMI categories and famine exposure = 0.0002 in the whole cohort), while there existed a gender difference (p = 0.0023 in females, p = 0.4484 in males). When evaluating the joint effects of the combination of famine exposure in early life and general obesity in adulthood on MetS, we observed the highest estimate in participants with both adulthood general obesity and fetal famine exposure (OR 17.52; 95% CI, 10.07–30.48) compared with those without famine exposure nor adulthood obesity.ConclusionsObesity in adulthood significantly further aggravated the risk of MetS in individuals who experienced early life undernutrition, especially in females.
Background Previous studies reported that famine exposure had an effect on metabolic syndrome (MetS). However, there is an inadequacy of study regarding the association between famine exposure, adulthood general obesity, and the risk of MetS. Methods A total of 8883 subjects aged ≥40 years from Jiading community in Shanghai were included. We defined famine exposure subgroups as nonexposed (1963–1974), fetal exposed (1959–1962), childhood exposed (1949–1958), and adolescence exposed (1941–1948). MetS was defined based on the National Cholesterol Education Program Adult Treatment Panel III (NCEP‐ATP III) criteria. Results Compared with the nonexposed group, the risks of MetS were increased in the fetal‐, childhood‐, and adolescence‐exposed groups with odds ratios (OR) and 95% confidence intervals (CI) of 1.48 (1.23–1.78), 1.89 (1.63–2.20), and 2.34 (1.99–2.74), respectively. After adjusting for sex, age, smoking status, drinking status, education, body mass index (BMI), and physical activity, the increased risk of MetS related to the fetal‐exposed and childhood‐exposed groups with OR and 95% CI of 1.42 (1.04–1.94) and 1.50 (1.02–2.21), respectively, were observed only in women. Famine exposure was significantly associated with MetS among individuals with a BMI < 23 kg/m2 (p for interaction between BMI categories and famine exposure = 0.0002 in the whole cohort), while there existed a gender difference (p = 0.0023 in females, p = 0.4484 in males). When evaluating the joint effects of the combination of famine exposure in early life and general obesity in adulthood on MetS, we observed the highest estimate in participants with both adulthood general obesity and fetal famine exposure (OR 17.52; 95% CI, 10.07–30.48) compared with those without famine exposure nor adulthood obesity. Conclusions Obesity in adulthood significantly further aggravated the risk of MetS in individuals who experienced early life undernutrition, especially in females. 摘要 背景 以前的研究报道了饥荒暴露对代谢综合征(MetS)有影响。然而, 关于饥荒暴露、成年期肥胖和 MetS 风险之间的关系则较少研究。 方法 纳入上海市嘉定社区年龄 >40岁的8883名受试者。我们将饥荒暴露亚组定义为未暴露(1963‐1974)、胎儿暴露(1959‐1962)、儿童暴露(1949‐1958)和青春期暴露(1941‐1948)。 MetS根据 NCEP‐ATP III标准定义。 结果 与未暴露组相比, 胎儿、儿童和青春期暴露组的 MetS 风险增加, OR 和 95% CI 分别为 1.48 (1.23‐1.78)、1.89 (1.632.20) 和 2.34 (1.99‐ 2.74)。在校正性别、年龄、吸烟状况、饮酒状况、教育程度、体重指数(BMI)和体力活动后, 女性中观察到胎儿暴露组和儿童暴露组发生 MetS 的风险增加, OR 和 95%CI 分别为 1.42( 1.04‐1.94) 和 1.50 (1.02‐2.21)。在 BMI<23 kg/m2 的个体中, 饥荒暴露与 MetS 显着相关(整个队列中 BMI 类别与饥荒暴露之间的交互作用 P = 0.0002), 但存在性别差异(女性 P=0.0023, 男性P=0.4484)。在评估生命早期饥荒暴露和成年期肥胖对 MetS 的联合影响时, 我们观察到与没有饥荒暴露或成年肥胖的人相比, 成年肥胖和胎儿饥荒暴露的参与者有最高估计值(OR, 95%CI:17.52, 10.07‐ 30.48)。 结论 成年期肥胖显著加剧了早年营养不良个体(尤其是女性)发生 MetS 的风险。 Highlights In a community‐dwelling Chinese population, famine exposure in early life, especially during the fetal and childhood stages, has an association with an increased risk of metabolic syndrome (MetS) in later life, but the above findings only applied to females, not males. Compared to nonexposed and nonobese participants, those with both fetal famine exposure and adulthood general obesity had a higher risk of MetS of more than 17‐folds. The coexistence of malnutrition in early life and adulthood overweight/obesity had an association with a higher risk of MetS.
Previous studies reported that famine exposure had an effect on metabolic syndrome (MetS). However, there is an inadequacy of study regarding the association between famine exposure, adulthood general obesity, and the risk of MetS.BACKGROUNDPrevious studies reported that famine exposure had an effect on metabolic syndrome (MetS). However, there is an inadequacy of study regarding the association between famine exposure, adulthood general obesity, and the risk of MetS.A total of 8883 subjects aged ≥40 years from Jiading community in Shanghai were included. We defined famine exposure subgroups as nonexposed (1963-1974), fetal exposed (1959-1962), childhood exposed (1949-1958), and adolescence exposed (1941-1948). MetS was defined based on the National Cholesterol Education Program Adult Treatment Panel III (NCEP-ATP III) criteria.METHODSA total of 8883 subjects aged ≥40 years from Jiading community in Shanghai were included. We defined famine exposure subgroups as nonexposed (1963-1974), fetal exposed (1959-1962), childhood exposed (1949-1958), and adolescence exposed (1941-1948). MetS was defined based on the National Cholesterol Education Program Adult Treatment Panel III (NCEP-ATP III) criteria.Compared with the nonexposed group, the risks of MetS were increased in the fetal-, childhood-, and adolescence-exposed groups with odds ratios (OR) and 95% confidence intervals (CI) of 1.48 (1.23-1.78), 1.89 (1.63-2.20), and 2.34 (1.99-2.74), respectively. After adjusting for sex, age, smoking status, drinking status, education, body mass index (BMI), and physical activity, the increased risk of MetS related to the fetal-exposed and childhood-exposed groups with OR and 95% CI of 1.42 (1.04-1.94) and 1.50 (1.02-2.21), respectively, were observed only in women. Famine exposure was significantly associated with MetS among individuals with a BMI < 23 kg/m2 (p for interaction between BMI categories and famine exposure = 0.0002 in the whole cohort), while there existed a gender difference (p = 0.0023 in females, p = 0.4484 in males). When evaluating the joint effects of the combination of famine exposure in early life and general obesity in adulthood on MetS, we observed the highest estimate in participants with both adulthood general obesity and fetal famine exposure (OR 17.52; 95% CI, 10.07-30.48) compared with those without famine exposure nor adulthood obesity.RESULTSCompared with the nonexposed group, the risks of MetS were increased in the fetal-, childhood-, and adolescence-exposed groups with odds ratios (OR) and 95% confidence intervals (CI) of 1.48 (1.23-1.78), 1.89 (1.63-2.20), and 2.34 (1.99-2.74), respectively. After adjusting for sex, age, smoking status, drinking status, education, body mass index (BMI), and physical activity, the increased risk of MetS related to the fetal-exposed and childhood-exposed groups with OR and 95% CI of 1.42 (1.04-1.94) and 1.50 (1.02-2.21), respectively, were observed only in women. Famine exposure was significantly associated with MetS among individuals with a BMI < 23 kg/m2 (p for interaction between BMI categories and famine exposure = 0.0002 in the whole cohort), while there existed a gender difference (p = 0.0023 in females, p = 0.4484 in males). When evaluating the joint effects of the combination of famine exposure in early life and general obesity in adulthood on MetS, we observed the highest estimate in participants with both adulthood general obesity and fetal famine exposure (OR 17.52; 95% CI, 10.07-30.48) compared with those without famine exposure nor adulthood obesity.Obesity in adulthood significantly further aggravated the risk of MetS in individuals who experienced early life undernutrition, especially in females.CONCLUSIONSObesity in adulthood significantly further aggravated the risk of MetS in individuals who experienced early life undernutrition, especially in females.
Highlights In a community‐dwelling Chinese population, famine exposure in early life, especially during the fetal and childhood stages, has an association with an increased risk of metabolic syndrome (MetS) in later life, but the above findings only applied to females, not males. Compared to nonexposed and nonobese participants, those with both fetal famine exposure and adulthood general obesity had a higher risk of MetS of more than 17‐folds. The coexistence of malnutrition in early life and adulthood overweight/obesity had an association with a higher risk of MetS.
Author Xu, Yu
Xu, Min
Zhang, Yi
Lu, Jieli
Hu, Chunyan
Wang, Shuangyuan
Zhao, Zhiyun
Bi, Yufang
Wang, Weiqing
Lin, Hong
Wang, Tiange
Lin, Lin
Qi, Hongyan
Zhu, Yuanyue
Chen, Yuhong
Zhang, Jie
Li, Mian
Ning, Guang
AuthorAffiliation 1 Department of Endocrine and Metabolic Diseases, Shanghai Institute of Endocrine and Metabolic Diseases, Ruijin Hospital Shanghai Jiao Tong University School of Medicine Shanghai China
2 Shanghai National Clinical Research Center for Metabolic Diseases, Key Laboratory for Endocrine and Metabolic Diseases of the National Health Commission of the PR China, Shanghai Key Laboratory for Endocrine Tumor, State Key Laboratory of Medical Genomics, Ruijin Hospital Shanghai Jiao Tong University School of Medicine Shanghai China
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– name: 1 Department of Endocrine and Metabolic Diseases, Shanghai Institute of Endocrine and Metabolic Diseases, Ruijin Hospital Shanghai Jiao Tong University School of Medicine Shanghai China
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Cites_doi 10.1210/jc.2016‐2477
10.1155/2020/3251275
10.1111/1753‐0407.12927
10.1136/bmj.315.7119.1342
10.2337/dc19‐2325
10.1098/rspb.2012.0320
10.1155/2019/7954856
10.1016/j.nut.2017.12.013
10.3945/jn.116.234575
10.1016/j.diabres.2004.07.022
10.1530/JOE‐13‐0099
10.1196/annals.1367.002
10.1016/j.ehb.2010.07.003
10.1038/s41430‐018‐0211‐1
10.1126/science.1095292
10.1161/JAHA.119.014175
10.1111/1753‐0407.12499
10.1677/JME‐08‐0025
10.1038/s41430‐020‐0561‐3
10.1056/NEJMra0708473
10.1249/01.MSS.0000078924.61453.FB
10.1093/nutrit/nux053
10.1093/hmg/ddp353
10.1159/000507356
10.2337/dc19‐S002
10.1111/1468‐0297.00494
10.1111/liv.14572
10.1001/jama.285.19.2486
10.1152/ajpendo.2000.279.1.E83
10.1152/ajpregu.90724.2008
10.1016/j.amjmed.2018.07.011
10.1186/s12902-016-0143-5
10.1016/S0140-6736(03)15268-3
10.3945/ajcn.2008.27038
10.1016/j.phrs.2017.05.013
10.2337/dc10‐2039
10.2337/dc14‐2391
10.1093/ajcn/86.4.1219
10.1002/dmrr.3322
10.1007/BF03345248
10.1016/S0140-6736(05)66378-7
10.1111/j.1479-828X.2006.00506.x
10.1210/jc.2011‐3010
10.1017/S2040174412000256
10.1016/j.clnu.2015.11.010
10.1007/s00125‐009‐1464‐y
10.1016/j.atherosclerosis.2005.07.020
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2022 The Authors. Journal of Diabetes published by Ruijin Hospital, Shanghai JiaoTong University School of Medicine and John Wiley & Sons Australia, Ltd.
Copyright_xml – notice: 2022 The Authors. published by Ruijin Hospital, Shanghai JiaoTong University School of Medicine and John Wiley & Sons Australia, Ltd.
– notice: 2022. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
– notice: 2022 The Authors. Journal of Diabetes published by Ruijin Hospital, Shanghai JiaoTong University School of Medicine and John Wiley & Sons Australia, Ltd.
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This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
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Notes Funding information
National Natural Science Foundation of China, Grant/Award Numbers: 81700764, 81970691, 81970728; Science and Technology Commission of Shanghai Municipality, Grant/Award Number: 19411964200; Shanghai Medical and Health Development Foundation, Grant/Award Number: DMRFP_I_01; Shanghai Outstanding Academic Leaders Plan, Grant/Award Number: 20XD1422800
Yi Zhang, Hongyan Qi and Chunyan Hu contributed equally to this work.
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Funding information National Natural Science Foundation of China, Grant/Award Numbers: 81700764, 81970691, 81970728; Science and Technology Commission of Shanghai Municipality, Grant/Award Number: 19411964200; Shanghai Medical and Health Development Foundation, Grant/Award Number: DMRFP_I_01; Shanghai Outstanding Academic Leaders Plan, Grant/Award Number: 20XD1422800
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References 2009; 89
2004; 363
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1997; 315
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2000; 279
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2019; 11
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2003; 35
2020; 36
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2020; 76
2016; 16
2004; 305
2017; 9
2012; 97
2005; 67
2006; 1083
2011; 9
2018; 131
2001; 110
2017; 75
2009; 52
2012; 3
2020; 2020
2019; 42
2013; 219
2006; 46
2017; 36
2020; 74
2005; 365
2020; 9
2003; 26
2006; 186
2008; 359
2008; 41
2020; 43
2017; 122
2007; 86
2012; 279
2017; 102
2018; 53
2008; 295
2009; 18
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References_xml – volume: 363
  start-page: 157
  issue: 9403
  year: 2004
  end-page: 163
  article-title: Appropriate body‐mass index for Asian populations and its implications for policy and intervention strategies
  publication-title: Lancet
– volume: 131
  start-page: 1515.e1
  issue: 12
  year: 2018
  end-page: 1515.e10
  article-title: Ideal cardiovascular health is inversely associated with nonalcoholic fatty liver disease: a prospective analysis
  publication-title: Am J Med
– volume: 26
  start-page: 941
  issue: 9
  year: 2003
  end-page: 945
  article-title: Maternal nutrition, fetal weight, body composition and disease in later life
  publication-title: J Endocrinol Invest
– volume: 52
  start-page: 2079
  issue: 10
  year: 2009
  end-page: 2086
  article-title: Insulin resistance, beta cell dysfunction and visceral adiposity as predictors of incident diabetes: the insulin resistance atherosclerosis study (IRAS) family study
  publication-title: Diabetologia
– volume: 75
  start-page: 951
  issue: 12
  year: 2017
  end-page: 970
  article-title: Developmental origins of health and disease: current knowledge and potential mechanisms
  publication-title: Nutr Rev
– volume: 86
  start-page: 1219
  issue: 4
  year: 2007
  end-page: 1224
  article-title: The metabolic syndrome in adults prenatally exposed to the Dutch famine
  publication-title: Am J Clin Nutr
– volume: 359
  start-page: 61
  issue: 1
  year: 2008
  end-page: 73
  article-title: Effect of in utero and early‐life conditions on adult health and disease
  publication-title: N Engl J Med
– volume: 40
  start-page: 2694
  issue: 11
  year: 2020
  end-page: 2705
  article-title: Early life famine exposure, adulthood obesity patterns and the risk of nonalcoholic fatty liver disease
  publication-title: Liver Int
– volume: 41
  start-page: 91
  issue: 2
  year: 2008
  end-page: 102
  article-title: Developmental origins of disease and determinants of chromatin structure: maternal diet modifies the primate fetal epigenome
  publication-title: J Mol Endocrinol
– volume: 36
  start-page: 253
  issue: 1
  year: 2017
  end-page: 259
  article-title: The famine exposure in early life and metabolic syndrome in adulthood
  publication-title: Clin Nutr
– volume: 315
  start-page: 1342
  issue: 7119
  year: 1997
  end-page: 1348
  article-title: Does malnutrition in utero determine diabetes and coronary heart disease in adulthood? Results from the Leningrad siege study, a cross sectional study
  publication-title: BMJ
– volume: 186
  start-page: 367
  issue: 2
  year: 2006
  end-page: 373
  article-title: Modification of the NCEP ATP III definitions of the metabolic syndrome for use in Asians identifies individuals at risk of ischemic heart disease
  publication-title: Atherosclerosis
– volume: 102
  start-page: 507
  issue: 2
  year: 2017
  end-page: 515
  article-title: Metabolic syndrome among adults in China: the 2010 China noncommunicable disease surveillance
  publication-title: J Clin Endocrinol Metab
– volume: 89
  start-page: 1737
  issue: 6
  year: 2009
  end-page: 1743
  article-title: Lipid profiles in middle‐aged men and women after famine exposure during gestation: the Dutch hunger winter families study
  publication-title: Am J Clin Nutr
– volume: 74
  start-page: 1229
  issue: 8
  year: 2020
  end-page: 1236
  article-title: Prenatal exposure to the Chinese famine and the risk of metabolic syndrome in adulthood across consecutive generations
  publication-title: Eur J Clin Nutr
– volume: 365
  start-page: 1415
  issue: 9468
  year: 2005
  end-page: 1428
  article-title: The metabolic syndrome
  publication-title: Lancet
– volume: 305
  start-page: 1733
  issue: 5691
  year: 2004
  end-page: 1736
  article-title: Living with the past: evolution, development, and patterns of disease
  publication-title: Science
– volume: 1083
  start-page: 1
  year: 2006
  end-page: 10
  article-title: Obesity and the metabolic syndrome: the stress on society
  publication-title: Ann N Y Acad Sci
– volume: 279
  start-page: 2883
  issue: 1739
  year: 2012
  end-page: 2890
  article-title: Does famine influence sex ratio at birth? Evidence from the 1959‐1961 great leap forward famine in China
  publication-title: Proc Biol Sci
– volume: 295
  start-page: R1941
  issue: 6
  year: 2008
  end-page: R1952
  article-title: Sex differences in the developmental origins of hypertension and cardiorenal disease
  publication-title: Am J Physiol Regul Integr Comp Physiol
– volume: 42
  start-page: S13
  issue: Suppl 1
  year: 2019
  end-page: S28
  article-title: 2. Classification and diagnosis of diabetes
  publication-title: Diabetes Care
– volume: 3
  start-page: 342
  issue: 5
  year: 2012
  end-page: 349
  article-title: Increased systolic blood pressure in rat offspring following a maternal low‐protein diet is normalized by maternal dietary choline supplementation
  publication-title: J Dev Orig Health Dis
– volume: 11
  start-page: 884
  issue: 11
  year: 2019
  end-page: 894
  article-title: Resting heart rate is associated with metabolic syndrome and predicted 10‐year risk of cardiovascular disease: a cross‐sectional study
  publication-title: J Diabetes
– volume: 2019
  start-page: 7954856
  year: 2019
  end-page: 7954859
  article-title: Famine exposure in early life and risk of metabolic syndrome in adulthood: comparisons of different metabolic syndrome definitions
  publication-title: J Diabetes Res
– volume: 36
  issue: 6
  year: 2020
  article-title: Association of bedtime with the risk of non‐alcoholic fatty liver disease among middle‐aged and elderly Chinese adults with pre‐diabetes and diabetes
  publication-title: Diabetes Metab Res Rev
– volume: 9
  issue: 7
  year: 2020
  article-title: Early‐life famine exposure and risk of cardiovascular diseases in later life: findings from the REACTION study
  publication-title: J Am Heart Assoc
– volume: 9
  start-page: 920
  issue: 10
  year: 2017
  end-page: 928
  article-title: Visceral adiposity is significantly associated with type 2 diabetes in middle‐aged and elderly Chinese women: a cross‐sectional study
  publication-title: J Diabetes
– volume: 67
  start-page: 251
  issue: 3
  year: 2005
  end-page: 257
  article-title: The US National Cholesterol Education Programme Adult Treatment Panel III (NCEP ATP III) prevalence of the metabolic syndrome in a Chinese population
  publication-title: Diabetes Res Clin Pract
– volume: 110
  start-page: 136
  issue: 460
  year: 2001
  end-page: 158
  article-title: Food availability, entitlements and the Chinese famine of 1959–61
  publication-title: Econ J
– volume: 285
  start-page: 2486
  issue: 19
  year: 2001
  end-page: 2497
  article-title: Executive summary of the third report of the National Cholesterol Education Program (NCEP) expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (adult treatment panel III)
  publication-title: Jama
– volume: 2020
  start-page: 3251275
  year: 2020
  end-page: 3251279
  article-title: Effect of exposure to famine during early life on risk of metabolic syndrome in adulthood: a meta‐analysis
  publication-title: J Diabetes Res
– volume: 219
  start-page: 159
  issue: 2
  year: 2013
  end-page: 171
  article-title: Pre‐ and postnatal nutrition in sheep affects β‐cell secretion and hypothalamic control
  publication-title: J Endocrinol
– volume: 43
  start-page: 1902
  issue: 8
  year: 2020
  end-page: 1909
  article-title: Early life famine exposure, ideal cardiovascular health metrics, and risk of incident diabetes: findings from the 4C study
  publication-title: Diabetes Care
– volume: 38
  start-page: 150
  issue: 1
  year: 2015
  end-page: 158
  article-title: BMI cut points to identify at‐risk Asian Americans for type 2 diabetes screening
  publication-title: Diabetes Care
– volume: 16
  start-page: 60
  issue: 1
  year: 2016
  article-title: Obesity and diabetes mellitus association in rural community of katana, south Kivu, in eastern Democratic Republic of Congo: Bukavu Observ cohort study results
  publication-title: BMC Endocr Disord
– volume: 53
  start-page: 20
  year: 2018
  end-page: 25
  article-title: Victims of Chinese famine in early life have increased risk of metabolic syndrome in adulthood
  publication-title: Nutrition
– volume: 122
  start-page: 1
  year: 2017
  end-page: 7
  article-title: Obesity and hypertension
  publication-title: Pharmacol Res
– volume: 76
  start-page: 140
  issue: 2
  year: 2020
  end-page: 146
  article-title: Association of Exposure to Chinese famine in early life with the risk of metabolic syndrome in adulthood
  publication-title: Ann Nutr Metab
– volume: 35
  start-page: 1381
  issue: 8
  year: 2003
  end-page: 1395
  article-title: International physical activity questionnaire: 12‐country reliability and validity
  publication-title: Med Sci Sports Exerc
– volume: 73
  start-page: 724
  issue: 5
  year: 2019
  end-page: 732
  article-title: Chinese famine exposure in infancy and metabolic syndrome in adulthood: results from the China health and retirement longitudinal study
  publication-title: Eur J Clin Nutr
– volume: 46
  start-page: 4
  issue: 1
  year: 2006
  end-page: 14
  article-title: The developmental origins of adult disease (barker) hypothesis
  publication-title: Aust N Z J Obstet Gynaecol
– volume: 146
  start-page: 2289
  issue: 11
  year: 2016
  end-page: 2295
  article-title: Exposure to the Chinese famine in childhood increases type 2 diabetes risk in adults
  publication-title: J Nutr
– volume: 97
  start-page: 2033
  issue: 6
  year: 2012
  end-page: 2038
  article-title: Association between nonalcoholic fatty liver disease (NAFLD) and osteoporotic fracture in middle‐aged and elderly Chinese
  publication-title: J Clin Endocrinol Metab
– volume: 9
  start-page: 92
  issue: 1
  year: 2011
  end-page: 105
  article-title: Why does the great Chinese famine affect the male and female survivors differently? Mortality selection versus son preference
  publication-title: Econ Hum Biol
– volume: 34
  start-page: 1014
  issue: 4
  year: 2011
  end-page: 1018
  article-title: Exposure to the chinese famine in early life and the risk of metabolic syndrome in adulthood
  publication-title: Diabetes Care
– volume: 279
  start-page: E83
  issue: 1
  year: 2000
  end-page: E87
  article-title: Fetal origins of hyperphagia, obesity, and hypertension and postnatal amplification by hypercaloric nutrition
  publication-title: Am J Physiol Endocrinol Metab
– volume: 18
  start-page: 4046
  issue: 21
  year: 2009
  end-page: 4053
  article-title: DNA methylation differences after exposure to prenatal famine are common and timing‐ and sex‐specific
  publication-title: Hum Mol Genet
– ident: e_1_2_8_3_1
  doi: 10.1210/jc.2016‐2477
– ident: e_1_2_8_34_1
  doi: 10.1155/2020/3251275
– ident: e_1_2_8_22_1
  doi: 10.1111/1753‐0407.12927
– ident: e_1_2_8_35_1
  doi: 10.1136/bmj.315.7119.1342
– ident: e_1_2_8_9_1
  doi: 10.2337/dc19‐2325
– ident: e_1_2_8_48_1
  doi: 10.1098/rspb.2012.0320
– ident: e_1_2_8_32_1
  doi: 10.1155/2019/7954856
– ident: e_1_2_8_14_1
  doi: 10.1016/j.nut.2017.12.013
– ident: e_1_2_8_17_1
  doi: 10.3945/jn.116.234575
– ident: e_1_2_8_29_1
  doi: 10.1016/j.diabres.2004.07.022
– ident: e_1_2_8_42_1
  doi: 10.1530/JOE‐13‐0099
– ident: e_1_2_8_6_1
  doi: 10.1196/annals.1367.002
– ident: e_1_2_8_47_1
  doi: 10.1016/j.ehb.2010.07.003
– ident: e_1_2_8_15_1
  doi: 10.1038/s41430‐018‐0211‐1
– ident: e_1_2_8_37_1
  doi: 10.1126/science.1095292
– ident: e_1_2_8_10_1
  doi: 10.1161/JAHA.119.014175
– ident: e_1_2_8_21_1
  doi: 10.1111/1753‐0407.12499
– ident: e_1_2_8_39_1
  doi: 10.1677/JME‐08‐0025
– ident: e_1_2_8_33_1
  doi: 10.1038/s41430‐020‐0561‐3
– ident: e_1_2_8_40_1
  doi: 10.1056/NEJMra0708473
– ident: e_1_2_8_23_1
  doi: 10.1249/01.MSS.0000078924.61453.FB
– ident: e_1_2_8_8_1
  doi: 10.1093/nutrit/nux053
– ident: e_1_2_8_45_1
  doi: 10.1093/hmg/ddp353
– ident: e_1_2_8_31_1
  doi: 10.1159/000507356
– ident: e_1_2_8_27_1
  doi: 10.2337/dc19‐S002
– ident: e_1_2_8_16_1
  doi: 10.1111/1468‐0297.00494
– ident: e_1_2_8_11_1
  doi: 10.1111/liv.14572
– ident: e_1_2_8_24_1
  doi: 10.1001/jama.285.19.2486
– ident: e_1_2_8_43_1
  doi: 10.1152/ajpendo.2000.279.1.E83
– ident: e_1_2_8_44_1
  doi: 10.1152/ajpregu.90724.2008
– ident: e_1_2_8_20_1
  doi: 10.1016/j.amjmed.2018.07.011
– ident: e_1_2_8_4_1
  doi: 10.1186/s12902-016-0143-5
– ident: e_1_2_8_25_1
  doi: 10.1016/S0140-6736(03)15268-3
– ident: e_1_2_8_38_1
  doi: 10.3945/ajcn.2008.27038
– ident: e_1_2_8_5_1
  doi: 10.1016/j.phrs.2017.05.013
– ident: e_1_2_8_13_1
  doi: 10.2337/dc10‐2039
– ident: e_1_2_8_26_1
  doi: 10.2337/dc14‐2391
– ident: e_1_2_8_36_1
  doi: 10.1093/ajcn/86.4.1219
– ident: e_1_2_8_18_1
  doi: 10.1002/dmrr.3322
– ident: e_1_2_8_12_1
  doi: 10.1007/BF03345248
– ident: e_1_2_8_2_1
  doi: 10.1016/S0140-6736(05)66378-7
– ident: e_1_2_8_7_1
  doi: 10.1111/j.1479-828X.2006.00506.x
– ident: e_1_2_8_19_1
  doi: 10.1210/jc.2011‐3010
– ident: e_1_2_8_41_1
  doi: 10.1017/S2040174412000256
– ident: e_1_2_8_30_1
  doi: 10.1016/j.clnu.2015.11.010
– ident: e_1_2_8_46_1
  doi: 10.1007/s00125‐009‐1464‐y
– ident: e_1_2_8_28_1
  doi: 10.1016/j.atherosclerosis.2005.07.020
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Snippet Background Previous studies reported that famine exposure had an effect on metabolic syndrome (MetS). However, there is an inadequacy of study regarding the...
BackgroundPrevious studies reported that famine exposure had an effect on metabolic syndrome (MetS). However, there is an inadequacy of study regarding the...
Previous studies reported that famine exposure had an effect on metabolic syndrome (MetS). However, there is an inadequacy of study regarding the association...
Highlights In a community‐dwelling Chinese population, famine exposure in early life, especially during the fetal and childhood stages, has an association with...
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SubjectTerms Body mass index
Child development
Diabetes
Famine
Metabolic syndrome
Obesity
Original
Teenagers
代谢综合征
肥胖
饥荒
Title Association between early life famine exposure and risk of metabolic syndrome in later life
URI https://onlinelibrary.wiley.com/doi/abs/10.1111/1753-0407.13319
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