Early growth, and coronary heart disease and type 2 diabetes: experiences from the Helsinki Birth Cohort Studies

被引:48
作者
Eriksson, J. G. [1 ]
机构
[1] Natl Publ Hlth Inst, Dept Epidemiol & Hlth Promot, Diabet & Genet Epidemiol Unit, SF-00300 Helsinki, Finland
关键词
coronary heart disease; type; 2; diabetes; fetal growth; childhood growth;
D O I
10.1038/sj.ijo.0803515
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Experiences during critical periods of development through the mechanisms of programming have consequences on later health outcomes. Observations worldwide linking a small body size at birth with adult health outcomes have greatly added to our understanding of the early origins of several non-communicable diseases like coronary heart disease (CHD) and type 2 diabetes. The pattern of growth predisposing to CHD is characterized by a small body size at birth and thinness through infancy up to 2 years of age, followed by accelerated gain in weight and body mass index (BMI) later in childhood. The early growth patterns of individuals who later develop type 2 diabetes very much resemble the growth patterns of CHD, that is, a small body size at birth and thinness at 1 year of age followed by higher body mass indices later in childhood. Numerous studies support the importance of events during critical periods of growth in the pathogenesis of many non-communicable diseases like CHD and type 2 diabetes. There are several possible mechanisms through which a non-optimal early growth associated with accelerated weight gain in childhood could lead to these diseases. To get a better understanding of the patterns of growth affecting adult health outcomes, a life-course approach to the development of chronic diseases needs to be taken.
引用
收藏
页码:S18 / S22
页数:5
相关论文
共 26 条
[1]  
Barker DJ., 1998, Mothers, babies, and health in later life, V2
[2]  
BARKER DJP, 1989, LANCET, V2, P577
[3]   Trajectories of growth among children who have coronary events as adults [J].
Barker, DJP ;
Osmond, C ;
Forsén, TJ ;
Kajantie, E ;
Eriksson, JG .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (17) :1802-1809
[4]   GROWTH IN-UTERO AND SERUM-CHOLESTEROL CONCENTRATIONS IN ADULT LIFE [J].
BARKER, DJP ;
MARTYN, CN ;
OSMOND, C ;
HALES, CN ;
FALL, CHD .
BRITISH MEDICAL JOURNAL, 1993, 307 (6918) :1524-1527
[5]  
Barker DJP, 2001, BRIT MED J, V323, P1
[6]   Relation of serial changes in childhood body-mass index to impaired glucose tolerance in young adulthood [J].
Bhargava, SK ;
Sachdev, HS ;
Fall, CHD ;
Osmond, C ;
Lakshmy, R ;
Barker, DJP ;
Biswas, SKD ;
Ramji, S ;
Prabhakaran, D ;
Reddy, KS .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (09) :865-875
[7]   Obesity from cradle to grave [J].
Eriksson, J ;
Forsén, T ;
Osmond, C ;
Barker, D .
INTERNATIONAL JOURNAL OF OBESITY, 2003, 27 (06) :722-727
[8]   The effects of the Pro12Ala polymorphism of the PPARγ-2 gene on lipid metabolism interact with body size at birth [J].
Eriksson, J ;
Lindi, V ;
Uusitupa, M ;
Forsén, T ;
Laakso, M ;
Osmond, C ;
Barker, D .
CLINICAL GENETICS, 2003, 64 (04) :366-370
[9]   Size at birth fat-free mass and resting metabolic rate in adult life [J].
Eriksson, J ;
Forsén, T ;
Tuomilehto, J ;
Osmond, C ;
Barker, D .
HORMONE AND METABOLIC RESEARCH, 2002, 34 (02) :72-76
[10]   Exercise protects against glucose intolerance in individuals with a small body size at birth [J].
Eriksson, JG ;
Ylihärsilä, H ;
Forsén, T ;
Osmond, C ;
Barker, DJP .
PREVENTIVE MEDICINE, 2004, 39 (01) :164-167