Sayer Avan Aihie, Syddall Holly, O'Dell Sandra D, Chen Xiao-He, Briggs Patricia J, Briggs R, Day Ian N M, Cooper Cyrus
MRC Environmental Epidemiology Unit, Southampton General Hospital, Southampton SO16 6YD, UK.
Age Ageing. 2002 Nov;31(6):468-70. doi: 10.1093/ageing/31.6.468.
Grip strength is a simple measure of skeletal muscle function but a powerful predictor of disability, morbidity and mortality. Recent evidence has shown that prenatal and infant growth influence grip strength in later life; this may reflect genetic influences on muscle size and function, although strong candidate genes have not been identified. IGF II has proliferative effects in adult muscle and is one of the major determinants of fetal growth; polymorphism in the IGF2 gene could therefore link early growth to adult grip strength.
To determine whether polymorphism of the IGF2 gene influences adult grip strength and mediates the association between size at birth and grip strength in later life.
Polymorphism of the ApaI marker in the IGF2 gene was determined for 693 Hertfordshire men and women born between 1920 and 1930 who had taken part in a study linking early growth to ageing. Grip strength was measured using isometric dynamometry. Genotyping assay development was undertaken in Southampton Genetic Epidemiology Laboratories (http://www.sgel.humgen.soton.ac.uk).
In univariate analyses, IGF2 genotype and birth weight were both significant predictors of adult grip strength in the men after adjustment for age and current height. Significant associations were not seen in the women. When IGF2 genotype and birth weight in men were studied simultaneously, both contributed significantly to grip strength after adjustment for age and adult height.
These results show that polymorphism of the IGF2 gene and birth weight have independent effects on adult grip strength in men and suggest that IGF2 polymorphism does not explain the association between size at birth and grip in later life. This study provides preliminary evidence for independent genetic and early environmental programming of adult muscle strength.
握力是骨骼肌功能的一项简单指标,但却是残疾、发病和死亡的有力预测因素。最近的证据表明,产前和婴儿期生长会影响成年后的握力;这可能反映了基因对肌肉大小和功能的影响,尽管尚未确定强有力的候选基因。胰岛素样生长因子II(IGF II)对成年肌肉有增殖作用,是胎儿生长的主要决定因素之一;因此,IGF2基因的多态性可能将早期生长与成年后的握力联系起来。
确定IGF2基因的多态性是否会影响成年后的握力,并介导出生时的体型与成年后握力之间的关联。
对693名出生于1920年至1930年之间、参与了一项将早期生长与衰老联系起来的研究的赫特福德郡男女,测定其IGF2基因中ApaI标记的多态性。使用等长测力法测量握力。基因分型检测在南安普敦遗传流行病学实验室(http://www.sgel.humgen.soton.ac.uk)进行。
在单变量分析中,在对年龄和当前身高进行调整后,IGF2基因型和出生体重均是男性成年后握力的显著预测因素。在女性中未发现显著关联。当同时研究男性的IGF2基因型和出生体重时,在对年龄和成年身高进行调整后,两者对握力均有显著贡献。
这些结果表明,IGF2基因的多态性和出生体重对男性成年后的握力有独立影响,并表明IGF2多态性无法解释出生时的体型与成年后握力之间的关联。本研究为成年肌肉力量的独立遗传和早期环境编程提供了初步证据。