The association of the K121Q polymorphism of the plasma cell glycoprotein-1 gene with type 2 diabetes and hypertension depends on size at birth

被引:51
作者
Kubaszek, A
Markkanen, A
Eriksson, JG
Forsen, T
Osmond, C
Barker, DJP
Laakso, M [1 ]
机构
[1] Univ Kuopio, Dept Med, SF-70210 Kuopio, Finland
[2] Natl Publ Hlth Inst, Dept Epidemiol & Hlth Promot, SF-00300 Helsinki, Finland
[3] Univ Helsinki, Dept Publ Hlth, Helsinki 00300, Finland
[4] Univ Southampton, Southampton Gen Hosp, MRC, Environm Epidemiol Unit, Southampton 5016 6YD, Hants, England
关键词
D O I
10.1210/jc.2003-031350
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Birth weight and length serve as indicators of the intrauterine environment, and a small body size at birth is a predictor of type 2 diabetes and hypertension. Insulin is one of the growth factors regulating fetal growth. The plasma cell glycoprotein 1 (PC-1) gene impairs insulin signaling at the insulin receptor level. Therefore, we investigated whether the K121Q polymorphism of the PC-1 gene association with insulin sensitivity, insulin levels, and the prevalence of diabetes and hypertension in adult life depends on size at birth in 489 subjects born in Helsinki during 1924-1933. We found that the effect of the PC-1 gene polymorphism on insulin levels and insulin sensitivity, measured as the homeostasis model assessment for insulin resistance, depended on birth length because fasting insulin levels and insulin resistance were highest in subjects carrying the 121Q allele who were small at birth ( P for interaction = 0.04 and 0.05). Additionally, in those whose birth length was up to 49 cm, the K121Q polymorphism of the PC-1 gene was associated with a 2-fold higher incidence of type 2 diabetes. Moreover, subjects who were short at birth and who had the 121Q allele had the highest incidence (31.6%) of type 2 diabetes together with hypertension. We conclude that the interaction between the K121Q polymorphism of the PC-1 gene and birth length affects insulin sensitivity and increases susceptibility to type 2 diabetes and hypertension in adulthood.
引用
收藏
页码:2044 / 2047
页数:4
相关论文
共 29 条
[1]   In utero programming of chronic disease [J].
Barker, DJP .
CLINICAL SCIENCE, 1998, 95 (02) :115-128
[2]   Purinergic signaling and vascular cell proliferation and death [J].
Burnstock, G .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2002, 22 (03) :364-373
[3]   SKELETAL-MUSCLE IS A PRIMARY SITE OF INSULIN RESISTANCE IN ESSENTIAL-HYPERTENSION [J].
CAPALDO, B ;
LEMBO, G ;
NAPOLI, R ;
RENDINA, V ;
ALBANO, G ;
SACCA, L ;
TRIMARCO, B .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1991, 40 (12) :1320-1322
[4]   The Q allele variant (GLN121) of membrane glycoprotein PC-1 interacts with the insulin receptor and inhibits insulin signaling more effectively than the common K allele variant (LYS121) [J].
Costanzo, BV ;
Trischitta, V ;
Di Paola, R ;
Spampinato, D ;
Pizzuti, A ;
Vigneri, R ;
Frittitta, L .
DIABETES, 2001, 50 (04) :831-836
[5]   INSULIN RESISTANCE - A MULTIFACETED SYNDROME RESPONSIBLE FOR NIDDM, OBESITY, HYPERTENSION, DYSLIPIDEMIA, AND ATHEROSCLEROTIC CARDIOVASCULAR-DISEASE [J].
DEFRONZO, RA ;
FERRANNINI, E .
DIABETES CARE, 1991, 14 (03) :173-194
[6]   DIABETES-MELLITUS AND HYPERTENSION [J].
EPSTEIN, M ;
SOWERS, JR .
HYPERTENSION, 1992, 19 (05) :403-418
[7]   Fetal and childhood growth and hypertension in adult life [J].
Eriksson, J ;
Forsén, T ;
Tuomilehto, J ;
Osmond, C ;
Barker, D .
HYPERTENSION, 2000, 36 (05) :790-794
[8]   The effects of the Pro12Ala polymorphism of the peroxisome proliferator-activated receptor-γ2 gene on insulin sensitivity and insulin metabolism interact with size at birth [J].
Eriksson, JG ;
Lindi, V ;
Uusitupa, M ;
Forsén, TJ ;
Laakso, M ;
Osmond, C ;
Barker, DJP .
DIABETES, 2002, 51 (07) :2321-2324
[9]   Effects of size at birth and childhood growth on the insulin resistance syndrome in elderly individuals [J].
Eriksson, JG ;
Forsén, T ;
Tuomilehto, J ;
Jaddoe, VWV ;
Osmond, C ;
Barker, DJP .
DIABETOLOGIA, 2002, 45 (03) :342-348
[10]   INSULIN RESISTANCE IN ESSENTIAL-HYPERTENSION [J].
FERRANNINI, E ;
BUZZIGOLI, G ;
BONADONNA, R ;
GIORICO, MA ;
OLEGGINI, M ;
GRAZIADEI, L ;
PEDRINELLI, R ;
BRANDI, L ;
BEVILACQUA, S .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 317 (06) :350-357