Identification of the BclI polymorphism in the glucocorticoid receptor gene:: association with sensitivity to glucocorticoids in vivo and body mass index

被引:260
作者
van Rossum, EFC
Koper, JW
van den Beld, AW
Uitterlinden, AG
Arp, P
Ester, W
Janssen, JAMJL
Brinkmann, AO
de Jong, FH
Grobbee, DE
Pols, HAP
Lamberts, SWJ
机构
[1] Erasmus Med Ctr, Dept Internal Med, NL-3000 CA Rotterdam, Netherlands
[2] Erasmus Med Ctr, Dept Endocrinol & Reprod, Rotterdam, Netherlands
[3] Univ Med Ctr Utrecht, Julius Ctr Hlth Sci & Primary Care, Utrecht, Netherlands
关键词
D O I
10.1046/j.1365-2265.2003.01888.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE Sensitivity to glucocorticoids differs between individuals, partially due to genetic variation in the glucocorticoid receptor (GR) gene. We studied the sequence alteration of a previously described intronic BclI polymorphism of the GR gene, and investigated whether there was an association with sensitivity to glucocorticoids and anthropometric parameters in a group of healthy elderly individuals. DESIGN AND MEASUREMENTS In study group 1, two overnight dexamethasone suppression tests (DSTs) were performed: with 1 mg dexamethasone, and 2.5 years later with 0.25 mg dexamethasone. Anthropometric parameters were measured in a larger population (study group 2), as well as in a third study group, in which we also measured body composition by dual-energy X-ray absorbtiometry (DEXA) scans. SUBJECTS Groups 1 and 2, respectively, 191 and 1963 male and female participants of the Rotterdam study, a population-based study in Dutch elderly. Study group 3: 370 elderly males (mean age 77.8 +/- 0.2 years) from Zoetermeer, the Netherlands. RESULTS We identified the BclI restriction site polymorphism as a C/G substitution in intron 2, 646 nucleotides downstream from exon 2. After both 1 mg and 0.25 mg DST, heterozygous (CG) and homozygous G-allele carriers (GG) had lower cortisol levels than CC-carriers (P = 0.01 and P = 0.02, respectively). In study group 2, we found a lower body mass index (BMI; P = 0.006) and waist-hip ratio (WHR; P = 0.02) in G-allele carriers. In study group 3, again we found a lower BMI (P = 0.05) in G-allele carriers. No differences were found in fat mass. However, lean mass tended to be lower in G-allele carriers (P = 0.07). CONCLUSIONS We characterized a BclI-RFLP (restriction fragment length polymorphism) of the GR gene as a C/G polymorphism in intron 2 of which the G-allele was associated with hypersensitivity to glucocorticoids. This resulted in a lower BMI in older individuals in general, while our study in elderly males suggests that the lower BMI is probably due to a greater loss of lean mass during the ageing process.
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页码:585 / 592
页数:8
相关论文
共 20 条
[1]  
Baxter J D, 1979, Monogr Endocrinol, V12, P1
[2]   Abdominal visceral fat is associated with a BclI restriction fragment length polymorphism at the glucocorticoid receptor gene locus [J].
Buemann, B ;
Vohl, MC ;
Chagnon, M ;
Chagnon, YC ;
Gagnon, J ;
Perusse, L ;
Dionne, F ;
Despres, JP ;
Tremblay, A ;
Nadeau, A ;
Bouchard, C .
OBESITY RESEARCH, 1997, 5 (03) :186-192
[3]   THE ASSOCIATION BETWEEN AGE AND BONE-MINERAL DENSITY IN MEN AND WOMEN AGED 55 YEARS AND OVER - THE ROTTERDAM STUDY [J].
BURGER, H ;
VANDAELE, PLA ;
ALGRA, D ;
VANDENOUWELAND, FA ;
GROBBEE, DE ;
HOFMAN, A ;
VANKUIJK, C ;
SCHUTTE, HE ;
BIRKENHAGER, JC ;
POLS, HAP .
BONE AND MINERAL, 1994, 25 (01) :1-13
[4]   Mechanisms of glucocorticoid action in bone: Implications to glucocorticoid-induced osteoporosis [J].
Canalis, E .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1996, 81 (10) :3441-3447
[5]  
Clement K, 1996, INT J OBESITY, V20, P507
[6]   RELATION BETWEEN BODY-SIZE AND BONE-MINERAL DENSITY IN ELDERLY MEN AND WOMEN [J].
EDELSTEIN, SL ;
BARRETTCONNOR, E .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1993, 138 (03) :160-169
[7]   MEASUREMENT OF LEAN BODY-MASS AND TOTAL-BODY FAT USING DUAL PHOTON-ABSORPTIOMETRY [J].
GOTFREDSEN, A ;
JENSEN, J ;
BORG, J ;
CHRISTIANSEN, C .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1986, 35 (01) :88-93
[8]   Interperson variability but intraperson stability of baseline plasma cortisol concentrations, and its relation to feedback sensitivity of the hypothalamo-pituitary-adrenal axis to a low dose of dexamethasone in elderly individuals [J].
Huizenga, NATM ;
Koper, JW ;
De Lange, P ;
Pols, HAP ;
Stolk, RP ;
Grobbee, DE ;
De Jong, FH ;
Lamberts, SWJ .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (01) :47-54
[9]   A polymorphism in the glucocorticoid receptor gene may be associated with an increased sensitivity to glucocorticoids in vivo [J].
Huizenga, NATM ;
Koper, JW ;
De Lange, P ;
Pols, HAP ;
Stolk, RP ;
Burger, H ;
Grobbee, DE ;
Brinkmann, AO ;
De Jong, FH ;
Lamberts, SWJ .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (01) :144-151
[10]   Lack of association between five polymorphisms in the human glucocorticoid receptor gene and glucocorticoid resistance [J].
Koper, JW ;
Stolk, RP ;
deLange, P ;
Huizenga, NATM ;
Molijn, GJ ;
Pols, HAP ;
Grobbee, DE ;
Karl, M ;
deJong, FH ;
Brinkmann, AO ;
Lamberts, SWJ .
HUMAN GENETICS, 1997, 99 (05) :663-668