The role of luteinizing hormone-beta gene polymorphism in the onset and progression of puberty in healthy boys

被引:63
作者
Raivio, T
Huhtaniemi, I
Anttila, R
Siimes, MA
Hagenas, L
Nilsson, C
Pettersson, K
Dunkel, L
机构
[1] UNIV HELSINKI, CHILDRENS HOSP, FIN-00290 HELSINKI, FINLAND
[2] UNIV TURKU, DEPT PHYSIOL, FIN-20520 TURKU, FINLAND
[3] UNIV TURKU, DEPT BIOTECHNOL, FIN-20520 TURKU, FINLAND
[4] KAROLINSKA UNIV HOSP, DEPT PEDIAT ENDOCRINOL, S-10401 STOCKHOLM, SWEDEN
关键词
D O I
10.1210/jc.81.9.3278
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
An immunologically anomalous LH with two point mutations in its beta-subunit gene (Trp(8)Arg and Ile(15)Thr) has recently been described. This polymorphism is common in Finland; 28% of the population are home- or heterozygous for the variant allele. To assess the effect of the LH variant on LH action, we correlated its presence in a group of 49 healthy boys with the onset and progression of puberty. This group was followed-up longitudinally from a mean age of 11.7 +/-. 0.1 yr for 3 yr at 3-month intervals. In addition, we studied the prevalence of the variant LR in boys with constitutional pubertal delay (testicular volume less than or equal to 4 mL after 13.5 yr of age). The LH beta gene status of each subject in this study was judged from a single venous blood sample using two immunofluorometric LH assays-with different combinations of monoclonal antibodies: one detecting both the variant and wild-type LH, and the other detecting only wild-type hormone. Of the boys with pubertal onset at a normal age, 36 (74%) were homozygous for the wild-type LH beta allele, 12 (24%) were heterozygous, and 1 (2%) was homozygous for the variant LH beta allele. Clear differences in pubertal parameters were found between the boys with normal and mutated (home- or heterozygous) LH genotypes. During the follow-up, the boys with the mutated genotype had smaller testicular volumes (P < 0.03), were shorter (P < 0.02), had slower growth rates (P < 0.04), and had lower serum insulin-like growth factor I-binding protein-3 levels (P < 0.03) than the boys with the normal LH genotype. In the boys with delayed onset of puberty, the frequency of the variant LH beta allele did not differ from that in the reference population, indicating that the variant LH is not associated with conditions due to disturbed control of the reactivation of GnRH secretion. We conclude that during the progression of puberty, the variant LH may be less active in stimulating testicular growth than wild-type LH. Thus, the gene may affect tempo, contributing to the wide normal variation in pubertal progression in healthy boys. Our results also suggest that the variant LH not only affects the course of puberty, but is already involved in the regulation of the GH-insulin-like growth factor I axis during childhood.
引用
收藏
页码:3278 / 3282
页数:5
相关论文
共 27 条
[1]   INSULIN-LIKE GROWTH-FACTOR-I AND INSULIN-LIKE GROWTH-FACTOR BINDING-PROTEIN-3 AS DETERMINANTS OF BLOOD HEMOGLOBIN CONCENTRATION IN HEALTHY-SUBJECTS [J].
ANTTILA, R ;
KOISTINEN, R ;
SEPPALA, M ;
KOISTINEN, H ;
SIIMES, MA .
PEDIATRIC RESEARCH, 1994, 36 (06) :745-748
[2]  
APTER D, 1976, CLIN CHEM, V22, P32
[3]  
BERTRAND J, 1993, PEDIAT ENDOCRINOLOGY, P746
[4]   LINEAR GROWTH AS A FUNCTION OF AGE AT ONSET OF PUBERTY AND SEX STEROID DOSAGE - THERAPEUTIC IMPLICATIONS [J].
BOURGUIGNON, JP .
ENDOCRINE REVIEWS, 1988, 9 (04) :467-488
[5]   SEX STEROIDS DO NOT INFLUENCE SOMATIC GROWTH IN CHILDHOOD [J].
CAMPOS, SP ;
MACGILLIVRAY, MH .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1989, 143 (08) :942-943
[6]   MATURATION OF GONADOTROPIN AND SEX STEROID-RESPONSES TO GONADOTROPIN-RELEASING-HORMONE AGONIST IN MALES [J].
CUTTLER, L ;
ROSENFIELD, RL ;
EHRMANN, DA ;
KREITER, M ;
BURSTEIN, S ;
CARA, JF ;
LEVITSKY, LL .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1993, 76 (02) :362-366
[7]   GONADAL CONTROL OF PULSATILE SECRETION OF LUTEINIZING-HORMONE AND FOLLICLE-STIMULATING-HORMONE IN PREPUBERTAL BOYS EVALUATED BY ULTRASENSITIVE TIME-RESOLVED IMMUNOFLUOROMETRIC ASSAYS [J].
DUNKEL, L ;
ALFTHAN, H ;
STENMAN, UH ;
PERHEENTUPA, J .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1990, 70 (01) :107-114
[8]   IDENTIFICATION OF 2 POINT MUTATIONS IN THE GENE CODING LUTEINIZING-HORMONE (LH) BETA-SUBUNIT, ASSOCIATED WITH IMMUNOLOGICALLY ANOMALOUS LH VARIANTS [J].
FURUI, K ;
SUGANUMA, N ;
TSUKAHARA, S ;
ASADA, Y ;
KIKKAWA, F ;
TANAKA, M ;
OZAWA, T ;
TOMODA, Y .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 78 (01) :107-113
[9]   MATURATION OF THE NORMAL PITUITARY-TESTICULAR AXIS, AS ASSESSED BY GONADOTROPIN-RELEASING-HORMONE AGONIST CHALLENGE [J].
GHAI, K ;
ROSENFIELD, RL .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 78 (06) :1336-1340
[10]   OCCURRENCE AND BIOLOGICAL PROPERTIES OF A COMMON GENETIC VARIANT OF LUTEINIZING-HORMONE [J].
HAAVISTO, AM ;
PETTERSSON, K ;
BERGENDAHL, M ;
VIRKAMAKI, A ;
HUHTANIEMI, I .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1995, 80 (04) :1257-1263