Genetics of risk factors for melanoma: An adult twin study of nevi and freckles

被引:102
作者
Bataille, V [1 ]
Snieder, H
MacGregor, AJ
Sasieni, P
Spector, TD
机构
[1] St Thomas Hosp, Twin Res & Genet Epidemiol Unit, London SE1 7EH, England
[2] St Thomas Hosp, St Johns Inst Dermatol, London SE1 7EH, England
[3] St Bartholomews & Royal London Sch Med, Skin Tumour Lab, Imperial Canc Res Fund, London, England
[4] St Bartholomews & Royal London Sch Med, Dept Dermatol, London, England
[5] Imperial Canc Res Fund, Math Stat & Epidemiol Dept, London, England
来源
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE | 2000年 / 92卷 / 06期
关键词
D O I
10.1093/jnci/92.6.457
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: We sought by use of an adult twin study to investigate the relative contribution of genetic and environmental effects on the expression of nevi and freckles, which are known risk factors for melanoma, and to determine if age and sun exposure influence the heritability of nevi, Design and Methods: Total nevus and freckle counts were conducted on 127 monozygotic twin pairs and 323 dizygotic twin pairs. Intraclass correlations were calculated by use of analysis of variance. Model-fitting analyses were performed to quantify the genetic and environmental components of the variance for nevus and freckle counts.Results: The intraclass correlation for total nevus counts was 83 in monozygotic pairs compared with 51 in dizygotic pairs. Quantitative genetic analyses showed that the contribution of genetic factors on nevi expression varied according to age. For twins less than 45 years old, the additive genetic variance on total nevus count was 36% (95% confidence interval [Cl] = 0.8%-63%), with 38% (95% CI = 14%-61%) and 26% (95% CI = 16%-42%) of the remaining variance attributed to common environment and unique environmental effects, respectively. In twins aged 45 years or older, common environmental effects on total nevus count became negligible, with the additive genetic variance increasing to 84% (95% CI = 77%-88%), Body site was also found to affect the heritability estimates for nevus counts, with a statistically significant difference between sun-exposed and sun-protected sites. The polychoric correlation (i.e., the correlation in liability within twins for more than two categories) for total freckle counts was .91 in monozygotic twin pairs compared with .54 in dizygotic twin pairs. Additive genetic effects explained 91% (95% CI = 86%-94%) of the variance in freckle counts. Conclusion: The contribution of genetic factors on the variance for total nevus counts increased with age, and sun exposure appears to influence the expression of nevi, The results of this study highlight the need to take into account the age and site of nevus counts for future genetic linkage or association studies in the search for new melanoma genes.
引用
收藏
页码:457 / 463
页数:7
相关论文
共 47 条
[1]  
[Anonymous], 1999, MOL CELL ENDOCRINOL
[2]  
ARMSTRONG BK, 1994, CANCER SURV, V20, P219
[3]  
AUGUSTSSON A, 1991, ACTA DERM-VENEREOL, V71, P518
[4]   Risk of cutaneous melanoma in relation to the numbers, types and sites of naevi: A case-control study [J].
Bataille, V ;
Bishop, JAN ;
Sasieni, P ;
Swerdlow, AJ ;
Pinney, E ;
Griffiths, K ;
Cuzickz, J .
BRITISH JOURNAL OF CANCER, 1996, 73 (12) :1605-1611
[5]   The association between naevi and melanoma in populations with different levels of sun exposure: a joint case-control study of melanoma in the UK and Australia [J].
Bataille, V ;
Grulich, A ;
Sasieni, P ;
Swerdlow, A ;
Bishop, JN ;
McCarthy, W ;
Hersey, P ;
Cuzick, J .
BRITISH JOURNAL OF CANCER, 1998, 77 (03) :505-510
[6]   FAMILY STUDIES IN MELANOMA - IDENTIFICATION OF THE ATYPICAL MOLE SYNDROME (AMS) PHENOTYPE [J].
BISHOP, JAN ;
BATAILLE, V ;
PINNEY, E ;
BISHOP, DT .
MELANOMA RESEARCH, 1994, 4 (04) :199-206
[7]   RISK OF CUTANEOUS MELANOMA-ASSOCIATED WITH PIGMENTATION CHARACTERISTICS AND FRECKLING - SYSTEMATIC OVERVIEW OF 10 CASE-CONTROL STUDIES [J].
BLISS, JM ;
FORD, D ;
SWERDLOW, AJ ;
ARMSTRONG, BK ;
CRISTOFOLINI, M ;
ELWOOD, JM ;
GREEN, A ;
HOLLY, EA ;
MACK, T ;
MACKIE, RM ;
OSTERLIND, A ;
WALTER, SD ;
PETO, J ;
EASTON, DF .
INTERNATIONAL JOURNAL OF CANCER, 1995, 62 (04) :367-376
[8]   Characterization of melanocyte stimulating hormone receptor variant alleles in twins with red hair [J].
Box, NF ;
Wyeth, JR ;
OGorman, LE ;
Martin, NG ;
Sturm, RA .
HUMAN MOLECULAR GENETICS, 1997, 6 (11) :1891-1897
[9]  
Briollais L, 1996, GENET EPIDEMIOL, V13, P385, DOI 10.1002/(SICI)1098-2272(1996)13:4<385::AID-GEPI7>3.0.CO
[10]  
2-3