Literature DB >> 1442963

Pathways to hysterectomy: insights from longitudinal twin research.

S A Treloar1, N G Martin, L Dennerstein, B Raphael, A C Heath.   

Abstract

OBJECTIVE: We hypothesized that genetic influences act on "liability" to hysterectomy, that secular influences might differentially affect relative importance of genetic and environmental influences, and that the sources of genetic influences could be identified from reported risk factors. STUDY
DESIGN: Hysterectomy data from an Australia-wide volunteer sample of female adult monozygotic and dizygotic twins are reported. In 1980 through 1982 a mailed questionnaire was completed by 1232 monozygotic female twin pairs and 751 dizygotic female twin pairs (3966 women) from the Australian Twin Register (wave 1). The same twins were surveyed by questionnaire 8 years later (wave 2).
RESULTS: A total of 366 had undergone hysterectomy by wave 1 and a further 198 at wave 2. The twin-pair correlations for liability to hysterectomy at wave 1 (0.61 +/- 0.06 for monozygotic and 0.20 +/- 0.11 for dizygotic) and wave 2 (0.65 +/- 0.05 for monozygotic and 0.32 +/- 0.09 for monozygotic) indicated a substantial genetic contribution. Reported risk factors accounted for only 15% of total variance.
CONCLUSION: Genetic influences on liability to hysterectomy were substantial and stable across birth cohorts, but the important sources of genetic influence on liability to hysterectomy are yet to be identified.

Entities:  

Mesh:

Year:  1992        PMID: 1442963     DOI: 10.1016/s0002-9378(11)91632-9

Source DB:  PubMed          Journal:  Am J Obstet Gynecol        ISSN: 0002-9378            Impact factor:   8.661


  22 in total

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Authors:  Karen L Huyck; Carolien I M Panhuysen; Karen T Cuenco; Jingmei Zhang; Hilary Goldhammer; Emlyn S Jones; Priya Somasundaram; Allison M Lynch; Bernard L Harlow; Hang Lee; Elizabeth A Stewart; Cynthia C Morton
Journal:  Am J Obstet Gynecol       Date:  2008-02       Impact factor: 8.661

Review 2.  Warner-Lambert/Parke-Davis Award lecture. Many tumors and many genes: genetics of uterine leiomyomata.

Authors:  C C Morton
Journal:  Am J Pathol       Date:  1998-10       Impact factor: 4.307

3.  A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids.

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4.  Genetic effects on variation in red-blood-cell folate in adults: implications for the familial aggregation of neural tube defects.

Authors:  L E Mitchell; D L Duffy; P Duffy; G Bellingham; N G Martin
Journal:  Am J Hum Genet       Date:  1997-02       Impact factor: 11.025

5.  BET1L and TNRC6B associate with uterine fibroid risk among European Americans.

Authors:  Todd L Edwards; Kara A Michels; Katherine E Hartmann; Digna R Velez Edwards
Journal:  Hum Genet       Date:  2013-04-19       Impact factor: 4.132

Review 6.  Epidemiological and genetic clues for molecular mechanisms involved in uterine leiomyoma development and growth.

Authors:  Arno E Commandeur; Aaron K Styer; Jose M Teixeira
Journal:  Hum Reprod Update       Date:  2015-07-03       Impact factor: 15.610

7.  Randomised trial comparing hysterectomy with endometrial ablation for dysfunctional uterine bleeding: psychiatric and psychosocial aspects.

Authors:  D A Alexander; A A Naji; S B Pinion; J Mollison; H C Kitchener; D E Parkin; D R Abramovich; I T Russell
Journal:  BMJ       Date:  1996-02-03

8.  African ancestry and genetic risk for uterine leiomyomata.

Authors:  Lauren A Wise; Edward A Ruiz-Narvaez; Julie R Palmer; Yvette C Cozier; Arti Tandon; Nick Patterson; Rose G Radin; Lynn Rosenberg; David Reich
Journal:  Am J Epidemiol       Date:  2012-11-15       Impact factor: 4.897

9.  Advances in the management of uterine fibroids.

Authors:  Kirsty I Munro; Hilary Od Critchley
Journal:  F1000 Med Rep       Date:  2009-09-28

Review 10.  Epidemiology of Uterine Fibroids: From Menarche to Menopause.

Authors:  Lauren A Wise; Shannon K Laughlin-Tommaso
Journal:  Clin Obstet Gynecol       Date:  2016-03       Impact factor: 2.190

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