Reproductive factors and gall-bladder cancer, and the effect of common genetic variants on these associations: a case–control study in India

Author:

Mhatre Sharayu12,Lacey Ben3,Sherliker Paul34,Chatterjee Nilanjan567,Rajaraman Preetha8,Goel Mahesh29,Patkar Shraddha29,Ostwal Vikas210,Patil Prachi211,Shrikhande Shailesh V29,Chitkara Garvit29,Badwe Rajendra29,Lewington Sarah3412ORCID,Dikshit Rajesh12

Affiliation:

1. Section of Molecular Epidemiology and Population Genetics, Centre for Cancer Epidemiology, Tata Memorial Centre, Kharghar, Navi Mumbai, India

2. Homi Bhabha National Institute (HBNI), Mumbai, India

3. Clinical Trial Service Unit and Epidemiological Studies Unit (CTSU), Nuffield Department of Population Health, University of Oxford, Oxford, UK

4. MRC Population Health Research Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK

5. Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD, USA

6. Department of Biostatistics, Bloomberg School of Public Health, John Hopkins University, Baltimore, MD, USA

7. Department of Oncology, School of Medicine, John Hopkins University, Baltimore, MD, USA

8. Office of Global Affairs, Department of Health and Human Services, Washington, DC, USA

9. Department of Surgical Oncology, Tata Memorial Hospital, Mumbai, Maharashtra, India

10. Department of Medical Oncology, Tata Memorial Hospital, Mumbai, Maharashtra, India

11. Department of Medical Gastroenterology, Tata Memorial Hospital, Mumbai, Maharashtra, India

12. UKM Medical Molecular Biology Institute (UMBI), Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia

Abstract

Abstract Background In India, as elsewhere, the incidence of gall-bladder cancer (GBC) is substantially higher in women than in men. Yet, the relevance of reproductive factors to GBC remains poorly understood. Methods We used logistic regression adjusted for age, education and area to examine associations between reproductive factors and GBC risk, using 790 cases of histologically confirmed GBC and group-matched 1726 visitor controls. We tested the interaction of these associations by genetic variants known to increase the risk of GBC. Results Parity was strongly positively associated with GBC risk: each additional pregnancy was associated with an ∼25% higher risk {odds ratio [OR] 1.26 [95% confidence interval (95% CI) 1.17–1.37]}. After controlling for parity, GBC risk was weakly positively associated with later age of menarche [postmenopausal women, OR 1.11 (95% CI 1.00–1.22) per year], earlier menopause [OR 1.03 (95% CI 1.00–1.06) per year] and shorter reproductive lifespan [OR 1.04 (95% CI 1.01–1.07) per year], but there was little evidence of an association with breastfeeding duration or years since last pregnancy. Risk alleles of single-nucleotide polymorphisms in the ABCB4 and ABCB1 genetic regions had a multiplicative effect on the association with parity, but did not interact with other reproductive factors. Conclusions We observed higher GBC risk with higher parity and shorter reproductive lifespan, suggesting an important role for reproductive and hormonal factors.

Funder

Department of Biotechnology

National Institute for Health Research Biomedical Research Centre

Publisher

Oxford University Press (OUP)

Subject

General Medicine,Epidemiology

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