| Literature DB >> 24861847 |
Lauren R Teras1, Cari M Kitahara, Brenda M Birmann, Patricia A Hartge, Sophia S Wang, Kim Robien, Alpa V Patel, Hans-Olov Adami, Elisabete Weiderpass, Graham G Giles, Pramil N Singh, Michael Alavanja, Laura E Beane Freeman, Leslie Bernstein, Julie E Buring, Graham A Colditz, Gary E Fraser, Susan M Gapstur, J Michael Gaziano, Edward Giovannucci, Jonathan N Hofmann, Martha S Linet, Gila Neta, Yikyung Park, Ulrike Peters, Philip S Rosenberg, Catherine Schairer, Howard D Sesso, Meir J Stampfer, Kala Visvanathan, Emily White, Alicja Wolk, Anne Zeleniuch-Jacquotte, Amy Berrington de González, Mark P Purdue.
Abstract
Multiple myeloma (MM) is a rare but highly fatal malignancy. High body weight is associated with this cancer, but several questions remain regarding the aetiological relevance of timing and location of body weight. To address these questions, we conducted a pooled analysis of MM mortality using 1·5 million participants (including 1388 MM deaths) from 20 prospective cohorts in the National Cancer Institute Cohort Consortium. Proportional hazards regression was used to calculate pooled multivariate hazard ratios (HRs) and 95% confidence intervals (CIs). Associations with elevated MM mortality were observed for higher early-adult body mass index (BMI; HR = 1·22, 95% CI: 1·09-1·35 per 5 kg/m(2) ) and for higher cohort-entry BMI (HR 1·09, 95% CI: 1·03-1·16 per 5 kg/m(2) ) and waist circumference (HR = 1·06, 95% CI: 1·02-1·10 per 5 cm). Women who were the heaviest, both in early adulthood (BMI 25+) and at cohort entry (BMI 30+) were at greater risk compared to those with BMI 18·5 ≤ 25 at both time points (HR = 1·95, 95% CI: 1·33-2·86). Waist-to-hip ratio and height were not associated with MM mortality. These observations suggest that overall, and possibly also central, obesity influence myeloma mortality, and women have the highest risk of death from this cancer if they remain heavy throughout adulthood.Entities:
Keywords: and anthropometry; body mass index; multiple myeloma; pooled analysis; prospective cohort study
Mesh:
Year: 2014 PMID: 24861847 PMCID: PMC4134758 DOI: 10.1111/bjh.12935
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998