| Literature DB >> 26921332 |
Jonathan N Hofmann1, Brenda M Birmann2, Lauren R Teras3, Ruth M Pfeiffer4, Ye Wang5, Demetrius Albanes4, Dalsu Baris4, Graham A Colditz6, Anneclaire J De Roos7, Graham G Giles8, H Dean Hosgood9, Qing Lan4, Ola Landgren10, Linda M Liao4, Nathaniel Rothman4, Stephanie J Weinstein4, Michael N Pollak5, Marian L Neuhouser11, Mark P Purdue4.
Abstract
The association between obesity and multiple myeloma risk may be partly attributed to reduced circulating levels of adiponectin in obese individuals. To prospectively evaluate multiple myeloma risk in relation to adiponectin levels overall and stratified by body mass index and other characteristics, we conducted a pooled investigation of pre-diagnosed peripheral blood samples from 624 multiple myeloma cases and 1,246 individually matched controls from seven cohorts participating in the Multiple Myeloma Cohort Consortium. Analysis of circulating analyte levels measured by ELISA revealed that higher total adiponectin levels were associated with reduced multiple myeloma risk overall [highest quartile vs. lowest: OR, 0.64; 95% confidence interval (CI) 0.47-0.85; Ptrend = 0.001]. This association was apparent among cases diagnosed six or more years after blood collection (OR, 0.60; 95% CI, 0.40-0.90; Ptrend = 0.004) and was similar in magnitude for men and women (OR, 0.59 and 0.66, respectively). Interestingly, we observed strong associations among subjects who were overweight (OR, 0.41; 95% CI, 0.26-0.65) or obese (OR, 0.41; 95% CI, 0.17-0.98) but not among those with normal weight (OR, 1.20; 95% CI, 0.73-2.00; overweight/obese vs. normal weight, Pinteraction = 0.04). Our findings provide the strongest epidemiologic evidence to date that adiponectin protects against multiple myeloma development, particularly among overweight and obese individuals, and offer a method for risk assessment in this susceptible population of heavier patients. Cancer Res; 76(7); 1935-41. ©2016 AACR. ©2016 American Association for Cancer Research.Entities:
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Year: 2016 PMID: 26921332 PMCID: PMC4878138 DOI: 10.1158/0008-5472.CAN-15-2406
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701