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Adiposity and Endometrial Cancer Risk in Postmenopausal Women: A Sequential Causal Mediation Analysis.

Authors :
Dashti SG
English DR
Simpson JA
Karahalios A
Moreno-Betancur M
Biessy C
Rinaldi S
Ferrari P
Tjønneland A
Halkjær J
Dahm CC
Vistisen HT
Menegaux F
Perduca V
Severi G
Aleksandrova K
Schulze MB
Masala G
Sieri S
Tumino R
Macciotta A
Panico S
Hiensch AE
May AM
Quirós JR
Agudo A
Sánchez MJ
Amiano P
Colorado-Yohar S
Ardanaz E
Allen NE
Weiderpass E
Fortner RT
Christakoudi S
Tsilidis KK
Riboli E
Kaaks R
Gunter MJ
Viallon V
Dossus L
Source :
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology [Cancer Epidemiol Biomarkers Prev] 2021 Jan; Vol. 30 (1), pp. 104-113. Date of Electronic Publication: 2020 Oct 02.
Publication Year :
2021

Abstract

Background: Adiposity increases endometrial cancer risk, possibly through inflammation, hyperinsulinemia, and increasing estrogens. We aimed to quantify the mediating effects of adiponectin (anti-inflammatory adipocytokine); IL6, IL1-receptor antagonist, TNF receptor 1 and 2, and C-reactive protein (inflammatory status biomarkers); C-peptide (hyperinsulinemia biomarker); and free estradiol and estrone (estrogen biomarkers) in the adiposity-endometrial cancer link in postmenopausal women.<br />Methods: We used data from a case-control study within the European Prospective Investigation into Cancer and Nutrition (EPIC). Eligible women did not have cancer, hysterectomy, and diabetes; did not use oral contraceptives or hormone therapy; and were postmenopausal at recruitment. Mediating pathways from adiposity to endometrial cancer were investigated by estimating natural indirect (NIE) and direct (NDE) effects using sequential mediation analysis.<br />Results: The study included 163 cases and 306 controls. The adjusted OR for endometrial cancer for body mass index (BMI) ≥30 versus ≥18.5-<25 kg/m <superscript>2</superscript> was 2.51 (95% confidence interval, 1.26-5.02). The ORs <superscript>NIE</superscript> were 1.95 (1.01-3.74) through all biomarkers [72% proportion mediated (PM)] decomposed as: 1.35 (1.06-1.73) through pathways originating with adiponectin (33% PM); 1.13 (0.71-1.80) through inflammation beyond (the potential influence of) adiponectin (13% PM); 1.05 (0.88-1.24) through C-peptide beyond adiponectin and inflammation (5% PM); and 1.22 (0.89-1.67) through estrogens beyond preceding biomarkers (21% PM). The OR <superscript>NDE</superscript> not through biomarkers was 1.29 (0.54-3.09). Waist circumference gave similar results.<br />Conclusions: Reduced adiponectin and increased inflammatory biomarkers, C-peptide, and estrogens mediated approximately 70% of increased odds of endometrial cancer in women with obesity versus normal weight.<br />Impact: If replicated, these results could have implications for identifying targets for intervention to reduce endometrial cancer risk in women with obesity.<br /> (©2020 American Association for Cancer Research.)

Details

Language :
English
ISSN :
1538-7755
Volume :
30
Issue :
1
Database :
MEDLINE
Journal :
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology
Publication Type :
Academic Journal
Accession number :
33008875
Full Text :
https://doi.org/10.1158/1055-9965.EPI-20-0965