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Details

Autor(en) / Beteiligte
Titel
Circulating Biomarker Score for Visceral Fat and Risks of Incident Colorectal and Postmenopausal Breast Cancer: The Multiethnic Cohort Adiposity Phenotype Study
Ist Teil von
  • Cancer epidemiology, biomarkers & prevention, 2020-05, Vol.29 (5), p.966-973
Ort / Verlag
United States
Erscheinungsjahr
2020
Link zum Volltext
Quelle
EZB Free E-Journals
Beschreibungen/Notizen
  • Visceral adipose tissue (VAT) may play a greater role than subcutaneous fat in increasing cancer risk but is poorly estimated in epidemiologic studies. We developed a VAT prediction score by regression equations averaged across 100 least absolute shrinkage and selection operator models in a cross-sectional study of 1,801 older adults in the Multiethnic Cohort (MEC). The score was then used as proxy for VAT in case-control studies of postmenopausal breast (950 case-control pairs) and colorectal (831 case-control pairs) cancer in an independent sample in MEC. Abdominal MRI-derived VAT; circulating biomarkers of metabolic, hormonal, and inflammation dysfunctions; and ORs for incident cancer adjusted for BMI and other risk factors were assessed. The final score, composed of nine biomarkers, BMI, and height, explained 11% and 15% more of the variance in VAT than BMI alone in men and women, respectively. The area under the receiver operator curve for VAT >150 cm was 0.90 in men and 0.86 in women. The VAT score was associated with risk of breast cancer [OR (95% confidence interval [CI]) by increasing tertiles: 1.00, 1.09 (0.86-1.39), 1.48 (1.16-1.89); = 0.002] but not with colorectal cancer ( = 0.84), although an association [1.00, 0.98 (0.68-1.39), 1.24 (0.88-1.76); = 0.08] was suggested for this cancer after excluding cases that occurred within 7 years of blood draw ( = 0.06). The VAT score predicted risks of postmenopausal breast cancer and can be used for risk assessment in diverse populations. These findings provide specific evidence for a role of VAT in breast cancer.
Sprache
Englisch
Identifikatoren
ISSN: 1055-9965
eISSN: 1538-7755
DOI: 10.1158/1055-9965.epi-19-1469
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7196505
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