A few simple questions could help doctors assess breast cancer risk

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Photo by CDC on Unsplash
Photo by CDC on Unsplash

Breast cancer risk could be linked to obesity status and different components of metabolic syndrome (such as obesity, high blood pressure, elevated blood sugar, and abnormal cholesterol), according to international researchers who say the findings could provide new tools to help doctors easily assess breast cancer risk. The team analysed data from 63,330 postmenopausal women without prior breast cancer. After a 23-year follow-up, the team found a higher metabolic syndrome score, regardless of obesity, was linked with more poor-prognosis breast cancers, and a 44% higher risk of death from breast cancer. Obesity, regardless of metabolic syndrome score, was associated with more good-prognosis cancers, and only women with severe obesity had a higher risk of breast cancer mortality.  The team says this higher metabolic syndrome score is a previously unrecognised breast cancer risk factor, and can be determined with three simple questions about cholesterol, diabetes and hypertension history, as well as waist circumference and blood pressure measurements, all of which are commonly determined during routine doctor visits.

Media release

From: Wiley

How do obesity and metabolic syndrome affect women’s risks of breast cancer and cancer-related death?  

Analysis reveals different adverse associations of obesity and metabolic syndrome with breast cancer subtypes and mortality risk. 

In the Women’s Health Initiative (WHI) randomized trial, a low-fat diet reduced breast cancer mortality, especially in women with more metabolic syndrome (MetS) components (obesity, high blood pressure, elevated blood sugar, and abnormal cholesterol). A recent analysis of WHI findings indicates that MetS and obesity each have different associations with breast cancer subtypes and mortality risk. The findings are published by Wiley online in CANCER, a peer-reviewed journal of the American Cancer Society. 

The analysis included 63,330 postmenopausal WHI clinical trial participants without prior breast cancer, as well as normal entry mammograms and MetS scores (0–4). After a median follow-up of 23.2 years, there were 4,562 incident breast cancers and 659 deaths from breast cancer (breast cancer mortality). 

A higher MetS score (3–4), regardless of obesity, was associated with more poor-prognosis, estrogen receptor (ER)-positive, progesterone receptor (PR)-negative breast cancers and a 44% higher risk of breast cancer mortality. Obesity, regardless of MetS score, was associated with more good-prognosis, ER-positive, PR-positive cancers. Only women with severe obesity (for example, a postmenopausal woman 5 feet, 6 inches tall, weighing >218 pounds) had a higher risk of breast cancer mortality.     

“Postmenopausal women with higher MetS scores are a previously unrecognized population at higher breast cancer mortality risk,” said lead author Rowan T. Chlebowski, MD, PhD of The Lundquist Institute. “Determination of MetS scores in the clinic requires only three questions regarding cholesterol, diabetes, and hypertension history as well as waist circumference and blood pressure measurements, which are commonly determined during routine visits.” 

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Cancer
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Organisation/s: The Lundquist Institute, USA
Funder: The development of this article is partially supported by National Cancer Institute Grants R01 CA119171 and R01 CA10921. The WHI program is funded by the National Heart, Lung, and Blood Institute, National Institutes of Health, US Department of Health and Human Services, via Contracts HHSN268201600018C and HHSN268201600001C. CONFLICT OF INTEREST STATEMENT: Rowan T. Chlebowski reports receiving personal fees from Novartis, AstraZeneca, Pfizer, and UpToDate during the conduct of the study. Joanne E. Mortimer has been a consultant for AstraZeneca and Novartis. Andrew M. Kaunitz has received grants from Bayer. Robert A. Wild has received grants from Boston Heart Diagnostics and Quest Medical and holds intellectual property with Partners Health Care. The other authors declare no conflicts of interest
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