News Release

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.

Peer-Reviewed Publication

Wiley

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.” 

 

Additional information
NOTE: The information contained in this release is protected by copyright. Please include journal attribution in all coverage. A free abstract of this article will be available via the CANCER Newsroom upon online publication. For more information or to obtain a PDF of any study, please contact: Sara Henning-Stout, newsroom@wiley.com 

Full Citation:
“Breast cancer incidence and mortality by metabolic syndrome and obesity: the Women’s Health Initiative.” Rowan T. Chlebowski, Aaron K. Aragaki, Kathy Pan, Michael S. Simon, Marian L. Neuhouser, Reina Haque, Thomas E. Rohan, Jean Wactawski-Wende, Tonya S. Orchard, Joanne E. Mortimer, Dorothy Lane, Andrew M. Kaunitz, Pinkal Desai, Robert A. Wild, Ana Barac, and JoAnn E. Manson. CANCER; Published Online: May 13, 2024 (DOI: 10.1002/cncr.35318). 

URL Upon Publication: http://doi.wiley.com/10.1002/cncr.35318

Author Contact: Rowan Chlebowski, MD, PhD, at rowanchlebowski@gmail.com or +1 310-748-7463

About the Journal 
CANCER is a peer-reviewed publication of the American Cancer Society integrating scientific information from worldwide sources for all oncologic specialties. The objective of CANCER is to provide an interdisciplinary forum for the exchange of information among oncologic disciplines concerned with the etiology, course, and treatment of human cancer. CANCER is published on behalf of the American Cancer Society by Wiley and can be accessed online. Follow CANCER on Twitter @JournalCancer and Instagram @ACSJournalCancer, and stay up to date with the American Cancer Society Journals on LinkedIn.

About Wiley      
Wiley is a knowledge company and a global leader in research, publishing, and knowledge solutions. Dedicated to the creation and application of knowledge, Wiley serves the world’s researchers, learners, innovators, and leaders, helping them achieve their goals and solve the world's most important challenges. For more than two centuries, Wiley has been delivering on its timeless mission to unlock human potential.  Visit us at Wiley.com. Follow us on Facebook, Twitter, LinkedIn and Instagram.


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