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Hanash uncovers protein effects of HRT

Study links estrogen hormone replacement therapy with serum levels of proteins involved in several major body processes

May 4, 2009
Dr. Samir Hanash

Dr. Samir Hanash's in-depth proteomic analysis of the sera of 50 participants from the Women’s Health Initiative hormone replacement therapy trial provides explanations for the trial’s clinical results.

Photo by Gordon Todd

An in-depth proteomic analysis of the sera of 50 participants from the Women’s Health Initiative (WHI) hormone replacement therapy trial provides some explanations for the trial’s clinical results. The study, led by Dr. Samir Hanash and published in Biomed Central’s open access journal Genome Medicine, shows that estrogen upregulates proteins involved in several major body processes.

Hanash, of the Public Health Sciences Division, worked with a team of researchers to identify and quantify proteins from 2,576,869 mass spectra, the largest serum protein data set obtained from a human observational study or clinical trial to date.

“Remarkably, as many as 10 percent of plasma proteins analyzed were found to be affected by estrogen hormone replacement therapy in post-menopausal women," Hanash said. "These changes indicate a substantial effect on coagulation and metabolic proteins that may explain the increased risk of venous thromboembolism and stroke, and the reduced risk of fracture, found in the WHI trial.”

The authors used baseline and one-year post-treatment sera samples from 50 women in the WHI trial, separated into five experimental pools. The average age of the subjects was 61.4 years. There were no statistically significant differences in any baseline characteristics between pools. Using samples gathered one year after the initiation of therapy, they identified changes in serum levels of proteins directly involved in processes as disparate as osteogenesis, blood vessel morphogenesis, blood pressure regulation, immunity, inflammation and coagulation.

This work demonstrates the utility of comprehensive profiling of the serum proteome for clinical investigations. “Our findings should encourage other investigators to include quantitative proteomic analysis as part of clinical trials of new therapies to better understand the effect of therapy and to identify surrogate markers of response to treatment,” Hanash said.

[Adapted from a news release from Genome Medicine.]

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