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In a new research paper BWH and MGH researchers identify a transcriptional biomarker that may assist in the monitoring of Huntington's disease activity and in the evaluation of new medications.

Biomarker for Huntington's disease identified

BWH and MGH researchers find transcriptional biomarker that could help monitor disease activity, evaluate potential treatments

03/Oct/2011

Huntington's disease, a devastating genetic disorder that causes degeneration of nerve cells in the brain, affects more than 15,000 Americans, and at least 150,000 are at risk of developing the disease.  There is no known cure or treatment for the disease – which starts with changes in mood, judgment, memory, and other cognitive functions and inevitably leads to increasing physical disability, dementia and death.  In a new research paper published online in the Proceedings of the National Academy of Sciences Early Edition, researchers identify a transcriptional biomarker that may assist in the monitoring of disease activity and in the evaluation of new medications.

The research, which is a collaboration between the laboratory of Clemens Scherzer, MD, in the Center for Neurologic Diseases at Brigham and Women's Hospital (BWH) and the laboratory of Steven Hersch, MD, PhD, at the MassGeneral Institute for Neurodegenerative Disease at Massachusetts General Hospital (MGH),  describes the discovery and validation of a blood test that could be used to follow the activity of Huntington's disease as well as the response patients might have to neuroprotective treatments.

Researchers analyzed 119 human blood samples from both Huntington's disease patients and others.  They found that individuals with Huntington's disease overexpressed the gene, H2AFY, in their blood.  The overexpression of this gene in both the blood and the brain was validated in blood samples from clinical studies involving 142 participants – including individuals with HD, some who were genetically destined to develop the disorder, and healthy controls – and postmortem autopsy samples from 12 individuals (including HD patients).  Specifically, the research demonstrates a 1.6-fold over-expression of H2AFY in patients with Huntington's disease.  

"We know how to diagnose HD. What we don't have, however, is a simple test to tell us whether the disease is active and progressing or responding to new medications. Such a test would be critical for making clinical trials more efficient. We are excited about the potential of our discovery" said Scherzer, who is also an assistant professor of Neurology at Harvard Medical School.  "The next challenge will be to develop this prototype biomarker into a test that is useful in drug trials."

To begin to evaluate the potential role H2AFY may play in monitoring the effectiveness of neuroprotective therapies, the researchers conducted experiments using genetic mouse models of Huntington's disease which were also discovered to over express H2AFY.  They found that animals receiving the neuroprotective drug sodium phenylbutyrate for two weeks had reduced expression of that gene in key areas of the brain. The investigators also tested human blood samples from a multicenter phase II clinical trial of sodium phenylbutyrate conducted by Dr. Hersch and the Huntington Study Group and found that the expression of H2AFY was diminished in participants who received the drug.  

"Our findings, taken along with previous research, suggest that Huntington's disease progression and patient responses to some treatments could be measured by a blood test and that this biomarker gene, H2AFY, could help to facilitate research into the effectiveness of potential treatments for this disease," said Hersch, who is also a professor of Neurology at Harvard Medical School.  "Even in very large studies lasting years, it is very difficult to use clinical measures to find evidence that a treatment might slow down Huntington's disease. Biomarkers like H2AFY can help considerably."

This research was funded through a National Institute of Health/National Institute of Neurological Disorders and Stroke supported program project, known as REVEAL-HD, which is a unique multi-disciplinary and multi-collaborative biomarker discovery and validation project.

Brigham and Women's Hospital is a 793-bed nonprofit teaching affiliate of Harvard Medical School. Through investigation and discovery conducted at its Biomedical Research Institute, BWH is an international leader in basic, clinical and translational research on human diseases, involving more than 900 physician-investigators and renowned biomedical scientists and faculty supported by more than $537 million in funding. BWH is also home to major landmark epidemiologic population studies, including the Nurses' and Physicians' Health Studies and the Women's Health Initiative.

Celebrating the 200th anniversary of its founding in 1811, Massachusetts General Hospital is the original and largest teaching hospital of Harvard Medical School. The MGH conducts the largest hospital-based research program in the United States, with an annual research budget of nearly $700 million and major research centers in AIDS, cardiovascular research, cancer, computational and integrative biology, cutaneous biology, human genetics, medical imaging, neurodegenerative disorders, regenerative medicine, systems biology, transplantation biology and photomedicine. 

MGH and BWH are founding members of Partners HealthCare System, a Boston-based integrated health care delivery system.  Both institutions are consistently ranked among the nation's top hospitals by US News and World Report.

Media Contacts: Mike Morrison, (617) 724-6425, mdmorrison@partners.org
Brigham and Women's Hospital: Lori J. Shanks, 617-534-1604, ljshanks@partners.org

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