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Alzheimer’s Disease

(current trial)

Can Lifestyle Changes Reverse Alzheimer’s Disease?

Dr. Dean Ornish and his colleagues are conducting the first randomized controlled trial to determine if the progression of early stage Alzheimer’s disease may be slowed, stopped, or perhaps even reversed by a comprehensive lifestyle medicine program, without drugs, devices, or surgery.

This lifestyle medicine program includes a whole foods low-fat, low-sugar plant-based diet; moderate exercise; stress management techniques including meditation; and psychosocial support.

*Patients must live in the greater San Francisco Bay area to be eligible.

 

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415-332-2525
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My colleagues and I are conducting the first randomized controlled trial to determine whether or not the progression of early Alzheimer’s disease may be reversed by a comprehensive lifestyle medicine program, based on pilot data as well as other relevant studies of less-intensive interventions.

This program includes a whole foods plant-based diet low in fat and sugar with nutritional supplements; moderate exercise; stress management techniques; and support groups.

This clinical research is being conducted via the non-profit Preventive Medicine Research Institute (a 501(c)(3) public foundation) in collaboration with other institutions.  The primary endpoint measure is cognitive function testing.

We are also studying changes in telomere length at Dr. Elizabeth Blackburn’s lab at UCSF; changes in the microbiome at Dr. Rob Knight’s lab at UCSD; inflammatory biomarkers; and measuring changes in gene expression and proteomics at Dr. David Sinclair’s lab at Harvard.  These will provide insight into mechanisms by which lifestyle changes may possibly affect the progression of Alzheimer’s disease.

In this study, 100 patients who have early Alzheimer’s disease in the San Francisco Bay area are being enrolled and are randomly-assigned to one of two groups.  Both groups will be tested at baseline using these state-of-the-art measures.

After baseline testing, the first group then receives this lifestyle medicine program for 20 weeks, four hours/day, three days/week.  The second group will not and will serve as a randomized control group during this phase of the study.  Both groups will be re-tested after 20 weeks.  Then, the second group will “cross over” and receive this lifestyle medicine program for 20 weeks and the first group will continue the lifestyle change program for 20 additional weeks.  After a total of 40 weeks, both groups will be re-tested again and compared.  This study has been approved by the Western Institutional Review Board.

All meals are provided (21 meals/week) during the study to each participant and their partner along with training in stress management, exercise, and support groups three days/week, four hours/session.  There are no costs to participants for the food, training, testing, or transportation.

For more than 40 years, we have conducted scientific research, including randomized control trials and demonstration projects, proving that the progression of many chronic diseases may be reversible by making these comprehensive lifestyle changes.

These include reversing coronary heart disease, type 2 diabetes, early stage prostate cancer, high blood pressure, elevated cholesterol levels, and obesity.  Medicare created a new benefit category to cover this lifestyle medicine program for reversing heart disease nationwide, which has essentially the same intervention.

The reason that these lifestyle changes are beneficial in slowing, stopping, or reversing the progression of so many chronic diseases is that they affect many of the same underlying biological mechanisms.  For example, we found that changing lifestyle changes gene expression—over 500 genes in only three months—upregulating genes that facilitate health, downregulating genes that cause chronic inflammation, oxidative stress, and oncogenes that promote prostate cancer, breast cancer, and colon cancer.  This study was published with J. Craig Venter, who first decoded the human genome.

We also conducted the first controlled study showing that these lifestyle changes may lengthen telomeres, the ends of our chromosomes that regulate aging (in collaboration with Dr. Elizabeth Blackburn, who received the Nobel Prize for her pioneering work with telomeres).  New research indicates that there may be a causal relationship between shorter telomeres and Alzheimer’s.

We are at a state of scientific evidence with respect to Alzheimer’s disease very similar to where we were 40 years ago regarding coronary heart disease.  In other words, epidemiological data, anecdotal clinical evidence, and animal studies suggest the possibility that early-stage Alzheimer’s disease may be slowed, stopped, or perhaps even reversed by making these comprehensive lifestyle changes, but no one has yet conducted this study.

For example, other studies (e.g., the MIND and FINGER studies) have shown that more moderate lifestyle changes may slow the rate of dementia.  We are studying if more intensive lifestyle changes may possibly reverse its progression.  Whatever we show will be of great interest.  If this study is successful, it will redefine what is possible, thereby giving many people new hope and new choices.  If we show the intervention is not beneficial, then that will be valuable to know as well.

Alzheimer’s disease currently affects over five million people at an annual cost of $259 billion in the U.S.  By 2050, 16 million people are projected to be affected at an annual cost of $1.1 trillion.  As our population ages, this will increase.  There are currently no highly effective drugs for either treating or preventing Alzheimer’s.  And when you lose your memories, you lose everything.

If you are interested in finding out more information about enrolling patients who live in the greater Bay area or in supporting this research, please call Colleen Kemp, RN, MSN at 415-332-2525 x-255 or via email at info@pmri.org.  Thank you very much for your consideration.

Dean Ornish, M.D., Principal Investigator
Founder & President, Preventive Medicine Research Institute [a 501 (c)(3) nonprofit]
Clinical Professor of Medicine, School of Medicine, University of California, San Francisco

If you or someone you know is interested in learning more about participating in this study, please submit: