Patients with amyotrophic lateral sclerosis (ALS) may be an exception to the rule that being overweight is a health hazard. In a retrospective study of over 400 ALS patients, MGH researchers found that those who were mildly obese survived longer than patients who were normal weight, underweight or even overweight.
Mild obesity appears to improve survival in ALS patients
Mass. General study finds survival predicted by body mass index, not lipid levels
Patients with amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease, may be an exception to the rule that being overweight is a health hazard. In a retrospective study of over 400 ALS patients, Massachusetts General Hospital (MGH) researchers found that those who were mildly obese survived longer than patients who were normal weight, underweight or even overweight. The study will appear in the journal Muscle & Nerve and has been published online.
"We have long known that being underweight shortens survival for ALS patients, and several studies in an animal model have shown that weight gain is associated with increased survival," says Anne-Marie Wills, MD, MPH, of the MGH Neurology Clinical Trials Unit, senior author of the report. "Our study was designed to investigate how cholesterol levels affect survival. We were surprised to find that body mass index or BMI – a measure of weight adjusted for height – made a large difference in survival. Patients with a BMI of 30 to 35, who would be considered mildly clinically obese, lived the longest; and patients who were overweight, with a BMI of 25 to 30, lived the second longest."
ALS is a progressive neurodegenerative disease affecting motor neurons in the brain and spinal cord. Death of these nerve cells stops the transmission of neural impulses to muscle fibers, leading to weakness, paralysis and usually death from respiratory failure. During the course of their disease ALS patients usually lose even more weight than can be attributed to the loss of muscle mass caused by nerve destruction and the related muscle inactivity. Studies have shown that ALS patients burn more calories than would be expected from their limited physical activity, but the mechanism for this metabolic change is currently unknown.
A previous smaller study suggested that ALS patients with higher levels of low-density lipoprotein (LDL) relative to high-density lipoprotein (HDL) might live longer. In order to test that association in a larger group of patients, the MGH team analyzed data on more than 400 patients who had participated in three clinical trials of potential ALS drugs. Along with the results of initial blood tests taken when participants entered the trials, the researchers had access to follow-up blood tests for almost 200 participants and information on how long each patient survived without needing mechanical ventilation assistance.
Depending on the particular clinical trial, survival data was available for one to two years after study initiation. While higher baseline cholesterol levels were associated with longer survival, that association disappeared when the results were controlled for BMI. As expected, the shortest survival was seen in malnourished or morbidly obese patients, but patients in the mildly obese range had the longest survival of any BMI group.
"While this finding needs further investigation, we hypothesize that it is due to increased energy reserves available to these patients," says Wills, an instructor of Neurology at Harvard Medical School. "We don't know whether actively putting on weight would be helpful, but right now I'm telling my patients with ALS they can eat anything they want."
The MGH team is leading a clinical trial to test the safety and tolerability of a high-fat, high-calorie diet for ALS patient. In order to precisely control participants' caloric intake, the study is limited to ALS patients who already have a feeding tube in place. Sponsored by the Muscular Dystrophy Association, the trial takes place at 12 sites around the country. More information is available at http://www.alsconsortium.org or at http://clinicaltrials.gov. At either site, search for "High-fat + ALS."
The lead author of the Muscle & Nerve study is Sabrina Paganoni, MD, PhD, of Spaulding Rehabilitation Hospital. Additional co-authors are Jing Deng, Matthew Jaffa and Merit Cudkowicz, MD, MSc, all of MGH Neurology. The study was supported by the Muscular Dystrophy Association and the Digiovanni ALS Research Fund.
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 more than $600 million and major research centers in AIDS, cardiovascular research, cancer, computational and integrative biology, cutaneous biology, human genetics, medical imaging, neurodegenerative disorders, regenerative medicine, reproductive biology, systems biology, transplantation biology and photomedicine.
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