Mediterranean diet does not delay onset of Huntington`s disease
Washington: Following a Mediterranean diet does not seem to be associated with the time of clinical onset of Huntington disease, according to a new study.
A prospective cohort study of 41 Huntington study group sites in the United States and Canada involving 1,001 participants enrolled in the Prospective Huntington at Risk Observational Study (PHAROS) between July 1999 and January 2004 who were followed up every nine months until 2010, completed a semi-quantitative food frequency questionnaire administered 33 months after baseline. A total of 211 participants ages 26 to 57 years had an expanded CAG repeat length (=37), a certain genetic characteristic).
The highest body mass index was associated with the lowest adherence to MedDi. Thirty-one participants phenoconverted. In a model adjusted for age, CAG repeat length, and caloric intake, MeDi was not associated with phenoconversion.
When individual components of MeDi were analyzed, higher dairy consumption (hazard ratio, 2.36) and higher caloric intake were associated with risk of phenoconversion, according to the study results.
Karen Marder, M.D., M.P.H., of Columbia University College of Physicians and Surgeons, New York, N.Y., and her colleagues wrote that their results suggest that studies of diet and energy expenditure in premanifest HD may provide data for both nonpharmacological interventions and pharmacological interventions to modify specific components of diet that may delay the onset of HD.
The study has been published in JAMA Neurology.
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