Dietary intake in adults at risk for Huntington disease

Objective: To examine caloric intake, dietary composition, and body mass index (BMI) in participants in the Prospective Huntington At Risk Observational Study (PHAROS). Methods: Caloric intake and macronutrient composition were measured using the National Cancer Institute Food Frequency Questionnaire (FFQ) in 652 participants at risk for Huntington disease (HD) who did not meet clinical criteria for HD. Logistic regression was used to examine the relationship between macronutrients, BMI, caloric intake, and genetic status (CAG <37 vs CAG ≥37), adjusting for age, gender, and education. Linear regression was used to determine the relationship between caloric intake, BMI, and CAG repeat length. Results: A total of 435 participants with CAG <37 and 217 with CAG ≥37 completed the FFQ. Individuals in the CAG ≥37 group had a twofold odds of being represented in the second, third, or fourth quartile of caloric intake compared to the lowest quartile adjusted for age, gender, education, and BMI. This relationship was attenuated in the highest quartile when additionally adjusted for total motor score. In subjects with CAG ≥37, higher caloric intake, but not BMI, was associated with both higher CAG repeat length (adjusted regression coefficient = 0.26, p = 0.032) and 5-year probability of onset of HD (adjusted regression coefficient = 0.024; p = 0.013). Adjusted analyses showed no differences in macronutrient composition between groups. Conclusions: Increased caloric intake may be necessary to maintain body mass index in clinically unaffected individuals with CAG repeat length ≥37. This may be related to increased energy expenditure due to subtle motor impairment or a hypermetabolic state.

[1]  Alexandra Durr,et al.  Early Energy Deficit in Huntington Disease: Identification of a Plasma Biomarker Traceable during Disease Progression , 2007, PloS one.

[2]  G Hu,et al.  Body mass index and the risk of Parkinson disease , 2006, Neurology.

[3]  E. Siemers,et al.  Rate of functional decline in Huntington’s disease , 2000, Neurology.

[4]  E. Almqvist At risk for Huntington disease : The PHAROS (Prospective Huntington At Risk Observational Study) cohort enrolled. , 2006 .

[5]  Zhao-Xue Yu,et al.  Lack of Huntingtin-Associated Protein-1 Causes Neuronal Death Resembling Hypothalamic Degeneration in Huntington's Disease , 2003, The Journal of Neuroscience.

[6]  Å. Petersén,et al.  Hypothalamic–endocrine aspects in Huntington's disease , 2006, The European journal of neuroscience.

[7]  A. Young,et al.  Interrater agreement in the assessment of motor manifestations of Huntington's disease , 2005, Movement disorders : official journal of the Movement Disorder Society.

[8]  R. Paffenbarger,et al.  Body mass index and risk of Parkinson's disease: a prospective cohort study. , 2007, American journal of epidemiology.

[9]  T. Stijnen,et al.  Weight loss in Huntington disease increases with higher CAG repeat number , 2008, Neurology.

[10]  Karen Marder,et al.  Energy balance in early-stage Huntington disease. , 2005, The American journal of clinical nutrition.

[11]  R. Barker,et al.  Weight changes in Huntington's disease , 2006, European journal of neurology.

[12]  S. Hersch At risk for Huntington disease: The PHAROS (Prospective Huntington At Risk Observational Study) cohort enrolled. , 2006, Archives of neurology.

[13]  David Broadhurst,et al.  Huntington disease patients and transgenic mice have similar pro-catabolic serum metabolite profiles. , 2006, Brain : a journal of neurology.

[14]  J. Willey,et al.  PRESTROKE PHYSICAL ACTIVITY IS ASSOCIATED WITH SEVERITY AND LONG-TERM OUTCOME FROM FIRST-EVER STROKE , 2009, Neurology.

[15]  A. Ochoa,et al.  Assessment of the nutrition status of patients with Huntington's disease. , 2004, Nutrition.

[16]  F. G. Benedict,et al.  A biometric study of basal metabolism in man , 2010 .

[17]  Gordon J. Gilbert WEIGHT LOSS IN HUNTINGTON DISEASE INCREASES WITH HIGHER CAG REPEAT NUMBER , 2009 .

[18]  L. M. Morales,et al.  Nutritional evaluation of Huntington disease patients. , 1989, The American journal of clinical nutrition.

[19]  J. Corey-Bloom,et al.  Rate and correlates of weight change in Huntington’s disease* , 2004, Journal of Neurology, Neurosurgery & Psychiatry.

[20]  G Block,et al.  A Reduced Dietary Questionnaire: Development and Validation , 1990, Epidemiology.

[21]  S. W. Davies,et al.  Transgenic models of Huntington's disease. , 1999, Human molecular genetics.

[22]  K. Kashihara Weight loss in Parkinson’s disease , 2006, Journal of Neurology.

[23]  Jane S. Paulsen,et al.  Detection of Huntington’s disease decades before diagnosis: the Predict-HD study , 2007, Journal of Neurology, Neurosurgery, and Psychiatry.

[24]  E. Ravussin,et al.  Higher sedentary energy expenditure in patients with Huntington's disease , 2000, Annals of neurology.

[25]  K. Marder,et al.  Weight loss in early stage of Huntington’s disease , 2002, Neurology.

[26]  G Block,et al.  Validation of a self-administered diet history questionnaire using multiple diet records. , 1990, Journal of clinical epidemiology.

[27]  Jane S. Paulsen,et al.  A new model for prediction of the age of onset and penetrance for Huntington's disease based on CAG length , 2004, Clinical genetics.