Literature DB >> 26443925

Abnormal Weight and Body Mass Index in Children with Juvenile Huntington's Disease.

Alexander Tereshchenko1, Michael McHugh1, Jessica K Lee1, Pedro Gonzalez-Alegre2, Kaitlin Crane3, Jeffrey Dawson3, Peg Nopoulos1,4,5.   

Abstract

BACKGROUND AND OBJECTIVES: The hallmark clinical manifestation of Huntington's disease (HD), namely lower weight and BMI has been reported in prodromal HD (PreHD) adults and also in PreHD children. Here, we aim to evaluate anthropometric measures of growth and development (height, weight, body mass index (BMI)) in a group of children, adolescents, and young adults diagnosed with Juvenile Onset Huntington's Disease (JHD).
METHODS: Growth measures for 18 JHD patients, documented prior to or shortly after diagnosis, were obtained through medical records. JHD growth measures were compared to a large sample (n = 274) of healthy children, as well as the Center for Disease Control (CDC) growth norms.
RESULTS: After controlling for sex and age, the JHD subjects had no significant differences in height. However, they were an average of 10% lower than controls in weight and BMI. Using CDC norms, the JHD subjects had the same pattern of normal height but decrement in weight. Length of cytosine-adenine-guanine (CAG) repeat in the huntingtin gene was significantly correlated to measures of weight with longer CAG repeats being associated with more severe weight reduction. A subset of 4 subjects had measures that pre-dated onset of any symptom and were therefore prodromal JHD (preJHD). These subjects also had a significant decrement in BMI compared to CDC norms.
CONCLUSIONS: Children with JHD have normal height, but significantly reduced weight and BMI, indicative of a specific deficit in body weight. As the preJHD subjects were also low in BMI, this suggests that these changes are directly due to the effect of the mutated gene on development, rather than symptom manifestation of the disease itself. Potential mechanisms of the weight decrement include energy deficiency due to mitochondrial dysfunction during development.

Entities:  

Keywords:  Huntington’s disease; body weight; growth; juvenile

Mesh:

Year:  2015        PMID: 26443925      PMCID: PMC4886713          DOI: 10.3233/JHD-150152

Source DB:  PubMed          Journal:  J Huntingtons Dis        ISSN: 1879-6397


  41 in total

1.  The relationship between CAG repeat length and age of onset differs for Huntington's disease patients with juvenile onset or adult onset.

Authors:  J Michael Andresen; Javier Gayán; Luc Djoussé; Simone Roberts; Denise Brocklebank; Stacey S Cherny; Lon R Cardon; James F Gusella; Marcy E MacDonald; Richard H Myers; David E Housman; Nancy S Wexler
Journal:  Ann Hum Genet       Date:  2006-12-19       Impact factor: 1.670

Review 2.  Energy deficit in Huntington disease: why it matters.

Authors:  Fanny Mochel; Ronald G Haller
Journal:  J Clin Invest       Date:  2011-02-01       Impact factor: 14.808

Review 3.  Hypothalamic dysfunction and neuroendocrine and metabolic alterations in Huntington's disease: clinical consequences and therapeutic implications.

Authors:  N A Aziz; D F Swaab; H Pijl; R A C Roos
Journal:  Rev Neurosci       Date:  2007       Impact factor: 4.353

4.  Mitochondrial cofactors in experimental Huntington's disease: behavioral, biochemical and histological evaluation.

Authors:  Arpit Mehrotra; Rajat Sandhir
Journal:  Behav Brain Res       Date:  2014-01-03       Impact factor: 3.332

Review 5.  Aerobic glycolysis in the primate brain: reconsidering the implications for growth and maintenance.

Authors:  Amy L Bauernfeind; Sarah K Barks; Tetyana Duka; Lawrence I Grossman; Patrick R Hof; Chet C Sherwood
Journal:  Brain Struct Funct       Date:  2013-11-02       Impact factor: 3.270

6.  The uncontrollable child: some general sociopsychological observations.

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Journal:  South Med J       Date:  1966-02       Impact factor: 0.954

7.  Abnormal in vivo skeletal muscle energy metabolism in Huntington's disease and dentatorubropallidoluysian atrophy.

Authors:  R Lodi; A H Schapira; D Manners; P Styles; N W Wood; D J Taylor; T T Warner
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8.  Mitochondrial impairment in patients and asymptomatic mutation carriers of Huntington's disease.

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9.  Systemic energy homeostasis in Huntington's disease patients.

Authors:  N Ahmad Aziz; Hanno Pijl; Marijke Frölich; Marieke Snel; Trea C M Streefland; Ferdinand Roelfsema; Raymund A C Roos
Journal:  J Neurol Neurosurg Psychiatry       Date:  2010-08-14       Impact factor: 10.154

10.  Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset.

Authors:  Nancy S Wexler; Judith Lorimer; Julie Porter; Fidela Gomez; Carol Moskowitz; Edith Shackell; Karen Marder; Graciela Penchaszadeh; Simone A Roberts; Javier Gayán; Denise Brocklebank; Stacey S Cherny; Lon R Cardon; Jacqueline Gray; Stephen R Dlouhy; Sandra Wiktorski; Marion E Hodes; P Michael Conneally; Jack B Penney; James Gusella; Jang-Ho Cha; Michael Irizarry; Diana Rosas; Steven Hersch; Zane Hollingsworth; Marcy MacDonald; Anne B Young; J Michael Andresen; David E Housman; Margot Mieja De Young; Ernesto Bonilla; Theresa Stillings; Americo Negrette; S Robert Snodgrass; Maria Dolores Martinez-Jaurrieta; Maria A Ramos-Arroyo; Jacqueline Bickham; Juan Sanchez Ramos; Frederick Marshall; Ira Shoulson; Gustavo J Rey; Andrew Feigin; Norman Arnheim; Amarilis Acevedo-Cruz; Leticia Acosta; Jose Alvir; Kenneth Fischbeck; Leslie M Thompson; Angela Young; Leon Dure; Christopher J O'Brien; Jane Paulsen; Adam Brickman; Denise Krch; Shelley Peery; Penelope Hogarth; Donald S Higgins; Bernhard Landwehrmeyer
Journal:  Proc Natl Acad Sci U S A       Date:  2004-03-01       Impact factor: 11.205

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  10 in total

1.  Quantifying the Onset of Unintended Weight Loss in Huntington's Disease: A Retrospective Analysis of Enroll-HD.

Authors:  Amy C Ogilvie; Peg C Nopoulos; Jordan L Schultz
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2.  Synaptic Dysfunction in Huntington's Disease: Lessons from Genetic Animal Models.

Authors:  Carlos Cepeda; Michael S Levine
Journal:  Neuroscientist       Date:  2020-11-16       Impact factor: 7.235

3.  Postnatal and adult consequences of loss of huntingtin during development: Implications for Huntington's disease.

Authors:  Eduardo E Arteaga-Bracho; Maria Gulinello; Michael L Winchester; Nandini Pichamoorthy; Jenna R Petronglo; Alicia D Zambrano; Julio Inocencio; Chirstopher D De Jesus; Joseph O Louie; Solen Gokhan; Mark F Mehler; Aldrin E Molero
Journal:  Neurobiol Dis       Date:  2016-09-10       Impact factor: 5.996

Review 4.  Juvenile-Onset Huntington Disease Pathophysiology and Neurodevelopment: A Review.

Authors:  Hannah S Bakels; Raymund A C Roos; Willeke M C van Roon-Mom; Susanne T de Bot
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Review 5.  Does Vitamin C Influence Neurodegenerative Diseases and Psychiatric Disorders?

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Review 6.  Huntington Disease as a Neurodevelopmental Disorder and Early Signs of the Disease in Stem Cells.

Authors:  Kalina Wiatr; Wojciech J Szlachcic; Marta Trzeciak; Marek Figlerowicz; Maciej Figiel
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7.  A genetic modifier suggests that endurance exercise exacerbates Huntington's disease.

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Journal:  Hum Mol Genet       Date:  2018-05-15       Impact factor: 6.150

Review 8.  Molecular Mechanisms Underlying Muscle Wasting in Huntington's Disease.

Authors:  Manuela Bozzi; Francesca Sciandra
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9.  Subcortical T1-Rho MRI Abnormalities in Juvenile-Onset Huntington's Disease.

Authors:  Alexander V Tereshchenko; Jordan L Schultz; Ansley J Kunnath; Joel E Bruss; Eric A Epping; Vincent A Magnotta; Peg C Nopoulos
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10.  Autonomic Changes in Juvenile-Onset Huntington's Disease.

Authors:  Jordan L Schultz; Peg C Nopoulos
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  10 in total

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