Reduced Telomere Length in Neurodegenerative Disorders May Suggest Shared Biology. Author: Kota LN1, Bharath S, Purushottam M, Moily NS, Sivakumar PT, Varghese M, Pal PK, Jain S. Affiliation: 1From the Dept. of Psychiatry (LNK, SB, MP, NSM, PTS, MV, SJ) and the Dept. of Neurology (PKP), National Institute of Mental Health and Neurosciences, Bangalore, Karnataka, India. Conference/Journal: J Neuropsychiatry Clin Neurosci. Date published: 2014 Dec 26 Other: Word Count: 111 Early cell death is a feature of neurodegenerative disorders. Telomere shortening is related to premature cellular senescence and could be a marker for cellular pathology in neurological diseases. Relative telomere length in dementia (N=70), Huntington's disease (N=35), ataxia telangiectasia (N=9), and age-group matched control samples (N=105) was measured as relative telomere copy/single copy gene ratios. Individuals with Huntington's disease had the lowest relative telomere copy/single copy gene ratio (0.21), followed by ataxia telangiectasia (0.31) and dementia (0.48). The younger control group had the highest relative telomere copy/single copy gene ratio (1.07). The reduced telomere length could be indicative of shared biological pathways across these disorders contributing to cellular senescence. PMID: 25541866 keyword biomarker