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Gene-Wise Association of Variants in Four Lysosomal Storage Disorder Genes in Neuropathologically Confirmed Lewy Body Disease

OBJECTIVE: Variants in GBA are associated with Lewy Body (LB) pathology. We investigated whether variants in other lysosomal storage disorder (LSD) genes also contribute to disease pathogenesis. METHODS: We performed a genetic analysis of four LSD genes including GBA, HEXA, SMPD1, and MCOLN1 in 231...

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Autores principales: Clark, Lorraine N., Chan, Robin, Cheng, Rong, Liu, Xinmin, Park, Naeun, Parmalee, Nancy, Kisselev, Sergey, Cortes, Etty, Torres, Paola A., Pastores, Gregory M., Vonsattel, Jean P., Alcalay, Roy, Marder, Karen, Honig, Lawrence L., Fahn, Stanley, Mayeux, Richard, Shelanski, Michael, Di Paolo, Gilbert, Lee, Joseph H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4416714/
https://www.ncbi.nlm.nih.gov/pubmed/25933391
http://dx.doi.org/10.1371/journal.pone.0125204
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author Clark, Lorraine N.
Chan, Robin
Cheng, Rong
Liu, Xinmin
Park, Naeun
Parmalee, Nancy
Kisselev, Sergey
Cortes, Etty
Torres, Paola A.
Pastores, Gregory M.
Vonsattel, Jean P.
Alcalay, Roy
Marder, Karen
Honig, Lawrence L.
Fahn, Stanley
Mayeux, Richard
Shelanski, Michael
Di Paolo, Gilbert
Lee, Joseph H.
author_facet Clark, Lorraine N.
Chan, Robin
Cheng, Rong
Liu, Xinmin
Park, Naeun
Parmalee, Nancy
Kisselev, Sergey
Cortes, Etty
Torres, Paola A.
Pastores, Gregory M.
Vonsattel, Jean P.
Alcalay, Roy
Marder, Karen
Honig, Lawrence L.
Fahn, Stanley
Mayeux, Richard
Shelanski, Michael
Di Paolo, Gilbert
Lee, Joseph H.
author_sort Clark, Lorraine N.
collection PubMed
description OBJECTIVE: Variants in GBA are associated with Lewy Body (LB) pathology. We investigated whether variants in other lysosomal storage disorder (LSD) genes also contribute to disease pathogenesis. METHODS: We performed a genetic analysis of four LSD genes including GBA, HEXA, SMPD1, and MCOLN1 in 231 brain autopsies. Brain autopsies included neuropathologically defined LBD without Alzheimer Disease (AD) changes (n = 59), AD without significant LB pathology (n = 71), Alzheimer disease and lewy body variant (ADLBV) (n = 68), and control brains without LB or AD neuropathology (n = 33). Sequencing of HEXA, SMPD1, MCOLN1 and GBA followed by ‘gene wise’ genetic association analysis was performed. To determine the functional effect, a biochemical analysis of GBA in a subset of brains was also performed. GCase activity was measured in a subset of brain samples (n = 64) that included LBD brains, with or without GBA mutations, and control brains. A lipidomic analysis was also performed in brain autopsies (n = 67) which included LBD (n = 34), ADLBV (n = 3), AD (n = 4), PD (n = 9) and control brains (n = 17), comparing GBA mutation carriers to non-carriers. RESULTS: In a ‘gene-wise’ analysis, variants in GBA, SMPD1 and MCOLN1 were significantly associated with LB pathology (p range: 0.03–4.14 x10(-5)). Overall, the mean levels of GCase activity were significantly lower in GBA mutation carriers compared to non-carriers (p<0.001). A significant increase and accumulation of several species for the lipid classes, ceramides and sphingolipids, was observed in LBD brains carrying GBA mutations compared to controls (p range: p<0.05-p<0.01). INTERPRETATION: Our study indicates that variants in GBA, SMPD1 and MCOLN1 are associated with LB pathology. Biochemical data comparing GBA mutation carrier to non-carriers support these findings, which have important implications for biomarker development and therapeutic strategies.
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spelling pubmed-44167142015-05-07 Gene-Wise Association of Variants in Four Lysosomal Storage Disorder Genes in Neuropathologically Confirmed Lewy Body Disease Clark, Lorraine N. Chan, Robin Cheng, Rong Liu, Xinmin Park, Naeun Parmalee, Nancy Kisselev, Sergey Cortes, Etty Torres, Paola A. Pastores, Gregory M. Vonsattel, Jean P. Alcalay, Roy Marder, Karen Honig, Lawrence L. Fahn, Stanley Mayeux, Richard Shelanski, Michael Di Paolo, Gilbert Lee, Joseph H. PLoS One Research Article OBJECTIVE: Variants in GBA are associated with Lewy Body (LB) pathology. We investigated whether variants in other lysosomal storage disorder (LSD) genes also contribute to disease pathogenesis. METHODS: We performed a genetic analysis of four LSD genes including GBA, HEXA, SMPD1, and MCOLN1 in 231 brain autopsies. Brain autopsies included neuropathologically defined LBD without Alzheimer Disease (AD) changes (n = 59), AD without significant LB pathology (n = 71), Alzheimer disease and lewy body variant (ADLBV) (n = 68), and control brains without LB or AD neuropathology (n = 33). Sequencing of HEXA, SMPD1, MCOLN1 and GBA followed by ‘gene wise’ genetic association analysis was performed. To determine the functional effect, a biochemical analysis of GBA in a subset of brains was also performed. GCase activity was measured in a subset of brain samples (n = 64) that included LBD brains, with or without GBA mutations, and control brains. A lipidomic analysis was also performed in brain autopsies (n = 67) which included LBD (n = 34), ADLBV (n = 3), AD (n = 4), PD (n = 9) and control brains (n = 17), comparing GBA mutation carriers to non-carriers. RESULTS: In a ‘gene-wise’ analysis, variants in GBA, SMPD1 and MCOLN1 were significantly associated with LB pathology (p range: 0.03–4.14 x10(-5)). Overall, the mean levels of GCase activity were significantly lower in GBA mutation carriers compared to non-carriers (p<0.001). A significant increase and accumulation of several species for the lipid classes, ceramides and sphingolipids, was observed in LBD brains carrying GBA mutations compared to controls (p range: p<0.05-p<0.01). INTERPRETATION: Our study indicates that variants in GBA, SMPD1 and MCOLN1 are associated with LB pathology. Biochemical data comparing GBA mutation carrier to non-carriers support these findings, which have important implications for biomarker development and therapeutic strategies. Public Library of Science 2015-05-01 /pmc/articles/PMC4416714/ /pubmed/25933391 http://dx.doi.org/10.1371/journal.pone.0125204 Text en © 2015 Clark et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Clark, Lorraine N.
Chan, Robin
Cheng, Rong
Liu, Xinmin
Park, Naeun
Parmalee, Nancy
Kisselev, Sergey
Cortes, Etty
Torres, Paola A.
Pastores, Gregory M.
Vonsattel, Jean P.
Alcalay, Roy
Marder, Karen
Honig, Lawrence L.
Fahn, Stanley
Mayeux, Richard
Shelanski, Michael
Di Paolo, Gilbert
Lee, Joseph H.
Gene-Wise Association of Variants in Four Lysosomal Storage Disorder Genes in Neuropathologically Confirmed Lewy Body Disease
title Gene-Wise Association of Variants in Four Lysosomal Storage Disorder Genes in Neuropathologically Confirmed Lewy Body Disease
title_full Gene-Wise Association of Variants in Four Lysosomal Storage Disorder Genes in Neuropathologically Confirmed Lewy Body Disease
title_fullStr Gene-Wise Association of Variants in Four Lysosomal Storage Disorder Genes in Neuropathologically Confirmed Lewy Body Disease
title_full_unstemmed Gene-Wise Association of Variants in Four Lysosomal Storage Disorder Genes in Neuropathologically Confirmed Lewy Body Disease
title_short Gene-Wise Association of Variants in Four Lysosomal Storage Disorder Genes in Neuropathologically Confirmed Lewy Body Disease
title_sort gene-wise association of variants in four lysosomal storage disorder genes in neuropathologically confirmed lewy body disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4416714/
https://www.ncbi.nlm.nih.gov/pubmed/25933391
http://dx.doi.org/10.1371/journal.pone.0125204
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