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Exemplar scoring identifies genetically separable phenotypes of lithium responsive bipolar disorder
Predicting lithium response (LiR) in bipolar disorder (BD) may inform treatment planning, but phenotypic heterogeneity complicates discovery of genomic markers. We hypothesized that patients with “exemplary phenotypes”—those whose clinical features are reliably associated with LiR and non-response (...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801503/ https://www.ncbi.nlm.nih.gov/pubmed/33431852 http://dx.doi.org/10.1038/s41398-020-01148-y |
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author | Nunes, Abraham Stone, William Ardau, Raffaella Berghöfer, Anne Bocchetta, Alberto Chillotti, Caterina Deiana, Valeria Degenhardt, Franziska Forstner, Andreas J. Garnham, Julie S. Grof, Eva Hajek, Tomas Manchia, Mirko Mattheisen, Manuel McMahon, Francis Müller-Oerlinghausen, Bruno Nöthen, Markus M. Pinna, Marco Pisanu, Claudia O’Donovan, Claire Rietschel, Marcella D. C. Rouleau, Guy Schulze, Thomas Severino, Giovanni Slaney, Claire M. Squassina, Alessio Suwalska, Aleksandra Turecki, Gustavo Uher, Rudolf Zvolsky, Petr Cervantes, Pablo del Zompo, Maria Grof, Paul Rybakowski, Janusz Tondo, Leonardo Trappenberg, Thomas Alda, Martin |
author_facet | Nunes, Abraham Stone, William Ardau, Raffaella Berghöfer, Anne Bocchetta, Alberto Chillotti, Caterina Deiana, Valeria Degenhardt, Franziska Forstner, Andreas J. Garnham, Julie S. Grof, Eva Hajek, Tomas Manchia, Mirko Mattheisen, Manuel McMahon, Francis Müller-Oerlinghausen, Bruno Nöthen, Markus M. Pinna, Marco Pisanu, Claudia O’Donovan, Claire Rietschel, Marcella D. C. Rouleau, Guy Schulze, Thomas Severino, Giovanni Slaney, Claire M. Squassina, Alessio Suwalska, Aleksandra Turecki, Gustavo Uher, Rudolf Zvolsky, Petr Cervantes, Pablo del Zompo, Maria Grof, Paul Rybakowski, Janusz Tondo, Leonardo Trappenberg, Thomas Alda, Martin |
author_sort | Nunes, Abraham |
collection | PubMed |
description | Predicting lithium response (LiR) in bipolar disorder (BD) may inform treatment planning, but phenotypic heterogeneity complicates discovery of genomic markers. We hypothesized that patients with “exemplary phenotypes”—those whose clinical features are reliably associated with LiR and non-response (LiNR)—are more genetically separable than those with less exemplary phenotypes. Using clinical data collected from people with BD (n = 1266 across 7 centers; 34.7% responders), we computed a “clinical exemplar score,” which measures the degree to which a subject’s clinical phenotype is reliably predictive of LiR/LiNR. For patients whose genotypes were available (n = 321), we evaluated whether a subgroup of responders/non-responders with the top 25% of clinical exemplar scores (the “best clinical exemplars”) were more accurately classified based on genetic data, compared to a subgroup with the lowest 25% of clinical exemplar scores (the “poor clinical exemplars”). On average, the best clinical exemplars of LiR had a later illness onset, completely episodic clinical course, absence of rapid cycling and psychosis, and few psychiatric comorbidities. The best clinical exemplars of LiR and LiNR were genetically separable with an area under the receiver operating characteristic curve of 0.88 (IQR [0.83, 0.98]), compared to 0.66 [0.61, 0.80] (p = 0.0032) among poor clinical exemplars. Variants in the Alzheimer’s amyloid–secretase pathway, along with G-protein-coupled receptor, muscarinic acetylcholine, and histamine H1R signaling pathways were informative predictors. This study must be replicated on larger samples and extended to predict response to other mood stabilizers. |
format | Online Article Text |
id | pubmed-7801503 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78015032021-01-21 Exemplar scoring identifies genetically separable phenotypes of lithium responsive bipolar disorder Nunes, Abraham Stone, William Ardau, Raffaella Berghöfer, Anne Bocchetta, Alberto Chillotti, Caterina Deiana, Valeria Degenhardt, Franziska Forstner, Andreas J. Garnham, Julie S. Grof, Eva Hajek, Tomas Manchia, Mirko Mattheisen, Manuel McMahon, Francis Müller-Oerlinghausen, Bruno Nöthen, Markus M. Pinna, Marco Pisanu, Claudia O’Donovan, Claire Rietschel, Marcella D. C. Rouleau, Guy Schulze, Thomas Severino, Giovanni Slaney, Claire M. Squassina, Alessio Suwalska, Aleksandra Turecki, Gustavo Uher, Rudolf Zvolsky, Petr Cervantes, Pablo del Zompo, Maria Grof, Paul Rybakowski, Janusz Tondo, Leonardo Trappenberg, Thomas Alda, Martin Transl Psychiatry Article Predicting lithium response (LiR) in bipolar disorder (BD) may inform treatment planning, but phenotypic heterogeneity complicates discovery of genomic markers. We hypothesized that patients with “exemplary phenotypes”—those whose clinical features are reliably associated with LiR and non-response (LiNR)—are more genetically separable than those with less exemplary phenotypes. Using clinical data collected from people with BD (n = 1266 across 7 centers; 34.7% responders), we computed a “clinical exemplar score,” which measures the degree to which a subject’s clinical phenotype is reliably predictive of LiR/LiNR. For patients whose genotypes were available (n = 321), we evaluated whether a subgroup of responders/non-responders with the top 25% of clinical exemplar scores (the “best clinical exemplars”) were more accurately classified based on genetic data, compared to a subgroup with the lowest 25% of clinical exemplar scores (the “poor clinical exemplars”). On average, the best clinical exemplars of LiR had a later illness onset, completely episodic clinical course, absence of rapid cycling and psychosis, and few psychiatric comorbidities. The best clinical exemplars of LiR and LiNR were genetically separable with an area under the receiver operating characteristic curve of 0.88 (IQR [0.83, 0.98]), compared to 0.66 [0.61, 0.80] (p = 0.0032) among poor clinical exemplars. Variants in the Alzheimer’s amyloid–secretase pathway, along with G-protein-coupled receptor, muscarinic acetylcholine, and histamine H1R signaling pathways were informative predictors. This study must be replicated on larger samples and extended to predict response to other mood stabilizers. Nature Publishing Group UK 2021-01-11 /pmc/articles/PMC7801503/ /pubmed/33431852 http://dx.doi.org/10.1038/s41398-020-01148-y Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Nunes, Abraham Stone, William Ardau, Raffaella Berghöfer, Anne Bocchetta, Alberto Chillotti, Caterina Deiana, Valeria Degenhardt, Franziska Forstner, Andreas J. Garnham, Julie S. Grof, Eva Hajek, Tomas Manchia, Mirko Mattheisen, Manuel McMahon, Francis Müller-Oerlinghausen, Bruno Nöthen, Markus M. Pinna, Marco Pisanu, Claudia O’Donovan, Claire Rietschel, Marcella D. C. Rouleau, Guy Schulze, Thomas Severino, Giovanni Slaney, Claire M. Squassina, Alessio Suwalska, Aleksandra Turecki, Gustavo Uher, Rudolf Zvolsky, Petr Cervantes, Pablo del Zompo, Maria Grof, Paul Rybakowski, Janusz Tondo, Leonardo Trappenberg, Thomas Alda, Martin Exemplar scoring identifies genetically separable phenotypes of lithium responsive bipolar disorder |
title | Exemplar scoring identifies genetically separable phenotypes of lithium responsive bipolar disorder |
title_full | Exemplar scoring identifies genetically separable phenotypes of lithium responsive bipolar disorder |
title_fullStr | Exemplar scoring identifies genetically separable phenotypes of lithium responsive bipolar disorder |
title_full_unstemmed | Exemplar scoring identifies genetically separable phenotypes of lithium responsive bipolar disorder |
title_short | Exemplar scoring identifies genetically separable phenotypes of lithium responsive bipolar disorder |
title_sort | exemplar scoring identifies genetically separable phenotypes of lithium responsive bipolar disorder |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801503/ https://www.ncbi.nlm.nih.gov/pubmed/33431852 http://dx.doi.org/10.1038/s41398-020-01148-y |
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