| Literature DB >> 33441847 |
William Stone1, Abraham Nunes1,2, Kazufumi Akiyama3, Nirmala Akula4, Raffaella Ardau5, Jean-Michel Aubry6,7, Lena Backlund8,9,10, Michael Bauer11, Frank Bellivier12,13, Pablo Cervantes14, Hsi-Chung Chen15, Caterina Chillotti5, Cristiana Cruceanu16, Alexandre Dayer6,17, Franziska Degenhardt18,19, Maria Del Zompo5,20, Andreas J Forstner18,21, Mark Frye22, Janice M Fullerton23, Maria Grigoroiu-Serbanescu24, Paul Grof25, Ryota Hashimoto26,27, Liping Hou4, Esther Jiménez28,29,30, Tadafumi Kato31, John Kelsoe32, Sarah Kittel-Schneider33,34, Po-Hsiu Kuo35,36, Ichiro Kusumi37, Catharina Lavebratt9,10, Mirko Manchia38,39, Lina Martinsson8, Manuel Mattheisen40, Francis J McMahon4, Vincent Millischer9,10, Philip B Mitchell23, Markus M Nöthen41, Claire O'Donovan2, Norio Ozaki42, Claudia Pisanu20, Andreas Reif33, Marcella Rietschel43, Guy Rouleau44, Janusz Rybakowski45, Martin Schalling9,10, Peter R Schofield23, Thomas G Schulze46, Giovanni Severino20, Alessio Squassina2,20, Julia Veeh33, Eduard Vieta28,29,30, Thomas Trappenberg1, Martin Alda47.
Abstract
Predicting lithium response prior to treatment could both expedite therapy and avoid exposure to side effects. Since lithium responsiveness may be heritable, its predictability based on genomic data is of interest. We thus evaluate the degree to which lithium response can be predicted with a machine learning (ML) approach using genomic data. Using the largest existing genomic dataset in the lithium response literature (n = 2210 across 14 international sites; 29% responders), we evaluated the degree to which lithium response could be predicted based on 47,465 genotyped single nucleotide polymorphisms using a supervised ML approach. Under appropriate cross-validation procedures, lithium response could be predicted to above-chance levels in two constituent sites (Halifax, Cohen's kappa 0.15, 95% confidence interval, CI [0.07, 0.24]; and Würzburg, kappa 0.2 [0.1, 0.3]). Variants with shared importance in these models showed over-representation of postsynaptic membrane related genes. Lithium response was not predictable in the pooled dataset (kappa 0.02 [- 0.01, 0.04]), although non-trivial performance was achieved within a restricted dataset including only those patients followed prospectively (kappa 0.09 [0.04, 0.14]). Genomic classification of lithium response remains a promising but difficult task. Classification performance could potentially be improved by further harmonization of data collection procedures.Entities:
Year: 2021 PMID: 33441847 PMCID: PMC7806976 DOI: 10.1038/s41598-020-80814-z
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379