Whole-genome sequencing reveals KRTAP1-1 as a novel genetic variant associated with antidepressant treatment outcomes
Abstract Achieving remission following initial antidepressant therapy in patients with major depressive disorder (MDD) is an important clinical result. Making predictions based on genetic markers holds promise for improving the remission rate. However, genetic variants found in previous genetic stud...
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doaj-cf984e96a1be4c26843a60ae3dc497762021-03-11T12:14:42ZengNature Publishing GroupScientific Reports2045-23222021-02-0111111010.1038/s41598-021-83887-6Whole-genome sequencing reveals KRTAP1-1 as a novel genetic variant associated with antidepressant treatment outcomesJong-Ho Park0Shinn-Won Lim1Woojae Myung2Inho Park3Hyeok-Jae Jang4Seonwoo Kim5Min-Soo Lee6Hun Soo Chang7DongHo Yum8Yeon-Lim Suh9Jong-Won Kim10Doh Kwan Kim11Department of Health Sciences and Technology, SAIHST, Sungkyunkwan UniversityDepartment of Health Sciences and Technology, SAIHST, Sungkyunkwan UniversityDepartment of Neuropsychiatry, Seoul National University Bundang HospitalPrecision Medicine Center, Gangnam Severance Hospital, Yonsei University College of MedicineDepartment of Health Sciences and Technology, SAIHST, Sungkyunkwan UniversityStatistics and Data Center, Research Institute for Future Medicine, Samsung Medical CenterDepartment of Psychiatry, College of Medicine, Korea UniversitySoonchunhyang Medical Institute, College of Medicine, Soonchunhyang UniversityDepartment of Pathology, Samsung Medical Center, Sungkyunkwan University School of MedicineDepartment of Pathology, Samsung Medical Center, Sungkyunkwan University School of MedicineDepartment of Health Sciences and Technology, SAIHST, Sungkyunkwan UniversityDepartment of Psychiatry, Samsung Medical Center, Sungkyunkwan University School of MedicineAbstract Achieving remission following initial antidepressant therapy in patients with major depressive disorder (MDD) is an important clinical result. Making predictions based on genetic markers holds promise for improving the remission rate. However, genetic variants found in previous genetic studies do not provide robust evidence to aid pharmacogenetic decision-making in clinical settings. Thus, the objective of this study was to perform whole-genome sequencing (WGS) using genomic DNA to identify genetic variants associated with the treatment outcomes of selective serotonin reuptake inhibitors (SSRIs). We performed WGS on 100 patients with MDD who were treated with escitalopram (discovery set: 36 remitted and 64 non-remitted). The findings were applied to an additional 553 patients with MDD who were treated with SSRIs (replication set: 185 remitted and 368 non-remitted). A novel loss-of-function variant (rs3213755) in keratin-associated protein 1–1 (KRTAP1-1) was identified in this study. This rs3213755 variant was significantly associated with remission following antidepressant treatment (p = 0.0184, OR 3.09, 95% confidence interval [CI] 1.22–7.80 in the discovery set; p = 0.00269, OR 1.75, 95% CI 1.22–2.53 in the replication set). Moreover, the expression level of KRTAP1-1 in surgically resected human temporal lobe samples was significantly associated with the rs3213755 genotype. WGS studies on a larger sample size in various ethnic groups are needed to investigate genetic markers useful in the pharmacogenetic prediction of remission following antidepressant treatment.https://doi.org/10.1038/s41598-021-83887-6 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jong-Ho Park Shinn-Won Lim Woojae Myung Inho Park Hyeok-Jae Jang Seonwoo Kim Min-Soo Lee Hun Soo Chang DongHo Yum Yeon-Lim Suh Jong-Won Kim Doh Kwan Kim |
spellingShingle |
Jong-Ho Park Shinn-Won Lim Woojae Myung Inho Park Hyeok-Jae Jang Seonwoo Kim Min-Soo Lee Hun Soo Chang DongHo Yum Yeon-Lim Suh Jong-Won Kim Doh Kwan Kim Whole-genome sequencing reveals KRTAP1-1 as a novel genetic variant associated with antidepressant treatment outcomes Scientific Reports |
author_facet |
Jong-Ho Park Shinn-Won Lim Woojae Myung Inho Park Hyeok-Jae Jang Seonwoo Kim Min-Soo Lee Hun Soo Chang DongHo Yum Yeon-Lim Suh Jong-Won Kim Doh Kwan Kim |
author_sort |
Jong-Ho Park |
title |
Whole-genome sequencing reveals KRTAP1-1 as a novel genetic variant associated with antidepressant treatment outcomes |
title_short |
Whole-genome sequencing reveals KRTAP1-1 as a novel genetic variant associated with antidepressant treatment outcomes |
title_full |
Whole-genome sequencing reveals KRTAP1-1 as a novel genetic variant associated with antidepressant treatment outcomes |
title_fullStr |
Whole-genome sequencing reveals KRTAP1-1 as a novel genetic variant associated with antidepressant treatment outcomes |
title_full_unstemmed |
Whole-genome sequencing reveals KRTAP1-1 as a novel genetic variant associated with antidepressant treatment outcomes |
title_sort |
whole-genome sequencing reveals krtap1-1 as a novel genetic variant associated with antidepressant treatment outcomes |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2021-02-01 |
description |
Abstract Achieving remission following initial antidepressant therapy in patients with major depressive disorder (MDD) is an important clinical result. Making predictions based on genetic markers holds promise for improving the remission rate. However, genetic variants found in previous genetic studies do not provide robust evidence to aid pharmacogenetic decision-making in clinical settings. Thus, the objective of this study was to perform whole-genome sequencing (WGS) using genomic DNA to identify genetic variants associated with the treatment outcomes of selective serotonin reuptake inhibitors (SSRIs). We performed WGS on 100 patients with MDD who were treated with escitalopram (discovery set: 36 remitted and 64 non-remitted). The findings were applied to an additional 553 patients with MDD who were treated with SSRIs (replication set: 185 remitted and 368 non-remitted). A novel loss-of-function variant (rs3213755) in keratin-associated protein 1–1 (KRTAP1-1) was identified in this study. This rs3213755 variant was significantly associated with remission following antidepressant treatment (p = 0.0184, OR 3.09, 95% confidence interval [CI] 1.22–7.80 in the discovery set; p = 0.00269, OR 1.75, 95% CI 1.22–2.53 in the replication set). Moreover, the expression level of KRTAP1-1 in surgically resected human temporal lobe samples was significantly associated with the rs3213755 genotype. WGS studies on a larger sample size in various ethnic groups are needed to investigate genetic markers useful in the pharmacogenetic prediction of remission following antidepressant treatment. |
url |
https://doi.org/10.1038/s41598-021-83887-6 |
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