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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Main Authors: 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
Format: Article
Language:English
Published: Nature Publishing Group 2021-02-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-83887-6
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spelling 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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