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Molecular autopsy: using the discovery of a novel de novo pathogenic variant in the KCNH2 gene to inform healthcare of surviving family
BACKGROUND: Molecular testing of the deceased (Molecular Autopsy) is an overlooked area in the United States healthcare system and is not covered by medical insurance, leading to ineffective care for surviving families of thousands of sudden unexpected natural deaths each year. We demonstrated the p...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288419/ https://www.ncbi.nlm.nih.gov/pubmed/30582040 http://dx.doi.org/10.1016/j.heliyon.2018.e01015 |
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author | Dong, Jingyun Williams, Nori Cerrone, Marina Borck, Christopher Wang, Dawei Zhou, Bo Eng, Lucy S. Subbotina, Ekaterina Um, Sung Yon Lin, Ying Ruiter, Kevin Rojas, Lisa Coetzee, William A. Sampson, Barbara A. Tang, Yingying |
author_facet | Dong, Jingyun Williams, Nori Cerrone, Marina Borck, Christopher Wang, Dawei Zhou, Bo Eng, Lucy S. Subbotina, Ekaterina Um, Sung Yon Lin, Ying Ruiter, Kevin Rojas, Lisa Coetzee, William A. Sampson, Barbara A. Tang, Yingying |
author_sort | Dong, Jingyun |
collection | PubMed |
description | BACKGROUND: Molecular testing of the deceased (Molecular Autopsy) is an overlooked area in the United States healthcare system and is not covered by medical insurance, leading to ineffective care for surviving families of thousands of sudden unexpected natural deaths each year. We demonstrated the precision management of surviving family members through the discovery of a novel de novo pathogenic variant in a decedent. METHODS: Forensic investigation and molecular autopsy were performed on an 18-year-old female who died suddenly and unexpectedly. Co-segregation family study of the first-degree relatives and functional characterization of the variant were conducted. FINDINGS: We identified a novel nonsense variant, NP_000229.1:p.Gln1068Ter, in the long QT syndrome type II gene KCNH2 in the decedent. This finding correlated with her ante-mortem electrocardiograms. Patch clamp functional studies using transfected COS-7 cells show that hERG-ΔQ1068 has a mixed phenotype, with both gain- (negative voltage shift of steady-state activation curve, the positive shift of the steady-state inactivation curve, and accelerated activation) and loss-of function (reduced current density, reduced surface expression and accelerated deactivation) hallmarks. Loss of cumulative activation during rapid pacing demonstrates that the loss-of-function phenotype predominates. The wild-type channel did not rescue the hERG-ΔQ1068 defects, demonstrating haploinsufficiency of the heterozygous state. Targeted variant testing in the family showed that the variant in KCNH2 arose de novo, which eliminated the need for exhaustive genome testing and annual cardiac follow-up for the parents and four siblings. INTERPRETATION: Molecular testing enables accurate determination of natural causes of death and precision care of the surviving family members in a time and cost-saving manner. We advocate for molecular autopsy being included under the healthcare coverage in US. |
format | Online Article Text |
id | pubmed-6288419 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-62884192018-12-21 Molecular autopsy: using the discovery of a novel de novo pathogenic variant in the KCNH2 gene to inform healthcare of surviving family Dong, Jingyun Williams, Nori Cerrone, Marina Borck, Christopher Wang, Dawei Zhou, Bo Eng, Lucy S. Subbotina, Ekaterina Um, Sung Yon Lin, Ying Ruiter, Kevin Rojas, Lisa Coetzee, William A. Sampson, Barbara A. Tang, Yingying Heliyon Article BACKGROUND: Molecular testing of the deceased (Molecular Autopsy) is an overlooked area in the United States healthcare system and is not covered by medical insurance, leading to ineffective care for surviving families of thousands of sudden unexpected natural deaths each year. We demonstrated the precision management of surviving family members through the discovery of a novel de novo pathogenic variant in a decedent. METHODS: Forensic investigation and molecular autopsy were performed on an 18-year-old female who died suddenly and unexpectedly. Co-segregation family study of the first-degree relatives and functional characterization of the variant were conducted. FINDINGS: We identified a novel nonsense variant, NP_000229.1:p.Gln1068Ter, in the long QT syndrome type II gene KCNH2 in the decedent. This finding correlated with her ante-mortem electrocardiograms. Patch clamp functional studies using transfected COS-7 cells show that hERG-ΔQ1068 has a mixed phenotype, with both gain- (negative voltage shift of steady-state activation curve, the positive shift of the steady-state inactivation curve, and accelerated activation) and loss-of function (reduced current density, reduced surface expression and accelerated deactivation) hallmarks. Loss of cumulative activation during rapid pacing demonstrates that the loss-of-function phenotype predominates. The wild-type channel did not rescue the hERG-ΔQ1068 defects, demonstrating haploinsufficiency of the heterozygous state. Targeted variant testing in the family showed that the variant in KCNH2 arose de novo, which eliminated the need for exhaustive genome testing and annual cardiac follow-up for the parents and four siblings. INTERPRETATION: Molecular testing enables accurate determination of natural causes of death and precision care of the surviving family members in a time and cost-saving manner. We advocate for molecular autopsy being included under the healthcare coverage in US. Elsevier 2018-12-08 /pmc/articles/PMC6288419/ /pubmed/30582040 http://dx.doi.org/10.1016/j.heliyon.2018.e01015 Text en © 2018 Published by Elsevier Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Dong, Jingyun Williams, Nori Cerrone, Marina Borck, Christopher Wang, Dawei Zhou, Bo Eng, Lucy S. Subbotina, Ekaterina Um, Sung Yon Lin, Ying Ruiter, Kevin Rojas, Lisa Coetzee, William A. Sampson, Barbara A. Tang, Yingying Molecular autopsy: using the discovery of a novel de novo pathogenic variant in the KCNH2 gene to inform healthcare of surviving family |
title | Molecular autopsy: using the discovery of a novel de novo pathogenic variant in the KCNH2 gene to inform healthcare of surviving family |
title_full | Molecular autopsy: using the discovery of a novel de novo pathogenic variant in the KCNH2 gene to inform healthcare of surviving family |
title_fullStr | Molecular autopsy: using the discovery of a novel de novo pathogenic variant in the KCNH2 gene to inform healthcare of surviving family |
title_full_unstemmed | Molecular autopsy: using the discovery of a novel de novo pathogenic variant in the KCNH2 gene to inform healthcare of surviving family |
title_short | Molecular autopsy: using the discovery of a novel de novo pathogenic variant in the KCNH2 gene to inform healthcare of surviving family |
title_sort | molecular autopsy: using the discovery of a novel de novo pathogenic variant in the kcnh2 gene to inform healthcare of surviving family |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288419/ https://www.ncbi.nlm.nih.gov/pubmed/30582040 http://dx.doi.org/10.1016/j.heliyon.2018.e01015 |
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