Deep sequencing of atrial fibrillation patients with mitral valve regurgitation shows no evidence of mosaicism but reveals novel rare germline variants

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Standard

Deep sequencing of atrial fibrillation patients with mitral valve regurgitation shows no evidence of mosaicism but reveals novel rare germline variants. / Gregers, Emilie; Ahlberg, Gustav; Christensen, Thea; Jabbari, Javad; Larsen, Kirstine O; Herfelt, Cecilie B; Henningsen, Kristoffer M; Andreasen, Laura; Thiis, Jens J; Lund, Jens; Holme, Susanne; Haunsø, Stig; Bentzen, Bo H; Schmitt, Nicole; Svendsen, Jesper H; Olesen, Morten S.

In: Heart Rhythm, Vol. 14, No. 10, 10.2017, p. 1531-1538.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Gregers, E, Ahlberg, G, Christensen, T, Jabbari, J, Larsen, KO, Herfelt, CB, Henningsen, KM, Andreasen, L, Thiis, JJ, Lund, J, Holme, S, Haunsø, S, Bentzen, BH, Schmitt, N, Svendsen, JH & Olesen, MS 2017, 'Deep sequencing of atrial fibrillation patients with mitral valve regurgitation shows no evidence of mosaicism but reveals novel rare germline variants', Heart Rhythm, vol. 14, no. 10, pp. 1531-1538. https://doi.org/10.1016/j.hrthm.2017.05.027

APA

Gregers, E., Ahlberg, G., Christensen, T., Jabbari, J., Larsen, K. O., Herfelt, C. B., Henningsen, K. M., Andreasen, L., Thiis, J. J., Lund, J., Holme, S., Haunsø, S., Bentzen, B. H., Schmitt, N., Svendsen, J. H., & Olesen, M. S. (2017). Deep sequencing of atrial fibrillation patients with mitral valve regurgitation shows no evidence of mosaicism but reveals novel rare germline variants. Heart Rhythm, 14(10), 1531-1538. https://doi.org/10.1016/j.hrthm.2017.05.027

Vancouver

Gregers E, Ahlberg G, Christensen T, Jabbari J, Larsen KO, Herfelt CB et al. Deep sequencing of atrial fibrillation patients with mitral valve regurgitation shows no evidence of mosaicism but reveals novel rare germline variants. Heart Rhythm. 2017 Oct;14(10):1531-1538. https://doi.org/10.1016/j.hrthm.2017.05.027

Author

Gregers, Emilie ; Ahlberg, Gustav ; Christensen, Thea ; Jabbari, Javad ; Larsen, Kirstine O ; Herfelt, Cecilie B ; Henningsen, Kristoffer M ; Andreasen, Laura ; Thiis, Jens J ; Lund, Jens ; Holme, Susanne ; Haunsø, Stig ; Bentzen, Bo H ; Schmitt, Nicole ; Svendsen, Jesper H ; Olesen, Morten S. / Deep sequencing of atrial fibrillation patients with mitral valve regurgitation shows no evidence of mosaicism but reveals novel rare germline variants. In: Heart Rhythm. 2017 ; Vol. 14, No. 10. pp. 1531-1538.

Bibtex

@article{c85687b0d736426b8d5d9446cf1fb269,

title = "Deep sequencing of atrial fibrillation patients with mitral valve regurgitation shows no evidence of mosaicism but reveals novel rare germline variants",

abstract = "BACKGROUND: Atrial fibrillation (AF) is the most common cardiac arrhythmia. Valvular heart disease is a strong predictor, yet the underlying molecular mechanisms are unknown.OBJECTIVE: The purpose of this study was to investigate the prevalence of somatic variants in AF candidate genes in an AF patient population undergoing surgery for mitral valve regurgitation (MVR) to determine whether these patients are genetically predisposed to AF.METHODS: DNA was extracted from blood and left atrial tissue from 44 AF patients with MVR. Using next-generation sequencing, we investigated 110 genes using the HaloPlex Target Enrichment System. MuTect software was used for identification of somatic point variants. We functionally characterized selected variants using electrophysiologic techniques.RESULTS: No somatic variants were identified in the cardiac tissue. Thirty-three patients (75%) had a rare germline variation in ≥1 candidate genes. Fourteen variants were novel. Fifteen variants were predicted damaging or likely damaging in ≥6 in silico predictions. We identified rare variants in genes never directly associated with AF: KCNE4, SCN4B, NEURL1, and CAND2. Interestingly, 7 patients (16%) had variants in genes involved in cellular potassium handling. The variants KCNQ1 (p.G272S) and KCNH2 (p.A913V) resulted in gain of function due to faster activation (KCNQ1) and slowed deactivation kinetics (KCNQ1, KCNH2).CONCLUSION: We did not find any somatic variants in patients with AF and MVR. Surprisingly, we found that our cohort of non-lone AF patients might, like lone AF patients, be predisposed to AF by rare germline variants. Our findings emphasize the extent of still unknown factors in the pathogenesis of AF.",

keywords = "Journal Article",

author = "Emilie Gregers and Gustav Ahlberg and Thea Christensen and Javad Jabbari and Larsen, {Kirstine O} and Herfelt, {Cecilie B} and Henningsen, {Kristoffer M} and Laura Andreasen and Thiis, {Jens J} and Jens Lund and Susanne Holme and Stig Hauns{\o} and Bentzen, {Bo H} and Nicole Schmitt and Svendsen, {Jesper H} and Olesen, {Morten S}",

year = "2017",

month = oct,

doi = "10.1016/j.hrthm.2017.05.027",

language = "English",

volume = "14",

pages = "1531--1538",

journal = "Heart Rhythm",

issn = "1547-5271",

publisher = "Elsevier",

number = "10",

}

RIS

TY - JOUR

T1 - Deep sequencing of atrial fibrillation patients with mitral valve regurgitation shows no evidence of mosaicism but reveals novel rare germline variants

AU - Gregers, Emilie

AU - Ahlberg, Gustav

AU - Christensen, Thea

AU - Jabbari, Javad

AU - Larsen, Kirstine O

AU - Herfelt, Cecilie B

AU - Henningsen, Kristoffer M

AU - Andreasen, Laura

AU - Thiis, Jens J

AU - Lund, Jens

AU - Holme, Susanne

AU - Haunsø, Stig

AU - Bentzen, Bo H

AU - Schmitt, Nicole

AU - Svendsen, Jesper H

AU - Olesen, Morten S

PY - 2017/10

Y1 - 2017/10

N2 - BACKGROUND: Atrial fibrillation (AF) is the most common cardiac arrhythmia. Valvular heart disease is a strong predictor, yet the underlying molecular mechanisms are unknown.OBJECTIVE: The purpose of this study was to investigate the prevalence of somatic variants in AF candidate genes in an AF patient population undergoing surgery for mitral valve regurgitation (MVR) to determine whether these patients are genetically predisposed to AF.METHODS: DNA was extracted from blood and left atrial tissue from 44 AF patients with MVR. Using next-generation sequencing, we investigated 110 genes using the HaloPlex Target Enrichment System. MuTect software was used for identification of somatic point variants. We functionally characterized selected variants using electrophysiologic techniques.RESULTS: No somatic variants were identified in the cardiac tissue. Thirty-three patients (75%) had a rare germline variation in ≥1 candidate genes. Fourteen variants were novel. Fifteen variants were predicted damaging or likely damaging in ≥6 in silico predictions. We identified rare variants in genes never directly associated with AF: KCNE4, SCN4B, NEURL1, and CAND2. Interestingly, 7 patients (16%) had variants in genes involved in cellular potassium handling. The variants KCNQ1 (p.G272S) and KCNH2 (p.A913V) resulted in gain of function due to faster activation (KCNQ1) and slowed deactivation kinetics (KCNQ1, KCNH2).CONCLUSION: We did not find any somatic variants in patients with AF and MVR. Surprisingly, we found that our cohort of non-lone AF patients might, like lone AF patients, be predisposed to AF by rare germline variants. Our findings emphasize the extent of still unknown factors in the pathogenesis of AF.

AB - BACKGROUND: Atrial fibrillation (AF) is the most common cardiac arrhythmia. Valvular heart disease is a strong predictor, yet the underlying molecular mechanisms are unknown.OBJECTIVE: The purpose of this study was to investigate the prevalence of somatic variants in AF candidate genes in an AF patient population undergoing surgery for mitral valve regurgitation (MVR) to determine whether these patients are genetically predisposed to AF.METHODS: DNA was extracted from blood and left atrial tissue from 44 AF patients with MVR. Using next-generation sequencing, we investigated 110 genes using the HaloPlex Target Enrichment System. MuTect software was used for identification of somatic point variants. We functionally characterized selected variants using electrophysiologic techniques.RESULTS: No somatic variants were identified in the cardiac tissue. Thirty-three patients (75%) had a rare germline variation in ≥1 candidate genes. Fourteen variants were novel. Fifteen variants were predicted damaging or likely damaging in ≥6 in silico predictions. We identified rare variants in genes never directly associated with AF: KCNE4, SCN4B, NEURL1, and CAND2. Interestingly, 7 patients (16%) had variants in genes involved in cellular potassium handling. The variants KCNQ1 (p.G272S) and KCNH2 (p.A913V) resulted in gain of function due to faster activation (KCNQ1) and slowed deactivation kinetics (KCNQ1, KCNH2).CONCLUSION: We did not find any somatic variants in patients with AF and MVR. Surprisingly, we found that our cohort of non-lone AF patients might, like lone AF patients, be predisposed to AF by rare germline variants. Our findings emphasize the extent of still unknown factors in the pathogenesis of AF.

KW - Journal Article

U2 - 10.1016/j.hrthm.2017.05.027

DO - 10.1016/j.hrthm.2017.05.027

M3 - Journal article

C2 - 28549997

VL - 14

SP - 1531

EP - 1538

JO - Heart Rhythm

JF - Heart Rhythm

SN - 1547-5271

IS - 10

ER -

ID: 183763006