A rare missense mutation in CHRNA4 associates with smoking behavior and its consequences

Using Icelandic whole-genome sequence data and an imputation approach we searched for rare sequence variants in CHRNA4 and tested them for association with nicotine dependence. We show that carriers of a rare missense variant (allele frequency = 0.24%) within CHRNA4, encoding an R336C substitution,...

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Main Authors: Thorgeirsson, T.E., Steinberg, S., Reginsson, G.W., Bjornsdottir, G., Rafnar, T., Jonsdottir, I., Helgadottir, A., Gretarsdottir, S., Helgadottir, H., Jonsson, S., Matthiasson, S.E., Gislason, T., Tyrfingsson, T., Gudbjartsson, T., Isaksson, H.J., Hardardottir, H., Sigvaldason, A., Kiemeney, L.A., Haugen, A., Zienolddiny, S., Wolf, H.J., Franklin, W.A., Panadero, A., Mayordomo, J.I., Hall, I.P., Rönmark, E., Lundbäck, B., Dirksen, A., Ashraf, H., Pedersen, J.H., Masson, G., Sulem, P., Thorsteinsdottir, U., Gudbjartsson, D.F., Stefansson, K.
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Published: Nature Publishing Group 2016
Online Access:https://eprints.nottingham.ac.uk/44362/
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author Thorgeirsson, T.E.
Steinberg, S.
Reginsson, G.W.
Bjornsdottir, G.
Rafnar, T.
Jonsdottir, I.
Helgadottir, A.
Gretarsdottir, S.
Helgadottir, H.
Jonsson, S.
Matthiasson, S.E.
Gislason, T.
Tyrfingsson, T.
Gudbjartsson, T.
Isaksson, H.J.
Hardardottir, H.
Sigvaldason, A.
Kiemeney, L.A.
Haugen, A.
Zienolddiny, S.
Wolf, H.J.
Franklin, W.A.
Panadero, A.
Mayordomo, J.I.
Hall, I.P.
Rönmark, E.
Lundbäck, B.
Dirksen, A.
Ashraf, H.
Pedersen, J.H.
Masson, G.
Sulem, P.
Thorsteinsdottir, U.
Gudbjartsson, D.F.
Stefansson, K.
author_facet Thorgeirsson, T.E.
Steinberg, S.
Reginsson, G.W.
Bjornsdottir, G.
Rafnar, T.
Jonsdottir, I.
Helgadottir, A.
Gretarsdottir, S.
Helgadottir, H.
Jonsson, S.
Matthiasson, S.E.
Gislason, T.
Tyrfingsson, T.
Gudbjartsson, T.
Isaksson, H.J.
Hardardottir, H.
Sigvaldason, A.
Kiemeney, L.A.
Haugen, A.
Zienolddiny, S.
Wolf, H.J.
Franklin, W.A.
Panadero, A.
Mayordomo, J.I.
Hall, I.P.
Rönmark, E.
Lundbäck, B.
Dirksen, A.
Ashraf, H.
Pedersen, J.H.
Masson, G.
Sulem, P.
Thorsteinsdottir, U.
Gudbjartsson, D.F.
Stefansson, K.
author_sort Thorgeirsson, T.E.
building Nottingham Research Data Repository
collection Online Access
description Using Icelandic whole-genome sequence data and an imputation approach we searched for rare sequence variants in CHRNA4 and tested them for association with nicotine dependence. We show that carriers of a rare missense variant (allele frequency = 0.24%) within CHRNA4, encoding an R336C substitution, have greater risk of nicotine addiction than non-carriers as assessed by the Fagerstrom Test for Nicotine Dependence (P= 1.2 × 10−4). The variant also confers risk of several serious smoking-related diseases previously shown to be associated with the D398N substitution in CHRNA5. We observed odds ratios (ORs) of 1.7–2.3 for lung cancer(LC;P= 4.0 × 10−4), chronic obstructive pulmonary disease (COPD;P= 9.3 × 10−4), peripheral artery disease (PAD;P= 0.090) and abdominal aortic aneurysms (AAAs; P= 0.12), and the variant associates strongly with the early-onset forms of LC (OR = 4.49,P= 2.2 × 10−4), COPD (OR = 3.22,P= 2.9 × 10−4), PAD (OR = 3.47,P= 9.2 × 10−3) and AAA (OR = 6.44, P= 6.3 × 10−3). Joint analysis of the four smoking-related diseases reveals significant association (P= 6.8 × 10−5), particularly for early-onset cases (P=2.1 × 10−7). Our results are in agreement with functional studies showing that the human α4β2 isoform of the channel containing R336C has less sensitivity for its agonists than the wild-type form following nicotine incubation.
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spelling nottingham-443622020-05-04T17:42:33Z https://eprints.nottingham.ac.uk/44362/ A rare missense mutation in CHRNA4 associates with smoking behavior and its consequences Thorgeirsson, T.E. Steinberg, S. Reginsson, G.W. Bjornsdottir, G. Rafnar, T. Jonsdottir, I. Helgadottir, A. Gretarsdottir, S. Helgadottir, H. Jonsson, S. Matthiasson, S.E. Gislason, T. Tyrfingsson, T. Gudbjartsson, T. Isaksson, H.J. Hardardottir, H. Sigvaldason, A. Kiemeney, L.A. Haugen, A. Zienolddiny, S. Wolf, H.J. Franklin, W.A. Panadero, A. Mayordomo, J.I. Hall, I.P. Rönmark, E. Lundbäck, B. Dirksen, A. Ashraf, H. Pedersen, J.H. Masson, G. Sulem, P. Thorsteinsdottir, U. Gudbjartsson, D.F. Stefansson, K. Using Icelandic whole-genome sequence data and an imputation approach we searched for rare sequence variants in CHRNA4 and tested them for association with nicotine dependence. We show that carriers of a rare missense variant (allele frequency = 0.24%) within CHRNA4, encoding an R336C substitution, have greater risk of nicotine addiction than non-carriers as assessed by the Fagerstrom Test for Nicotine Dependence (P= 1.2 × 10−4). The variant also confers risk of several serious smoking-related diseases previously shown to be associated with the D398N substitution in CHRNA5. We observed odds ratios (ORs) of 1.7–2.3 for lung cancer(LC;P= 4.0 × 10−4), chronic obstructive pulmonary disease (COPD;P= 9.3 × 10−4), peripheral artery disease (PAD;P= 0.090) and abdominal aortic aneurysms (AAAs; P= 0.12), and the variant associates strongly with the early-onset forms of LC (OR = 4.49,P= 2.2 × 10−4), COPD (OR = 3.22,P= 2.9 × 10−4), PAD (OR = 3.47,P= 9.2 × 10−3) and AAA (OR = 6.44, P= 6.3 × 10−3). Joint analysis of the four smoking-related diseases reveals significant association (P= 6.8 × 10−5), particularly for early-onset cases (P=2.1 × 10−7). Our results are in agreement with functional studies showing that the human α4β2 isoform of the channel containing R336C has less sensitivity for its agonists than the wild-type form following nicotine incubation. Nature Publishing Group 2016-03-08 Article PeerReviewed Thorgeirsson, T.E., Steinberg, S., Reginsson, G.W., Bjornsdottir, G., Rafnar, T., Jonsdottir, I., Helgadottir, A., Gretarsdottir, S., Helgadottir, H., Jonsson, S., Matthiasson, S.E., Gislason, T., Tyrfingsson, T., Gudbjartsson, T., Isaksson, H.J., Hardardottir, H., Sigvaldason, A., Kiemeney, L.A., Haugen, A., Zienolddiny, S., Wolf, H.J., Franklin, W.A., Panadero, A., Mayordomo, J.I., Hall, I.P., Rönmark, E., Lundbäck, B., Dirksen, A., Ashraf, H., Pedersen, J.H., Masson, G., Sulem, P., Thorsteinsdottir, U., Gudbjartsson, D.F. and Stefansson, K. (2016) A rare missense mutation in CHRNA4 associates with smoking behavior and its consequences. Molecular Psychiatry, 21 (5). pp. 594-600. ISSN 1359-4184 https://www.nature.com/mp/journal/v21/n5/full/mp201613a.html doi:10.1038/mp.2016.13 doi:10.1038/mp.2016.13
spellingShingle Thorgeirsson, T.E.
Steinberg, S.
Reginsson, G.W.
Bjornsdottir, G.
Rafnar, T.
Jonsdottir, I.
Helgadottir, A.
Gretarsdottir, S.
Helgadottir, H.
Jonsson, S.
Matthiasson, S.E.
Gislason, T.
Tyrfingsson, T.
Gudbjartsson, T.
Isaksson, H.J.
Hardardottir, H.
Sigvaldason, A.
Kiemeney, L.A.
Haugen, A.
Zienolddiny, S.
Wolf, H.J.
Franklin, W.A.
Panadero, A.
Mayordomo, J.I.
Hall, I.P.
Rönmark, E.
Lundbäck, B.
Dirksen, A.
Ashraf, H.
Pedersen, J.H.
Masson, G.
Sulem, P.
Thorsteinsdottir, U.
Gudbjartsson, D.F.
Stefansson, K.
A rare missense mutation in CHRNA4 associates with smoking behavior and its consequences
title A rare missense mutation in CHRNA4 associates with smoking behavior and its consequences
title_full A rare missense mutation in CHRNA4 associates with smoking behavior and its consequences
title_fullStr A rare missense mutation in CHRNA4 associates with smoking behavior and its consequences
title_full_unstemmed A rare missense mutation in CHRNA4 associates with smoking behavior and its consequences
title_short A rare missense mutation in CHRNA4 associates with smoking behavior and its consequences
title_sort rare missense mutation in chrna4 associates with smoking behavior and its consequences
url https://eprints.nottingham.ac.uk/44362/
https://eprints.nottingham.ac.uk/44362/
https://eprints.nottingham.ac.uk/44362/