Genotype-phenotype correlation between the cardiac myosin binding protein C mutation A31P and hypertrophic cardiomyopathy in a cohort of Maine Coon cats: a longitudinal study

Sara Magdalena Rebecca Granström; M. T. N. Godiksen; M. Christiansen; Christian Bressen Pipper; Torben Martinussen; Rasmus Møgelvang; P. Søgaard; Jakob Willesen; Jørgen Koch

doi:10.1016/j.jvc.2015.10.005

Genotype-phenotype correlation between the cardiac myosin binding protein C mutation A31P and hypertrophic cardiomyopathy in a cohort of Maine Coon cats: a longitudinal study

Sara Magdalena Rebecca Granström, M. T. N. Godiksen, M. Christiansen, Christian Bressen Pipper, Torben Martinussen, Rasmus Møgelvang, P. Søgaard, Jakob Willesen, Jørgen Koch

Section of Biostatistics

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

15 Citations (Scopus)

Abstract

OBJECTIVES: A missense mutation (A31P) in the cardiac myosin binding protein C gene has been associated with hypertrophic cardiomyopathy (HCM) in Maine Coon cats. The aim of this study was to investigate the effect of A31P on development of HCM, myocardial diastolic dysfunction detected by color tissue Doppler imaging and occurrence of cardiac death during longitudinal follow-up in a cohort of Maine Coon cats.

ANIMALS: The original cohort comprised 282 cats (158 of wild-type genotype, 99 heterozygous for A31P and 25 homozygous for A31P).

METHODS: Prospective longitudinal study including echocardiography and registration of survival.

RESULTS: The median age at the initial examination was 1.7 years (range, 0.8-9.2 years) and 6.4% (18/282) of the cats were diagnosed with HCM. One hundred sixty-five cats were eligible for echocardiographic re-examination, and during an average follow-up period of 2.7 years an additional 6.7% (11/165) of the cats developed HCM. Survival data could be obtained for 262 of the cats originally included, and among these 9.2% (24/262) died of causes that met the study criteria for cardiac death. In the homozygous group 80% (20/25) of cats included were diagnosed with HCM and 48% (12/25) suffered cardiac death during follow-up. These results corresponded to a significantly higher risk for cats homozygous for A31P to develop HCM (p<0.001) and die from cardiac-related causes compared with both other genotypes (p<0.001).

CONCLUSIONS: Homozygosity for A31P was associated with a high penetrance of HCM and a substantial risk for cardiac death in the study population.

Original language	English
Journal	Journal of Veterinary Cardiology
Volume	17
Issue number	Suppl. 1
Pages (from-to)	S268-S281
Number of pages	14
ISSN	1760-2734
DOIs	https://doi.org/10.1016/j.jvc.2015.10.005
Publication status	Published - Dec 2015

Access to Document

10.1016/j.jvc.2015.10.005Licence: Other

Cite this

Granström, S. M. R., Godiksen, M. T. N., Christiansen, M., Pipper, C. B., Martinussen, T., Møgelvang, R., Søgaard, P., Willesen, J., & Koch, J. (2015). Genotype-phenotype correlation between the cardiac myosin binding protein C mutation A31P and hypertrophic cardiomyopathy in a cohort of Maine Coon cats: a longitudinal study. Journal of Veterinary Cardiology, 17 (Suppl. 1), S268-S281. https://doi.org/10.1016/j.jvc.2015.10.005

Genotype-phenotype correlation between the cardiac myosin binding protein C mutation A31P and hypertrophic cardiomyopathy in a cohort of Maine Coon cats : a longitudinal study. / Granström, Sara Magdalena Rebecca; Godiksen, M. T. N.; Christiansen, M.; Pipper, Christian Bressen; Martinussen, Torben; Møgelvang, Rasmus; Søgaard, P.; Willesen, Jakob ; Koch, Jørgen.

In: Journal of Veterinary Cardiology, Vol. 17 , No. Suppl. 1, 12.2015, p. S268-S281.

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

Granström, SMR, Godiksen, MTN, Christiansen, M, Pipper, CB, Martinussen, T, Møgelvang, R, Søgaard, P, Willesen, J & Koch, J 2015, 'Genotype-phenotype correlation between the cardiac myosin binding protein C mutation A31P and hypertrophic cardiomyopathy in a cohort of Maine Coon cats: a longitudinal study', Journal of Veterinary Cardiology, vol. 17 , no. Suppl. 1, pp. S268-S281. https://doi.org/10.1016/j.jvc.2015.10.005

Granström SMR, Godiksen MTN, Christiansen M, Pipper CB, Martinussen T, Møgelvang R et al. Genotype-phenotype correlation between the cardiac myosin binding protein C mutation A31P and hypertrophic cardiomyopathy in a cohort of Maine Coon cats: a longitudinal study. Journal of Veterinary Cardiology. 2015 Dec;17 (Suppl. 1):S268-S281. https://doi.org/10.1016/j.jvc.2015.10.005

Granström, Sara Magdalena Rebecca ; Godiksen, M. T. N. ; Christiansen, M. ; Pipper, Christian Bressen ; Martinussen, Torben ; Møgelvang, Rasmus ; Søgaard, P. ; Willesen, Jakob ; Koch, Jørgen. / Genotype-phenotype correlation between the cardiac myosin binding protein C mutation A31P and hypertrophic cardiomyopathy in a cohort of Maine Coon cats : a longitudinal study. In: Journal of Veterinary Cardiology. 2015 ; Vol. 17 , No. Suppl. 1. pp. S268-S281.

@article{baceae9d3f5246e1891ff6d84ed5d3e2,

title = "Genotype-phenotype correlation between the cardiac myosin binding protein C mutation A31P and hypertrophic cardiomyopathy in a cohort of Maine Coon cats: a longitudinal study",

abstract = "OBJECTIVES: A missense mutation (A31P) in the cardiac myosin binding protein C gene has been associated with hypertrophic cardiomyopathy (HCM) in Maine Coon cats. The aim of this study was to investigate the effect of A31P on development of HCM, myocardial diastolic dysfunction detected by color tissue Doppler imaging and occurrence of cardiac death during longitudinal follow-up in a cohort of Maine Coon cats.ANIMALS: The original cohort comprised 282 cats (158 of wild-type genotype, 99 heterozygous for A31P and 25 homozygous for A31P).METHODS: Prospective longitudinal study including echocardiography and registration of survival.RESULTS: The median age at the initial examination was 1.7 years (range, 0.8-9.2 years) and 6.4% (18/282) of the cats were diagnosed with HCM. One hundred sixty-five cats were eligible for echocardiographic re-examination, and during an average follow-up period of 2.7 years an additional 6.7% (11/165) of the cats developed HCM. Survival data could be obtained for 262 of the cats originally included, and among these 9.2% (24/262) died of causes that met the study criteria for cardiac death. In the homozygous group 80% (20/25) of cats included were diagnosed with HCM and 48% (12/25) suffered cardiac death during follow-up. These results corresponded to a significantly higher risk for cats homozygous for A31P to develop HCM (p<0.001) and die from cardiac-related causes compared with both other genotypes (p<0.001).CONCLUSIONS: Homozygosity for A31P was associated with a high penetrance of HCM and a substantial risk for cardiac death in the study population.",

author = "Granstr{\"o}m, {Sara Magdalena Rebecca} and Godiksen, {M. T. N.} and M. Christiansen and Pipper, {Christian Bressen} and Torben Martinussen and Rasmus M{\o}gelvang and P. S{\o}gaard and Jakob Willesen and J{\o}rgen Koch",

year = "2015",

month = dec,

doi = "10.1016/j.jvc.2015.10.005",

language = "English",

volume = "17 ",

pages = "S268--S281",

journal = "Journal of Veterinary Cardiology",

issn = "1760-2734",

publisher = "Elsevier",

number = "Suppl. 1",

}

TY - JOUR

T1 - Genotype-phenotype correlation between the cardiac myosin binding protein C mutation A31P and hypertrophic cardiomyopathy in a cohort of Maine Coon cats

T2 - a longitudinal study

AU - Granström, Sara Magdalena Rebecca

AU - Godiksen, M. T. N.

AU - Christiansen, M.

AU - Pipper, Christian Bressen

AU - Martinussen, Torben

AU - Møgelvang, Rasmus

AU - Søgaard, P.

AU - Willesen, Jakob

AU - Koch, Jørgen

PY - 2015/12

Y1 - 2015/12

N2 - OBJECTIVES: A missense mutation (A31P) in the cardiac myosin binding protein C gene has been associated with hypertrophic cardiomyopathy (HCM) in Maine Coon cats. The aim of this study was to investigate the effect of A31P on development of HCM, myocardial diastolic dysfunction detected by color tissue Doppler imaging and occurrence of cardiac death during longitudinal follow-up in a cohort of Maine Coon cats.ANIMALS: The original cohort comprised 282 cats (158 of wild-type genotype, 99 heterozygous for A31P and 25 homozygous for A31P).METHODS: Prospective longitudinal study including echocardiography and registration of survival.RESULTS: The median age at the initial examination was 1.7 years (range, 0.8-9.2 years) and 6.4% (18/282) of the cats were diagnosed with HCM. One hundred sixty-five cats were eligible for echocardiographic re-examination, and during an average follow-up period of 2.7 years an additional 6.7% (11/165) of the cats developed HCM. Survival data could be obtained for 262 of the cats originally included, and among these 9.2% (24/262) died of causes that met the study criteria for cardiac death. In the homozygous group 80% (20/25) of cats included were diagnosed with HCM and 48% (12/25) suffered cardiac death during follow-up. These results corresponded to a significantly higher risk for cats homozygous for A31P to develop HCM (p<0.001) and die from cardiac-related causes compared with both other genotypes (p<0.001).CONCLUSIONS: Homozygosity for A31P was associated with a high penetrance of HCM and a substantial risk for cardiac death in the study population.

AB - OBJECTIVES: A missense mutation (A31P) in the cardiac myosin binding protein C gene has been associated with hypertrophic cardiomyopathy (HCM) in Maine Coon cats. The aim of this study was to investigate the effect of A31P on development of HCM, myocardial diastolic dysfunction detected by color tissue Doppler imaging and occurrence of cardiac death during longitudinal follow-up in a cohort of Maine Coon cats.ANIMALS: The original cohort comprised 282 cats (158 of wild-type genotype, 99 heterozygous for A31P and 25 homozygous for A31P).METHODS: Prospective longitudinal study including echocardiography and registration of survival.RESULTS: The median age at the initial examination was 1.7 years (range, 0.8-9.2 years) and 6.4% (18/282) of the cats were diagnosed with HCM. One hundred sixty-five cats were eligible for echocardiographic re-examination, and during an average follow-up period of 2.7 years an additional 6.7% (11/165) of the cats developed HCM. Survival data could be obtained for 262 of the cats originally included, and among these 9.2% (24/262) died of causes that met the study criteria for cardiac death. In the homozygous group 80% (20/25) of cats included were diagnosed with HCM and 48% (12/25) suffered cardiac death during follow-up. These results corresponded to a significantly higher risk for cats homozygous for A31P to develop HCM (p<0.001) and die from cardiac-related causes compared with both other genotypes (p<0.001).CONCLUSIONS: Homozygosity for A31P was associated with a high penetrance of HCM and a substantial risk for cardiac death in the study population.

U2 - 10.1016/j.jvc.2015.10.005

DO - 10.1016/j.jvc.2015.10.005

M3 - Journal article

C2 - 26776585

VL - 17

SP - S268-S281

JO - Journal of Veterinary Cardiology

JF - Journal of Veterinary Cardiology

SN - 1760-2734

IS - Suppl. 1

ER -