Evidence map›Paper›PMID 39241028›Full record

ArticlePloS one2024

Increased risk of cardiac arrhythmia in Hailey-Hailey disease patients.

William Jebril, Philip Curman, Daniel C Andersson, Henrik Larsson, Etty Bachar-Wikstrom, Martin Cederlöf, Jakob D Wikstrom

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Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

William JebrilDermatology and Venereology Division, Department of Medicine (Solna), Karolinska Institutet, Stockholm, Sweden.
Philip CurmanDermatology and Venereology Division, Department of Medicine (Solna), Karolinska Institutet, Stockholm, Sweden.
Daniel C AnderssonDepartment of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
Henrik LarssonSchool of Medical Sciences, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
Etty Bachar-WikstromDermatology and Venereology Division, Department of Medicine (Solna), Karolinska Institutet, Stockholm, Sweden.
Martin CederlöfDepartment of Medical Epidemiology and Biostatistics (Solna), Karolinska Institutet, Stockholm, Sweden.
Jakob D WikstromDermatology and Venereology Division, Department of Medicine (Solna), Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0002-4287-1774

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHailey-Hailey disease (HHD) is a rare autosomal dominant skin disease caused by mutations in the ATP2C1 gene, which encodes the secretory Ca2+/Mn2+-ATPase (SPCA1) pump in the Golgi apparatus. Although ATP2C1 is ubiquitously expressed in the body, possible extracutaneous manifestations of HHD are unknown. However, dysfunction of the Golgi apparatus not specifically coupled to ATP2C1 has been associated with heart disease.

objectiveTo investigate the association between HHD and common heart disease in a Swedish, population-based cohort.

methodsWe conducted a population-based cohort study based on a linkage of Swedish nationwide registers to investigate the relationship between HHD and heart disease. We have been granted ethical approval from the Swedish Ethical Review Authority to conduct this study. The patients in this manuscript have given written informed consent to the publication of their case details. A total of 342 individuals with an ICD-10 diagnosis of HHD (Q82.8E) were identified and matched with randomly selected comparison individuals without HHD on a 1:100 ratio. Furthermore, in a separate clinical cohort we matched 23 HHD patients for age, sex, and BMI with control subjects to examine electrocardiogram parameters, electrolytes, and cardiovascular biomarkers.

resultsCompared with individuals without HHD, individuals with HHD had an excess risk of arrhythmia (RR 1.4, CI 1.0-2.0), whereas no increased risks of myocardial infarction (RR 1.1, CI 0.6-1.7) or heart failure (RR 1.0, CI 0.6-1.6; Table 1) were found. We found no difference in ECG parameters, cardiovascular biomarkers, and electrolytes in the clinical subset.

conclusionThis study reveals that HHD is associated with an increased risk of arrhythmia and represents the first data of any extracutaneous comorbidity in HHD. Thus, HHD may be a systemic disease. Our findings also shed light on the importance of the Golgi apparatus' Ca2+/Mn2+ homeostasis in common heart disease.

Indexed as

Arrhythmias, CardiacPemphigus, Benign FamilialAdultAgedCalcium-Transporting ATPasesCase-Control StudiesCohort StudiesFemaleHumansMaleMiddle AgedRisk FactorsSwedenATP2C1 protein, humanCalcium-Transporting ATPases

Identifiers

PMID39241028
PMCPMC11379163

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.