Comorbidity and long-term outcome in patients with congenital heart block and their siblings exposed to Ro/SSA autoantibodies in utero.


Journal

Annals of the rheumatic diseases
ISSN: 1468-2060
Titre abrégé: Ann Rheum Dis
Pays: England
ID NLM: 0372355

Informations de publication

Date de publication:
05 2019
Historique:
received: 06 09 2018
revised: 26 01 2019
accepted: 01 02 2019
pubmed: 28 2 2019
medline: 31 12 2019
entrez: 28 2 2019
Statut: ppublish

Résumé

Congenital heart block (CHB) may develop in fetuses of Ro/SSA autoantibody-positive women. Given the rarity of CHB, information on comorbidity and complications later in life is difficult to systematically collect for large groups of patients. We therefore used nation-wide healthcare registers to investigate comorbidity and outcomes in patients with CHB and their siblings. Data from patients with CHB (n= 119) and their siblings (n= 128), all born to anti-Ro/SSA-positive mothers, and from matched healthy controls (n= 1,190) and their siblings (n= 1,071), were retrieved from the Swedish National Patient Register. Analyses were performed by Cox proportional hazard modelling. Individuals with CHB had a significantly increased risk of cardiovascular comorbidity, with cardiomyopathy and/or heart failure observed in 20 (16.8%) patients versus 3 (0.3%) controls, yielding a HR of 70.0 (95% CI 20.8 to 235.4), and with a HR for cerebral infarction of 39.9 (95% CI 4.5 to 357.3). Patients with CHB also had a higher risk of infections. Pacemaker treatment was associated with a decreased risk of cerebral infarction but increased risks of cardiomyopathy/heart failure and infection. The risk of systemic connective tissue disorder was also increased in patients with CHB (HR 11.8, 95% CI 4.0 to 11.8), and both patients with CHB and their siblings had an increased risk to develop any of 15 common autoimmune conditions (HR 5.7, 95% CI 2.83 to 11.69 and 3.6, 95% CI 1.7 to 8.0, respectively). The data indicate an increased risk of several cardiovascular, infectious and autoimmune diseases in patients with CHB, with the latter risk shared by their siblings.

Identifiants

pubmed: 30808622
pii: annrheumdis-2018-214406
doi: 10.1136/annrheumdis-2018-214406
doi:

Substances chimiques

Antibodies, Antinuclear 0
Autoantibodies 0
SS-A antibodies 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

696-703

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

© Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Johannes Mofors (J)

Department of Medicine, Karolinska Institutet, Stockholm, Sweden.

Håkan Eliasson (H)

Department of Women's and Children's Health, Karolinska Universitetssjukhuset, Stockholm, Sweden.

Aurelie Ambrosi (A)

Department of Medicine, Karolinska Institutet, Stockholm, Sweden.

Stina Salomonsson (S)

Department of Medicine, Karolinska Institutet, Stockholm, Sweden.

Amanda Skog (A)

Department of Medicine, Karolinska Institutet, Stockholm, Sweden.

Michael Fored (M)

Department of Medicine, Karolinska Institutet, Stockholm, Sweden.

Anders Ekbom (A)

Department of Medicine, Karolinska Institutet, Stockholm, Sweden.

Gunnar Bergman (G)

Department of Women's and Children's Health, Karolinska Universitetssjukhuset, Stockholm, Sweden.

Sven-Erik Sonesson (SE)

Department of Women's and Children's Health, Karolinska Universitetssjukhuset, Stockholm, Sweden.

Marie Wahren-Herlenius (M)

Department of Medicine, Karolinska Institutet, Stockholm, Sweden marie.wahren@ki.se.

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Classifications MeSH