Comorbidity and long-term outcome in patients with congenital heart block and their siblings exposed to Ro/SSA autoantibodies in utero.
Adolescent
Adult
Antibodies, Antinuclear
/ immunology
Autoantibodies
/ immunology
Autoimmune Diseases
/ immunology
Child
Child, Preschool
Comorbidity
Female
Heart Block
/ congenital
Humans
Infant
Infant, Newborn
Male
Maternal Exposure
/ adverse effects
Middle Aged
Pedigree
Pregnancy
Pregnancy Complications
/ immunology
Prenatal Exposure Delayed Effects
/ immunology
Registries
Siblings
Sweden
Young Adult
congenital heart block
pacemaker
sjögren’s syndrome
sle
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
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
696-703Commentaires 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.