Risk of Sudden Infant Death Syndrome Among Siblings of Children Who Died of Sudden Infant Death Syndrome in Denmark

被引:9
|
作者
Glinge, Charlotte [1 ,2 ]
Rossetti, Sara [1 ]
Oestergaard, Louise Bruun [3 ,4 ]
Stampe, Niels Kjaer [1 ]
Lynge, Thomas Hadberg [1 ]
Skals, Regitze [4 ]
Winkel, Bo Gregers [1 ]
Lodder, Elisabeth M. [2 ]
Bezzina, Connie R. [2 ]
Gislason, Gunnar [3 ,5 ]
Banner, Jytte [6 ]
Behr, Elijah R. [7 ,8 ,9 ]
Torp-Pedersen, Christian [4 ,10 ,11 ]
Jabbari, Reza [1 ]
Tfelt-Hansen, Jacob [1 ,6 ]
机构
[1] Copenhagen Univ Hosp, Dept Cardiol, Ctr Heart, Rigshosp, Copenhagen, Denmark
[2] Univ Amsterdam, Amsterdam UMC, Dept Clin & Expt Cardiol, Ctr Heart,Amsterdam Cardiovasc Sci, Amsterdam, Netherlands
[3] Copenhagen Univ Hosp Herlev & Gentofte, Dept Cardiol, Copenhagen, Denmark
[4] Aalborg Univ Hosp, Dept Cardiol, Aalborg, Denmark
[5] Danish Heart Fdn, Copenhagen, Denmark
[6] Copenhagen Univ Hosp, Dept Forens Med, Rigshosp, Copenhagen, Denmark
[7] St Georges Univ London, Cardiol Sect, Cardiol Clin Acad Grp, London, England
[8] St Georges Univ Hosp NHS Fdn Trust, London, England
[9] Mayo Clin Healthcare, London, England
[10] North Zealand Univ Hosp, Dept Cardiol, Hillerod, Denmark
[11] Univ Copenhagen, Dept Publ Hlth, Copenhagen, Denmark
基金
欧盟地平线“2020”; 荷兰研究理事会;
关键词
UNITED-STATES; SMOKING; REGISTERS; TRENDS; COHORT;
D O I
10.1001/jamanetworkopen.2022.52724
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Key PointsQuestionIs a family history of sudden infant death syndrome (SIDS) associated with increased risk of subsequent SIDS compared with the general population? FindingsIn this cohort study of more than 2.6 million consecutive births in Denmark between 1978 and 2016, a total of 1540 infants died of SIDS. A higher rate of SIDS was observed among siblings of children who died of SIDS compared with the general population. MeaningThese findings suggest that any sibling of a child who died of SIDS should be investigated with great care to exclude genetic and environmental factors. This cohort study evaluates whether having a sibling who died of sudden infant death syndrome (SIDS) is associated with increased risk of SIDS compared with the general pediatric population among infants in Denmark. Importance Sudden infant death syndrome (SIDS) remains a leading cause of death during the first year of life. The etiology of SIDS is complex and remains largely unknown. Objective To evaluate whether siblings of children who died of SIDS have a higher risk of SIDS compared with the general pediatric population. Design, Setting, and Participants This register-based cohort study used Danish nationwide registers. Participants were all infants (<1 year) in Denmark between January 1, 1978, and December 31, 2016, including siblings of children who died of SIDS. Siblings were followed up from the index cases' date of SIDS, date of birth, or immigration, whichever came first, and until age 1 year, emigration, developing SIDS, death, or study end. The median (IQR) follow-up was 1 (1-1) year. Data analysis was conducted from January 2017 to October 2022. Main Outcomes and Measures Standardized incidence ratios (SIRs) of SIDS were calculated with Poisson regression models relative to the general population. Results In a population of 2666834 consecutive births (1395199 [52%] male), 1540 infants died of SIDS (median [IQR] age at SIDS, 3 [2-4] months) during a 39-year study period. A total of 2384 younger siblings (cases) to index cases (first sibling with SIDS) were identified. A higher rate of SIDS was observed among siblings compared with the general population, with SIRs of 4.27 (95% CI, 2.13-8.53) after adjustment for sex, age, and calendar year and of 3.50 (95% CI, 1.75-7.01) after further adjustment for mother's age (<29 years vs >= 29 years) and education (high school vs after high school). Conclusions and Relevance In this nationwide study, having a sibling who died of SIDS was associated with a 4-fold higher risk of SIDS compared with the general population. Shared genetic and/or environmental factors may contribute to the observed clustering of SIDS. The family history of SIDS should be considered when assessing SIDS risk in clinical settings. A multidisciplinary genetic evaluation of families with SIDS could provide additional evidence.
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页数:11
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