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Familial Aggregation of Childhood‐ and Adulthood‐Onset Systemic Lupus Erythematosus
Author(s) -
Sinicato Nailú Angélica,
Oliveira Luciana,
Lapa AlineTamires,
Postal Mariana,
Peliçari Karinade Oliveira,
Costallat Lilian T. L.,
Marini Roberto,
GildaSilvaLopes Vera Lúcia,
Niewold Timothy B.,
Appenzeller Simone
Publication year - 2020
Publication title -
arthritis care and research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.032
H-Index - 163
eISSN - 2151-4658
pISSN - 2151-464X
DOI - 10.1002/acr.23931
Subject(s) - medicine , first degree relatives , cohort , age of onset , lupus erythematosus , systemic lupus erythematosus , young adult , connective tissue disease , pediatrics , offspring , family history , disease , immunology , autoimmune disease , pregnancy , genetics , biology , antibody
Objective To assess the familial occurrence of systemic lupus erythematosus ( SLE ) in a large Brazilian cohort. Methods Consecutive patients with SLE were recruited and stratified according to age at disease onset into childhood‐onset SLE or adult‐onset SLE . Each patient was personally interviewed regarding the history of SLE across 3 generations (first‐, second‐, and third‐degree relatives). Recurrence rates were analyzed for each degree of relation. Results We included 392 patients with SLE (112 with childhood‐onset SLE and 280 with adult‐onset SLE ). We identified 2,574 first‐degree relatives, 5,490 second‐degree relatives, and 6,805 third‐degree relatives. In the combined overall SLE cohort, we observed a familial SLE recurrence rate of 19.4 in first‐degree relatives, 5.4 in second‐degree relatives, and 3.0 in third‐degree relatives. Recurrence rates were higher for first‐ and second‐degree relatives of patients with childhood‐onset SLE than for first‐ and second‐degree relatives of patients with adult‐onset SLE (25.2 versus 18.4 for first‐degree, and 8.5 versus 4.5 for second‐degree), while in third‐degree relatives, recurrence rates were higher in adult‐onset SLE than in childhood‐onset SLE ( P = 2.2 × 10 –4 for differences in recurrence proportions between childhood‐onset SLE and adult‐onset SLE ). There were no phenotypic differences in patients from multicase versus single‐case families, and there was no sex‐skewing observed in the offspring of patients with SLE . Conclusion The greater decline in SLE recurrence rate by generation in childhood‐onset SLE versus adult‐onset SLE suggests a more polygenic and epistatic inheritance and suggests that adult‐onset SLE may be characterized by fewer risk factors that are individually stronger. This finding suggests a higher genetic load in childhood‐onset SLE versus adult‐onset SLE and a difference in the genetic architecture of the disease based on age at onset.