Parental rheumatoid arthritis and childhood epilepsy
Autor: | Damini Jawaheer, Bent Ottesen, Merete Lund Hetland, Lina Steinrud Mørch, Chunsen Wu, Jørn Olsen, Ane Lilleøre Rom, Jakob Christensen |
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Rok vydání: | 2016 |
Předmět: |
Adult
Male Parents medicine.medical_specialty Pediatrics Adolescent Offspring Arthritis Rheumatoid Cohort Studies 03 medical and health sciences Epilepsy 0302 clinical medicine Pregnancy Risk Factors Journal Article Humans Medicine Registries Early childhood Child Proportional Hazards Models 030203 arthritis & rheumatology business.industry Proportional hazards model Hazard ratio medicine.disease Confidence interval Child Preschool Prenatal Exposure Delayed Effects Physical therapy Female Neurology (clinical) business 030217 neurology & neurosurgery Cohort study |
Zdroj: | Rom, A L, Wu, C, Olsen, J, Jawaheer, D, Hetland, M L, Christensen, J, Ottesen, B & Mørch, L S 2016, ' Parental rheumatoid arthritis and childhood epilepsy : A nationwide cohort study ', Neurology, vol. 87, no. 24, pp. 2510-2516 . https://doi.org/10.1212/WNL.0000000000003424 Rom, A L, Wu, C, Olsen, J, Jawaheer, D, Hetland, M L, Christensen, J, Ottesen, B & Mørch, L S 2016, ' Parental rheumatoid arthritis and childhood epilepsy: A nationwide cohort study ', Neurology, vol. 87, no. 24, pp. 2510-2516 . https://doi.org/10.1212/WNL.0000000000003424 |
ISSN: | 1526-632X 0028-3878 |
DOI: | 10.1212/wnl.0000000000003424 |
Popis: | OBJECTIVE: To assess the influence of parental rheumatoid arthritis (RA) on risk of epilepsy.METHODS: We performed a nationwide cohort study including all singletons born in Denmark from 1977 to 2008 (n = 1,917,723) through individual linkage to nationwide Danish registries. The children were followed for an average of 16 years. Main outcome measures were adjusted hazard ratios (HRs) for epilepsy with onset in early childhood (29 days-4 years), late childhood (5-15 years), adolescence/adulthood (≥15 years), and at any age until the end of follow-up (December 31, 2010).RESULTS: Compared to unexposed children, children exposed to maternal RA had an increased risk of early and late childhood epilepsy (adjusted HRs 1.34 [95% confidence interval (CI) 1.13-1.60] and 1.26 [95% CI 1.13-1.41]), while children exposed to maternal RA had no increased risk of epilepsy in adolescence/adulthood (HR 1.15 [95% CI 0.92-1.45]). Paternal RA was not associated with an overall risk of epilepsy in the offspring (HR 0.96 [95% CI 0.81-1.15]) or at any age. Children exposed to maternal RA in utero had a more pronounced increased risk of early childhood epilepsy than children exposed to mothers who were diagnosed with RA after childbirth (HR 1.90 [95% CI 1.26-2.86] vs HR 1.26 [95% CI 1.03-1.52], respectively [p = 0.16]).CONCLUSIONS: Exposure to maternal RA was associated with an increased risk of childhood epilepsy, while exposure to paternal RA was not, which indicates that changes in the intrauterine environment may play a role. OBJECTIVE: To assess the influence of parental rheumatoid arthritis (RA) on risk of epilepsy.METHODS: We performed a nationwide cohort study including all singletons born in Denmark from 1977 to 2008 (n = 1,917,723) through individual linkage to nationwide Danish registries. The children were followed for an average of 16 years. Main outcome measures were adjusted hazard ratios (HRs) for epilepsy with onset in early childhood (29 days-4 years), late childhood (5-15 years), adolescence/adulthood (≥15 years), and at any age until the end of follow-up (December 31, 2010).RESULTS: Compared to unexposed children, children exposed to maternal RA had an increased risk of early and late childhood epilepsy (adjusted HRs 1.34 [95% confidence interval (CI) 1.13-1.60] and 1.26 [95% CI 1.13-1.41]), while children exposed to maternal RA had no increased risk of epilepsy in adolescence/adulthood (HR 1.15 [95% CI 0.92-1.45]). Paternal RA was not associated with an overall risk of epilepsy in the offspring (HR 0.96 [95% CI 0.81-1.15]) or at any age. Children exposed to maternal RA in utero had a more pronounced increased risk of early childhood epilepsy than children exposed to mothers who were diagnosed with RA after childbirth (HR 1.90 [95% CI 1.26-2.86] vs HR 1.26 [95% CI 1.03-1.52], respectively [p = 0.16]).CONCLUSIONS: Exposure to maternal RA was associated with an increased risk of childhood epilepsy, while exposure to paternal RA was not, which indicates that changes in the intrauterine environment may play a role. |
Databáze: | OpenAIRE |
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