Natalie V Scime, Sonia M Grandi, Joel G Ray, Cindy-Lee Dennis, Mary A De Vera, Hailey R Banack, Simone N Vigod, Alexa Boblitz, Hilary K Brown
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Royston-Parmar models were used to estimate the time-varying association between pregnancy complications and a composite of 25 autoimmune diseases from date of delivery to date of autoimmune disease diagnosis or censoring at death, loss of health insurance, or 31 March 2021. Models were adjusted for baseline socio-demographics, parity and comorbidities.</p><p><strong>Results: </strong>At 19 years (median = 10.9 years of follow-up), cumulative incidence of autoimmune disease was 3.1% in those with a pregnancy complication and 2.6% in those without complications. Adjusted hazard ratio (AHR) curves as a function of time since birth were generally L-shaped. Universally, risks were most elevated within the first 3 years after birth [at 1 year: preeclampsia AHR 1.22, 95% confidence interval (CI) 1.09-1.36; stillbirth AHR 1.36, 95% CI 0.99-1.85; spontaneous preterm birth AHR 1.30, 95% CI 1.18-1.44; severe SGA AHR 1.14, 95% CI 0.99-1.31] and plateaued but remained elevated thereafter.</p><p><strong>Conclusions: </strong>Prior history of pregnancy complications may be an important female-specific risk factor to consider during clinical assessment of females for possible autoimmune disease to facilitate timely detection and treatment.</p>","PeriodicalId":14147,"journal":{"name":"International journal of epidemiology","volume":"53 5","pages":""},"PeriodicalIF":6.4000,"publicationDate":"2024-08-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11349189/pdf/","citationCount":"0","resultStr":"{\"title\":\"Pregnancy complications and new-onset maternal autoimmune disease.\",\"authors\":\"Natalie V Scime, Sonia M Grandi, Joel G Ray, Cindy-Lee Dennis, Mary A De Vera, Hailey R Banack, Simone N Vigod, Alexa Boblitz, Hilary K Brown\",\"doi\":\"10.1093/ije/dyae115\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Autoimmune diseases disproportionately impact women and female-specific aspects of reproduction are thought to play a role. We investigated the time-varying association between pregnancy complications and new-onset autoimmune disease in females during the reproductive and midlife years.</p><p><strong>Methods: </strong>We conducted a population-based cohort study of 1 704 553 singleton births to 1 072 445 females in Ontario, Canada (2002-17) with no pre-existing autoimmune disease. Pregnancy complications were preeclampsia, stillbirth, spontaneous preterm birth and severe small for gestational age (SGA). Royston-Parmar models were used to estimate the time-varying association between pregnancy complications and a composite of 25 autoimmune diseases from date of delivery to date of autoimmune disease diagnosis or censoring at death, loss of health insurance, or 31 March 2021. Models were adjusted for baseline socio-demographics, parity and comorbidities.</p><p><strong>Results: </strong>At 19 years (median = 10.9 years of follow-up), cumulative incidence of autoimmune disease was 3.1% in those with a pregnancy complication and 2.6% in those without complications. Adjusted hazard ratio (AHR) curves as a function of time since birth were generally L-shaped. 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引用次数: 0
摘要
背景:自身免疫性疾病对女性的影响尤为严重,而女性特有的生殖问题被认为是其中的一个因素。我们研究了女性在生育期和中年时期妊娠并发症与新发自身免疫性疾病之间的时变关系:我们对加拿大安大略省(2002-17 年)1 704 553 例单胎分娩和 1 072 445 例未患自身免疫性疾病的女性进行了基于人群的队列研究。妊娠并发症包括子痫前期、死胎、自发性早产和严重胎龄过小 (SGA)。罗伊斯顿-帕尔马模型用于估计妊娠并发症与 25 种自身免疫性疾病复合体之间的时变关系,时间跨度为分娩日期至自身免疫性疾病诊断日期或死亡、失去医疗保险或 2021 年 3 月 31 日。模型根据基线社会人口统计学、奇偶性和合并症进行了调整:19年(中位数=10.9年随访)后,妊娠并发症患者的自身免疫性疾病累积发病率为3.1%,无并发症患者的自身免疫性疾病累积发病率为2.6%。调整后危险比(AHR)曲线与出生后时间的关系一般呈 L 型。总体而言,产后头 3 年的风险最高[1 年时:子痫前期 AHR 1.22,95% 置信区间(CI)1.09-1.36;死胎 AHR 1.36,95% CI 0.99-1.85;自发性早产 AHR 1.30,95% CI 1.18-1.44;严重 SGA AHR 1.14,95% CI 0.99-1.31],之后风险趋于平稳,但仍然较高:在对可能患有自身免疫性疾病的女性进行临床评估时,既往妊娠并发症史可能是一个重要的女性特异性风险因素,以便及时发现和治疗。
Pregnancy complications and new-onset maternal autoimmune disease.
Background: Autoimmune diseases disproportionately impact women and female-specific aspects of reproduction are thought to play a role. We investigated the time-varying association between pregnancy complications and new-onset autoimmune disease in females during the reproductive and midlife years.
Methods: We conducted a population-based cohort study of 1 704 553 singleton births to 1 072 445 females in Ontario, Canada (2002-17) with no pre-existing autoimmune disease. Pregnancy complications were preeclampsia, stillbirth, spontaneous preterm birth and severe small for gestational age (SGA). Royston-Parmar models were used to estimate the time-varying association between pregnancy complications and a composite of 25 autoimmune diseases from date of delivery to date of autoimmune disease diagnosis or censoring at death, loss of health insurance, or 31 March 2021. Models were adjusted for baseline socio-demographics, parity and comorbidities.
Results: At 19 years (median = 10.9 years of follow-up), cumulative incidence of autoimmune disease was 3.1% in those with a pregnancy complication and 2.6% in those without complications. Adjusted hazard ratio (AHR) curves as a function of time since birth were generally L-shaped. Universally, risks were most elevated within the first 3 years after birth [at 1 year: preeclampsia AHR 1.22, 95% confidence interval (CI) 1.09-1.36; stillbirth AHR 1.36, 95% CI 0.99-1.85; spontaneous preterm birth AHR 1.30, 95% CI 1.18-1.44; severe SGA AHR 1.14, 95% CI 0.99-1.31] and plateaued but remained elevated thereafter.
Conclusions: Prior history of pregnancy complications may be an important female-specific risk factor to consider during clinical assessment of females for possible autoimmune disease to facilitate timely detection and treatment.
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