Capone Kristin, Rosenberg Harry J, Wroblewski Kristen, Gokhale Ranjana, Kirschner Barbara S
Department of Pediatrics, Section of Gastroenterology, Hepatology, and Nutrition.
Department of Public Health Sciences, University of Chicago Medicine, Chicago, IL.
J Pediatr Gastroenterol Nutr. 2019 Jun;68(6):829-834. doi: 10.1097/MPG.0000000000002253.
The aim of the study was to prospectively study changes in prevalence of positive family history (FH+) in pediatric-onset inflammatory bowel disease (IBD) in contrast to previously published cross-sectional data.
An observational cohort study was performed using a prospective pediatric-onset IBD database including 485 patients with disease duration ≥10 years as of December 2016. Proband characteristics and FH+ were obtained at diagnosis and subsequently from the database, medical records, and follow-up telephone interviews in 2006 and 2016.
Updated 2016 information was obtained from 322 (66%) patients and included in analysis with median follow-up of 18 years (interquartile range 14, 26). Prevalence of FH+ increased from 13.7% at diagnosis to 26.6% at 20 years for first-degree relatives and from 38.5% to 52.2% for all relatives. At 20-year follow-up, an additional 10.0% of probands had a sibling, 6.1% had a parent, 1.9% had a grandparent, and 4.5% had a cousin diagnosed with IBD. FH+ at diagnosis was associated with greater risk for additional FH+ at 20 years (43% vs 22%, P < 0.001). Non-Jewish Caucasians had significantly lower risk of a FH+ compared to Jewish Caucasians (P = 0.002), but similar risk to African Americans (P = 0.55). FH+ at diagnosis was not associated with disease type (P = 0.33) or age at diagnosis (P = 0.24).
This prospective study documents changes in family history of IBD in pediatric-onset IBD patients over time. Prevalence of FH+ increased for first-degree and all relatives at 20 years by 12.9% and 13.7%, respectively. FH+ at diagnosis was associated with a 2-fold greater likelihood of subsequent FH+ at 20 years.
本研究旨在前瞻性地研究儿童期起病的炎症性肠病(IBD)中阳性家族史(FH+)患病率的变化,并与先前发表的横断面数据进行对比。
采用前瞻性儿童期起病的IBD数据库进行一项观察性队列研究,该数据库包括截至2016年12月疾病病程≥10年的485例患者。在诊断时以及随后于2006年和2016年从数据库、病历和随访电话访谈中获取先证者特征和FH+情况。
从322例(66%)患者获得了2016年的更新信息,并纳入分析,中位随访时间为18年(四分位间距14, 26)。一级亲属的FH+患病率从诊断时的13.7%增加到20岁时的26.6%,所有亲属的FH+患病率从38.5%增加到52.2%。在20年随访时,另外10.0%的先证者有一个患IBD的兄弟姐妹,6.1%有一个患IBD的父母,1.9%有一个患IBD的祖父母,4.5%有一个患IBD的表亲。诊断时的FH+与20岁时出现额外FH+的风险更高相关(43%对22%,P<0.001)。与犹太裔白种人相比,非犹太裔白种人FH+的风险显著更低(P = 0.002),但与非裔美国人风险相似(P = 0.55)。诊断时的FH+与疾病类型(P = 0.33)或诊断年龄(P = 0.24)无关。
这项前瞻性研究记录了儿童期起病的IBD患者家族史随时间的变化。20岁时,一级亲属和所有亲属的FH+患病率分别增加了12.9%和13.7%。诊断时的FH+与20岁时后续出现FH+的可能性高出2倍相关。