Population Health Unit, Finnish Institute for Health and Welfare, Helsinki, Finland; Department of Public Health, University of Turku, Turku, Finland; Centre for Population Health Research, University of Turku and Turku University Hospital, Turku, Finland.
Population Health Unit, Finnish Institute for Health and Welfare, Helsinki, Finland.
Lancet Public Health. 2023 Sep;8(9):e680-e690. doi: 10.1016/S2468-2667(23)00145-7.
Multimorbidity affects people of all ages, but the risk factors of multimorbidity in adolescence are unclear. The aim of this study was to examine preterm birth (<37 weeks) as a shared risk factor for multiple health outcomes and the role of gestational age (degree of prematurity) in the development of increasingly complex multimorbidity (two, three, or four health outcomes) in adolescence (age 10-18 years).
We used population-wide data from Finland (1 187 610 adolescents born 1987-2006) and Norway (555 431 adolescents born 1998-2007). Gestational age at birth was ascertained from medical birth registers and categorised as 23-27 weeks (extremely preterm), 28-31 weeks (very preterm), 32-33 weeks (moderately preterm), 34-36 weeks (late preterm), 37-38 weeks (early term), 39-41 weeks (term, reference category) and 42-44 weeks (post-term). Children who died or emigrated before their 10th birthday, and those with missing or implausible data on gestational age, birthweight, or covariates, were excluded. Health outcomes at age 10-18 years were ascertained from specialised health care and mortality registers. We calculated hazard ratios (HRs) and population attributable fractions (PAFs) with 95% CIs for multiple health outcomes during adolescence.
Individuals were followed up from age 10 to 18 years (mean follow-up: 6 years, SD: 3 years). Preterm birth was associated with increased risks of 20 hospital-treated malignant, cardiovascular, endocrinological, neuropsychiatric, respiratory, genitourinary, and congenital health outcomes, after correcting for multiple testing and ignoring small effects (HR <1·2). Confounder-adjusted HRs comparing preterm with term-born adolescents were 2·29 (95% CI 2·19-2·39) for two health outcomes (PAF 9·0%; 8·3-9·6), and 4·22 (3·66-4·87) for four health outcomes (PAF 22·7%; 19·4-25·8) in the Finnish data. Results in the Norwegian data showed a similar pattern. We observed a consistent dose-response relationship between an earlier gestational age and elevated risks of increasingly complex multimorbidity in both datasets.
Preterm birth is associated with increased risks of diverse multimorbidity patterns at age 10-18 years. Adolescents with a preterm-born background could benefit from diagnostic vigilance directed at multimorbidity and a multidisciplinary approach to health care.
European Union Horizon 2020, Academy of Finland, Foundation for Pediatric Research, Sigrid Jusélius Foundation, Signe and Ane Gyllenberg Foundation.
多种疾病影响着各个年龄段的人群,但青少年多种疾病的风险因素尚不清楚。本研究旨在探讨早产(<37 周)是否为多种健康结果的共同危险因素,以及胎龄(早产程度)在青少年(10-18 岁)中发展为越来越复杂的多种疾病(两种、三种或四种健康结果)中的作用。
我们使用了来自芬兰(1187610 名 1987-2006 年出生的青少年)和挪威(555431 名 1998-2007 年出生的青少年)的全人群数据。出生时的胎龄通过医疗出生登记确定,并分为 23-27 周(极早产)、28-31 周(早产)、32-33 周(中度早产)、34-36 周(早产)、37-38 周(足月,参考类别)、39-41 周(足月)和 42-44 周(过期)。10 岁生日前死亡或移民的儿童,以及胎龄、出生体重或协变量缺失或不可信的儿童,均被排除在外。10-18 岁的健康结果通过专门的医疗保健和死亡率登记确定。我们计算了青少年时期多种健康结果的风险比(HRs)和人群归因分数(PAFs)及其 95%置信区间。
个体从 10 岁到 18 岁(平均随访时间:6 年,标准差:3 年)进行随访。在校正了多重检验和忽略小效应后,与足月出生的青少年相比,早产与 20 种医院治疗的恶性、心血管、内分泌、神经精神、呼吸、泌尿生殖和先天性健康结果的风险增加有关(HR<1.2)。在芬兰数据中,与足月出生的青少年相比,早产儿的校正 HR 为 2.29(95%CI 2.19-2.39),有两种健康结果(PAF 9.0%;8.3-9.6),4.22(3.66-4.87)有四种健康结果(PAF 22.7%;19.4-25.8)。挪威数据中的结果显示出类似的模式。我们在两个数据集均观察到胎龄与日益复杂的多种疾病风险之间存在一致的剂量-反应关系。
早产与 10-18 岁时多种疾病模式的风险增加有关。有早产背景的青少年可能受益于针对多种疾病的诊断监测以及多学科的医疗保健方法。
欧盟地平线 2020、芬兰科学院、儿科研究基金会、西格德·朱塞利乌斯基金会、西涅和安妮·吉伦伯格基金会。