Department of Epidemiology and Prevention, Wake Forest University School of Medicine, Winston-Salem, North Carolina.
Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, Ontario, Canada.
JAMA Netw Open. 2024 Nov 4;7(11):e2445871. doi: 10.1001/jamanetworkopen.2024.45871.
Preterm birth (PTB) is a leading cause of neonatal mortality. However, evidence on mortality beyond the neonatal period is limited, especially in North America.
To examine associations of PTB with all-cause and cause-specific mortality from birth through 23 to 36 years of age.
DESIGN, SETTING, AND PARTICIPANTS: This population-based matched cohort study of live births in Canada included individuals born between January 1, 1983, and December 31, 1996, and followed up until December 31, 2019. Data were analyzed from June 1, 2023, to April 30, 2024.
PTBs, between 24 and 37 weeks' gestation (with gestational age [GA]-specific subcategories of 24 to 27 weeks, 28 to 31 weeks, 32 to 33 weeks, and 34 to 36 weeks) compared with term births (37-41 weeks' gestation).
All-cause mortality and cause-specific mortality were the main outcomes. Risk differences (RDs) and risk ratios (RRs) were estimated for all-cause mortality using log-binomial regressions and hazard ratios were estimated for cause-specific mortality using Cox proportional hazards regression models (censoring individuals who died from other causes) within prespecified age intervals (ages 0-11 months and ages 1-5, 6-12, 13-17, 18-28, and 29-36 years). Observed confounding was accounted for using coarsened exact matching on baseline characteristics.
Of 4 998 560 births (54.2% male), 6.9% were born preterm (with GA-specific subcategories of 0.3% born at 24-27 weeks, 0.6% at 28-31 weeks, 0.8% at 32-33 weeks, and 5.1% at 34-36 weeks). During a median of 29 years of follow-up, 72 662 individuals died (14 312 born preterm and 58 350 at term). PTB was associated with an increased risk of death in all age intervals, with the highest RDs and RRs from birth through infancy (ages 0-11 months) (RD, 2.29% [95% CI, 2.23%-2.35%]; RR, 11.61 [95% CI, 11.09-12.15]) and in early childhood (ages 1-5 years) (RD, 0.34% [95% CI, 0.31%-0.36%]; RR, 2.79 [95% CI, 2.61-2.98]) and the lowest RDs and RRs among those between ages 18 and 28 years (RD, 0.07% [95% CI, 0.04%-0.10%]; RR, 1.13 [95% CI, 1.07-1.19]). We identified increased risks of mortality associated with several causes, including respiratory, circulatory, and digestive system disorders; nervous system, endocrine, and infectious diseases; cancers; congenital malformations; and conditions originating in the perinatal period. No associations were found for external causes of deaths. Associations by GA categories suggested lower risks with higher GA.
The findings of this population-based matched cohort study suggest that individuals born preterm were at an increased risk of death from birth until their third and fourth decades of life, with higher risks as GA decreased. Some of these associations may have been partly due to underlying health determinants that affected PTB and mortality. These findings suggest that PTB should be recognized as a risk factor for mortality and could inform preventive strategies.
早产 (PTB) 是新生儿死亡的主要原因。然而,关于新生儿期后死亡率的证据有限,尤其是在北美。
研究 PTB 与从出生到 23 至 36 岁期间所有原因和特定原因死亡率之间的关系。
设计、地点和参与者:这项基于人群的匹配队列研究包括 1983 年 1 月 1 日至 1996 年 12 月 31 日期间出生的活产儿,并随访至 2019 年 12 月 31 日。数据分析于 2023 年 6 月 1 日至 2024 年 4 月 30 日进行。
PTB,妊娠 24 至 37 周(具有特定的 GA 亚分类,即 24 至 27 周、28 至 31 周、32 至 33 周和 34 至 36 周)与足月出生(37-41 周)相比。
全因死亡率和特定原因死亡率是主要结局。使用对数二项式回归估计全因死亡率的风险差异(RD)和风险比(RR),并使用 Cox 比例风险回归模型(对死于其他原因的个体进行删失)估计特定原因死亡率的风险比(在预先指定的年龄间隔内),年龄间隔为 0-11 个月和 1-5 岁、6-12 岁、13-17 岁、18-28 岁和 29-36 岁。通过对基线特征进行粗糙化精确匹配来解释观察到的混杂因素。
在 4998560 例分娩(54.2%为男性)中,6.9%为早产儿(具有特定的 GA 亚分类,即 0.3%出生于 24-27 周、0.6%出生于 28-31 周、0.8%出生于 32-33 周和 5.1%出生于 34-36 周)。在中位 29 年的随访期间,有 72662 人死亡(14312 人出生于早产儿,58350 人在足月时出生)。PTB 与所有年龄间隔的死亡风险增加相关,从出生到婴儿期(0-11 个月)(RD,2.29%[95%CI,2.23%-2.35%];RR,11.61[95%CI,11.09-12.15])和幼儿期(1-5 岁)(RD,0.34%[95%CI,0.31%-0.36%];RR,2.79[95%CI,2.61-2.98])的风险最高,而在 18 至 28 岁的人群中风险最低(RD,0.07%[95%CI,0.04%-0.10%];RR,1.13[95%CI,1.07-1.19])。我们发现与几种原因相关的死亡率风险增加,包括呼吸系统、循环系统和消化系统疾病;神经系统、内分泌和传染病;癌症;先天性畸形;以及围产期起源的疾病。外部原因死亡无关联。按 GA 类别进行的关联表明,GA 越高,风险越低。
这项基于人群的匹配队列研究的结果表明,出生时为早产儿的个体从出生到 30 岁和 40 岁期间死亡的风险增加,随着 GA 降低,风险增加。这些关联中的一些可能部分归因于影响 PTB 和死亡率的潜在健康决定因素。这些发现表明,PTB 应被视为死亡率的一个危险因素,并为预防策略提供信息。