Unger Holger W, Dadi Abel, Brown Kiarna, Simon David, Guthridge Steven
Menzies School of Health Research, Charles Darwin University, Darwin, NT, Australia.
Department of Obstetrics and Gynaecology, Royal Darwin Hospital, Darwin, NT, Australia.
BMC Pregnancy Childbirth. 2024 Dec 24;24(1):855. doi: 10.1186/s12884-024-07053-2.
PTB increases the risk of health problems such as chronic renal disease and diabetes in later life and adverse impacts are inversely correlated with gestational age at birth. Rates of PTB in the Northern Territory (NT) of Australia are amongst the highest nationally and globally, with First Nations babies most affected. This study assessed the magnitude and potential drivers of intergenerational PTB recurrence in the NT.
A retrospective intergenerational cohort study (1986-2017) was conducted amongst 5,366 mothers born singleton who had 9,571 singleton live births (7,673 First Nations, and 1,898 non-First Nations babies). Maternal and offspring PTB was categorised as early (< 34 weeks) and late (34-36 gestational weeks). Modified Poisson regression was used to estimate the relative risk (RR) of PTB associated with maternal PTB, adjusting for moderators such as receipt of antenatal care prior to the offspring PTB. Secondary analyses assessed the impact of additional adjustment for conditions with a familial component, or that PTB predisposes to, on the risk estimate. Mediation analysis assessed the degree of mediation of maternal-offspring PTB relationships by these conditions.
Overall, First Nations women born preterm (< 37 weeks) had an increased risk of delivering before 37 gestational weeks (aRR 1.28; 95%CI 1.08, 1.51). Women born preterm had a higher risk of delivering early (< 34 gestational weeks) but not late preterm (34-36 weeks): the risk of early offspring PTB was increased amongst women themselves born early preterm (aRR 1.95, 95%CI 1.17, 3.24) or late preterm (aRR 1.41, 95%CI 1.01, 1.97). Adjustment for pre-eclampsia, intrauterine growth restriction, and hypertensive renal disease attenuated the observed intergenerational PTB associations. Mediation analysis suggested these conditions may mediate up to 26% of the observed intergenerational PTB recurrence. Similar trends were observed when first-time mothers were considered only. Maternal PTB status was not associated with PTB amongst non-First Nations women.
First Nations women born preterm have an increased risk of early PTB. This association is in part driven by pre-eclampsia and hypertensive renal disease. Routine inquiry of maternal birth status may be a useful tool to identify NT First Nations women who may benefit from preventative measures.
早产会增加日后患慢性肾病和糖尿病等健康问题的风险,且不良影响与出生时的孕周呈负相关。澳大利亚北领地(NT)的早产率在全国乃至全球都名列前茅,原住民婴儿受影响最大。本研究评估了北领地早产代际复发的程度和潜在驱动因素。
对5366名单胎出生的母亲及其9571名单胎活产婴儿(7673名原住民婴儿和1898名非原住民婴儿)进行了一项回顾性代际队列研究(1986 - 2017年)。将母亲和后代的早产分为早期(<34周)和晚期(34 - 36孕周)。采用修正泊松回归估计与母亲早产相关的早产相对风险(RR),并对后代早产前接受产前护理等调节因素进行调整。二次分析评估了对具有家族成分或早产易引发的疾病进行额外调整对风险估计的影响。中介分析评估了这些疾病对母婴早产关系的中介程度。
总体而言,早产(<37周)出生的原住民女性在37孕周前分娩的风险增加(调整后风险比1.28;95%置信区间1.08,1.51)。早产出生的女性早期(<34孕周)分娩风险较高,但晚期早产(34 - 36周)风险不高:自身早期早产(调整后风险比1.95,95%置信区间1.17,3.24)或晚期早产(调整后风险比1.41,95%置信区间1.01,1.97)的女性,其后代早期早产风险增加。对先兆子痫、宫内生长受限和高血压肾病进行调整后,观察到的代际早产关联减弱。中介分析表明,这些疾病可能介导了高达26%观察到的代际早产复发。仅考虑初产妇时也观察到类似趋势。非原住民女性中,母亲的早产状态与早产无关。
早产出生的原住民女性早期早产风险增加。这种关联部分由先兆子痫和高血压肾病驱动。常规询问母亲的出生状况可能是识别北领地原住民女性中哪些人可能从预防措施中受益的有用工具。