Evidence map›Paper›PMID 42071193›Full record

ArticleBMC pregnancy and childbirth2026

Assessment of albumin-related inflammatory indices in preeclampsia and their relationship with composite adverse perinatal outcomes.

Aykut Kından, Goncagül Kından, Dilara Sarikaya Kurt, Ayberk Çakır, Özgür Volkan Akbulut, Şevki Çelen

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Article in BMC pregnancy and childbirth, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Aykut KındanDepartment of Obstetrics and Gynecology, Nurdağı State Hospital, Gaziantep, Turkey. aykutkindan33@hotmail.com.ORCID http://orcid.org/0000-0002-0962-1036
Goncagül KındanDepartment of Obstetrics and Gynecology, Atatürk Sanatoryum Training and Research Hospital, Ankara, Turkey.ORCID http://orcid.org/0009-0001-7547-4695
Dilara Sarikaya KurtDepartment of Obstetrics and Gynecology, Mudanya State Hospital, Bursa, Turkey.ORCID http://orcid.org/0000-0002-1492-0305
Ayberk ÇakırDepartment of Obstetrics and Gynecology, Acıbadem University Atakent Hospital, Istanbul, Turkey.ORCID http://orcid.org/0000-0001-5749-4556
Özgür Volkan AkbulutDepartment of Perinatology, Etlik City Hospital, Ankara, Turkey.ORCID http://orcid.org/0000-0002-1960-2146
Şevki ÇelenDepartment of Perinatology, Etlik City Hospital, Ankara, Turkey.ORCID http://orcid.org/0000-0001-7033-3474

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPreeclampsia is characterized by systemic inflammation, endothelial dysfunction, and multi-organ involvement, contributing to increased risk of adverse perinatal outcomes. Albumin-based inflammatory and nutritional indices have recently gained interest as easily accessible biomarkers in high-risk pregnancies. This study aimed to compare albumin-related indices between preeclamptic and normotensive pregnancies and to evaluate their predictive value for composite adverse perinatal outcomes (CAPO) in preeclampsia.

methodsThis retrospective case-control study included 186 preeclamptic patients and 186 healthy controls matched for maternal age, BMI, gravidity, and gestational age. Laboratory parameters measured at delivery and calculated indices (NAR, FAR, sACR, HALP, and BAR) were compared. The preeclampsia cohort was further classified into CAPO (+) and CAPO (-) groups. Logistic regression models were used to identify independent predictors of CAPO, and receiver operating characteristic (ROC) analysis assessed predictive performance.

resultsAlbumin-based indices differed significantly between preeclamptic and healthy pregnancies, with higher NAR, FAR, and BAR values and lower sACR levels in the preeclampsia group (all p < 0.001). Among preeclamptic patients, CAPO developed in 44.1% (n = 82). CAPO (+) patients demonstrated higher NAR, BAR, and HALP values and lower sACR levels compared to CAPO (-) patients. In multivariable logistic regression, only the blood urea nitrogen-to-albumin ratio (BAR) remained independently associated with CAPO (aOR = 1.157, p = 0.015). BAR demonstrated moderate discriminative performance for CAPO (AUC = 0.718; cut-off > 0.61; sensitivity 67.1%; specificity 69.2%; p < 0.001).

conclusionAll albumin-based indices showed significant alterations in preeclampsia; however, only BAR independently predicted adverse perinatal outcomes. BAR is a simple, inexpensive biomarker derived from routine laboratory parameters and may support risk stratification and neonatal outcome prediction in preeclamptic pregnancies. Prospective multicenter studies are warranted to validate its clinical applicability.

Indexed as

InflammationPre-EclampsiaSerum AlbuminAdultBiomarkersCase-Control StudiesFemaleHumansInfant, NewbornLogistic ModelsPredictive Value of TestsPregnancyPregnancy OutcomeRetrospective StudiesROC CurveBiomarkersSerum AlbuminAlbumin-based inflammatory indicesBlood urea nitrogen-to-albumin ratio (BAR)Composite adverse perinatal outcomeNeonatal outcomesPreeclampsia

Identifiers

PMID42071193
PMCPMC13285206

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.