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Peer-reviewedCC BYBMC pregnancy and childbirth

Association of a second-trimester alpha-fetoprotein-to-transaminase ratio with preeclampsia: an exploratory retrospective cohort study.

  1. 1Department of Perinatology, Ankara Bilkent City Hospital, University of Health Sciences, Ankara, Türkiye.
  2. 2Department of Perinatology, Ankara Bilkent City Hospital, University of Health Sciences, Ankara, Türkiye. [email protected].

Abstract

Background

Maternal serum alpha-fetoprotein (AFP) is related to placental dysfunction, whereas aminotransferases are routinely available biochemical measures. We evaluated an empirically constructed AFP/(AST×ALT) index measured during second-trimester screening as an exploratory marker associated with subsequent preeclampsia. We specifically examined whether the index showed a consistent severity gradient and whether it provided clinically meaningful discrimination.Methods

This retrospective cohort study included 164 singleton pregnancies followed at a tertiary referral center between January 2022 and June 2024: 81 pregnancies without preeclampsia, 42 with preeclampsia without severe features, and 41 with preeclampsia with severe features. AFP, aspartate aminotransferase (AST), and alanine aminotransferase (ALT) measured at 16-18 weeks were retrieved. The AFP/(AST×ALT) index was calculated. Group comparisons were performed using variance-robust methods with post-hoc pairwise testing. Candidate diagnostic performance was explored using receiver-operating-characteristic analysis, and logistic regression was scaled per 0.1-unit increase in the index. Multivariable models included maternal age, body mass index, parity, and gestational age at sampling.Results

The index showed a non-monotonic pattern across groups: 0.200 ± 0.188 in pregnancies without preeclampsia, 0.801 ± 0.422 in preeclampsia without severe features, and 0.229 ± 0.239 in preeclampsia with severe features. The comparison between pregnancies without preeclampsia and preeclampsia with severe features was not significant, whereas both comparisons involving preeclampsia without severe features were significant. This pattern was driven largely by lower second-trimester AST and ALT values in the group without severe features. For preeclampsia presence, ROC analysis yielded an AUC of 0.738 (95% CI 0.654-0.812). A cutoff of 0.328 provided 61.4% sensitivity and 86.4% specificity. In multivariable analysis adjusted for maternal age, BMI, parity, and gestational age at sampling, the adjusted OR was 1.46 (95% CI 1.25-1.71) per 0.1-unit increase in the index.Conclusions

AFP/(AST×ALT) demonstrated an association with preeclampsia in this retrospective cohort, but the relationship was non-monotonic across clinical phenotypes and appeared strongly influenced by low transaminase values in the group without severe features. The index should therefore be regarded as exploratory rather than as a validated severity biomarker or stand-alone clinical test. Independent prospective validation is required.

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BibTeX
@article{haksever2026association,
  title = {{Association of a second-trimester alpha-fetoprotein-to-transaminase ratio with preeclampsia: an exploratory retrospective cohort study.}},
  author = {Murat Haksever and Uğurcan Zorlu and Sadık Orhun Aktaş and Hakkı Şerbetci and Şükrü Bakırcı and Dilek Şahin},
  journal = {BMC pregnancy and childbirth},
  year = {2026},
  month = sep,
  doi = {10.1186/s12884-026-09876-7},
  url = {https://europepmc.org/article/MED/42958157},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Association of a second-trimester alpha-fetoprotein-to-transaminase ratio with preeclampsia: an exploratory retrospective cohort study.
AU  - Murat Haksever
AU  - Uğurcan Zorlu
AU  - Sadık Orhun Aktaş
AU  - Hakkı Şerbetci
AU  - Şükrü Bakırcı
AU  - Dilek Şahin
PY  - 2026
DA  - 2026/09/11
JO  - BMC pregnancy and childbirth
DO  - 10.1186/s12884-026-09876-7
UR  - https://europepmc.org/article/MED/42958157
AB  - Background  Maternal serum alpha-fetoprotein (AFP) is related to placental dysfunction, whereas aminotransferases are routinely available biochemical measures. We evaluated an empirically constructed AFP/(AST×ALT) index measured during second-trimester screening as an exploratory marker associated with subsequent preeclampsia. We specifically examined whether the index showed a consistent severity gradient and whether it provided clinically meaningful discrimination.Methods  This retrospective cohort study included 164 singleton pregnancies followed at a tertiary referral center between January 2022 and June 2024: 81 pregnancies without preeclampsia, 42 with preeclampsia without severe features, and 41 with preeclampsia with severe features. AFP, aspartate aminotransferase (AST), and alanine aminotransferase (ALT) measured at 16-18 weeks were retrieved. The AFP/(AST×ALT) index was calculated. Group comparisons were performed using variance-robust methods with post-hoc pairwise testing. Candidate diagnostic performance was explored using receiver-operating-characteristic analysis, and logistic regression was scaled per 0.1-unit increase in the index. Multivariable models included maternal age, body mass index, parity, and gestational age at sampling.Results  The index showed a non-monotonic pattern across groups: 0.200 ± 0.188 in pregnancies without preeclampsia, 0.801 ± 0.422 in preeclampsia without severe features, and 0.229 ± 0.239 in preeclampsia with severe features. The comparison between pregnancies without preeclampsia and preeclampsia with severe features was not significant, whereas both comparisons involving preeclampsia without severe features were significant. This pattern was driven largely by lower second-trimester AST and ALT values in the group without severe features. For preeclampsia presence, ROC analysis yielded an AUC of 0.738 (95% CI 0.654-0.812). A cutoff of 0.328 provided 61.4% sensitivity and 86.4% specificity. In multivariable analysis adjusted for maternal age, BMI, parity, and gestational age at sampling, the adjusted OR was 1.46 (95% CI 1.25-1.71) per 0.1-unit increase in the index.Conclusions  AFP/(AST×ALT) demonstrated an association with preeclampsia in this retrospective cohort, but the relationship was non-monotonic across clinical phenotypes and appeared strongly influenced by low transaminase values in the group without severe features. The index should therefore be regarded as exploratory rather than as a validated severity biomarker or stand-alone clinical test. Independent prospective validation is required.
SN  - 1471-2393
ER  -