Evidence map›Paper›PMID 42062971›Full record

ArticleBMC pregnancy and childbirth2026

Serum visinin-like protein-1 levels in preeclampsia: a cross-sectional pilot study.

Neslihan Aslan, Cigdem Akcabay, Necip Ilhan, Miray Onat, Ebru Celik Kavak, Ibrahim Batmaz, Salih Burcin Kavak

Abstract read
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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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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Neslihan AslanGynecology and Obstetrics Clinic, Fethi Sekin City Hospital, Elazig, Turkey.ORCID http://orcid.org/0009-0005-0437-1700
Cigdem AkcabayDepartment of Obstetrics and Gynecology, School of Medicine, Firat University Faculty of Medicine, Elazig, 23000, Turkey.ORCID http://orcid.org/0000-0003-2068-7412
Necip IlhanDepartment of Medical Biochemistry, Firat University Faculty of Medicine, Elazig, Turkey.ORCID http://orcid.org/0000-0001-9997-0418
Miray OnatDepartment of Obstetrics and Gynecology, School of Medicine, Firat University Faculty of Medicine, Elazig, 23000, Turkey.ORCID http://orcid.org/0009-0008-8085-3703
Ebru Celik KavakGynecology and Obstetrics Specialist, Elazig, Turkey.ORCID http://orcid.org/0000-0002-7447-8264
Ibrahim BatmazDepartment of Obstetrics and Gynecology, Faculty of Medicine, Mardin Artuklu University, Mardin, Turkey.ORCID http://orcid.org/0000-0001-9492-2783
Salih Burcin KavakDepartment of Obstetrics and Gynecology, School of Medicine, Firat University Faculty of Medicine, Elazig, 23000, Turkey. burcinkavak1@gmail.com.ORCID http://orcid.org/0000-0002-6318-5175

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo evaluate serum Visinin-like protein-1 (VILIP-1) levels in normotensive pregnant women and in patients with preeclampsia across the severity spectrum, and to investigate the association between VILIP-1 levels and disease severity.

methodsIn this prospective cross-sectional pilot study, a total of 60 pregnant women were allocated into three groups: normotensive controls (n = 20), preeclampsia without severe features (n = 20), and preeclampsia with severe features (n = 20). Baseline clinical and laboratory characteristics were recorded. Serum VILIP-1 levels were measured and compared among groups. Statistical analyses were performed using non-parametric tests with adjustment for multiple comparisons.

resultsBaseline demographic and obstetric characteristics were comparable among groups. Gestational age at delivery and neonatal birth weight were significantly lower in the preeclampsia with severe features group. Markers of hepatic and renal dysfunction were significantly elevated in this group, whereas hematological parameters did not differ significantly. Serum VILIP-1 levels were significantly higher in patients with preeclampsia with severe features compared with both normotensive pregnant women and those with preeclampsia without severe features (24.75 ± 18.27 ng/mL vs. 10.23 ± 7.98 ng/mL and 7.91 ± 4.97 ng/mL, respectively; adjusted p < 0.05).

conclusionsSerum VILIP-1 levels are significantly increased in preeclampsia with severe features and appear to be associated with disease severity and maternal organ involvement. These findings suggest that VILIP-1 may reflect disease severity rather than serving as a diagnostic biomarker; however, larger prospective studies are warranted to clarify its clinical utility.

Indexed as

NeurocalcinPre-EclampsiaAdultBiomarkersBirth WeightCase-Control StudiesCross-Sectional StudiesFemaleGestational AgeHumansInfant, NewbornPilot ProjectsPregnancyProspective StudiesSeverity of Illness IndexBiomarkersNeurocalcinBiomarkersDisease severityPreeclampsiaPregnancyVisinin-like protein-1

Identifiers

PMID42062971
PMCPMC13277192

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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.