Publicación:
Biomarker role of maternal soluble human leukocyte antigen G in pre-eclampsia: A meta-analysis

dc.contributor.authorBhattarai, Abhinav
dc.contributor.authorShah, Sangam
dc.contributor.authorDahal, Krishna Prasad
dc.contributor.authorNeupane, Raksha
dc.contributor.authorThapa, Sangharsha R.
dc.contributor.authorNeupane, Niraj
dc.contributor.authorBarboza, Joshuan J.
dc.contributor.authorShrestha, Anisha K.
dc.contributor.authorSah, Ranjit Kumar
dc.contributor.authorApostolopoulos, Vasso
dc.date.accessioned2025-09-05T16:32:13Z
dc.description.abstractIntroduction: Human leukocyte antigen-G (HLA-G) is a non-classical class I HLA molecule shown to regulate the immunomodulation of maternal immune cells to prevent fetal tissue destruction. Low levels of freely circulating maternal soluble HLA-G (sHLA-G) have been observed in pre-eclampsia, however, no pooled evidence exists. This meta-analysis aimed to generate pooled findings on the association of sHLA-G levels with pre-eclampsia and is the first study to perform a trimester-wise comparison of the levels of sHLA-G in preeclamptic cases and normal pregnant controls. Methods: The databases PubMed, Emba, Web of Science, and Google Scholar through May 31, 2023. Preeclamptic women were defined as cases and normal pregnancies as controls. Data on the level of sHLA-G in cases and controls was extracted and subjected to a meta-analysis using a random-effects model. The pooled effect was expressed in terms of standardized mean difference (SMD). Sensitivity analysis was performed to investigate the effect of the exclusion of each study on the pooled results. Publication bias was assessed statistically. Results: Nine studies with altogether 567 PE cases and 1132 normal pregnancy controls were included in the meta-analysis. The first and third trimester levels of sHLA-G in PE cases were significantly lower than that of normal pregnant controls: (SMD: −0.84 [−1.29; −0.38]; p =.003; I2 = 54%) and (SMD: −0.39 [−0.71; −0.06]; p =.02; I2 = 79%) respectively. Sensitivity analysis revealed significant fluctuations in the pooled findings when few studies were excluded, raising questions on the consistency of results among studies. Conclusion: Although we found that first and third-trimester sHLA-G levels in pre-eclampsia are significantly lower, taking into consideration the inconsistent results from the sensitivity analysis, our findings advocate the demand for more studies with larger sample sizes to generate solid ground pooled evidence on the predictive role of sHLA-G in pre-eclampsia. © 2024 Elsevier B.V., All rights reserved.
dc.identifier.doi10.1002/iid3.1254
dc.identifier.scopus2-s2.0-85190860009
dc.identifier.urihttps://cris.uwiener.edu.pe/handle/001/146
dc.identifier.uuidfe6dff16-3fae-4a79-b229-c3f96758aa45
dc.language.isoen
dc.publisherJohn Wiley and Sons Inc
dc.relation.citationissue4
dc.relation.citationvolume12
dc.relation.ispartofseriesImmunity, Inflammation and Disease
dc.relation.issn20504527
dc.rightshttp://purl.org/coar/access_right/c_abf2
dc.titleBiomarker role of maternal soluble human leukocyte antigen G in pre-eclampsia: A meta-analysis
dc.typehttp://purl.org/coar/resource_type/c_2df8fbb1
dspace.entity.typePublication

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