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. 2022 Aug 10:13:966400.
doi: 10.3389/fphar.2022.966400. eCollection 2022.

Association of LEPTIN and other inflammatory markers with preeclampsia: A systematic review

Affiliations

Association of LEPTIN and other inflammatory markers with preeclampsia: A systematic review

Eduardo Carvalho de Arruda Veiga et al. Front Pharmacol. .

Abstract

Background: Preeclampsia is a serious pregnancy complication that affects 5%-10% of the obstetric population. Objective: To study inflammatory markers associated with preeclampsia. Search Strategy: Searches of articles on the topic published over a 10-year period (2009-2019) were performed in three databases (PubMed, Cochrane, and Embase) using the keywords preeclampsia and inflammatory markers. The PubMed search using 10 years and humans as filters retrieved 124 articles. Using an advanced search strategy, 0 articles were identified in Embase and 10 articles in Cochrane. After screening and eligibility assessment, 13 articles were included in the systematic review and meta-analysis. Meta-analysis and quality assessment of the studies were performed using the Review Manager 5.3 program. Results: For meta-analysis, women with preeclampsia were compared to control women, i.e., pregnancies without arterial hypertension. Leptin levels were significantly higher (p < 0.0002) in women with preeclampsia compared to controls. Total cholesterol was also significantly elevated in women with preeclampsia (p < 0.0001). There was no significant difference in HDL between groups, but women with preeclampsia had significantly increased LDL (p < 0.01). The same was observed for triglycerides, which were significantly increased in women with preeclampsia (p < 0.04) compared to controls. Analysis of TNF-alpha, an important inflammatory marker, showed higher levels in women with preeclampsia (p < 0.03) compared to controls. The same was observed for another important inflammatory marker, interleukin 6, which was significantly increased in women with preeclampsia (p < 0.0002). There was a significant increase of C-reactive protein in women with preeclampsia (p < 0.003) compared to controls. Conclusion: Women with preeclampsia have increased levels of inflammatory markers compared to control women.

Keywords: C reaction protein; HDL; inflammatory; markers; preeclaimpsia.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

FIGURE 1
FIGURE 1
Flowchart for selection of studies.
FIGURE 2
FIGURE 2
Meta-analyses of inflammatory markers among pregnant women with preeclampsia and control pregnant women (control), that is, without preeclampsia. (A)—Meta-analyses of Leptin (ng/ml) among preeclampsia (woman pregnant with preeclampsia) and control (woman pregnant without preeclampsia). (B)—Meta-analyses of Total cholesterol (mg/dl) among preeclampsia (woman pregnant with preeclampsia) and control (woman pregnant without preeclampsia). (C)—Meta-analyses of HDL (mg/dl) among preeclampsia (woman pregnant with preeclampsia) and control (woman pregnant without preeclampsia). (D)—Meta-analysis of LDL (mg/dl) among preeclampsia (woman pregnant with preeclampsia) and control (woman pregnant without preeclampsia).
FIGURE 3
FIGURE 3
Meta-analyses of inflammatory markers among pregnant women with preeclampsia and control pregnant women (control), that is, without preeclampsia. (A)—Meta-analysis of Triglycerides (mg/dl) among preeclampsia (woman pregnant with preeclampsia) and control (woman pregnant without preeclampsia). (B)—Meta-analysis of TNFα (pg/ml) among preeclampsia (woman pregnant with preeclampsia) and control (woman pregnant without preeclampsia). (C)—Meta-analysis of IL6 (pg/ml) among preeclampsia (woman pregnant with preeclampsia) and control (woman pregnant without preeclampsia). (D)—Meta-analysis of C-reactive protein (mg/dl) among preeclampsia (woman pregnant with preeclampsia) and control (woman pregnant without preeclampsia).
FIGURE 4
FIGURE 4
Risk of bias graph: review authors’ judgements about each risk of bias item presented as percentages across all included studies.
FIGURE 5
FIGURE 5
Risk of bias summary: review authors’ judgements about each risk of bias item for each included study.

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References

    1. Abraham T., Romani A. M. P. (2022). The relationship between obesity and pre-eclampsia: Incidental risks and identification of potential biomarkers for pre-eclampsia. Cells 11. 10.3390/cells11091548 - DOI - PMC - PubMed
    1. Alahakoon T. I., Medbury H. J., Williams H., Lee V. W. (2020). Lipid profiling in maternal and fetal circulations in preeclampsia and fetal growth restriction-A prospective case control observational study. BMC Pregnancy Childbirth 20, 61. 10.1186/s12884-020-2753-1 - DOI - PMC - PubMed
    1. Bawah A. T., Seini M. M., Abaka-Yawason A., Alidu H., Nanga S. (2019). Leptin, resistin and visfatin as useful predictors of gestational diabetes mellitus. Lipids Health Dis. 18, 221. 10.1186/s12944-019-1169-2 - DOI - PMC - PubMed
    1. Beneventi F., Locatelli E., de Amici M., Cavagnoli C., Bellingeri C., de Maggio I., et al. (2020). Maternal and fetal Leptin and interleukin 33 concentrations in pregnancy complicated by obesity and preeclampsia. J. Maternal-Fetal Neonatal Med. 33, 3942–3948. 10.1080/14767058.2019.1593359 - DOI - PubMed
    1. Berstock J. R., Whitehouse M. R. (2019). How to prepare and manage a systematic review and meta-analysis of clinical studies. EFORT Open Rev. 4, 213–220. 10.1302/2058-5241.4.180049 - DOI - PMC - PubMed

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