# Higher Circulating Lymphocytes and the Incidence of Pre-eclampsia and Eclampsia

**Authors:** Qiuping Zhao, Rongmei Liu, Hui Chen, Xiaomo Yang, Jiajia Dong, Minfu Bai, MingYang Yu, Zeying Feng, Dingyuan Zeng

PMC · DOI: 10.1155/2024/8834312 · Journal of Pregnancy · 2024-03-19

## TL;DR

Higher levels of certain immune cells, like lymphocytes and T cells, are linked to an increased risk of pre-eclampsia and eclampsia during pregnancy.

## Contribution

This study identifies a causal relationship between specific immune cell counts and pre-eclampsia/eclampsia using genetic data.

## Key findings

- Genetically higher lymphocyte counts are associated with increased risk of eclampsia and pre-eclampsia.
- T cell and CD28- CD25+ CD8+ T cell counts also show a causal link to these conditions.
- Colocalization analysis confirms shared genetic variants between immune cell traits and pre-eclampsia/eclampsia.

## Abstract

Excessive immune activation contributes to the onset of early dysfunction of the maternal-fetal interface, and it is closely linked to the development of pre-eclampsia. However, the effect of specific immune cells on the risk of pre-eclampsia and eclampsia remains controversial. We investigated the causal relationship between immune cells and pre-eclampsia and eclampsia. For exposure, we extracted genetic variants associated with immune cell-related traits, and for outcomes, we used summary genetic data of pre-eclampsia/eclampsia. A two-sample Mendelian randomization (MR) analysis was then performed to assess the causal relationship. Robustness of the MR results was then evaluated through colocalization analysis. We found that genetically proxied circulating lymphocyte absolute count was causally associated with total eclampsia (odds ratio (OR) = 1.53, 95% confidence interval (CI) (1.31-1.79), p = 1.15E − 07) and pre-eclampsia (OR = 1.50, 95% CI (1.28-1.77), p = 9.18E − 07); T cell absolute count was causally associated with total eclampsia (OR = 1.49, 95% CI (1.28-1.73), p = 2.73E − 07) and pre-eclampsia (OR = 1.47, 95% CI (1.25-1.72), p = 1.76E − 06). And CD28- CD25+ CD8+ T cell absolute count was causally associated with total eclampsia (OR = 1.83, 95% CI (1.44-2.32), p = 7.11E − 07) and pre-eclampsia (OR = 1.77, 95% CI (1.38-2.26), p = 6.55E − 06). Colocalization analysis revealed that immune cell-related traits shared the same variant with pre-eclampsia/eclampsia. Our study suggested causal effects of genetic predisposition to high lymphocyte absolute count levels, T cell absolute count, and CD28- CD25+ CD8+ T cell absolute count on eclampsia, particularly pre-eclampsia risk, providing crucial new insights into the potential prevention target for eclampsia and pre-eclampsia.

## Linked entities

- **Diseases:** pre-eclampsia (MONDO:0005081), eclampsia (MONDO:0001754)

## Full-text entities

- **Genes:** IL2RA (interleukin 2 receptor subunit alpha) [NCBI Gene 3559] {aka CD25, IDDM10, IL2R, IMD41, TCGFR, p55}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, CD28 (CD28 molecule) [NCBI Gene 940] {aka IMD123, Tp44}
- **Diseases:** Pre-eclampsia (MESH:D011225), Eclampsia (MESH:D004461)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC10965280/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10965280/full.md

## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC10965280/full.md

---
Source: https://tomesphere.com/paper/PMC10965280