# The Genetic Link Between Primary Immune Thrombocytopenia and Depression/Anxiety Disorders: A Two‐Sample Mendelian Randomization Study

**Authors:** Le Jiang, Ya‐jing Zhao, Shou‐qing Han, Zhen‐yu Yan, Xin‐guang Liu

PMC · DOI: 10.1002/jcla.70176 · Journal of Clinical Laboratory Analysis · 2026-02-11

## TL;DR

This study finds a genetic link between immune thrombocytopenia and depression, but not anxiety, suggesting ITP may increase depression risk.

## Contribution

The study provides novel genetic evidence of a causal link between ITP and depression using robust Mendelian randomization methods.

## Key findings

- ITP shows a positive causal effect on depression (OR = 1.007, p = 0.014).
- No genetic link was found between ITP and anxiety.
- Results were consistent across sensitivity and multivariable analyses.

## Abstract

Primary immune thrombocytopenia (ITP) is an autoimmune bleeding disorder with complex immunopathogenesis. Its major symptoms, such as bleeding tendency and fatigue, may predispose patients to depression and anxiety. Although psychiatric comorbidities are increasingly recognized in ITP management, whether ITP causally contributes to these conditions remains unclear.

We conducted a two‐sample Mendelian randomization (MR) study to investigate the potential genetically causal links between ITP and depression/anxiety. To ensure robustness, complementary MR approaches were performed, including pleiotropy‐robust methods (MR‐Corr and MRMix), multivariable MR adjusting for inflammatory biomarkers (C‐reactive protein and interleukin‐6), the robust adjusted profile score (RAPS) model, reverse MR, and colocalization analysis.

MR analysis revealed a positive causal effect of ITP on depression (OR = 1.007, 95% CI: 1.001–1.013; p = 0.014), whereas no genetic predisposition of ITP on anxiety was observed. Multivariable and pleiotropy‐robust sensitivity analyses supported the stability and consistency of the ITP‐depression association, indicating that the result was unlikely driven by pleiotropy, instrument weakness, or inflammatory confounding.

These findings provided novel genetic evidence supporting ITP‐associated mental health issues and highlighted the importance of integrated psycho‐hematological interventions for ITP in clinical practice. Future research was needed to elucidate the biological underpinning between ITP and psychiatric disorders, which might provide more options for ITP patients to improve life quality.

A two‐sample Mendelian randomization study revealed a positive genetic association between primary immune thrombocytopenia (ITP) and major depressive disorder (MDD), but not with anxiety. Results remained consistent across sensitivity and multivariable analyses, indicating that ITP may causally increase susceptibility to depression.

## Linked entities

- **Diseases:** depression (MONDO:0002050), anxiety (MONDO:0005618), major depressive disorder (MONDO:0002009)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}
- **Diseases:** inflammatory (MESH:D007249), anxiety (MESH:D001007), bleeding tendency (MESH:C536965), Anxiety Disorders (MESH:D001008), Depression (MESH:D003866), fatigue (MESH:D005221), psychiatric (MESH:D001523), ITP (MESH:D016553), autoimmune bleeding disorder (MESH:D001327)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13042916/full.md

## References

50 references — full list in the complete paper: https://tomesphere.com/paper/PMC13042916/full.md

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Source: https://tomesphere.com/paper/PMC13042916