# Intestinal Permeability and Depression—A Narrative Review of Selected Blood-Based Biomarkers

**Authors:** Anca C. Bibolar, Bianca D. Crecan-Suciu, Ramona L. Păunescu, Vlad-I. Nechita, Olivia Verisezan-Roșu, Ioana V. Micluția

PMC · DOI: 10.3390/ijms262010076 · 2025-10-16

## TL;DR

This review explores blood-based markers of intestinal permeability in depression, highlighting their potential role in identifying inflammation-related subtypes.

## Contribution

The paper provides a narrative review of selected biomarkers linking intestinal permeability to depression, emphasizing their potential for patient stratification.

## Key findings

- Altered intestinal permeability markers are reported in depression, but results are inconsistent.
- Biomarker levels correlate with disease severity and treatment response in some cases.
- Current evidence does not support routine clinical use of these markers.

## Abstract

The intestinal barrier has recently gained attention as a contributor to the pathophysiology of depression. This narrative review examines the current literature on blood-based markers of intestinal permeability in patients with depression. A structured search of PubMed and EMBASE was performed. Both recent and older studies were included to capture key mechanisms and theoretical foundations. We focused on zonulin, intestinal fatty acid-binding protein (I-FABP), lipopolysaccharides (LPS), LPS-binding protein (LBP), and soluble CD14 (sCD14). While several studies report altered intestinal permeability markers in individuals with depression, results remain inconsistent. Factors such as small sample sizes and variability in measurement procedures complicate interpretation. In some cases, altered biomarker levels were associated with disease severity or response to antidepressant treatment, suggesting a potential role in patient stratification. However, current evidence does not support their routine use in clinical settings. Further research is needed to clarify their value in psychiatric populations. If validated, these markers may help identify inflammation-related depression subtypes and guide more precise treatment strategies.

## Linked entities

- **Proteins:** Hp (haptoglobin), FABP2 (fatty acid binding protein 2), LBP (lipopolysaccharide binding protein), Scd1_1 (acyl-CoA Delta-9 desaturase)
- **Diseases:** depression (MONDO:0002050)

## Full-text entities

- **Genes:** FABP2 (fatty acid binding protein 2) [NCBI Gene 2169] {aka FABPI, I-FABP}, CD14 (CD14 molecule) [NCBI Gene 929], HP (haptoglobin) [NCBI Gene 3240] {aka HP2ALPHA2, HPA1S}, LBP (lipopolysaccharide binding protein) [NCBI Gene 3929] {aka BPIFD2}
- **Diseases:** Depression (MESH:D003866), psychiatric (MESH:D001523), inflammation (MESH:D007249)
- **Chemicals:** LPS (MESH:D008070)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12563369/full.md

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Source: https://tomesphere.com/paper/PMC12563369