# Serum brain-derived neurotrophic factor, micronutrient status, and inflammatory cytokines in type 2 diabetes with nephropathy: a case–control analysis

**Authors:** Huda Jaber Waheed, Nawfal A. Numan

PMC · DOI: 10.7717/peerj.20086 · PeerJ · 2025-10-20

## TL;DR

This study found that brain-derived neurotrophic factor (BDNF) levels are significantly lower in type 2 diabetes patients with nephropathy compared to healthy individuals and those without complications.

## Contribution

The study identifies BDNF as a potential biomarker for diabetic nephropathy and links its levels to vitamin deficiencies and inflammation.

## Key findings

- Serum BDNF levels were significantly lower in diabetic nephropathy patients compared to controls and diabetic patients without complications.
- BDNF levels correlated with vitamin deficiencies and inflammatory markers in diabetic nephropathy patients.
- BDNF showed strong diagnostic potential with an AUC of 0.938 for distinguishing diabetic nephropathy from healthy controls.

## Abstract

Brain-derived neurotrophic factor (BDNF) levels are lower in diabetic patients compared to healthy individuals, and may be further affected by nephropathy. This study aimed to evaluate serum BDNF levels in diabetic patients with nephropathy without complications and compare them to levels in healthy control subjects.

A case–control study was conducted involving three groups: healthy individuals (controls), diabetic patients without complications (DM), and diabetic nephropathy patients (DN). Serum BDNF levels were measured using the sandwich Enzyme-Linked Immunosorbent Assay (ELISA) technique, alongside serum levels of interleukin (IL)-12, IL-16, folic acid, vitamin B12, vitamin D3, total cholesterol, triglycerides, high density lipoprotein (HDL), hemoglobin A1c (HbA1c), urea, creatinine, total calcium, and zinc.

Serum BDNF levels were significantly lower in the DN group compared to the DM and control groups (42.1, 34.1, and 27.23 ng/mL, respectively). In the DM group, BDNF showed a direct correlation with HbA1c and urea (r = 0.26 and r = 0.35, respectively), and an inverse correlation with fasting plasma glucose (FPG) (r =  − 0.30). In the DN group, BDNF was directly correlated with FPG (r = 0.31) and serum creatinine (r = 0.27). The area under the curve (AUC) for BDNF in distinguishing DN from controls was 0.938, and 0.738 for DN versus DM.

Serum BDNF levels are markedly reduced in type 2 diabetic patients with nephropathy and correlate with deficiencies in vitamins D, B12, folate, and zinc, as well as elevated IL-6 and IL-12. BDNF may serve as a biomarker for diabetic kidney disease, highlighting the importance of nutritional status, inflammation control, and neurotrophic support.

## Linked entities

- **Proteins:** BDNF (brain derived neurotrophic factor)
- **Chemicals:** folic acid (PubChem CID 135398658), vitamin B12 (PubChem CID 73415824), vitamin D3 (PubChem CID 5280795), urea (PubChem CID 1176), creatinine (PubChem CID 588), zinc (PubChem CID 23994)
- **Diseases:** type 2 diabetes (MONDO:0005148)

## Full-text entities

- **Genes:** IL12B (interleukin 12B) [NCBI Gene 3593] {aka CLMF, CLMF2, IL-12B, IMD28, IMD29, NKSF}, IL16 (interleukin 16) [NCBI Gene 3603] {aka LCF, NIL16, PRIL16, prIL-16}, BDNF (brain derived neurotrophic factor) [NCBI Gene 627] {aka ANON2, BULN2}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}
- **Diseases:** type 2 diabetes (MESH:D003924), diabetic (MESH:D003920), inflammation (MESH:D007249), nephropathy (MESH:D007674), diabetic kidney disease (MESH:D003928)
- **Chemicals:** cholesterol (MESH:D002784), glucose (MESH:D005947), folate (MESH:D005492), vitamin B12 (MESH:D014805), zinc (MESH:D015032), urea (MESH:D014508), FPG (-), vitamin D3 (MESH:D002762), creatinine (MESH:D003404), calcium (MESH:D002118), triglycerides (MESH:D014280)
- **Species:** Homo sapiens (human, species) [taxon 9606], Debaryomyces sp. NRRL Y-7804 (species) [taxon 27303]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12548638/full.md

## References

73 references — full list in the complete paper: https://tomesphere.com/paper/PMC12548638/full.md

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Source: https://tomesphere.com/paper/PMC12548638