# Therapeutic and Diagnostic Landscape of Diabetic Neuropathy: A Systematic Review of Clinical Studies

**Authors:** Jay Prakash S Rajput, Rahul Deb, Sajidali S Saiyad, Zayan Jamal, Santosh Kumar Sah, Alkeshkumar R Vara, Nadia Sandhu, Dimpal Rochlani, Tanzila A Saiyed, Arin A Pathan, Ashok Sagar, Tejal Virola

PMC · DOI: 10.7759/cureus.102825 · Cureus · 2026-02-02

## TL;DR

This review summarizes recent clinical studies on diagnosing and treating diabetic neuropathy, highlighting effective strategies and areas needing more research.

## Contribution

The paper provides a comprehensive synthesis of recent clinical evidence on DN therapies and diagnostics from 2020 to 2025.

## Key findings

- Pregabalin, duloxetine, and α-lipoic acid showed consistent efficacy in reducing pain and improving nerve function.
- High-frequency spinal cord stimulation and structured rehabilitation improved outcomes in refractory and mobility-related cases.
- Biomarker-based and microvascular measures are emerging as useful diagnostic adjuncts alongside nerve conduction studies.

## Abstract

Diabetic neuropathy (DN) is one of the most prevalent complications of diabetes mellitus, affecting up to half of patients and contributing to disability, poor quality of life, and the risk of foot ulceration. Despite extensive research, its heterogeneous manifestations and complex pathophysiology continue to challenge timely diagnosis and effective treatment. This systematic review aimed to synthesize recent clinical evidence on diagnostic and therapeutic strategies for DN.

A comprehensive search of PubMed, EMBASE, CENTRAL, and Web of Science identified 76 eligible clinical studies published between 2020 and 2025, including randomized controlled trials, observational studies, and case reports. Data extraction and risk-of-bias assessment were performed according to PRISMA guidelines.

Pharmacological agents, particularly pregabalin, duloxetine, and α-lipoic acid, demonstrated the most consistent efficacy, with significant pain reduction and improvements in nerve conduction velocity. Neuromodulation with high-frequency spinal cord stimulation provided sustained pain relief in refractory cases, while structured, exercise-based rehabilitation improved gait velocity and balance. Advanced wound care strategies, such as platelet-rich plasma dressings and bioengineered skin substitutes, accelerated ulcer healing. Complementary therapies (e.g., acupuncture and balneotherapy) and emerging biologics (e.g., gene- and cell-based interventions) showed preliminary promise but require further validation.

Nerve conduction studies and validated scoring instruments remain the most reliable diagnostic tools, with biomarker- and microvascular-based measures emerging as valuable adjuncts. Current evidence underscores the value of integrating pharmacological, device-based, and rehabilitative strategies, while highlighting critical gaps in small-fiber and autonomic neuropathies. Robust, multicenter trials are needed to establish disease-modifying therapies and optimize comprehensive care pathways for DN.

## Linked entities

- **Chemicals:** pregabalin (PubChem CID 4715169), duloxetine (PubChem CID 60835), α-lipoic acid (PubChem CID 864)
- **Diseases:** diabetic neuropathy (MONDO:0006626), diabetes mellitus (MONDO:0005015)

## Full-text entities

- **Genes:** CSF3 (colony stimulating factor 3) [NCBI Gene 1440] {aka C17orf33, CSF3OS, GCSF}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, MRC1 (mannose receptor C-type 1) [NCBI Gene 4360] {aka CD206, CLEC13D, CLEC13DL, MMR, MRC1L1, bA541I19.1}, CD68 (CD68 molecule) [NCBI Gene 968] {aka GP110, LAMP4, SCARD1}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, HGF (hepatocyte growth factor) [NCBI Gene 3082] {aka DFNB39, F-TCF, HGFB, HPTA, SF}
- **Diseases:** nerve damage (MESH:D000080902), painful neuropathy (MESH:C564945), Pain (MESH:D010146), acute and chronic diabetes (MESH:D001930), Optic (MESH:D009901), hyperglycemia (MESH:D006943), small fiber neuropathy (MESH:D000071075), inflammatory demyelinating polyneuropathy (MESH:D020277), diabetic foot complications (MESH:D017719), inflammatory (MESH:D007249), DM (MESH:D009223), ulcer (MESH:D014456), vitamin deficiencies (MESH:D014802), polyneuropathy (MESH:D011115), Diabetes mellitus (MESH:D003920), neuropathic symptoms (MESH:D001750), acute motor axonal neuropathy (MESH:D020275), infections (MESH:D007239), DN (MESH:D003929), sensory loss (MESH:C580162), Diabetic Peripheral Neuropathy (MESH:D010523), neuropathic disorders (MESH:D009437), sensory neuropathy (MESH:D009477), Peripheral Artery Disease (MESH:D058729), skin dryness (MESH:D014987), focal and multifocal neuropathies (MESH:D005490), autonomic (MESH:D001342), Neuropathy (MESH:D009422), Bruns-Garland syndrome (MESH:D013132), foot ulceration (MESH:D016523), hypoglycemic neuropathy (MESH:C000721848), impaired glucose tolerance (MESH:D018149), metabolic disorder (MESH:D008659)
- **Chemicals:** oxygen (MESH:D010100), tocotrienol (MESH:D024508), Pregabalin (MESH:D000069583), DFU (-), gamma-linolenic acid (MESH:D017965), Duloxetine (MESH:D000068736), vitamin E (MESH:D014810), alpha-Lipoic acid (MESH:D008063), polyol (MESH:C024617), trazodone (MESH:D014196), amitriptyline (MESH:D000639), tapentadol (MESH:D000077432), capsaicin (MESH:D002211), glutathione (MESH:D005978), Creatinine (MESH:D003404), alcohol (MESH:D000438), acetyl-L-carnitine (MESH:D000108), DPN (MESH:D009243)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

86 references — full list in the complete paper: https://tomesphere.com/paper/PMC12958784/full.md

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Source: https://tomesphere.com/paper/PMC12958784