Retinal Neurodegeneration in Diabetic Peripheral Neuropathy by Optical Coherence Tomography: A Systematic Review and Meta-analysis

ABSTRACT

Purpose

The optical coherence tomography (OCT) has been used to evaluate the changes of retinal degeneration in patients with diabetic peripheral neuropathy (DPN) in recent years, but the results of previous studies were controversial. Therefore, systematic review and meta-analysis were performed to evaluate the degree of retinal neurodegeneration in DPN measured by OCT.

Methods

A comprehensive search of PubMed, Embase, Web of Science, Scopus, China Biomedical Literature (CBM), China National Knowledge Infrastructure (CNKI), VIP, and Wanfang databases were performed to identify studies that evaluate retinal neurodegeneration in DPN by using OCT. The included studies were critically reviewed and meta-analyses were performed to evaluate differences of the OCT-derived parameters between the DPN and non-DPN patients.

Results

Twelve studies were included in the final meta-analysis, involving a total of 1,807 eyes (573 in the DPN group and 1,229 in the non-DPN group). The mean peripapillary retinal nerve fiber layer (pRNFL) thickness was significantly lower in the DPN group than in the non-DPN group (weighted mean difference [WMD] = −8.37 μm; 95% CI: −11.00, −5.74). The reduction of pRNFL thickness was the most pronounced in the inferior quadrant, and the differences in the nasal and temporal quadrants were also statistically significant, with WMD (95% CI) being −4.63 μm (−7.51, −1.76) and −3.92 μm (−6.86, −0.98), respectively. Similar results were observed for macular parameters, with WMD and 95% CI being −1.0 μm (−1.5, −0.5) for macular retinal nerve fiber layer (mRNFL), −2.7 μm (−10.7, −5.3) for macular ganglion cell-inner plexiform layer (mGCIPL), and −2.2 μm (−4.4, −0.04) for macular ganglion cell complex (mGCC), respectively.

Conclusions

Patients with DPN present with significant retinal neurodegeneration, with reduced pRNFL, mRNFL, mGCIPL, and mGCC thickness. Measurements of OCT parameters may serve as a biomarker for diagnosing and monitoring DPN.

KEYWORDS:

• Diabetic peripheral neuropathy
• optical coherence tomography
• retinal ganglion cell
• retinal nerve fiber layer

Declaration of interest

There are no conflicts of interest. None of the authors has financial or other conflicts of interest concerning this study.

Supplemental material

Supplemental data for this article can be accessed on the publisher’s website.

Additional information

Funding

This study was supported by the National Natural Science Foundation of China [82000901]. The sponsor had no role in the design or conduct of this research.