EC Ophthalmology

Research Article Volume 14 Issue 10 - 2023

Long-Term Visual Outcomes in Diabetic Patients with Diabetic Foot Ulcers with and without Peripheral Vasculopathy and Diabetic Neuropathy

Christopher Zhu* and Joanna Sohn

Department of Ophthalmology, University of Texas Health at San Antonio, USA
*Corresponding Author: Christopher Zhu, Department of Ophthalmology, University of Texas Health at San Antonio, USA.
Received: August 15, 2023; Published: September 08, 2023



Introduction: Diabetes affects 11.6% of South Texans, leading to disabling conditions including diabetic foot ulcers (DFU) and diabetic retinopathy (DR). Peripheral vasculopathy (PV) and diabetic neuropathy (DN) have been reported as independent risk factors for developing DFU. However, the relationship between systemic parameters of DFU (PV and DN) and ocular outcomes of DR (visual acuity) remain unknown. Therefore, we investigated visual outcomes of diabetic patients with DFU alone compared to patients with additional PV or DN in relation to diabetic retinopathy (DR).

Methods: A retrospective review was done on patients visiting a tertiary center in San Antonio that were diagnosed with DFU and underwent ophthalmic and neurovascular examinations within the past 10 years; 144 diabetic eyes were included. The prevalence of DR with DFU with or without concomitant PV or DN was assessed using visual acuity (Log MAR) as the primary endpoint.

Results: The study group of 144 eyes (72 subjects) had an average age of 59.9 and was 54.2% male. At the final visit, proliferative diabetic retinopathy (PDR) was found in 73.4% of the DFU-only group, 75.0% of the DFU-with-PV group, and 73.4% of the DFU-with-DN group. New onset of PDR was noted in 43.3% of DFU-only, 63.3% of DFU-with-PV, and 54.1% of DFU-with-DN during the follow-up period (p > 0.05). Initial average visual acuity, represented by Log MAR, was 0.627 for the DFU-only, 0.491 for DFU-with-PV, and 0.514 for the DFU-with-DN. Final average visual acuity was 0.429 for DFU-only, 0.515 for DFU-with-PV, and 0.593 for DFU-with- DN. With an average follow-up period of 50.7 months, the DFU-only group demonstrated an average Log MAR change of -0.198 compared to +0.024 in the DFU-with-PV group and +0.078 in the DFU-with-DN group (p = 0.036). Furthermore, diabetic patients with DFU were more likely to require panretinal photocoagulation (PRP) during the follow-up period if they experienced concomitant PV (72.9%) compared to DFU alone (60.9%) or with concomitant DN (29.7%, p = 0.0007).

Conclusion: Most patients with DFU experienced a progression of DR to PDR. DFU patients with DN experienced significant declining visual acuity despite necessary treatment for DR. Those with PV were slightly more likely to develop PDR and were significantly more likely to receive PRP treatment. All patients with DFU should undergo timely retinal examinations and management to prevent premature blindness from DR-in particular those with PV and DN.

 Keywords: Diabetic Retinopathy; Peripheral Vasculopathy; Foot Ulcer; Neuropathy; Diabetes; Proliferative Diabetic Retinopathy

  1. Ramirez AG., et al. The South Texas Health Status Review: A Health Disparities Roadmap (2013).
  2. Moss SE., et al. “The prevalence and incidence of lower extremity amputation in a diabetic population”. Archives of Internal Medicine3 (1992): 610-616.
  3. Borssen B., et al. “The epidemiology of foot lesions in diabetic patients aged 15-50 years”. Diabetic Medicine5 (1990): 438-444.
  4. Karam T., et al. “Diabetic retinopathy in patients with diabetic foot syndrome in South India”. Indian Journal of Ophthalmology4 (2018): 547-550.
  5. Serban D., et al. “Diabetic Retinopathy in Patients with Diabetic Foot Ulcer: A Systematic Review”. The International Journal of Lower Extremity Wounds2 (2021): 98-103.
  6. Yunus YM and Rajbhandari SM. “Insensate foot of diabetic foot ulcer can have underlying silent neuropathic pain”. International Wound Journal3 (2011): 301-305.
  7. Rahman AMM., et al. “Vasculopathy in patients with diabetic foot using doppler ultrasound”. Pakistan Journal of Medical Sciences3 (2009): 428-433.
  8. Sosenko JM., et al. “Comparison of quantitative sensory-threshold measures for their association with foot ulceration in diabetic patients”. Diabetes Care10 (1990): 1057-1061.
  9. McNeely MJ., et al. “The independent contributions of diabetic neuropathy and vasculopathy in foot ulceration. How great are the risks?” Diabetes Care2 (1995): 216-219.
  10. Cusick M., et al. “Associations of mortality and diabetes complications in patients with type 1 and type 2 diabetes: early treatment diabetic retinopathy study report no. 27”. Diabetes Care3 (2005): 617-625.
  11. Hwang DJ., et al. “Association between diabetic foot ulcer and diabetic retinopathy”. PLoS One4 (2017): e0175270.
  12. Joshi D., et al. “A clinical study of the association and risk factors for lower limb neuropathy in patients with diabetic retinopathy”. Journal of Family Medicine and Primary Care4 (2020): 1891-1895.
  13. Shahbazian H., et al. “Risk assessment of patients with diabetes for foot ulcers according to risk classification consensus of International Working Group on Diabetic Foot (IWGDF)”. Pakistan Journal of Medical Sciences3 (2013): 730-734.
  14. Rasheed R., et al. “Relationship between diabetic retinopathy and diabetic peripheral neuropathy - Neurodegenerative and microvascular changes”. Indian Journal of Ophthalmology11 (2021): 3370-3375.
  15. Simo R., et al. “Diabetic Retinopathy: Role of Neurodegeneration and Therapeutic Perspectives”. The Asia-Pacific Journal of Ophthalmology2 (2022): 160-167.
  16. Barber AJ and Baccouche B. “Neurodegeneration in diabetic retinopathy: Potential for novel therapies”. Vision Research 139 (2017): 82-92.
  17. Kadlubowska J., et al. “Neurodegeneration and Neuroinflammation in Diabetic Retinopathy: Potential Approaches to Delay Neuronal Loss”. Current Neuropharmacology8 (2016): 831-839.
  18. Wang W and Lo ACY. “Diabetic Retinopathy: Pathophysiology and Treatments”. International Journal of Molecular Sciences6 (2018).
  19. Ejaz S., et al. “Importance of pericytes and mechanisms of pericyte loss during diabetes retinopathy”. Diabetes, Obesity and Metabolism1 (2008): 53-63.
  20. Beltramo E and Porta M. “Pericyte loss in diabetic retinopathy: mechanisms and consequences”. Current Medicinal Chemistry26 (2013): 3218-3225.
  21. Bloomgarden ZT. “Diabetic retinopathy and neuropathy”. Diabetes Care4 (2005): 963-970.
  22. Lee CM., et al. “Insufficient early detection of peripheral neurovasculopathy and associated factors in rural diabetes residents of Taiwan: a cross-sectional study”. BMC Endocrine Disorders 14 (2014): 89.
  23. Dal Monte M., et al. “Effects of somatostatin analogues on retinal angiogenesis in a mouse model of oxygen-induced retinopathy: involvement of the somatostatin receptor subtype 2”. Investigative Ophthalmology and Visual Science8 (2009): 3596-606.
  24. Dal Monte M., et al. “Protective role of somatostatin receptor 2 against retinal degeneration in response to hypoxia”. Naunyn-Schmiedeberg's Archives of Pharmacology5 (2012): 481-494.
  25. Simo R., et al. “Deficit of somatostatin-like immunoreactivity in the vitreous fluid of diabetic patients: possible role in the development of proliferative diabetic retinopathy”. Diabetes Care12 (2002): 2282-2286.
  26. Hernandez C., et al. “Topical administration of somatostatin prevents retinal neurodegeneration in experimental diabetes”. Diabetes7 (2013): 2569-2578.
  27. Zhang SX., et al. “Pigment epithelium-derived factor (PEDF) is an endogenous antiinflammatory factor”. The FASEB Journal2 (2006): 323-325.
  28. Spranger J., et al. “Loss of the antiangiogenic pigment epithelium-derived factor in patients with angiogenic eye disease”. Diabetes12 (2001): 2641-2645.
  29. Becerra SP., et al. “Pigment epithelium-derived factor behaves like a noninhibitory serpin. Neurotrophic activity does not require the serpin reactive loop”. Journal of Biological Chemistry43 (1995): 25992-25999.
  30. Lovshin JA., et al. “Extrahypothalamic expression of the glucagon-like peptide-2 receptor is coupled to reduction of glutamate-induced cell death in cultured hippocampal cells”. Endocrinology7 (2004): 3495-3506.
  31. Chen S., et al. “Glucagon-like peptide-1 protects hippocampal neurons against advanced glycation end product-induced tau hyperphosphorylation”. Neuroscience 256 (2014): 137-146.
  32. Hernandez C., et al. “Topical Administration of GLP-1 Receptor Agonists Prevents Retinal Neurodegeneration in Experimental Diabetes”. Diabetes1 (2016): 172-187.
  33. Forrester JV., et al. “The Role of Inflammation in Diabetic Retinopathy”. Frontiers in Immunology 11 (2020): 583687.

Christopher Zhu and Joanna Sohn. “Long-Term Visual Outcomes in Diabetic Patients with Diabetic Foot Ulcers with and without Peripheral Vasculopathy and Diabetic Neuropathy” ”. EC Ophthalmology  14.10 (2023): 01-07.