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Neuroretinal dysfunction revealed by a flicker electroretinogram correlated with peripheral nerve dysfunction and parameters of atherosclerosis in patients with diabetes
- Source :
- Journal of Diabetes Investigation, Vol 12, Iss 7, Pp 1236-1243 (2021), Journal of Diabetes Investigation
- Publication Year :
- 2020
- Publisher :
- Wiley, 2020.
-
Abstract
- Aims/Introduction Diabetic polyneuropathy (DPN) develops in the early stage of diabetes. However, no common diagnostic protocol has yet been established. Here, to verify that the flicker electroretinogram using a hand‐held device can detect the early dysfunction of the peripheral nervous system in patients with diabetes, we investigated the correlation between the progression of DPN and neuroretinal dysfunction. Materials and Methods In total, 184 participants with type 1 or 2 diabetes underwent a flicker electroretinogram (ERG) using a hand‐held device RETeval™ and nerve conduction study. Participants were also evaluated for intima‐media thickness, ankle‐brachial index, toe brachial index and brachial‐ankle pulse wave velocity. Parameters of the nerve conduction study were used to diagnose the severity according to Baba’s classification. A multiple regression analysis was used to examine the associations of ERG parameters with the severity of DPN categorized by Baba’s classification. Diagnostic properties of the device in DPN were evaluated using a receiver operating characteristic curve. Results A multiple regression model to predict the severity of DPN was generated using ERG. In the model, moderate‐to‐severe DPN was effectively diagnosed (area under the receiver operating characteristic curve 0.692, sensitivity 56.5%, specificity 78.3%, positive predictive value 70.6%, negative predictive value 66.1%, positive likelihood ratio 2.60, negative likelihood ratio 0.56). In the patients without diabetic retinopathy, the implicit time and amplitude in ERG significantly correlated with the parameters of the nerve conduction study, brachial‐ankle pulse wave velocity and intima‐media thickness. Conclusions Electroretinogram parameters obtained by the hand‐held device successfully predict the severity of DPN. The device might be useful to evaluate DPN.<br />The progression of diabetic retinopathy and the dysfunction of neuroretina evaluated using the mydriasis‐free flicker electroretinogram showed a significant correlation. In patients without apparent diabetic retinopathy, the electroretinogram data correlated with parameters indicating vascular dysfunction, and with parameters indicating diabetic polyneuropathy, such as data of a nerve conduction study. Therefore, the electroretinogram data might reflect the neural and vascular impairments of the retina in patients with diabetes. The electroretinogram data were able to be used to predict the severity of diabetic polyneuropathy.
- Subjects :
- Male
medicine.medical_specialty
Endocrinology, Diabetes and Metabolism
Neural Conduction
030209 endocrinology & metabolism
Pulse Wave Analysis
Carotid Intima-Media Thickness
Severity of Illness Index
Likelihood ratios in diagnostic testing
Diseases of the endocrine glands. Clinical endocrinology
03 medical and health sciences
0302 clinical medicine
Predictive Value of Tests
Diabetes mellitus
Internal medicine
Electroretinography
Internal Medicine
medicine
Humans
Ankle Brachial Index
Peripheral Nerves
Pulse wave velocity
Aged
Diabetic Retinopathy
Receiver operating characteristic
medicine.diagnostic_test
business.industry
Articles
General Medicine
Diabetic retinopathy
Middle Aged
Atherosclerosis
RC648-665
medicine.disease
Diabetes Mellitus, Type 1
Clinical Science and Care
Diabetes Mellitus, Type 2
ROC Curve
030221 ophthalmology & optometry
Nerve conduction study
Cardiology
Female
Original Article
business
Erg
Point‐of‐care testing
Diabetic neuropathies
Subjects
Details
- ISSN :
- 20401124 and 20401116
- Volume :
- 12
- Database :
- OpenAIRE
- Journal :
- Journal of Diabetes Investigation
- Accession number :
- edsair.doi.dedup.....35b795cd0d926743dbaeb0f94147a6ae
- Full Text :
- https://doi.org/10.1111/jdi.13465