This observational cross-sectional study aims to investigate the effects of glycemic control and clinical parameters on tibial nerve conduction latency in individuals with diabetic peripheral neuropathy. Adults aged 45 to 76 years with diabetic peripheral neuropathy will be evaluated at a neurology and clinical neurophysiology clinic. Data collection will include demographic and clinical characteristics, diabetes type and duration, fasting blood glucose, and HbA1c values obtained from routine clinical records. Participants will also be assessed using the Michigan Neuropathy Screening Instrument (MNSI), including both the questionnaire and physical examination components. Nerve conduction studies will be performed using standard electromyography procedures, and tibial nerve conduction latency will be recorded. The study will examine the relationship between tibial nerve conduction latency and glycemic control parameters, neuropathy screening scores, and diabetes duration. The findings may help improve early identification and clinical evaluation of diabetic peripheral neuropathy.
Diabetic peripheral neuropathy is one of the most common chronic complications of diabetes mellitus and is associated with sensory loss, pain, and sensorimotor impairment, particularly in the distal extremities. Persistent hyperglycemia may contribute to structural and functional damage in peripheral nerves through metabolic and microvascular mechanisms. Electrophysiological abnormalities such as prolonged latency and reduced conduction velocity are commonly observed in affected individuals. Tibial nerve conduction latency may provide clinically relevant information for the evaluation of diabetic peripheral neuropathy. The aim of this observational, cross-sectional, analytical study is to investigate the effects of glycemic control parameters and clinical variables on tibial nerve conduction latency in individuals with diabetic peripheral neuropathy. The study will be conducted at Uzm. Dr. Gaye Yildirim Neurology and Clinical Neurophysiology Clinic. Participants will include individuals aged 45 to 76 years with diabetic peripheral neuropathy diagnosed on the basis of laboratory findings, clinical findings, and nerve conduction test results. Individuals with autoimmune disease, cerebrovascular disease, chronic infectious disease, cancer, history of chemotherapy or radiotherapy, radicular neuropathy, chronic kidney failure, liver failure, alcoholism or substance dependence, mental or physical disability, or inability to speak Turkish will be excluded. Data will be collected through face-to-face assessment, clinical evaluation, and review of routine clinical records. Demographic and clinical variables will include age, height, weight, education level, diabetes type, and diabetes duration. Glycemic control parameters will include fasting blood glucose and HbA1c values obtained from routine laboratory tests; no additional laboratory testing will be requested specifically for the study. Neuropathy assessment will include the Michigan Neuropathy Screening Instrument (MNSI), consisting of both the questionnaire and physical examination components. The questionnaire will be completed by participants, and the examination component will be performed by the researcher. Clinical assessment will include vibration sensation, ankle reflexes, and the presence of foot ulceration or deformity. Nerve conduction studies will be performed in the clinical neurophysiology laboratory using standard electromyography procedures. Motor and sensory conduction parameters of upper and lower extremity nerves will be evaluated, and tibial nerve conduction latency will be recorded as the main electrophysiological outcome. Peripheral neuropathy will be defined on the basis of abnormalities in at least two different nerves, including changes in conduction velocity, reduced amplitude, and/or prolonged F-wave latency. The primary analysis will examine the relationship between tibial nerve conduction latency and fasting blood glucose, HbA1c, MNSI questionnaire score, MNSI examination score, and diabetes duration using multiple linear regression analysis. Descriptive statistics will be presented as mean, standard deviation, number, and percentage, and statistical significance will be set at p\<0.05. The planned sample size is at least 50 participants, based on an a priori power analysis for multiple linear regression. The study is expected to contribute to the early identification, risk evaluation, and clinical follow-up of diabetic peripheral neuropathy.
Study Type
OBSERVATIONAL
Enrollment
50
Fenerbahçe University
Istanbul, Ataşehir, Turkey (Türkiye)
RECRUITINGTibial Nerve Conduction Latency
Tibial nerve conduction latency measured by standard nerve conduction study/electromyography procedures in individuals with diabetic peripheral neuropathy. The study will evaluate its relationship with glycemic control parameters, Michigan Neuropathy Screening Instrument scores, and diabetes duration.
Time frame: At baseline
Michigan Neuropathy Screening Instrument Questionnaire Score
The Michigan Neuropathy Screening Instrument (MNSI) Questionnaire is a participant-reported measure used to assess neuropathic symptoms in individuals with diabetic peripheral neuropathy. The questionnaire consists of 15 yes/no items. Responses are scored according to the standard MNSI scoring approach, and the total score is calculated by summing the scored items. In this study, a score of 4 or higher will be interpreted as indicating neuropathic symptom involvement. Higher scores indicate a greater burden of neuropathic symptoms, whereas lower scores indicate fewer reported neuropathic symptoms. The questionnaire score will be analyzed in relation to tibial nerve conduction latency.
Time frame: At baseline
Michigan Neuropathy Screening Instrument Examination Score
The Michigan Neuropathy Screening Instrument (MNSI) Examination is a researcher-administered clinical assessment used to evaluate signs of diabetic peripheral neuropathy. The examination includes assessment of vibration sensation, ankle reflexes, and the presence of foot ulceration or deformity. Each examination component is scored according to predefined criteria, and the total score is calculated on an 8-point scale. In this study, a total score of 2.5 or higher will be considered abnormal. Higher scores indicate more severe clinical findings consistent with peripheral neuropathy, whereas lower scores indicate fewer abnormal examination findings. The examination score will be analyzed in relation to tibial nerve conduction latency.
Time frame: At baseline
Hemoglobin A1c (HbA1c)
HbA1c value obtained from routine clinical laboratory records as an indicator of glycemic control.
Time frame: At baseline
Fasting Blood Glucose
Fasting blood glucose value obtained from routine clinical laboratory records.
Time frame: At baseline
Diabetes Duration
Duration of diabetes recorded from clinical history and patient records.
Time frame: At baseline
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