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Jens Randel Nyengaard

Redefining distal symmetrical polyneuropathy features in type 1 diabetes: a systematic review

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Diabetic neuropathy is among the most frequent complications of both type 1 (T1DM) and type 2 diabetes (T2DM) and commonly manifests as a distal symmetrical polyneuropathy (DSPN). Despite evidence that T1DM- and T2DM-related DSPN are separate entities, most of our knowledge on diabetic DSPN derives from studies focused on type 2 diabetes. This systematic review provides an overview of current evidence on DSPN in T1DM, including its epidemiological, pathophysiological and clinical features, along with principal diagnostic tests findings. This review included 182 clinical and preclinical studies. The results indicate that DSPN is a less frequent complication in T1DM compared with T2DM and that distinctive pathophysiological mechanisms underlie T1DM-related DSPN development, with hyperglycemia as a major determinant. T1DM-related DSPN more frequently manifests with non-painful than painful symptoms, with lower neuropathic pain prevalence compared with T2DM-associated DSPN. The overt clinical picture seems characterized by a higher prevalence of large fiber-related clinical signs (e.g., ankle reflexes reduction and vibration hypoesthesia) and to a lesser extent small fiber damage (e.g., thermal or pinprick hypoesthesia). These findings as a whole suggest that large fibers impairment plays a dominant role in the clinical picture of symptomatic T1DM-related DSPN. Nevertheless, small fiber diagnostic testing shows high diagnostic accuracy in detecting early nerve damage and may be an appropriate diagnostic tool for disease monitoring and screening.

Original languageEnglish
JournalActa Diabetologica
Volume59
Issue1
Pages (from-to)1-19
Number of pages19
ISSN0940-5429
DOIs
Publication statusPublished - Jan 2022

    Research areas

  • Distal symmetrical polyneuropathy, Neuropathic pain, Neuropathy, Type 1 diabetes, SUBCLINICAL NEUROPATHY, RISK-FACTORS, MICROVASCULAR COMPLICATIONS, SENSORY NEUROPATHY, NERVE DYSFUNCTION, SENSORIMOTOR POLYNEUROPATHY, LARGE-FIBER NEUROPATHY, PERIPHERAL NEUROPATHY, CORNEAL CONFOCAL MICROSCOPY, DIAGNOSTIC-CRITERIA

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