scholarly journals Diagnosing and managing diabetic somatic and autonomic neuropathy

2019 ◽  
Vol 10 ◽  
pp. 204201881982689 ◽  
Author(s):  
Shazli Azmi ◽  
Maryam Ferdousi ◽  
Alise Kalteniece ◽  
Hamad Al-Muhannadi ◽  
Abdulrahman Al-Mohamedi ◽  
...  

The diagnosis and management of diabetic neuropathy can be a major challenge. Late diagnosis contributes to significant morbidity in the form of painful diabetic neuropathy, foot ulceration, amputation, and increased mortality. Both hyperglycaemia and cardiovascular risk factors are implicated in the development of somatic and autonomic neuropathy and an improvement in these risk factors can reduce their rate of development and progression. There are currently no US Food and Drug Administration (FDA)-approved disease-modifying treatments for either somatic or autonomic neuropathy, as a consequence of multiple failed phase III clinical trials. While this may be partly attributed to premature translation, there are major shortcomings in trial design and outcome measures. There are a limited number of partially effective FDA-approved treatments for the symptomatic relief of painful diabetic neuropathy and autonomic neuropathy.

Author(s):  
Georgios Ponirakis ◽  
Tarik Elhadd ◽  
Subitha Chinnaiyan ◽  
Abdul H Hamza ◽  
Sanaulla Sheik ◽  
...  

Author(s):  
◽  

Introduction: Alzheimer’s disease is a more common neurodegenerative disease, affecting 25 million people worldwide, or accounting for about 60 to 70% of all dementia cases. There is currently no exact mechanism to explain the pathophysiology of Alzheimer’s disease, however, cascading metabolic amyloid and post-translational review of tau protein are used as major hypotheses. Objective: To demonstrate in the literature new approaches in the development of Alzheimer’s disease modifiers. Methodology: For the accomplishment of this study made in the bibliographical survey of scientific literature and respect to the approached subject, in the databases PUBMED, ScienceDirect, Scielo and Scopus. Results: Alzheimer’s disease-modifying drugs are not yet available, but many patients may, however, develop phase III clinical trials and are intended to modify as pathological stages leading to the disease. As disease-modifying therapies under study, these changes also affect Aβ and tau protein and also cause inflammation and oxidative damage. The results obtained in the clinical trials performed were positive and promising and are still under study. The results show that there is still a long way to go in the development of Alzheimer’s disease modifying drugs. Conclusion: The results demonstrated that there is still a long way to go in the development of Alzheimer’s disease modifying drugs, but nevertheless levels at the research level should be continued in order to improve the pathophysiology of the disease and find an effective treatment for this disease the same.


1999 ◽  
Vol 89 (9) ◽  
pp. 468-471 ◽  
Author(s):  
RC Wilson

Thirty-one adult diabetic patients with painful distal symmetrical polyneuropathy were treated with low doses of oral trazodone (50 or 100 mg/day). After 2 weeks of therapy, 19 patients (61.3%) experienced symptomatic relief, and 7 (22.6%) experienced complete relief. Although 8 patients (25.8%) discontinued the drug because of side effects, these were relatively minor (dizziness, headache, insomnia). Low-dose trazodone is recommended as an effective treatment option for painful diabetic neuropathy.


Pain ◽  
2017 ◽  
Vol 158 (12) ◽  
pp. 2340-2353 ◽  
Author(s):  
Jana Raputova ◽  
Iva Srotova ◽  
Eva Vlckova ◽  
Claudia Sommer ◽  
Nurcan Üçeyler ◽  
...  

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