Efficacy and safety of the combined metabolic medication, containing inosine, nicotinamide, riboflavin and succinic acid, for the treatment of diabetic neuropathy: a multicenter randomized, double-blind, placebo-controlled parallel group clinical trial (CYLINDER)

被引:10
|
作者
Kharitonova, Tatiana [1 ]
Shvarts, Yury G. [2 ]
Verbovoy, Andrey F. [3 ]
Orlova, Natalia S. [4 ]
Puzyreva, Valentina P. [5 ]
Strokov, Igor A. [6 ]
机构
[1] St Peterburgskij Naucno Issledovatelskij Inst Sko, Dept Acute Cerebrovasc Pathol & Emergency Neurol, St Petersburg, Russia
[2] City Clin Hosp, Dept Fac Therapy, Saratov, Russia
[3] Ltd Liabil Co Ctr Diabet, Dept Endocrinil, Samara, Russia
[4] EcoSafety Med Ctr, St Petersburg, Russia
[5] City Hosp 4, City Endocrinol Ctr, Rostov Na Donu, Russia
[6] Sechenov Univ, Dept Nervous Dis & Neurosurg, Moscow, Russia
关键词
ALPHA-LIPOIC ACID; PERIPHERAL NEUROPATHY; END-POINTS;
D O I
10.1136/bmjdrc-2022-002785
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Antioxidants may have positive impact on diabetic polyneuropathy (DPN), presumably due to alleviation of oxidative stress. We aimed to evaluate the efficacy and safety of combination of antioxidants: succinic acid, inosine, nicotinamide, and riboflavin (SINR) in the treatment of DPN. Research design and methods In a double-blind, placebo-controlled clinical trial, men and women aged 45-74 years with type 2 diabetes and symptomatic DPN, with initial Total Symptom Score (TSS) >5, were randomized into experimental (n=109) or placebo (n=107) group. Patients received study medication/placebo intravenously for 10 days, followed by oral administration for 75 days. Statistical significance was defined as a two-tailed p<0.05. Results In SINR group, mean TSS change after 12 weeks was -2.65 (+/- 1.46) vs -1.73 (+/- 1.51) in the placebo group (p<0.0001; t-test). Reduction of symptoms in the SINR group was achieved regardless of hemoglobin Al c levels, but better results were observed in patients with initial TSS <7.5. The analysis of TSS subscores revealed statistically significant between-group differences by dynamics of the intensity of paresthesia and of numbness starting from day 11 (p=0.035 and p=0.001, respectively; mixed model); by day 57, statistically significant between-group differences were detected also by dynamics of burning intensity (p=0.005; mixed model). Study limitations are small effect size, moderate proportion of patients with severe DPN symptoms, subjective assessment of outcomes, exclusion of participants who received injectable glucose-lowering medications other than insulins, and patients with uncontrolled and type 1 diabetes. Conclusions The combination of SINR effectively alleviates DPN symptoms in patients with type 2 diabetes.
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页数:9
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