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High vs Low Dose Vitamin D in Patients With Diabetic Peripheral Neuropathy

High-dose Vitamin D Supplementation Reduces Inflammation and Improves Microcirculation in Patients With Diabetic Peripheral Neuropathy

Aim. To assess the effect of different doses of vitamin D supplementation on peripheral neuropathy in patients with type 2 diabetes mellitus (T2DM).

68 patients with T2DM and peripheral neuropathy will be randomized into two treatment groups: cholecalciferol 5,000 IU once/week and cholecalciferol 40,000 IU once/week orally for 24 weeks. Severity of neuropathy (neuropathy symptom score (NSS), neuropathy disability score (NDS), visual analog scale (VAS)), body mass index (BMI), glycated hemoglobin (HbA1c), 25-hydroxycalciferol (25(OH)D), parathyroid hormone (PTH), serum interleukins (IL) 1β, 6 and 10, C-reactive protein, tumor necrosis factor α and microcirculation (MC) parameters assessed before and after treatment. The initial and final indicators of the skin blood flow (M, σ, Kv) and MC parameters after postural and occlusal tests by laser Doppler flowmetry (LDF). Sixteen subjects without diabetes will represent the control group.

Studieöversikt

Status

Avslutad

Intervention / Behandling

Detaljerad beskrivning

It is well known that vitamin D deficiency along with type 2 diabetes mellitus (T2DM) is a modern pandemic. Development of microvascular complications in T2DM worsens both the prognosis and the patients' quality of life. There is increasing evidence of a possible contribution of vitamin D deficiency to the pathogenesis of diabetes and its complications. Large-scale studies have shown 40% increased risk of developing diabetes in individuals with a reduced 25(OH)D level. A recent interventional prospective study demonstrated no decrease in the risk of T2DM development in patients with prediabetes after two-year treatment with 4,000 IU of vitamin D per day. But, some experts suggested that 4,000 IU is not sufficient supplementation dose for patients with already existing impaired glucose metabolism and on the other hand most study participants had normal basal 25(OH)D level. Along with immune-mediated mechanisms, microcirculation deterioration in patients with diabetes has been found to play an important role in the pathogenesis of microvascular complications including peripheral neuropathy (DPN).

It is believed that vitamin D deficiency also plays a role in the progression of DPN. Thus, the correction of vitamin D deficiency in patients with T2DM is becoming increasingly attractive for the prevention and treatment of microvascular complications. However, the question of the required vitamin D dose and the treatment duration remain highly debatable. The aim of this study was to assess the effect of therapy with different doses of cholecalciferol for 24 weeks on clinical manifestations of peripheral neuropathy, inflammatory markers, and parameters of microcirculation in patients with T2DM.

Patients and Methods: Baseline characteristics will be recorded for all patients including Height, weight, BMI, diabetes status and biochemical parameters. All will be repeated at 24 weeks. Blood will be collected after an overnight fast and stored at -20 degrees until analysis.

Patients will be recruited from the Almazov Research centre, St Petersburg, Russia Federation.

68 patients with T2DM and peripheral neuropathy will be randomized into two treatment groups: cholecalciferol 5,000 IU once/week and cholecalciferol 40,000 IU once/week orally for 24 weeks. Severity of neuropathy (neuropathy symptom score (NSS), neuropathy disability score (NDS), visual analog scale (VAS)), body mass index (BMI), glycated hemoglobin (HbA1c), 25-hydroxycalciferol (25(OH)D), parathyroid hormone (PTH), serum interleukins (IL) 1β, 6 and 10, C-reactive protein, tumor necrosis factor α and microcirculation (MC) parameters assessed before and after treatment. The initial and final indicators of the skin blood flow (M, σ, Kv) and MC parameters after postural and occlusal tests by laser Doppler flowmetry (LDF). Sixteen subjects without diabetes will represent the control group.

Studietyp

Interventionell

Inskrivning (Faktisk)

68

Fas

  • Fas 4

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

      • Saint Petersburg, Ryska Federationen, 197143
        • Almazov National Medical Research Centre

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år till 65 år (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Ja

Kön som är behöriga för studier

Allt

Beskrivning

Inclusion Criteria:

  • males and females with T2DM aged 18 to 65 years
  • diabetes duration ≥5 years,
  • HbA1c <9%,
  • stable hypoglycemic,
  • hypotensive and hypolipidemic therapy
  • neurological deficit 4 points and more according to the neuropathy disability score (NDS).

Exclusion Criteria:

  • patients with type 1 diabetes
  • hypothyroidism
  • glomerular filtration rate (GFR) <45 ml/min/1.73 m2
  • current and former smokers
  • obliterating atherosclerosis
  • diabetic foot or Charcot osteoarthropathy
  • inflammatory joint diseases
  • oncological diseases
  • ongoing infectious diseases or in the preceding four weeks
  • alcohol and drug addiction
  • history of В12 deficiency
  • anemia or current therapy with vitamin B12
  • regular use of glucocorticoids
  • vitamin D supplements
  • anticoagulants
  • antidepressants
  • tricyclic antidepressants
  • anticonvulsants
  • opiates
  • non-steroidal anti-inflammatory drugs
  • vasoprotective and microcirculation correctors
  • alpha lipoic acid
  • group B vitamins.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Aktiv komparator: high dose
vitamin D (40,000 IU weekly) for 24 weeks
Patients will be randomised to receive either high dose vitamin D (40,000 IU weekly) or low dose vitamin D (5,000 IU weekly) for 24 weeks
Aktiv komparator: Low dose
vitamin D (5,000 IU weekly) for 24 weeks
Patients will be randomised to receive either high dose vitamin D (40,000 IU weekly) or low dose vitamin D (5,000 IU weekly) for 24 weeks

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Microcirculation
Tidsram: Baseline and 24 weeks
Assessment of microcirculatory changes using laser doppler
Baseline and 24 weeks

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Interleukins
Tidsram: Baseline and 24 weeks
Serum interleukins (IL) will be determined by enzyme-linked immunosorbent assay (Bio-Rad 680 Microplate Reader, USA) using the appropriate sets of reagents for enzyme immunoassay to determine the concentration of IL-1β (reference values 0-5.0 pg/ml), IL-6 (reference values 0-7.0 pg/ml), IL-10 (reference values 0-9.1 pg/ml), (Vector-Best, Novosibirsk, Russia) compared from baseline
Baseline and 24 weeks
Tumor necrosis factor-α (TNFα)
Tidsram: Baseline and 24 weeks
Tumor necrosis factor-α (TNFα) will be determined by enzyme-linked immunosorbent assay (Bio-Rad 680 Microplate Reader, USA) using the appropriate sets of reagents for enzyme immunoassay to determine the concentration of TNFα (reference values 0-8.21 pg/ml) (Vector-Best, Novosibirsk, Russia)
Baseline and 24 weeks
Neuropathy disability score
Tidsram: Baseline and 24 weeks
Using standard scoring systems and questionnaires. Scoring is: Neuropathy disability score (0-10),
Baseline and 24 weeks
Pain score
Tidsram: Baseline and 24 weeks
Patients will be asked to score pain on a visual analog scale 0-10 with 10 being the worst pain ever
Baseline and 24 weeks
Neuropathic symptom score
Tidsram: Baseline and 24 weeks
This will be scored using standard questionnaire 0-9
Baseline and 24 weeks

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Utredare

  • Huvudutredare: Tatiana Karonova, PhD, Almazov National Medical Research Centre

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

10 januari 2018

Primärt slutförande (Faktisk)

20 juni 2019

Avslutad studie (Faktisk)

25 januari 2020

Studieregistreringsdatum

Först inskickad

29 april 2020

Först inskickad som uppfyllde QC-kriterierna

5 maj 2020

Första postat (Faktisk)

6 maj 2020

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

6 maj 2020

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

5 maj 2020

Senast verifierad

1 maj 2020

Mer information

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