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Abstract Title:

Impact of Rutin and Vitamin C combination on oxidative stress and glycemic control in patients with type 2 diabetes.

Abstract Source:

Clin Nutr ESPEN. 2020 02 ;35:128-135. Epub 2019 Nov 14. PMID: 31987106

Abstract Author(s):

Sara Ramzy Ragheb, Lamia Mohamed El Wakeel, Merhan Samy Nasr, Nagwa Ali Sabri

Article Affiliation:

Sara Ramzy Ragheb

Abstract:

AIM: This study aimed to investigate the effect of Vitamin C alone and in combination with Rutin on the glycemic control, insulin resistance, lipid profile and oxidative stress markers in patients with type 2 diabetes.

METHODS: A prospective, randomized, controlled study conducted on 53 type 2 diabetes patients randomized into 3 groups; (group A) 20 received Rutin with vitamin C, (group B) 20receivedvitamin C and (group C)13 received antidiabetic treatment only. Fasting Blood Glucose (FBG), Hemoglobin A1c (HbA1c), fasting insulin, Malondialdehyde, Superoxide dismutase, Lipid profile and patients' quality of life (QOL) using SF-36 questionnaire were assessed in all patients at baseline and after 8 weeks.

RESULTS: At baseline, the 3 groups were comparable while FBG was lower in group C versus group A and B (p = 0.0021). After 8 weeks, a significant reduction was observed in % change of FBG in groups A and B versus group C (p = 0.0165, 0.0388 respectively). Low Density Lipoprotien-cholesterol (LDL-c) and Total cholesterol (TC) levels significantly improved in group B versus baseline (p = 0.0239,0.0166 respectively). QOL, physical functioning and energy domains improved significantly in group A versus group C (p = 0.0049, 0.0253 respectively), while role limitation to physical health and to emotional problem improved significantly in group B versus group C (p = 0.0267,0.0280 respectively).

CONCLUSION: Vitamin C supplementation alone or with Rutin significantly reduced the % change of FBG compared to controls but had no effect on HbA1c, FBG,TC, fasting insulin and HOMA-IR or oxidative stress in T2DMpatients.

CLINICAL TRIAL REGISTRATION NUMBER: NCT03437902.

Study Type : Human Study

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