Metabolic and clinical responses to Bunium Persicum (black caraway) supplementation in overweight and obese patients with type 2 diabetes: a double-blind, randomized placebo-controlled clinical trial.

Saber Jafari-Maskouni, Mansour Shahraki, Milad Daneshi-Maskooni, Alireza Dashipour, Ali Shamsi-Goushki, Zinat Mortazavi
Author Information
  1. Saber Jafari-Maskouni: Department of Nutrition, School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran.
  2. Mansour Shahraki: Department of Nutrition, School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran.
  3. Milad Daneshi-Maskooni: Department of Nutrition, School of Medicine, Jiroft University of Medical Sciences, Jiroft, Iran. ORCID
  4. Alireza Dashipour: Department of Food Science and Nutrition, Cellular and Molecular Research Center, Department of Clinical Biochemistry, Zahedan University of Medical Sciences, Zahedan, Iran.
  5. Ali Shamsi-Goushki: Department of Nutrition, School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran.
  6. Zinat Mortazavi: Department of Nutrition, School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran.

Abstract

BACKGROUND: Diabetes mellitus is the most common metabolic disorder worldwide. We aimed to determine the metabolic and clinical responses to Bunium Persicum (Black Caraway) supplementation in overweight and obese patients with T2DM.
METHODS: Participant recruitment took place in the diabetic clinic of Bu-Ali hospital in Zahedan. Due to the eligibility criteria, 60 participants were randomly placed into two groups, namely placebo ( = 30) and BP ( = 30). The supplementation was considered one 1000 mg capsule 2 times /day BP by meals (lunch and dinner) for 8 weeks. Physical activity levels, dietary intakes, anthropometric measurements [weight, height, and waist circumference], glycemic indices [fasting blood glucose (FBG) and insulin (FBI)], blood lipids [triglyceride (TG), total cholesterol (TC), high-density lipoprotein cholesterol (HDL-c), and low-density lipoprotein cholesterol (LDL-c)], and serum nesfatin-1 level were determined. Homeostasis model assessment-insulin resistance (HOMA-IR), Quantitative insulin sensitivity checks index (QUICKI), and Body Mass Index (BMI) were computed.
RESULTS: In comparison with placebo, BP significantly decreased FBG, HOMA-IR, and BMI (). The differences in the FBI, QUICKI, TG, TC, LDL, HDL, WC, and Nesfatin-1 were not significant ().
CONCLUSION: BP supplementation improved serum glucose indices and BMI among overweight and obese T2DM patients. Further trials are needed to confirm results.
TRIAL REGISTRATION: Iranian Registry of Clinical Trials (IRCT), IRCT20181207041876N1, Registered 18/01/2019, https://irct.ir/trial/35752.

Keywords

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Word Cloud

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