Startseite Benefits of metformin add-on insulin therapy (MAIT) for HbA1c and lipid profile in adolescents with type 1 diabetes mellitus: preliminary report from a double-blinded, placebo-controlled, randomized clinical trial
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Benefits of metformin add-on insulin therapy (MAIT) for HbA1c and lipid profile in adolescents with type 1 diabetes mellitus: preliminary report from a double-blinded, placebo-controlled, randomized clinical trial

  • Ali Sheikhy , Zahra Eydian , Aida Fallahzadeh , Marjan Shakiba , Mahmoud Hajipour , Mohammadreza Alaei , Asieh Mosallanejad und Hedyeh Saneifard EMAIL logo
Veröffentlicht/Copyright: 7. März 2022

Abstract

Objectives

Metabolic control during puberty is impaired in Type 1 Diabetes Mellitus (T1DM) patients due to increased insulin resistance. Metformin is one of the oral medications typically used in type 2 diabetes mellitus to reduce insulin resistance. We aimed to examine the effect of metformin on glycemic indices and insulin daily dosage in adolescents with T1DM.

Methods

The present clinical trial was carried out on 50 adolescents aged 10–20 years with T1DM referred to the Endocrinology Clinic of Mofid Children’s Hospital in Tehran for nine months. The patients were randomly divided into two groups. In the first group, metformin was added to insulin therapy, while the second group continued routine insulin therapy combined with placebo. Hemoglobin A1c (HbA1c), weight, BMI, insulin dosage, and blood pressure were measured at the beginning of the study and repeated every three months. Serum lipid profile, creatinine, blood urea nitrogen, and liver enzymes were also measured twice: At the beginning and end of the study (after nine months).

Results

The HbA1c level (p<0.001) and insulin dosage (p=0.04) were lower in the metformin group than in the placebo group after nine months. Daily insulin dosage variability was significantly lower in the metformin recipient group (p=0.041). Serum triglyceride, cholesterol, and creatinine were significantly lower in the metformin arm than in the placebo arm (p<0.05). However, metformin did not affect LDL, HDL, liver enzymes, and BUN.

Conclusions

Adjunctive metformin therapy reduces insulin dosage by inhibiting insulin resistance and weight gain. It helps decrease daily insulin dosage variability, which may prevent hypoglycemia. Also, metformin reduces creatinine, preventing renal failure in the long term.


Corresponding author: Hedyeh Saneifard, MD, Assistant Professor of Pediatric Endocrinology, Mofid Children Hospital, Shahid Beheshti University of Medical Sciences, Shariati Ave., Tehran, Iran; and Pediatric Gastroenterology, Hepatology and Nutrition Research Center, Research Institute for Children’s Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran, Phone: +98 912 2185679, E-mail:
Ali Sheikhy and Zahra Eydian contributed equally as the first author

Acknowledgment

The authors wish to thank patients for their participation and kind cooperation.

  1. Research funding: None declared.

  2. Author contribution: A.S and A.F contributed in drafting. Z.E contributed in data gathering and drafting. M.S, M.A, and A.M contributed in final revision. M.H contributed in formal analysis. H.S contributed in design, supervision, conceptualization, and final revision. All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: Authors state no conflict of interest.

  4. Informed consent: Informed consent was obtained from all individuals included in this study.

  5. Ethical approval: Shahid Beheshti University of Medical Sciences’ Board of Ethics approved the study protocol (IR.SBMU.MSP.REC.1398.869) registered at IRCT with the code IRCT20201207049638N1 (https://www.irct.ir/trial/52867). The study was performed as per the Declaration of Helsinki.

  6. Availability of data and materials: The datasets generated and analyzed during the current study are available from the corresponding author.

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Supplementary Material

The online version of this article offers supplementary material (https://doi.org/10.1515/jpem-2021-0704).


Received: 2021-11-22
Revised: 2022-02-12
Accepted: 2022-02-13
Published Online: 2022-03-07
Published in Print: 2022-04-26

© 2022 Walter de Gruyter GmbH, Berlin/Boston

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