Evidence mapPaperPMID 35268481Full record

ArticleJournal of clinical medicine2022

A New Approach to Overcome Insulin Resistance in Patients with Impaired Glucose Tolerance: The Results of a Multicenter, Double-Blind, Placebo-Controlled, Randomized Clinical Trial of Efficacy and Safety of Subetta.

Ashot Mkrtumyan, Alexander Ametov, Tatiana Demidova, Anna Volkova, Ekaterina Dudinskaya, Arkady Vertkin, Sergei Vorobiev

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.4field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 6 institutions in 1 country.

Ashot MkrtumyanDepartment of Endocrinology, Moscow Clinical Scientific and Practical Center Named after A. S. Loginov, 111123 Moscow, Russia.
Alexander AmetovDepartment of Endocrinology, Faculty of Medicine, Medical Academy of Continuing Professional Education, 125993 Moscow, Russia.
Tatiana DemidovaDepartment of Endocrinology, City Clinical Hospital Named after V. P. Demikhova, 117463 Moscow, Russia.
Anna VolkovaDepartment of Faculty Therapy, Faculty of Medicine, Pavlov First Saint Petersburg State Medical University, 197022 St. Petersburg, Russia.
Ekaterina DudinskayaDepartment of Age-Related Metabolic and Endocrine Disorders, Russian Gerontological Research and Clinical Center, Pirogov Russian National Research Medical University, 129226 Moscow, Russia.
Arkady VertkinDepartment of Therapy, Clinical Pharmacology and Emergency Medicine, A. I. Evdokimov Moscow State University of Medicine and Dentistry, 127473 Moscow, Russia.
Sergei VorobievDepartment of Endocrinology, Rostov State Medical University, 344022 Rostov-on-Don, Russia.
City Clinical Hospital · RUFirst Pavlov State Medical University of St. Petersburg · RUMoscow State University of Medicine and Dentistry · RUPirogov Russian National Research Medical University · RURostov State Medical University · RURussian Medical Academy of Continuous Professional Education · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Impaired glucose tolerance (IGT) is a common carbohydrate metabolism disorder world-wide. To evaluate the efficacy and safety of 12-week Subetta therapy in correcting 2-h plasma glucose in patients with IGT, a multicenter, double-blind, placebo-controlled, randomized clinical trial was performed. Derived by technological treatment of antibodies to insulin receptor β-subunit and endothelial NO synthase, Subetta increases the sensitivity of insulin receptors by activating the insulin signaling pathway. Oral glucose tolerance test (OGTT), fasting plasma glucose (FPG), and glycated hemoglobin (HbA1c) were examined at screening, after 4 and 12 weeks. In Per Protocol population, 2-h plasma glucose in the Subetta group decreased by 2.05 ± 2.11 mmol/L (versus 0.56 ± 2.55 mmol/L in the Placebo group) after 12 weeks. The difference between the two groups was 1.49 ± 2.33 mmol/L (p < 0.0001). After 12 weeks, 65.2% of patients had 2-h plasma glucose <7.8 mmol/L. FPG remained almost unchanged. HbA1c tended to decrease. The number of adverse events did not differ in both groups. Subetta treatment is beneficial for patients with IGT; it also prevents progression of carbohydrate metabolism disorders.

Indexed as

2-h plasma glucoseglycated hemoglobinimpaired glucose tolerance

Identifiers

PMID35268481
PMCPMC8910875
OpenAlexW4214951073

What Socratic holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.