Evidence mapPaperPMID 39902162Full record

ReviewFrontiers in endocrinology2024

Current views on etiology, diagnosis, epidemiology and gene therapy of maturity onset diabetes in the young.

Lilya U Dzhemileva, Elena N Zakharova, Anna O Goncharenko, Maria V Vorontsova, S A Rumyantsev, Natalia G Mokrysheva, Marina Y Loguinova, Vladimir P Chekhonin

Abstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
field-weighted citation impact
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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Case Report: Identification of aFrontiers in endocrinology · 2026
    Article
  8. The Role of Gene Therapy and RNA-Based Therapeutic Strategies in Diabetes.International journal of molecular sciences · 2025
    Review
  9. Review
  10. Review
  11. Article
  12. Article
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

8 authors.

Lilya U DzhemilevaEndocrinology Research Centre, Moscow, Russia.
Elena N ZakharovaEndocrinology Research Centre, Moscow, Russia.
Anna O GoncharenkoEndocrinology Research Centre, Moscow, Russia.
Maria V VorontsovaEndocrinology Research Centre, Moscow, Russia.
S A RumyantsevEndocrinology Research Centre, Moscow, Russia.
Natalia G MokryshevaEndocrinology Research Centre, Moscow, Russia.
Marina Y LoguinovaEndocrinology Research Centre, Moscow, Russia.
Vladimir P ChekhoninEndocrinology Research Centre, Moscow, Russia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MODY, or maturity-onset diabetes of the young, is a group of monogenic diseases characterized by autosomal dominant inheritance of a non-insulin-dependent form of diabetes that classically manifests in adolescence or in young adults under 25 years of age. MODY is a rare cause of diabetes, accounting for 1% of all cases, and is often misdiagnosed as type 1 or type 2 diabetes. It is of great importance to accurately diagnose MODY, as this allows for the most appropriate treatment of patients and facilitates early diagnosis for them and their families. This disease has a high degree of phenotypic and genetic polymorphism. The most prevalent forms of the disease are attributed to mutations in three genes: GCK (MODY 2) and (HNF)1A/4A (MODY 3 and MODY 1). The remaining MODY subtypes, which are less prevalent, have been identified by next generation sequencing (NGS) in the last decade. Mutations in the GCK gene result in asymptomatic, stable fasting hyperglycemia, which does not require specific treatment. Mutations in the HNF1A and HNF4A genes result in pancreatic β-cell dysfunction, which in turn causes hyperglycemia. This often leads to diabetic angiopathy. The most commonly prescribed drugs for the treatment of hyperglycemia are sulfonylurea derivatives. Nevertheless, with advancing age, some patients may require insulin therapy due to the development of resistance to sulfonylurea drugs. The strategy of gene therapy for monogenic forms of MODY is still an experimental approach, and it is unlikely to be widely used in the clinic due to the peculiarities of MODY structure and the high genetic polymorphism and clinical variability even within the same form of the disease. Furthermore, there is a lack of clear gene-phenotypic correlations, and there is quite satisfactory curability in the majority of patients. This review presents the main clinical and genetic characteristics and mutation spectrum of common and rarer forms of MODY, with a detailed analysis of the field of application of AVV vectors in the correction of hyperglycemia and insulin resistance.

Indexed as

Diabetes Mellitus, Type 2Genetic TherapyAdolescentAdultHepatocyte Nuclear Factor 1-alphaHepatocyte Nuclear Factor 4HumansMutationYoung AdultHepatocyte Nuclear Factor 1-alphaHepatocyte Nuclear Factor 4AAV-vectorsautosomal dominant inheritancediabetes monogenic formsEuropean and Asian populationsgene therapymaturity-onset diabetes of the young (MODY)

Identifiers

PMID39902162
PMCPMC11788143

What Socratic holds

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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.