Evidence map›Paper›PMID 22996131›Full record

ReviewCurrent diabetes reports2012

Monogenic models: what have the single gene disorders taught us?

Tomasz Klupa, Jan Skupien, Maciej T Malecki

Open access · hybridAbstract readReview
In one paragraph

Review in Current diabetes reports, 2012. 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
3.8field-weighted citation impact, top 7% 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

12 citing papers in PubMed, 26 citations in OpenAlex.

  1. Variants influencing age at diagnosis of HNF1A-MODY.Molecular medicine (Cambridge, Mass.) · 2022
    Article
  2. Article
  3. Transient Neonatal Diabetes due to a Mutation in KCNJ11 in a Child with Klinefelter Syndrome.Journal of clinical research in pediatric endocrinology · 2018
    Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Genetic insights into cardiometabolic risk factors.The Clinical biochemist. Reviews · 2014
    Review
  10. Complications of diabetes therapy.Endocrinology and metabolism clinics of North America · 2013
    Review
  11. Article
  12. Dysfunctional mitochondrial bioenergetics and oxidative stress in Akita(+/Ins2)-derived β-cells.American journal of physiology. Endocrinology and metabolism · 2013
    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

3 authors at 3 institutions in 2 countries.

Tomasz KlupaDepartment of Metabolic Diseases, Jagiellonian University, Medical College, 15 Kopernika Street, 31-501, Krakow, Poland.
Jan Skupien
Maciej T Malecki
Jagiellonian University · PLJoslin Diabetes Center · USKrakow Cardiovascular Research Institute · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monogenic diabetes constitutes a heterogeneous group of single gene disorders. The molecular background and clinical picture of many of these diseases have been described. While each of these forms is much less prevalent than multifactorial type 1 and type 2 diabetes mellitus (T2DM), together they affect millions of patients worldwide. Genetic diagnosis, which has become widely available, is of great clinical importance for patients with single gene diabetes. It helps to fully understand the pathophysiology of the disease, tailor the optimal hypoglycemic treatment, and define the prognosis for the entire family. Monogenic diabetes forms can be divided into 2 large groups, resulting from impaired insulin secretion or from an abnormal response to insulin. There are several lessons we have been taught by single-gene diabetes. We learned that the gene responsible for the occurrence of diabetes can be identified if an appropriate search strategy is used. In addition, discoveries of genes responsible for monogenic disorders pointed to them as susceptibility candidates for T2DM. Moreover, establishing that some families of proteins or biological pathways, such as transcription factors or potassium channel subunits, are involved in monogenic diabetes sparked research on their involvement in multifactorial diabetes. Finally, the example of single gene diabetes, particularly HNF1A MODY and permanent neonatal diabetes associated with the KCNJ11 and ABCC8 genes, all efficiently controlled on sulfonylurea, inspires us to continue the efforts to tailor individual treatment for T2DM patients. In this review paper, we summarize the impact of single gene disease discoveries on diabetes research and clinical practice.

Indexed as

ATP-Binding Cassette TransportersDiabetes Mellitus, Type 1Diabetes Mellitus, Type 2FemaleGenetic Predisposition to DiseaseGenetic TestingGenotypeHepatocyte Nuclear Factor 1-alphaHumansHyperglycemiaHypoglycemic AgentsKcnj11 ChannelMaleModels, BiologicalMutationPharmacogeneticsATP-Binding Cassette TransportersHepatocyte Nuclear Factor 1-alphaHNF1A protein, humanHypoglycemic AgentsKcnj11 ChannelPotassium Channels, Inwardly RectifyingReceptors, DrugSulfonylurea CompoundsSulfonylurea Receptors

Identifiers

PMID22996131
PMCPMC3488607
OpenAlexW2067448094

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 OpenQuestion graph.