Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

[Diabetes and heredity].

P Froguel1, P Passa

  • 1Service d'Endocrinologie-Diabétologie, Hôpital Saint-Louis, Paris.

La Revue De Medecine Interne
|March 1, 1991
PubMed
Summary
This summary is machine-generated.

Genetic factors play a crucial role in both insulin-dependent diabetes (IDD) and non-insulin-dependent diabetes (NIDD). Understanding these genetic links, particularly HLA region associations for IDD, is key for future detection and prevention strategies.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Transmission of Type 2 diabetes to sons and daughters: the D.E.S.I.R. cohort.

Diabetic medicine : a journal of the British Diabetic Association·2017
Same author

Interaction between GPR120 p.R270H loss-of-function variant and dietary fat intake on incident type 2 diabetes risk in the D.E.S.I.R. study.

Nutrition, metabolism, and cardiovascular diseases : NMCD·2016
Same author

Placental antiangiogenic prolactin fragments are increased in human and rat maternal diabetes.

Biochimica et biophysica acta·2014
Same author

A nonsense loss-of-function mutation in PCSK1 contributes to dominantly inherited human obesity.

International journal of obesity (2005)·2014
Same author

Transcription factor gene MNX1 is a novel cause of permanent neonatal diabetes in a consanguineous family.

Diabetes & metabolism·2013
Same author

Macrophage gene expression in adipose tissue is associated with insulin sensitivity and serum lipid levels independent of obesity.

Obesity (Silver Spring, Md.)·2013
Same journal

[Abdominal pain, fever and arthralgia in a 49-year-old woman].

La Revue de medecine interne·2026
Same journal

[Cardiorespiratory functional disorders: A transnosologic approach].

La Revue de medecine interne·2026
Same journal

[Diagnostic evaluation for suspected polycythemia].

La Revue de medecine interne·2026
Same journal

Heart involvements in systemic sclerosis beyond pulmonary hypertension: From conduction, rhythm and function defects to coronary artery disease.

La Revue de medecine interne·2026
Same journal

[Acute intermittent porphyria: When diagnostic errance jeopardizes patient health].

La Revue de medecine interne·2026
Same journal

Autosomal dominant polycystic kidney disease: Current perspectives in 2026.

La Revue de medecine interne·2026
See all related articles

Area of Science:

  • Genetics
  • Molecular Biology
  • Immunology

Context:

  • Diabetes mellitus, encompassing both insulin-dependent diabetes (IDD) and non-insulin-dependent diabetes (NIDD), has a significant hereditary component.
  • Environmental factors act as facilitators in genetically susceptible individuals.
  • Advances in molecular biology are crucial for unraveling the genetic underpinnings of diabetes.

Purpose:

  • To explore the genetic factors contributing to the development of IDD and NIDD.
  • To highlight the role of the HLA region and specific HLA DQ conformations in IDD pathogenesis.
  • To identify potential genetic markers for NIDD and discuss the implications for early detection and prevention.

Summary:

  • IDD is strongly associated with the HLA region on chromosome 6, with 90% of cases linked to DR3 or DR4 groups. A specific HLA DQ molecule conformation facilitates antigen presentation to T-cells, contributing to IDD development.

Related Experiment Videos

  • NIDD exhibits a higher degree of heritability, but its genetic basis is less defined due to the absence of a clear marker. Genes related to insulin, insulin receptor, and glucose transporter are implicated in some NIDD forms.
  • Further family studies are essential for pinpointing the specific genes responsible for NIDD, paving the way for early detection and potential prevention strategies.
  • Impact:

    • Improved understanding of diabetic heredity can lead to the identification of individuals at high risk.
    • Discovery of specific genetic markers may enable early diagnosis and targeted interventions for both IDD and NIDD.
    • Genetic insights hold the potential for developing novel strategies for diabetes prevention and management.