Familial aggregation and segregation analysis in families presenting Autoimmunity, Polyautoimmunity, and Multiple Autoimmune Syndrome
Studies documenting increased risk of developing autoimmune diseases (ADs) have shown that these conditions share several immunogenetic mechanisms (i.e., the autoimmune tautology). This report explored familial aggregation and segregation of AD, polyautoimmunity, and multiple autoimmune syndrome (MA...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2015
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- eng
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/21887
- Acceso en línea:
- https://doi.org/10.1155/2015/572353
https://repository.urosario.edu.co/handle/10336/21887
- Palabra clave:
- Ciencias médicas, Medicina
Enfermedades
adult
Article
Autoimmune disease
Female
Human
Age
Autoimmunity
Codominance
Colombia
Disease transmission
Familial aggregation
First degree relative
Genetic analysis
Major clinical study
Major gene
Mendelian transmission
Male
Multiple Autoimmune Syndrome
Onset Age
Pedigree
Polyautoimmunity
- Rights
- License
- Abierto (Texto Completo)
Summary: | Studies documenting increased risk of developing autoimmune diseases (ADs) have shown that these conditions share several immunogenetic mechanisms (i.e., the autoimmune tautology). This report explored familial aggregation and segregation of AD, polyautoimmunity, and multiple autoimmune syndrome (MAS) in 210 families. Familial aggregation was examined for first-degree relatives. Segregation analysis was implemented as in S.A.G.E. release 6.3. Data showed differences between late- and early-onset families regarding their age, age of onset, and sex. Familial aggregation of AD in late- and early-onset families was observed. For polyautoimmunity as a trait, only aggregation was observed between sibling pairs in late-onset families. No aggregation was observed for MAS. Segregation analyses for AD suggested major gene(s) with no clear discernible classical known Mendelian transmission in late-onset families, while for polyautoimmunity and MAS no model was implied. Data suggest that polyautoimmunity and MAS are not independent traits and that gender, age, and age of onset are interrelated factors influencing autoimmunity. © 2015 John Castiblanco et al. |
---|