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Is the CD14 C159T polymorphism effective in the development of secondary amyloidosis in Familial Mediterranean fever?
- Source :
- Rheumatology International. 27:691-694
- Publication Year :
- 2006
- Publisher :
- Springer Science and Business Media LLC, 2006.
-
Abstract
- The most important complication of FMF is the development of amyloidosis. It is more common in the eastern Mediterranean compared to the US. The individual response to endotoxin may have a significant effect on the development of amyloidosis in FMF patients. To investigate the association between CD14 promotor C-159T polymorphism and development of amyloidosis, one hundred and forty-six patients who had FMF and had not developed amyloidosis; 26 with FMF and secondary amyloidosis and 92 controls were genotyped at the CD14-C159T locus. There was no difference between the genotype distribution of FMF patients (CC 30.0%, CT 50.0%, TT 20.0%) and controls (CC 29.2%, CT 45.8%, TT 25%); or between FMF patients with amyloidosis (CC 30.8%, CT 53.8%, TT 15.4%) or without amyloidosis (CC 29.2%, CT 45.8%, TT 25%). Our study shows that the CD14-C159T polymorphism is not associated with FMF or development of amyloidosis in the population studied. The effect of the genetic variations in the endotoxin signaling pathway under different environmental conditions such as high and low endotoxin exposure remain to be determined.
- Subjects :
- Adult
Male
medicine.medical_specialty
Adolescent
CD14
Immunology
Population
Lipopolysaccharide Receptors
Familial Mediterranean fever
Polymorphism, Single Nucleotide
Gastroenterology
Rheumatology
Internal medicine
Genotype
medicine
Humans
Immunology and Allergy
Child
Promoter Regions, Genetic
education
education.field_of_study
Secondary amyloidosis
business.industry
Amyloidosis
Infant
medicine.disease
Familial Mediterranean Fever
Case-Control Studies
Child, Preschool
Female
business
Complication
Subjects
Details
- ISSN :
- 1437160X and 01728172
- Volume :
- 27
- Database :
- OpenAIRE
- Journal :
- Rheumatology International
- Accession number :
- edsair.doi.dedup.....efef133f55ae069904d4dfce2d4a5143