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Epidemiology of systemic sclerosis
1University of Manchester, ARC Epidemiology Research Unit, School of Epidemiology and Health Sciences, UK.
Current Opinion in Rheumatology
|November 1, 1996
Summary
Recent systemic sclerosis research indicates the limited form is more prevalent. While genetic links are unclear, organic solvents may contribute to disease development in some individuals.
Area of Science:
- Rheumatology
- Epidemiology
- Immunology
Background:
- Systemic sclerosis epidemiology shows a rising prevalence of the limited form.
- Identifying genetic susceptibility alleles for systemic sclerosis has yielded limited success.
- Previous research on occupational and environmental factors has focused on silicone gel breast implants without proven association.
Purpose of the Study:
- To review recent findings on systemic sclerosis epidemiology.
- To discuss the current understanding of genetic and environmental factors in systemic sclerosis.
- To highlight the limited success in identifying disease susceptibility genes.
Main Methods:
- Literature review of recent epidemiological studies on systemic sclerosis.
- Analysis of molecular genetic investigations for susceptibility alleles.
- Evaluation of studies on occupational and environmental influences, including silicone gel breast implants and organic solvents.
Main Results:
- The limited form of systemic sclerosis appears more prominent in recent studies.
- Human Leukocyte Antigen (HLA) class II allele associations (DP, DQ, DR) are more related to autoimmune response than susceptibility.
- Studies on silicone gel breast implants have failed to establish an association; however, organic solvents remain implicated in some cases.
Conclusions:
- The epidemiology of systemic sclerosis is evolving, with a notable increase in the limited subtype.
- Genetic factors, particularly HLA associations, offer insights into the autoimmune response but not disease susceptibility.
- Environmental factors, specifically organic solvents, continue to be investigated as potential contributors to systemic sclerosis etiology.