Abstract | OBJECTIVE: METHODS: RESULTS:
Etanercept treatment resulted in initial clinical resolution of nephrotic syndrome in the 27 year old female. Both subjects demonstrated improvements in GFR and initial reduction or stabilisation of amyloid deposits on SAP scanning. CONCLUSION:
Etanercept may reverse or slow the progression of systemic AA amyloidosis in subjects with C33Y TNFRSF1A mutation. Treatment may however need to be continuous and life-long to prevent progression to end stage disease.
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Authors | E Drewe, M L Huggins, A G Morgan, M J D Cassidy, R J Powell |
Journal | Rheumatology (Oxford, England)
(Rheumatology (Oxford))
Vol. 43
Issue 11
Pg. 1405-8
(Nov 2004)
ISSN: 1462-0324 [Print] England |
PMID | 15316120
(Publication Type: Case Reports, Journal Article)
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Chemical References |
- Cytokines
- Immunoglobulin G
- Immunosuppressive Agents
- Receptors, Tumor Necrosis Factor
- Receptors, Tumor Necrosis Factor, Type I
- Serum Amyloid A Protein
- Etanercept
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Topics |
- Adult
- Amyloidosis
(drug therapy, genetics)
- Cytokines
(blood)
- Etanercept
- Familial Mediterranean Fever
(drug therapy, genetics)
- Female
- Humans
- Immunoglobulin G
(therapeutic use)
- Immunosuppressive Agents
(therapeutic use)
- Male
- Middle Aged
- Mutation
- Nephrotic Syndrome
(drug therapy, genetics)
- Receptors, Tumor Necrosis Factor
(therapeutic use)
- Receptors, Tumor Necrosis Factor, Type I
(genetics)
- Serum Amyloid A Protein
(metabolism)
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