Abstract | OBJECTIVES: METHODS: The effects of PSL (0.2-0.5 mg/kg/day) and TAC (3 mg/day) or AZA (1-2 mg/kg/day) therapies (n = 18) were evaluated for short (12 months) and long (36 months or more) periods. RESULTS: In the short period, IP improved in 6 and 5 patients and was stable in 12 and 13 patients in the TAC and AZA groups, respectively. In the long period, 11 patients were followed up in the TAC group and 12 in the AZA group. IP improved in 4 and 2 patients and was stable in seven and nine in the TAC and AZA groups, respectively. The rates of evolution of total fibrosis score, and those corrected by disease duration for the long period, in the TAC group were significantly lower than those in the AZA group (p = .017 and .025, respectively). CONCLUSION: The inhibitory effect of PSL and TAC combination therapy on the progression of fibrosis in SSc-PIP may be superior to that of PSL and AZA in the long period.
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Authors | Takao Kiboshi, Takuya Kotani, Junichi Konma, Hidehiko Makino, Shogo Matsuda, Takayasu Suzuka, Yumiko Wada, Hideyuki Shiba, Kenichiro Hata, Takeshi Shoda, Tohru Takeuchi |
Journal | Modern rheumatology
(Mod Rheumatol)
Vol. 32
Issue 2
Pg. 358-364
(Feb 28 2022)
ISSN: 1439-7609 [Electronic] England |
PMID | 33896348
(Publication Type: Comparative Study, Journal Article)
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Copyright | © 2021 Japan College of Rheumatology. |
Chemical References |
- Immunosuppressive Agents
- Prednisolone
- Azathioprine
- Tacrolimus
|
Topics |
- Azathioprine
(therapeutic use)
- Drug Therapy, Combination
- Fibrosis
- Humans
- Immunosuppressive Agents
(therapeutic use)
- Lung Diseases, Interstitial
(complications, drug therapy)
- Prednisolone
(therapeutic use)
- Retrospective Studies
- Scleroderma, Systemic
(complications, drug therapy)
- Tacrolimus
(therapeutic use)
- Treatment Outcome
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