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Lupus flare and recurrent lupus nephritis following kidney transplantation in patients with lupus nephritis
被引:0
|作者:
Kim, Young-Eun
[1
]
Kim, Jin-Myung
[2
]
Ahn, Soo Min
[1
]
Oh, Ji Seon
[1
,3
]
Kim, Yong-Gil
[1
]
Lee, Chang-Keun
[1
]
Yoo, Bin
[1
]
Shin, Sung
[2
]
Hong, Seokchan
[1
]
机构:
[1] Univ Ulsan, Asan Med Ctr, Dept Internal Med, Div Rheumatol,Coll Med, 88,Olymp Ro 43 Gil, Seoul 05505, South Korea
[2] Univ Ulsan, Asan Med Ctr, Dept Surg, Div Kidney & Pancreas Transplantat,Coll Med, 88,Olymp Ro 43 Gil, Seoul 05505, South Korea
[3] Asan Med Ctr, Big Data Res Ctr, Informat Med, Seoul, South Korea
基金:
新加坡国家研究基金会;
关键词:
kidney transplantation;
lupus nephritis;
systemic lupus erythematosus;
STAGE RENAL-DISEASE;
REPLACEMENT THERAPY;
UNITED-STATES;
ERYTHEMATOSUS;
CLASSIFICATION;
SECONDARY;
DIALYSIS;
OUTCOMES;
TIME;
D O I:
10.1111/1756-185X.15349
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Background: Clinical manifestations and risk factors associated with systemic lupus erythematosus (SLE) flares, including recurrent lupus nephritis (LN), in patients with LN who undergo kidney transplantation have been unclear. Methods: Kidney transplant recipients with LN from January 1995 to December 2021 were included in this study. A disease flare was defined as either an increase in the non-renal SLE disease activity index score or the presence of biopsy-proven recurrent LN. Results: Among a total of 93 patients with LN who underwent kidney transplantation, 11 patients (11.8%) experienced SLE flares during a median follow-up period of 76.9 months (IQR, 43.0-122.4). The most common clinical manifestations of SLE flares were recurrent LN (4/11, 36.4%) and hematologic manifestations (4/11, 36.4%). Patients who had flares had significantly higher anti-double-stranded DNA (anti-dsDNA) antibody titers both before and after transplantation. Furthermore, an increased anti-dsDNA antibody level before transplantation was associated with a high risk of an SLE flare (HR, 1.030; p = .008). Conversely, preemptive transplantation was associated with a lower risk of a flare (HR, 0.617; p = .026). The rate of patient death-censored graft survival was found to be considerably lower in patients with recurrent LN than in those without LN. Conclusions: Approximately 10% of patients with LN experienced an SLE flare after transplantation, with recurrent LN being the most frequent manifestation. Anti-dsDNA antibody titers before transplantation were significantly related to the risk of an SLE flare. Notably, preemptive transplantation was associated with a reduced risk of flares following transplantation.
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