Clinical and laboratory characteristics of early-onset and delayed-onset lupus nephritis patients: A single-center retrospective study

被引:9
作者
Kosalka-Wegiel, Joanna [1 ,2 ]
Dziedzic, Radoslaw [3 ]
Siwiec-Kozlik, Andzelika [2 ]
Spalkowska, Magdalena [4 ]
Milewski, Mamert [2 ]
Zuk-Kuwik, Joanna [5 ]
Zareba, Lech [6 ]
Bazan-Socha, Stanislawa [2 ,7 ]
Korkosz, Mariusz [1 ,2 ]
机构
[1] Jagiellonian Univ, Med Coll, Dept Rheumatol & Immunol, Jakubowskiego 2, PL-30688 Krakow, Poland
[2] Univ Hosp, Dept Rheumatol Immunol & Internal Med, Jakubowskiego 2, PL-30688 Krakow, Poland
[3] Jagiellonian Univ, Med Coll, Doctoral Sch Med & Hlth Sci, Sw Lazarza 16, PL-31530 Krakow, Poland
[4] Jagiellonian Universitym Med Coll, Dept Dermatol, Dept Neurol, Bot 3, PL-31501 Krakow, Poland
[5] Jagiellonian Univ, Med Coll, Dept Hematol, Jakubowskiego 2, PL-30688 Krakow, Poland
[6] Univ Rzeszow, Inst Comp Sci, Coll Nat Sci, Pigon 1, PL-35310 Rzeszow, Poland
[7] Jagiellonian Univ, Med Coll, Fac Med, Dept Internal Med, Jakubowskiego 2, PL-30688 Krakow, Poland
关键词
Systemic lupus erythematosus; Lupus nephritis; Prognostic factors; ERYTHEMATOSUS; DISEASE; MULTICENTER; DIAGNOSIS; ANEMIA;
D O I
10.1007/s00296-024-05579-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Lupus nephritis (LN) manifests systemic lupus erythematosus (SLE) and is characterized by various clinical and laboratory features. This study aimed to comprehensively evaluate the characteristics of LN patients according to the time of LN diagnosis: early-onset (LN diagnosed within one year from SLE diagnosis) vs. delayed-onset (LN diagnosed more than one year after SLE diagnosis).Methods We conducted a retrospective analysis of medical records from all SLE patients treated at the University Hospital in Krakow, Poland, from 2012 to 2022. We collected data on demographic, clinical, and laboratory characteristics, including histological findings, treatment modalities, and disease outcomes. Statistical analyses were performed to identify factors impacting LN development and prognosis.Results Among 331 LN patients, early-onset was diagnosed in 207 (62.54%) and delayed-onset was documented in 122 cases (36.86%). In 2 (0.6%) LN cases, the time of first kidney manifestation in the SLE course was unknown. Delayed-onset LN had a higher female-to-male ratio and younger age at SLE diagnosis. This group was associated with more severe clinical manifestations. In turn, studied subgroups did not differ in internist comorbidities, kidney histopathology, and family history regarding autoimmune diseases. Delayed-onset LN exhibited a higher frequency of anti-dsDNA, anti-Smith, anti-Ro, anti-RNP, and anti-cardiolipin IgG autoantibodies. During a 14-year follow-up period, 16 patients died. Mortality rate and causes of death were comparable in both analyzed subgroups.Conclusions More severe clinical manifestations in delayed-onset LN prompt strict monitoring of non-LN SLE patients to diagnose and treat kidney involvement early. Also, recognizing the higher frequency of autoantibodies such as anti-dsDNA or anti-Smith in delayed-onset LN underscores the potential value of autoantibody profiling as a diagnostic and prognostic tool.
引用
收藏
页码:1283 / 1294
页数:12
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