Session Information
Session Type: Abstract Submissions (ACR)
Background/Purpose
To describe the profile of patients included in RELESSER with histologically confirmed lupus nephritis (LN).
Methods RELESSER is a multicentre cross-sectional study, with information retrospectively collected from the charts of patients with SLE followed up at participant rheumatology units. Globally, 359 variables including demographic and clinical data, activity, severity, comorbidities, treatments and mortality were recorded. The following renal data were included: WHO LN histological type, proteinuria, haematuria, leukocyturia, cellular casts and creatinine clearance, treatment response, recurrence, development of ESRD and/or the need for dialysis or renal transplantation. We performed a descriptive analysis by calculating means ± SD for numerical variables and frequencies for qualitative variables. Chi-square or t-Student tests were applied to analyse their relationship with LN. Odds ratio and confidence intervals were calculated by using simple logistic regression. Statistical significance was p<0.05.
Results
LN was confirmed in 1092 patients (31%). Most patients were female (86%), Caucasian (90%), and the mean age at disease onset was 33±14 years. Most patients developed LN in the first year after SLE diagnosis. Most had LN proliferative forms (70%), and there were only 16 cases of thrombotic microangiopathy (TMA). The risk of LN development was significantly lower among women (p<0.001), and higher as lower was the age of the disease onset and among hispanic ethnicity (p<0.001). Complete response to treatment was achieved in 68.3% of patients, whereas 17.9% remained with renal activity. A higher risk for persistence of renal activity was found with higher levels of baseline serum creatinine (1 vs 0.91, p=0.004) and proteinuria (2.76 vs 2.4, p=0.006). ESRD was clinically associated with positive a-dsDNA, low complement, pleuropericarditis, seizures (all p<0.001), and haemolytic anemia (p=0.015).TMA was a risk factor for ESRD, and the necessity of dialysis or renal transplantation (all p<0.05).ESRD was an independent mortality risk factor (p<0.001).326 recurrences were recorded, with a mean time to first recurrence of 47 months (0-28),regardless of histology.The lower was the serum creatinine and older was the age at LN onset,the lower was the recurrence risk.TMA was a risk factor for recurrence (p=0.016). Recurrences were related with persistent lupus activity and ESRD (both, p<0.001). During the follow up, the LN development associations are described in Table 1. LN was a poor prognostic factor associated with increased mortality risk OR 2.4 (1.81-3.22), p<0.001.
Table 1.
|
OR (CI) |
Malar rash Pleurisy Pericarditis Alveolar and interstitial lung disease: Alveolar hemorrhage Seizures Psychosis Haemolytic anemia Leukolymphopenia Thrombocytopenia a-dsDNA a-Sm Antiphospholipid syndrome: lupus anticoagulant arterial/venous thrombosis Low complement levels |
1.54 (1.33-1.78)** 1.95 (1.66-2.29)** 2.07 (1.73-2.50)** 1.73 (1.23-2.44)* 3.56 (1.77-7.19)** 2.40 (1.84-3.13)** 1.88 (1.20-2.94)* 2.39 (1.89-3.03)** 1.38 (1.19-1.61)** 1.49 (1.26-1.76)** 4.77 (3.82-5.95)** 1.73 (1.45-2.05)** 1.57 (1.29-1.92)** 1.28 (1.06-1.55)* 1.84 (1.35-2.51)**/ 1.60 (1.27-2.01)** 4.48 (3.53-5.68)** |
*: p<0.05; **: p<0.001
Conclusion
LN, mainly proliferative forms, affects almost one third of patients with SLE,and is often associated with the occurrence of other severe lupus manifestations, being a poor prognostic factor. TMA and relapses are associated with worse outcome in renal function.
Disclosure:
M. Galindo Izquierdo,
None;
E. Rodriguez-Almaraz,
None;
S. Perez,
None;
J. M. Pego-Reigosa,
Governmental research grant,
2,
European Union Research grant,
2;
J. Calvo-Alen,
MSD, GlaxoSmithKline, Eli Lilly,
5;
F. J. López-Longo,
None;
I. Rúa-Figueroa,
None;
A. Olivé,
None;
V. Martínez Taboada,
None;
P. Vela Casasempere,
None;
M. Freire,
None;
J. Narváez,
None;
A. Fernandez Nebro,
None;
J. Rosas,
None;
M. Ibanez Barcelo,
None;
E. Uriarte,
None;
E. Tomero,
None;
A. Zea,
None;
M. L. Horcada,
None;
V. Torrente,
None;
I. Castellvi,
None;
J. Calvet,
None;
R. Menor Almagro,
Abbvie,
2;
M. A. Aguirre,
None;
E. Raya,
None;
E. Diez Alvarez,
None;
T. Vázquez Rodríguez,
None;
P. García de la Peña,
None;
A. Movasat,
None;
J. L. Andreu,
None;
P. Richi,
None;
C. Marras Fernandez-Cid,
None;
C. A. Montilla Morales,
None;
B. Hernández-Cruz,
None;
J. L. Marenco de la Fuente,
None;
M. Gantes,
None;
E. Ucar,
None;
J. J. Alegre,
None;
J. Manero,
None;
J. Ibañez Ruán,
None;
M. Rodríguez-Gómez,
None;
V. Quevedo,
None;
J. Hernández Beiraín,
None;
L. Silva Fernández,
None.
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