Session Information
Date: Sunday, November 8, 2015
Title: Systemic Lupus Erythematosus - Clinical Aspects and Treatment Poster Session I
Session Type: ACR Poster Session A
Session Time: 9:00AM-11:00AM
Background/Purpose: To describe the demographic, clinical and immunological manifestations in patients with late onset systemic lupus erythematosus (SLE)
Methods: Patients diagnosed of SLE in the RELESSER data base (National Registry of Patients with Systemic Lupus Erythematosus of the Spanish Society of Rheumatology) were included. Late-onset was defined as >50 years of age at time of first SLE-related symptom. Design: multicenter retrospective cross-sectional study. Socio-demographic variables, comorbidities, classification, clinical and immunological manifestations were evaluated. Pearson´s chi-square test, t-Student
Results: Of the 3628 patients included: 566 (15.6%) patients had late-onset SLE, 3062 (84.4%) patients were younger than 50 years. The mean age at diagnosis was 60.7(Sd 8.5) years in the late-onset SLE and 30.5 (Sd 9.96) years in the younger onset group. In the late onset group: 91 (16.1%) were male and 475 (83.9%) women. The male/female ratio was 5/1. Diagnosis in the younger onset group was sooner than in late-onset group (28.2 Sd 48.9 days compared with 45.3 Sd 70.3 days with P <0.0001).
Comparing comorbidities by age group, it was found that SLE patients over 50 years of age had more comorbidities with p<0.0001. Secondary Sjogren’s syndrome was more frequent in the older age group (p<0.001). Table 1: Clinical manifestations. During follow-up 205 patients died: 74 (14.3%) with late-onset SLE and 131 (4.7%) younger than 50 years (P <0.0001). Evaluating the cause of death, the group of younger patients had higher mortality due to SLE with statistical significance. The cause of death from severe infections and cancer was higher in patients over 50 years, but without statistical significance
Clinical manifestation
|
Older than 50 years. N (%) |
Younger than 50 years. N (%) |
Missing N (%) |
VALUE OF P |
|
Systemic Manifestations |
Lymphadenopathy |
36(6,5%) |
332(11%) |
95 (2,6%) |
0,002 |
Cutáneous Manifestations |
Inflamatory rash |
286(51,9%) |
2076(87,9%) |
84 (2,3%) |
<0,0001 |
Alopecia |
115(21%) |
1161(38,7%) |
108 (3,0%) |
<0,0001 |
|
Osteoarticular Manifestations |
Avascular bone necrosis |
9(1,6%) |
140(4,7%) |
89 (2,4%) |
0,001 |
Arthritis |
74(13,2%) |
285(9,4%) |
81 (2,2%) |
0,007 |
|
Osteoporosis |
94(17,3%) |
164(5,5%) |
141 (3,9%) |
<0,0001 |
|
Pulmonary Manifestations |
Pleural fibrosis |
19(3,4%) |
52(1,7%) |
64 (1,7%) |
0,009 |
Pulmonary thromboembolism |
24(4,3%) |
79(2,6%) |
55 (1,5%) |
0,030 |
|
Cardiovascular Manifestations |
Valvular disease |
68(12,3%) |
150(5%) |
113 (3,1%) |
<0,0001 |
Valvular dysfunction |
31(5,9%) |
90(3,1%) |
245 (6,7%) |
0,001 |
|
Angina |
31(5,5%) |
37(1,2%) |
75 (2,1%) |
<0,0001 |
|
Acute myocardial infarction |
26(4,7%) |
45(1,5%) |
83 (2,3%) |
<0,0001 |
|
Cardiomyopathy |
41(7,4%) |
63(2,1%) |
100 (2,7%) |
<0,0001 |
|
Peripheral vascular Manifestations |
Raynaud |
131(24,1%) |
1055(35,7%) |
160 (4,4%) |
<0,0001 |
Renal Manifestations |
Lupus nephritis |
78(14,3%) |
1003(33,4%) |
110 (3,0%) |
<0,0001 |
HTA in the first outbreak |
39(7,1%) |
360(12,4%) |
201 (5,5%) |
<0,0001 |
|
Hematuria |
94(17,7%) |
940(32,8%) |
264 (7,2%) |
<0,0001 |
|
Pyuria |
47(9%) |
687(24,6%) |
337 (9,2%) |
<0,0001 |
|
Creatinine clearance = 50 irreversible |
41 (7,4%) |
150 (5%) |
131 (3,6%) |
0,025 |
|
Proteinuria = 3,5g/24hs |
6(1,1%) |
127(4,3%) |
145 (4,0%) |
<0,0001 |
|
End stage renal disease |
8(1,5%) |
89(3%) |
164 (4,5%) |
0,039 |
|
Neuro psychiatric Manifestations |
Lupus headache |
13(2,4%) |
199(6,6%) |
110 (3,0%) |
<0,0001 |
Depression |
122(22,2%) |
481(16%) |
111 (3,0%) |
<0,0001 |
|
Ocular Manifestations |
Cataract |
111(20,3%) |
201(6,7%) |
123 (3,4%) |
<0,0001 |
Immunology |
Complement |
327(59,2%) |
2433(81,2%) |
108 (3,0%) |
<0,0001 |
Ac anti RNP positive |
84(15,2%) |
792(26,9%) |
162 (4,4%) |
<0,0001 |
Conclusion: Patients with late-onset SLE have a higher risk of mortality than the younger-onset SLE. The diagnostic delay is higher in patients over 50 years. This group of patients have more comorbidities and higher risk of joint, pulmonary and cardiovascular involvement, on the contrary renal involvement is less common
To cite this abstract in AMA style:
Riveros Frutos A, Martínez-Morillo M, Casas I, Rúa-Figueroa I, Pego-Reigosa J, García de Yebenes MJ, Olivé A, Rosas J, Vela Casasempere P, Ibanez Barcelo M, Torrente V, Castellvi I, Narváez J, Moreno M, Blanco R, Martínez Taboada V, Calvo J, Aguirre Zamorano , Freire M, Raya E, Erausquin C, Uriarte E, Diez Alvarez E, Vázquez Rodríguez T, Fernandez-Nebro A, Tomero E, García de la Peña P, Sánchez Atrio A, Fernandez Castro M, Zea A, Richi P, López Longo FJ, Galindo M, Carreira PE, Bonilla G, Marras Fernandez-Cid C, Horcada ML, Montilla Morales CA, Hernández-Cruz B, Marenco de la Fuente JL, Gantes M, Fernández Berrizbeitia O, Alegre JJ, Pecondón Español , Rodríguez-Gómez M, Quevedo V, Hernández Beiraín J, Silva Fernández L. Late Onset Systemic Lupus Erythematosus: A Different Disease Subset? [abstract]. Arthritis Rheumatol. 2015; 67 (suppl 10). https://acrabstracts.org/abstract/late-onset-systemic-lupus-erythematosus-a-different-disease-subset/. Accessed .« Back to 2015 ACR/ARHP Annual Meeting
ACR Meeting Abstracts - https://acrabstracts.org/abstract/late-onset-systemic-lupus-erythematosus-a-different-disease-subset/