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Risk factors associated with mortality in systemic lupus erythematosus. A case-control study in a tertiary care center in Mexico City

Identifieur interne : 000057 ( PascalFrancis/Corpus ); précédent : 000056; suivant : 000058

Risk factors associated with mortality in systemic lupus erythematosus. A case-control study in a tertiary care center in Mexico City

Auteurs : B. Hernandez-Cruz ; N. Tapia ; A. R. Villa-Romero ; E. Reyes ; M. H. Cardiel

Source :

RBID : Pascal:02-0044020

Descripteurs français

English descriptors

Abstract

Objective To identify the mortality risk factors in a group of Mexican patients with SLE. Methods A case-control autopsy study in a tertiary care center in Mexico, City. Patients with SLE who died during 1958 to 1994 with an autopsy study were selected as cases, and alive patients matched by age (±3 years), decade of SLE onset, and disease duration (±5 years) were defined as controls. Clinical charts were reviewed looking at clinical variables. SLE disease activity was evaluated with the MexSledai index, and SLE disease severity with the Severity Index. Variables were classified as present at any moment during the follow-up and 3 months before death in cases or cut-off date in controls. Statistical analysis: matched univariate and multivariate analysis by multiple logistic regression were performed, and the results were presented as odds ratio and 95% confidence intervals (OR, 95%CI). Results 76 matched pairs of patients were studied. Age, gender; and years of formal education were similar in the cases and controls. Variables associated with mortality three months before death were: lung involvement OR=15.6, 95%CI (4.8-50.3), p<0.001; severe thrombocytopenia 9.6 (2.9-31.7), p<0.001; heart involvement 5.8 (2.6-13.0), p<0.001; and the severity index (cases 8.8 μ, 2.4 σ vs controls 3.5, 2.0, respectively) 2.2 (1.5-3.4), p<0.001. Variables associated with mortality detected at any moment before death were kidney involvement 2. 16 (1.09-4.29), p<0.02; the steroid therapeutic index 2.3 (1.2-4.5), p<0.001; number of previous admissions 2.4 (1.4-4.3), p<0.001; the MEX-SLEDAI index (cases 21.6 μ, 6.3 σ vs controls 12.6, 5.8), 1.2 (1.1-1.3), p<0.001; and the number of severe infections 14.4 (4.4-46.2), p<0.001. Protective variables were skin involvement 0.1 (0.3-0.6), p<0.001; daily dose of chloroquine (cases 3.9 μ, 24.1 σ vs controls 39.4, 60.0 mg), p<0.0001 and the time from the first SLE symptom to the patient's demise or the cut-off date 0.7(0.6-0.9), p<0.001. Multiple logistic regression showed that the model which best explained mortality consisted of a severity index 2.6 (1.7-3.8), p<0.001; heart disease 6.5 (1.5-28.2), p=0.01, and steroid therapeutic index 3.3 (1.6-6.6), p=0.001. Conclusions An active SLE with multi-organic involvement, steroids and infections were associated with mortality in Mexican patients with lupus attended in a tertiary care center. A protective effect of cutaneous disease and chloroquine use was observed.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

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A08 01  1  ENG  @1 Risk factors associated with mortality in systemic lupus erythematosus. A case-control study in a tertiary care center in Mexico City
A11 01  1    @1 HERNANDEZ-CRUZ (B.)
A11 02  1    @1 TAPIA (N.)
A11 03  1    @1 VILLA-ROMERO (A. R.)
A11 04  1    @1 REYES (E.)
A11 05  1    @1 CARDIEL (M. H.)
A14 01      @1 Department of Internal Medicine, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirdn @2 Mexico City @3 MEX @Z 1 aut. @Z 2 aut.
A14 02      @1 Clinical Epidemiology Unit, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirdn @2 Mexico City @3 MEX @Z 3 aut.
A14 03      @1 Department of Pathology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirdn @2 Mexico City @3 MEX @Z 4 aut.
A14 04      @1 Department of Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirdn @2 Mexico City @3 MEX @Z 5 aut.
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A61       @0 A
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C01 01    ENG  @0 Objective To identify the mortality risk factors in a group of Mexican patients with SLE. Methods A case-control autopsy study in a tertiary care center in Mexico, City. Patients with SLE who died during 1958 to 1994 with an autopsy study were selected as cases, and alive patients matched by age (±3 years), decade of SLE onset, and disease duration (±5 years) were defined as controls. Clinical charts were reviewed looking at clinical variables. SLE disease activity was evaluated with the MexSledai index, and SLE disease severity with the Severity Index. Variables were classified as present at any moment during the follow-up and 3 months before death in cases or cut-off date in controls. Statistical analysis: matched univariate and multivariate analysis by multiple logistic regression were performed, and the results were presented as odds ratio and 95% confidence intervals (OR, 95%CI). Results 76 matched pairs of patients were studied. Age, gender; and years of formal education were similar in the cases and controls. Variables associated with mortality three months before death were: lung involvement OR=15.6, 95%CI (4.8-50.3), p<0.001; severe thrombocytopenia 9.6 (2.9-31.7), p<0.001; heart involvement 5.8 (2.6-13.0), p<0.001; and the severity index (cases 8.8 μ, 2.4 σ vs controls 3.5, 2.0, respectively) 2.2 (1.5-3.4), p<0.001. Variables associated with mortality detected at any moment before death were kidney involvement 2. 16 (1.09-4.29), p<0.02; the steroid therapeutic index 2.3 (1.2-4.5), p<0.001; number of previous admissions 2.4 (1.4-4.3), p<0.001; the MEX-SLEDAI index (cases 21.6 μ, 6.3 σ vs controls 12.6, 5.8), 1.2 (1.1-1.3), p<0.001; and the number of severe infections 14.4 (4.4-46.2), p<0.001. Protective variables were skin involvement 0.1 (0.3-0.6), p<0.001; daily dose of chloroquine (cases 3.9 μ, 24.1 σ vs controls 39.4, 60.0 mg), p<0.0001 and the time from the first SLE symptom to the patient's demise or the cut-off date 0.7(0.6-0.9), p<0.001. Multiple logistic regression showed that the model which best explained mortality consisted of a severity index 2.6 (1.7-3.8), p<0.001; heart disease 6.5 (1.5-28.2), p=0.01, and steroid therapeutic index 3.3 (1.6-6.6), p=0.001. Conclusions An active SLE with multi-organic involvement, steroids and infections were associated with mortality in Mexican patients with lupus attended in a tertiary care center. A protective effect of cutaneous disease and chloroquine use was observed.
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Format Inist (serveur)

NO : PASCAL 02-0044020 INIST
ET : Risk factors associated with mortality in systemic lupus erythematosus. A case-control study in a tertiary care center in Mexico City
AU : HERNANDEZ-CRUZ (B.); TAPIA (N.); VILLA-ROMERO (A. R.); REYES (E.); CARDIEL (M. H.)
AF : Department of Internal Medicine, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirdn/Mexico City/Mexique (1 aut., 2 aut.); Clinical Epidemiology Unit, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirdn/Mexico City/Mexique (3 aut.); Department of Pathology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirdn/Mexico City/Mexique (4 aut.); Department of Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirdn/Mexico City/Mexique (5 aut.)
DT : Publication en série; Niveau analytique
SO : Clinical and experimental rheumatology; ISSN 0392-856X; Italie; Da. 2001; Vol. 19; No. 4; Pp. 395-401; Bibl. 34 ref.
LA : Anglais
EA : Objective To identify the mortality risk factors in a group of Mexican patients with SLE. Methods A case-control autopsy study in a tertiary care center in Mexico, City. Patients with SLE who died during 1958 to 1994 with an autopsy study were selected as cases, and alive patients matched by age (±3 years), decade of SLE onset, and disease duration (±5 years) were defined as controls. Clinical charts were reviewed looking at clinical variables. SLE disease activity was evaluated with the MexSledai index, and SLE disease severity with the Severity Index. Variables were classified as present at any moment during the follow-up and 3 months before death in cases or cut-off date in controls. Statistical analysis: matched univariate and multivariate analysis by multiple logistic regression were performed, and the results were presented as odds ratio and 95% confidence intervals (OR, 95%CI). Results 76 matched pairs of patients were studied. Age, gender; and years of formal education were similar in the cases and controls. Variables associated with mortality three months before death were: lung involvement OR=15.6, 95%CI (4.8-50.3), p<0.001; severe thrombocytopenia 9.6 (2.9-31.7), p<0.001; heart involvement 5.8 (2.6-13.0), p<0.001; and the severity index (cases 8.8 μ, 2.4 σ vs controls 3.5, 2.0, respectively) 2.2 (1.5-3.4), p<0.001. Variables associated with mortality detected at any moment before death were kidney involvement 2. 16 (1.09-4.29), p<0.02; the steroid therapeutic index 2.3 (1.2-4.5), p<0.001; number of previous admissions 2.4 (1.4-4.3), p<0.001; the MEX-SLEDAI index (cases 21.6 μ, 6.3 σ vs controls 12.6, 5.8), 1.2 (1.1-1.3), p<0.001; and the number of severe infections 14.4 (4.4-46.2), p<0.001. Protective variables were skin involvement 0.1 (0.3-0.6), p<0.001; daily dose of chloroquine (cases 3.9 μ, 24.1 σ vs controls 39.4, 60.0 mg), p<0.0001 and the time from the first SLE symptom to the patient's demise or the cut-off date 0.7(0.6-0.9), p<0.001. Multiple logistic regression showed that the model which best explained mortality consisted of a severity index 2.6 (1.7-3.8), p<0.001; heart disease 6.5 (1.5-28.2), p=0.01, and steroid therapeutic index 3.3 (1.6-6.6), p=0.001. Conclusions An active SLE with multi-organic involvement, steroids and infections were associated with mortality in Mexican patients with lupus attended in a tertiary care center. A protective effect of cutaneous disease and chloroquine use was observed.
CC : 002B07
FD : Lupus érythémateux; Disséminé; Facteur risque; Epidémiologie; Mortalité; Etiologie; Evolutivité; Anatomopathologie; Postmortem; Mexique; Adulte; Etude cas témoin
FG : Amérique Centrale; Amérique; Homme; Peau pathologie; Tissu conjonctif pathologie; Maladie système; Maladie autoimmune; Immunopathologie; Santé publique
ED : Lupus erythematosus; Disseminated; Risk factor; Epidemiology; Mortality; Etiology; Evolutivity; Pathology; Postmortem; Mexico; Adult; Case control study
EG : Central America; America; Human; Skin disease; Connective tissue disease; Systemic disease; Autoimmune disease; Immunopathology; Public health
SD : Lupus eritematoso; Diseminado; Factor riesgo; Epidemiología; Mortalidad; Etiología; Evolutividad; Anatomía patológica; Postmortem; México; Adulto; Estudio caso control
LO : INIST-20920.354000095792370060
ID : 02-0044020

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<div type="abstract" xml:lang="en">Objective To identify the mortality risk factors in a group of Mexican patients with SLE. Methods A case-control autopsy study in a tertiary care center in Mexico, City. Patients with SLE who died during 1958 to 1994 with an autopsy study were selected as cases, and alive patients matched by age (±3 years), decade of SLE onset, and disease duration (±5 years) were defined as controls. Clinical charts were reviewed looking at clinical variables. SLE disease activity was evaluated with the MexSledai index, and SLE disease severity with the Severity Index. Variables were classified as present at any moment during the follow-up and 3 months before death in cases or cut-off date in controls. Statistical analysis: matched univariate and multivariate analysis by multiple logistic regression were performed, and the results were presented as odds ratio and 95% confidence intervals (OR, 95%CI). Results 76 matched pairs of patients were studied. Age, gender; and years of formal education were similar in the cases and controls. Variables associated with mortality three months before death were: lung involvement OR=15.6, 95%CI (4.8-50.3), p<0.001; severe thrombocytopenia 9.6 (2.9-31.7), p<0.001; heart involvement 5.8 (2.6-13.0), p<0.001; and the severity index (cases 8.8 μ, 2.4 σ vs controls 3.5, 2.0, respectively) 2.2 (1.5-3.4), p<0.001. Variables associated with mortality detected at any moment before death were kidney involvement 2. 16 (1.09-4.29), p<0.02; the steroid therapeutic index 2.3 (1.2-4.5), p<0.001; number of previous admissions 2.4 (1.4-4.3), p<0.001; the MEX-SLEDAI index (cases 21.6 μ, 6.3 σ vs controls 12.6, 5.8), 1.2 (1.1-1.3), p<0.001; and the number of severe infections 14.4 (4.4-46.2), p<0.001. Protective variables were skin involvement 0.1 (0.3-0.6), p<0.001; daily dose of chloroquine (cases 3.9 μ, 24.1 σ vs controls 39.4, 60.0 mg), p<0.0001 and the time from the first SLE symptom to the patient's demise or the cut-off date 0.7(0.6-0.9), p<0.001. Multiple logistic regression showed that the model which best explained mortality consisted of a severity index 2.6 (1.7-3.8), p<0.001; heart disease 6.5 (1.5-28.2), p=0.01, and steroid therapeutic index 3.3 (1.6-6.6), p=0.001. Conclusions An active SLE with multi-organic involvement, steroids and infections were associated with mortality in Mexican patients with lupus attended in a tertiary care center. A protective effect of cutaneous disease and chloroquine use was observed.</div>
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<s1>Risk factors associated with mortality in systemic lupus erythematosus. A case-control study in a tertiary care center in Mexico City</s1>
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<s1>Department of Internal Medicine, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirdn</s1>
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<s1>Department of Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirdn</s1>
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<s0>Objective To identify the mortality risk factors in a group of Mexican patients with SLE. Methods A case-control autopsy study in a tertiary care center in Mexico, City. Patients with SLE who died during 1958 to 1994 with an autopsy study were selected as cases, and alive patients matched by age (±3 years), decade of SLE onset, and disease duration (±5 years) were defined as controls. Clinical charts were reviewed looking at clinical variables. SLE disease activity was evaluated with the MexSledai index, and SLE disease severity with the Severity Index. Variables were classified as present at any moment during the follow-up and 3 months before death in cases or cut-off date in controls. Statistical analysis: matched univariate and multivariate analysis by multiple logistic regression were performed, and the results were presented as odds ratio and 95% confidence intervals (OR, 95%CI). Results 76 matched pairs of patients were studied. Age, gender; and years of formal education were similar in the cases and controls. Variables associated with mortality three months before death were: lung involvement OR=15.6, 95%CI (4.8-50.3), p<0.001; severe thrombocytopenia 9.6 (2.9-31.7), p<0.001; heart involvement 5.8 (2.6-13.0), p<0.001; and the severity index (cases 8.8 μ, 2.4 σ vs controls 3.5, 2.0, respectively) 2.2 (1.5-3.4), p<0.001. Variables associated with mortality detected at any moment before death were kidney involvement 2. 16 (1.09-4.29), p<0.02; the steroid therapeutic index 2.3 (1.2-4.5), p<0.001; number of previous admissions 2.4 (1.4-4.3), p<0.001; the MEX-SLEDAI index (cases 21.6 μ, 6.3 σ vs controls 12.6, 5.8), 1.2 (1.1-1.3), p<0.001; and the number of severe infections 14.4 (4.4-46.2), p<0.001. Protective variables were skin involvement 0.1 (0.3-0.6), p<0.001; daily dose of chloroquine (cases 3.9 μ, 24.1 σ vs controls 39.4, 60.0 mg), p<0.0001 and the time from the first SLE symptom to the patient's demise or the cut-off date 0.7(0.6-0.9), p<0.001. Multiple logistic regression showed that the model which best explained mortality consisted of a severity index 2.6 (1.7-3.8), p<0.001; heart disease 6.5 (1.5-28.2), p=0.01, and steroid therapeutic index 3.3 (1.6-6.6), p=0.001. Conclusions An active SLE with multi-organic involvement, steroids and infections were associated with mortality in Mexican patients with lupus attended in a tertiary care center. A protective effect of cutaneous disease and chloroquine use was observed.</s0>
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<s0>Lupus érythémateux</s0>
<s5>01</s5>
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<s0>Lupus erythematosus</s0>
<s5>01</s5>
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<s0>Lupus eritematoso</s0>
<s5>01</s5>
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<s5>02</s5>
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<s5>02</s5>
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<s0>Diseminado</s0>
<s5>02</s5>
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<s5>03</s5>
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<s0>Mortality</s0>
<s5>05</s5>
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<s5>06</s5>
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<s5>06</s5>
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<s5>07</s5>
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<s5>08</s5>
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<s5>08</s5>
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<s0>Anatomía patológica</s0>
<s5>08</s5>
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<s0>Postmortem</s0>
<s5>09</s5>
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<s0>Postmortem</s0>
<s5>09</s5>
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<s0>Postmortem</s0>
<s5>09</s5>
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<s2>NG</s2>
<s5>10</s5>
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<s5>10</s5>
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<s2>NG</s2>
<s5>10</s5>
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<s5>11</s5>
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<s5>11</s5>
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<s5>12</s5>
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<s2>NG</s2>
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<s2>NG</s2>
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<s0>Hombre</s0>
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<s0>Peau pathologie</s0>
<s5>37</s5>
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<fC07 i1="04" i2="X" l="ENG">
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<s5>37</s5>
</fC07>
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<s5>37</s5>
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<s0>Tissu conjonctif pathologie</s0>
<s5>38</s5>
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<s5>38</s5>
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<s5>38</s5>
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<s0>Maladie système</s0>
<s5>39</s5>
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<s0>Systemic disease</s0>
<s5>39</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA">
<s0>Enfermedad sistémica</s0>
<s5>39</s5>
</fC07>
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<s0>Maladie autoimmune</s0>
<s5>40</s5>
</fC07>
<fC07 i1="07" i2="X" l="ENG">
<s0>Autoimmune disease</s0>
<s5>40</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA">
<s0>Enfermedad autoinmune</s0>
<s5>40</s5>
</fC07>
<fC07 i1="08" i2="X" l="FRE">
<s0>Immunopathologie</s0>
<s5>41</s5>
</fC07>
<fC07 i1="08" i2="X" l="ENG">
<s0>Immunopathology</s0>
<s5>41</s5>
</fC07>
<fC07 i1="08" i2="X" l="SPA">
<s0>Inmunopatología</s0>
<s5>41</s5>
</fC07>
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<s0>Santé publique</s0>
<s5>45</s5>
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<s0>Public health</s0>
<s5>45</s5>
</fC07>
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<s5>45</s5>
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<fN21>
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<NO>PASCAL 02-0044020 INIST</NO>
<ET>Risk factors associated with mortality in systemic lupus erythematosus. A case-control study in a tertiary care center in Mexico City</ET>
<AU>HERNANDEZ-CRUZ (B.); TAPIA (N.); VILLA-ROMERO (A. R.); REYES (E.); CARDIEL (M. H.)</AU>
<AF>Department of Internal Medicine, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirdn/Mexico City/Mexique (1 aut., 2 aut.); Clinical Epidemiology Unit, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirdn/Mexico City/Mexique (3 aut.); Department of Pathology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirdn/Mexico City/Mexique (4 aut.); Department of Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirdn/Mexico City/Mexique (5 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Clinical and experimental rheumatology; ISSN 0392-856X; Italie; Da. 2001; Vol. 19; No. 4; Pp. 395-401; Bibl. 34 ref.</SO>
<LA>Anglais</LA>
<EA>Objective To identify the mortality risk factors in a group of Mexican patients with SLE. Methods A case-control autopsy study in a tertiary care center in Mexico, City. Patients with SLE who died during 1958 to 1994 with an autopsy study were selected as cases, and alive patients matched by age (±3 years), decade of SLE onset, and disease duration (±5 years) were defined as controls. Clinical charts were reviewed looking at clinical variables. SLE disease activity was evaluated with the MexSledai index, and SLE disease severity with the Severity Index. Variables were classified as present at any moment during the follow-up and 3 months before death in cases or cut-off date in controls. Statistical analysis: matched univariate and multivariate analysis by multiple logistic regression were performed, and the results were presented as odds ratio and 95% confidence intervals (OR, 95%CI). Results 76 matched pairs of patients were studied. Age, gender; and years of formal education were similar in the cases and controls. Variables associated with mortality three months before death were: lung involvement OR=15.6, 95%CI (4.8-50.3), p<0.001; severe thrombocytopenia 9.6 (2.9-31.7), p<0.001; heart involvement 5.8 (2.6-13.0), p<0.001; and the severity index (cases 8.8 μ, 2.4 σ vs controls 3.5, 2.0, respectively) 2.2 (1.5-3.4), p<0.001. Variables associated with mortality detected at any moment before death were kidney involvement 2. 16 (1.09-4.29), p<0.02; the steroid therapeutic index 2.3 (1.2-4.5), p<0.001; number of previous admissions 2.4 (1.4-4.3), p<0.001; the MEX-SLEDAI index (cases 21.6 μ, 6.3 σ vs controls 12.6, 5.8), 1.2 (1.1-1.3), p<0.001; and the number of severe infections 14.4 (4.4-46.2), p<0.001. Protective variables were skin involvement 0.1 (0.3-0.6), p<0.001; daily dose of chloroquine (cases 3.9 μ, 24.1 σ vs controls 39.4, 60.0 mg), p<0.0001 and the time from the first SLE symptom to the patient's demise or the cut-off date 0.7(0.6-0.9), p<0.001. Multiple logistic regression showed that the model which best explained mortality consisted of a severity index 2.6 (1.7-3.8), p<0.001; heart disease 6.5 (1.5-28.2), p=0.01, and steroid therapeutic index 3.3 (1.6-6.6), p=0.001. Conclusions An active SLE with multi-organic involvement, steroids and infections were associated with mortality in Mexican patients with lupus attended in a tertiary care center. A protective effect of cutaneous disease and chloroquine use was observed.</EA>
<CC>002B07</CC>
<FD>Lupus érythémateux; Disséminé; Facteur risque; Epidémiologie; Mortalité; Etiologie; Evolutivité; Anatomopathologie; Postmortem; Mexique; Adulte; Etude cas témoin</FD>
<FG>Amérique Centrale; Amérique; Homme; Peau pathologie; Tissu conjonctif pathologie; Maladie système; Maladie autoimmune; Immunopathologie; Santé publique</FG>
<ED>Lupus erythematosus; Disseminated; Risk factor; Epidemiology; Mortality; Etiology; Evolutivity; Pathology; Postmortem; Mexico; Adult; Case control study</ED>
<EG>Central America; America; Human; Skin disease; Connective tissue disease; Systemic disease; Autoimmune disease; Immunopathology; Public health</EG>
<SD>Lupus eritematoso; Diseminado; Factor riesgo; Epidemiología; Mortalidad; Etiología; Evolutividad; Anatomía patológica; Postmortem; México; Adulto; Estudio caso control</SD>
<LO>INIST-20920.354000095792370060</LO>
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