ADULT- AND CHILDHOOD-ONSET SYSTEMIC LUPUS ERYTHEMATOSUS: A COMPARISON OF ONSET, CLINICAL FEATURES, SEROLOGY, AND OUTCOME
Identifieur interne : 000E25 ( Istex/Corpus ); précédent : 000E24; suivant : 000E26ADULT- AND CHILDHOOD-ONSET SYSTEMIC LUPUS ERYTHEMATOSUS: A COMPARISON OF ONSET, CLINICAL FEATURES, SEROLOGY, AND OUTCOME
Auteurs : L. B. Tucker ; S. Menon ; J. G. Schaller ; D. A. IsenbergSource :
- Rheumatology [ 1462-0324 ] ; 1995.
Abstract
This study examines the differences which may distinguish systemic lupus erythematosus (SLE) presenting in adult life or childhood. A common database was established, with analysis of clinical, serological and outcome features of a cohert of patients with SLE, with disease diagnosed before the age of 16 (n = 39) or after the age of 16 (n = 165). Disease onset was generally more severe in the childhood-onset patients. Cardiopulmonary disease was more common in the older-onset group, but major haematological manifestations were more frequent in the childhood-onset group. Serologically, anti-DNA, anti-Sm and anti-RNP antibodies and a low C3 were all found more frequently in the younger patients. Twice as many adult-onset cases had died at the time of the last follow-up (10 vs 5%), but this group had been followed for a longer period (average 7.5 yr, S.D. 3.9 for adults vs average 4.8 yr, S.D. 3.2 for children). However, the younger patients were twice as likely (82 vs 40%) to require high-dose prednisone, although the requirement for immunosuppressive agents was similar in the two groups. Clinicians should anticipate that children with SLE have a more severe disease onset than adults in general.
Url:
DOI: 10.1093/rheumatology/34.9.866
Links to Exploration step
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<front><div type="abstract">This study examines the differences which may distinguish systemic lupus erythematosus (SLE) presenting in adult life or childhood. A common database was established, with analysis of clinical, serological and outcome features of a cohert of patients with SLE, with disease diagnosed before the age of 16 (n = 39) or after the age of 16 (n = 165). Disease onset was generally more severe in the childhood-onset patients. Cardiopulmonary disease was more common in the older-onset group, but major haematological manifestations were more frequent in the childhood-onset group. Serologically, anti-DNA, anti-Sm and anti-RNP antibodies and a low C3 were all found more frequently in the younger patients. Twice as many adult-onset cases had died at the time of the last follow-up (10 vs 5%), but this group had been followed for a longer period (average 7.5 yr, S.D. 3.9 for adults vs average 4.8 yr, S.D. 3.2 for children). However, the younger patients were twice as likely (82 vs 40%) to require high-dose prednisone, although the requirement for immunosuppressive agents was similar in the two groups. Clinicians should anticipate that children with SLE have a more severe disease onset than adults in general.</div>
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<profileDesc><abstract><p>This study examines the differences which may distinguish systemic lupus erythematosus (SLE) presenting in adult life or childhood. A common database was established, with analysis of clinical, serological and outcome features of a cohert of patients with SLE, with disease diagnosed before the age of 16 (<hi rend="italic">n</hi>
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<journal-id journal-id-type="publisher-id">brheum</journal-id>
<journal-id journal-id-type="pmc">rheumatology</journal-id>
<journal-title>Rheumatology</journal-title>
<issn pub-type="epub">1462-0332</issn>
<issn pub-type="ppub">1462-0324</issn>
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<article-id pub-id-type="doi">10.1093/rheumatology/34.9.866</article-id>
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<subject>Paediatric Rheumatology</subject>
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<article-title>ADULT- AND CHILDHOOD-ONSET SYSTEMIC LUPUS ERYTHEMATOSUS: A COMPARISON OF ONSET, CLINICAL FEATURES, SEROLOGY, AND OUTCOME</article-title>
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<name><surname>TUCKER</surname>
<given-names>L. B.</given-names>
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<xref ref-type="aff" rid="au1"><sup>*</sup>
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<name><surname>MENON</surname>
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<xref ref-type="aff" rid="au2"><sup>†</sup>
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<name><surname>SCHALLER</surname>
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<xref ref-type="aff" rid="au1"><sup>*</sup>
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<name><surname>ISENBERG</surname>
<given-names>D. A.</given-names>
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<xref ref-type="aff" rid="au2"><sup>†</sup>
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<institution>Division of Pediatric Rheumatology, The Floating Hospital, New England Medical Center and Tufts University School of Medicine</institution>
<addr-line>Boston, MA, USA</addr-line>
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<aff id="au2"><sup>†</sup>
<institution>The Bloomsbury Rheumatology Unit, Department of Medicine, University College</institution>
<addr-line>London</addr-line>
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<corresp id="cor1">Correspondence to: L. B. Tucker, Division of Pediatric Rheumatology, Box 286, New England Medical Center, 750 Washington Street, Boston, MA 02111, USA.</corresp>
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<pub-date pub-type="ppub">
<month>9</month>
<year>1995</year>
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<volume>34</volume>
<issue>9</issue>
<fpage>866</fpage>
<lpage>872</lpage>
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<day>19</day>
<month>1</month>
<year>1995</year>
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<date date-type="accepted">
<day>09</day>
<month>5</month>
<year>1995</year>
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<copyright-statement>© 1995 British Society of Rheumatology</copyright-statement>
<copyright-year>1995</copyright-year>
<abstract>
<p>This study examines the differences which may distinguish systemic lupus erythematosus (SLE) presenting in adult life or childhood. A common database was established, with analysis of clinical, serological and outcome features of a cohert of patients with SLE, with disease diagnosed before the age of 16 (<italic>n</italic>
= 39) or after the age of 16 (<italic>n</italic>
= 165). Disease onset was generally more severe in the childhood-onset patients. Cardiopulmonary disease was more common in the older-onset group, but major haematological manifestations were more frequent in the childhood-onset group. Serologically, anti-DNA, anti-Sm and anti-RNP antibodies and a low C3 were all found more frequently in the younger patients. Twice as many adult-onset cases had died at the time of the last follow-up (10 <italic>vs</italic>
5%), but this group had been followed for a longer period (average 7.5 yr, S.D. 3.9 for adults <italic>vs</italic>
average 4.8 yr, S.D. 3.2 for children). However, the younger patients were twice as likely (82 <italic>vs</italic>
40%) to require high-dose prednisone, although the requirement for immunosuppressive agents was similar in the two groups. Clinicians should anticipate that children with SLE have a more severe disease onset than adults in general.</p>
</abstract>
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<abstract>This study examines the differences which may distinguish systemic lupus erythematosus (SLE) presenting in adult life or childhood. A common database was established, with analysis of clinical, serological and outcome features of a cohert of patients with SLE, with disease diagnosed before the age of 16 (n = 39) or after the age of 16 (n = 165). Disease onset was generally more severe in the childhood-onset patients. Cardiopulmonary disease was more common in the older-onset group, but major haematological manifestations were more frequent in the childhood-onset group. Serologically, anti-DNA, anti-Sm and anti-RNP antibodies and a low C3 were all found more frequently in the younger patients. Twice as many adult-onset cases had died at the time of the last follow-up (10 vs 5%), but this group had been followed for a longer period (average 7.5 yr, S.D. 3.9 for adults vs average 4.8 yr, S.D. 3.2 for children). However, the younger patients were twice as likely (82 vs 40%) to require high-dose prednisone, although the requirement for immunosuppressive agents was similar in the two groups. Clinicians should anticipate that children with SLE have a more severe disease onset than adults in general.</abstract>
<note type="author-notes">Correspondence to: L. B. Tucker, Division of Pediatric Rheumatology, Box 286, New England Medical Center, 750 Washington Street, Boston, MA 02111, USA.</note>
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