Source:http://linkedlifedata.com/resource/pubmed/id/12729053
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2003-5-5
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pubmed:abstractText |
The benefit of combining quinacrine (Qn) with hydroxychloroquine (HCQ) in the treatment of systemic lupus erythematosus (SLE) was previously re-evaluated by us. In our current study we observed that, in 11 active SLE patients (SLEDAI score 5-12), the addition of Qn (100 mg/day) to their existing ongoing therapeutic regimens resulted in a significant attenuation of their previously persistent anticardiolipin antibody (aCL) response. This was in comparison with a matched non-Qn treated control group composed of 14 randomly chosen aCL-positive SLE patients with a similar SLEDAI score 6-10. Prior to Qn treatment the therapeutic regimens of 12 months' duration, included in all cases HCQ (400 mg/day), in many cases prednisone (P, 10-20 mg/day) and in some additional cases immunosuppressive drugs. SLEDAI scores and aCL levels were monitored during the entire follow-up period which totaled 24 months in the study group and 15-18 months in the controls. Along with the beneficial effect of the added Qn on SLEDAI scores, aCL disappearance was documented in eight of 11 patients and remained negative during 8-12 months of follow-up (P = 0.004), compared with such a change in only three of 14 non-Qn treated aCL-positive patients (P = 0.18). We conclude that the added Qn treatment to former established therapeutic protocols may eliminate aCL response in SLE patients. Whether this agent's effect is permanent needs further elucidation.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Anti-Inflammatory Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Anticardiolipin,
http://linkedlifedata.com/resource/pubmed/chemical/Antimalarials,
http://linkedlifedata.com/resource/pubmed/chemical/Hydroxychloroquine,
http://linkedlifedata.com/resource/pubmed/chemical/Prednisone,
http://linkedlifedata.com/resource/pubmed/chemical/Quinacrine
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pubmed:status |
MEDLINE
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pubmed:issn |
0961-2033
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
12
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
297-301
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:12729053-Adult,
pubmed-meshheading:12729053-Anti-Inflammatory Agents,
pubmed-meshheading:12729053-Antibodies, Anticardiolipin,
pubmed-meshheading:12729053-Antimalarials,
pubmed-meshheading:12729053-Drug Therapy, Combination,
pubmed-meshheading:12729053-Female,
pubmed-meshheading:12729053-Humans,
pubmed-meshheading:12729053-Hydroxychloroquine,
pubmed-meshheading:12729053-Lupus Erythematosus, Systemic,
pubmed-meshheading:12729053-Male,
pubmed-meshheading:12729053-Middle Aged,
pubmed-meshheading:12729053-Prednisone,
pubmed-meshheading:12729053-Quinacrine,
pubmed-meshheading:12729053-Severity of Illness Index
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pubmed:year |
2003
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pubmed:articleTitle |
Quinacrine added to ongoing therapeutic regimens attenuates anticardiolipin antibody production in SLE.
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pubmed:affiliation |
Division of Clinical Immunology, Bnai-Zion Medical Center, Haifa, Israel.
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pubmed:publicationType |
Journal Article,
Clinical Trial
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