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Antiphospholipid antibodies and the risk of thrombocytopenia in patients with systemic lupus erythematosus: A systematic review and meta-analysis
被引:38
|作者:
Chock, Yu Pei
[1
]
Moulinet, Thomas
[2
,3
]
Dufrost, Virginie
[3
,4
,5
]
Erkan, Doruk
[6
]
Wahl, Denis
[3
,4
,5
]
Zuily, Stephane
[3
,4
,5
]
机构:
[1] Yale Sch Med, Sect Rheumatol, New Haven, CT USA
[2] CHRU Nancy, Dept Internal Med, F-54000 Nancy, France
[3] Univ Lorraine, Inserm UMR S 1116, F-54000 Nancy, France
[4] CHRU Nancy, Vasc Med Div, F-54000 Nancy, France
[5] CHRU Nancy, Reg Competence Ctr Rare Vasc & Syst Autoimmune Di, F-54000 Nancy, France
[6] Hosp Special Surg, Barbara Volcker Ctr Women & Rheumat Dis, Weill Cornell Med, 535 E 70th St, New York, NY 10021 USA
关键词:
Antiphospholipid antibodies;
Systemic lupus erythematosus;
Thrombocytopenia;
IgM;
ANTICARDIOLIPIN ANTIBODIES;
CLINICAL-SIGNIFICANCE;
I ANTIBODIES;
CLASSIFICATION CRITERIA;
LIVEDO-RETICULARIS;
DISEASE-ACTIVITY;
ANTICOAGULANT;
ASSOCIATION;
MANIFESTATIONS;
PREVALENCE;
D O I:
10.1016/j.autrev.2019.102395
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Background: According to criteria for the classification of Systemic Lupus Erythematosus (SLE), thrombocytopenia is one of the disease-defining hematologic disorders. Since the recognition of Antiphospholipid Syndrome (APS), thrombocytopenia was frequently reported but several studies yielded contradictory results on the association between aPL-positivity and thrombocytopenia. Methods: We evaluated the role of antiphospholipid antibodies (aPL) and different aPL profiles on the risk of thrombocytopenia in SLE patients by conducting a systematic review and meta-analysis of available literature from 1987 to 2018. MEDLINE, EMBASE, Cochrane Library, congress abstracts, and reference lists of eligible studies were searched. Studies were selected if they included SLE patients with descriptions of the exposure to aPL and the outcomes (thrombocytopenia). Two reviewers extracted study characteristics and outcome data from published reports. Estimates were pooled using random effects models and sensitivity analyses. We followed the PRISMA guidelines for all stages of the meta-analysis. PROSPERO registration number: CRD42015027378. Results: From 3278 articles identified, 53 studies met inclusion criteria amounting to 9019 SLE patients. Twenty-nine percent of aPL-positive SLE patients had thrombocytopenia compared to 15.1% in aPL-negative SLE patients. The overall pooled Odds Ratio (OR) for thrombocytopenia in aPL positive patients was 2.48 (95% CI; 2.10-2.93). Among aPL subtypes, the risk of thrombocytopenia was highest for lupus anticoagulant (OR = 3.56 [95% CI, 2.57-5.25]), IgM anti-beta(2)-GP1(OR = 2.87 [95% CI; 2.57-5.25]), IgG and IgM anticardiolipin antibodies (OR = 1.87 [95% CI; 1.52-2.31] and OR = L73 [95% CI; 1.36-2.19] respectively). Conclusions: The occurrence of thrombocytopenia was strongly determined by various aPL profiles in SLE patients. While the association between IgM antibodies and other APS manifestations including thrombosis is debated, IgM isotypes are helpful in the risk stratification of thrombocytopenia in SLE.
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