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Predictors and clinical complications associated with antiphospholipid antibodies in sickle cell disease
被引:1
|作者:
Rivera, Claudia Rodriguez
[1
]
Srisuwananukorn, Andrew
[2
]
Bajwa, Rizma Jalees
[1
]
Gordeuk, Victor R.
[3
]
Rauch, Joyce
[4
]
Levine, Jerrold S.
[1
,5
]
Saraf, Santosh L.
[3
]
机构:
[1] Univ Illinois, Dept Med, Div Nephrol, 1740 W Taylor St, Chicago, IL 60607 USA
[2] Mt Sinai Hlth Syst, Dept Med, Div Hematol & Oncol, New York, NY USA
[3] Univ Illinois, Dept Med, Div Hematol & Oncol, 1740 W Taylor St, Chicago, IL 60607 USA
[4] McGill Univ, Res Inst, Hlth Ctr, Dept Med, Montreal, PQ, Canada
[5] Vet Affairs Med Ctr, Dept Med, Div Nephrol, Jesse Brown, Chicago, IL USA
来源:
EJHAEM
|
2023年
/
4卷
/
01期
基金:
美国国家卫生研究院;
关键词:
antiphospholipid antibody;
antiphospholipid syndrome;
multiorgan failure;
sickle cell disease;
systemic lupus erythematosus;
RISK;
D O I:
10.1002/jha2.643
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Although a higher prevalence of antiphospholipid autoantibodies (aPL) has been observed in some cohorts of sickle cell disease (SCD) patients, the clinical risk factors for the development of aPL and its associated complications remain unclear. In a retrospective study of 63 SCD patients, a lower hemoglobin concentration and higher white blood cell count were independently associated with an elevated aPL. SCD patients with elevated aPL had increased pregnancy complications (>= 3 miscarriages, preterm delivery, pre-eclampsia) and venous thrombotic events. Our findings suggest that SCD may predispose to the generation of aPL and that aPL itself may contribute to the vasculopathy of SCD. Prospective testing for aPL is warranted in patients with SCD.
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页码:211 / 215
页数:5
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