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抗甲状腺抗体阳性对儿童原发性免疫性血小板减少症的影响。

The effect of anti-thyroid antibodies positivity on children with primary immune thrombocytopenia.

作者信息

Mousa Suzan O, Soliman Gamal T, Saedii Ahmed A-F, Hameed Emad N

机构信息

a Pediatric Department , Minia University Hospital , El-Minya , Egypt.

b Pediatric Department , Minia University Hospital , El-Minya , Egypt.

出版信息

Pediatr Hematol Oncol. 2017 Aug;34(5):298-307. doi: 10.1080/08880018.2017.1400136. Epub 2017 Nov 30.

DOI:10.1080/08880018.2017.1400136
PMID:29190168
Abstract

Primary immune thrombocytopenia (ITP) is the most common cause of acquired thrombocytopenia in children. Anti-thyroid antibodies (aTA) have previously been found to be present in various autoimmune diseases. Our aim was to study the effect of aTA positivity (which are anti-thyroid peroxidase (aTPo) and/or anti-thyroglobulin (aTg)) on children with primary immune thrombocytopenia and their relation to treatment response. Sixty-one children with primary ITP were enrolled in the present study. They were further subdivided into: ND&P group (newly diagnosed and persistent) and chronic ITP group. Seventy-five apparently healthy children were enrolled as control group. aTPo and aTg antibodies were significantly higher and more frequently positive in all children with ITP and in each ITP group than the control group (P <.05 in all). But, there were no statistically significant differences between the two ITP subgroups (P >.05). aTA positive children with ITP had significantly lower platelet count: at the start of treatment (P =.009), after receiving methylprednisolone or intravenous immunoglobulin (P =.02) and at one month follow-up (P =.003) than aTA negative children with ITP. Lastly, aTA positive children had more relapses (P =.03), continued more frequently to have relapses after one year in the ND&P group (P =.02) and required immunosuppressive therapy more frequently in the chronic ITP group (P =.005).

摘要

原发性免疫性血小板减少症(ITP)是儿童获得性血小板减少症最常见的病因。抗甲状腺抗体(aTA)此前已在多种自身免疫性疾病中被发现。我们的目的是研究aTA阳性(即抗甲状腺过氧化物酶(aTPo)和/或抗甲状腺球蛋白(aTg))对原发性免疫性血小板减少症患儿的影响及其与治疗反应的关系。本研究纳入了61例原发性ITP患儿。他们被进一步细分为:新诊断并持续存在组(ND&P组)和慢性ITP组。75名明显健康的儿童被纳入作为对照组。与对照组相比,所有ITP患儿及各ITP组中的aTPo和aTg抗体均显著更高且更频繁呈阳性(所有P均<.05)。但是,两个ITP亚组之间无统计学显著差异(P>.05)。ITP患儿中aTA阳性者的血小板计数显著更低:在治疗开始时(P =.009)、接受甲泼尼龙或静脉注射免疫球蛋白后(P =.02)以及随访1个月时(P =.003)均低于ITP患儿中aTA阴性者。最后,aTA阳性患儿复发更多(P =.03),在ND&P组中1年后更频繁持续复发(P =.02),在慢性ITP组中更频繁需要免疫抑制治疗(P =.005)。

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