Effect of iron supplementation on platelet count in adult patients with iron deficiency anemia.

IF 2.5 3区 医学 Q3 CELL BIOLOGY
Platelets Pub Date : 2022-11-17 Epub Date: 2022-09-01 DOI:10.1080/09537104.2022.2091772
Xue Li, Nanyi Li, Guangjie Zhao, Xiaoqin Wang
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引用次数: 2

Abstract

Iron deficiency anemia (IDA) affects more than 1.2 billion individuals globally. In addition to anemia, reactive thrombocytosis is also a common clinical hematological condition in patients with IDA. However, some case reports have described the thrombotic complications in association with IDA-induced thrombocytosis. Patients with a high risk of thrombosis need prompt identification and effective treatment to prevent thrombotic complications. While iron replacement treatment has been shown to decrease platelet count in this context, there is limited published evidence on how iron supplementation affects the thrombocytosis caused by IDA. We retrospectively examined the clinical records of 440 patients with IDA from an RCT completed from 1 January 2016, to 30 December 2017, and data obtained from this study was used for post hoc analysis to examine the effect of iron on platelet count in IDA-induced thrombocytosis.The mean ± standard deviation (SD) platelet counts of the 440 patients with IDA was 310.23 ± 98.72 × 109/L. With baseline platelet counts>450 × 109 /L as the cutoff for thrombocytosis, patients were divided into 2 groups: 36 (8.1%) in the IDA with thrombocytosis group (mean ± SD platelet count, 521.67 ± 73.85 × 109/L) and the remaining 404 in the IDA without thrombocytosis group (mean ± SD platelet count, 291.39 ± 76.11 × 109/L).Differences were found in baseline characteristics including white blood cell (WBC) count, hemoglobin (Hb) level, mean corpuscular volume (MCV), transferrin saturation (TSAT), serum iron (SI) level, and total iron-binding capacity (TIBC) between the two groups (P < .05). From baseline to 8 weeks of continuous iron supplementation treatment, the mean platelet counts in both groups were decreased at 2-week treatment intervals. And in the IDA with thrombocytosis group, half of the patients resolved thrombocytosis after 2 weeks of iron supplementation, and the counts of all patients with thrombocytosis decreased below 450 × 109 /L within 6 weeks.In conclusion, the rate of reactive thrombocytosis in patients with IDA was 8.1%. IDA patients with thrombocytosis showed more severe anemia, lower ferritin, and more advanced iron deficiency than those without thrombocytosis. Platelet counts of half of the patients with thrombocytosis reduced below cut off of 450 × 109/L for thrombocytosis after 2 weeks of treatment, and all patients resolved thrombocytosis after 6 weeks. Our study provided clinical evidence for more effective and individualized iron management in the future. IDA patients with thrombocytosis should take active iron treatment and increase follow-up frequency to prevent thrombotic events. For patients with persistent thrombocytosis, a concomitant clonal process should be considered.

补铁对成年缺铁性贫血患者血小板计数的影响。
缺铁性贫血(IDA)影响全球超过12亿人。除了贫血,反应性血小板增多也是IDA患者常见的临床血液学症状。然而,一些病例报告描述了与ida诱导的血小板增多症相关的血栓性并发症。血栓形成的高风险患者需要及时识别和有效治疗,以防止血栓并发症。虽然在这种情况下,铁替代治疗已被证明可以减少血小板计数,但关于铁补充如何影响IDA引起的血小板增多的已发表证据有限。我们从2016年1月1日至2017年12月30日完成的一项随机对照试验中回顾性检查了440例IDA患者的临床记录,并将该研究获得的数据用于事后分析,以检查铁对IDA诱导的血小板增多症血小板计数的影响。440例IDA患者的平均±标准差(SD)血小板计数为310.23±98.72 × 109/L。以基线血小板计数>450 × 109/L作为血小板增多的临界值,将患者分为两组:有血小板增多组36例(8.1%)(平均±SD血小板计数,521.67±73.85 × 109/L),无血小板增多组404例(平均±SD血小板计数,291.39±76.11 × 109/L)。6周内,两组患者在白细胞(WBC)计数、血红蛋白(Hb)水平、平均红细胞体积(MCV)、转铁蛋白饱和度(TSAT)、血清铁(SI)水平和总铁结合能力(TIBC)等基线特征上存在差异(p9 /L)。总之,IDA患者的反应性血小板增多率为8.1%。有血小板增多的IDA患者比没有血小板增多的患者表现出更严重的贫血、更低的铁蛋白和更严重的缺铁。半数血小板增多患者在治疗2周后血小板计数降至450 × 109/L以下,6周后血小板增多均消失。我们的研究为将来更有效和个性化的铁管理提供了临床依据。IDA伴血小板增多的患者应积极接受铁治疗,并增加随访频率以预防血栓事件。对于持续性血小板增多的患者,应考虑伴随的克隆过程。
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来源期刊
Platelets
Platelets 医学-细胞生物学
CiteScore
6.70
自引率
3.00%
发文量
79
审稿时长
1 months
期刊介绍: Platelets is an international, peer-reviewed journal covering all aspects of platelet- and megakaryocyte-related research. Platelets provides the opportunity for contributors and readers across scientific disciplines to engage with new information about blood platelets. The journal’s Methods section aims to improve standardization between laboratories and to help researchers replicate difficult methods. Research areas include: Platelet function Biochemistry Signal transduction Pharmacology and therapeutics Interaction with other cells in the blood vessel wall The contribution of platelets and platelet-derived products to health and disease The journal publishes original articles, fast-track articles, review articles, systematic reviews, methods papers, short communications, case reports, opinion articles, commentaries, gene of the issue, and letters to the editor. Platelets operates a single-blind peer review policy. Authors can choose to publish gold open access in this journal.
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