Department of Pediatric Neurology, Emma Children's Hospital, Academic Medical Center, University of Amsterdam, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands.
Department of Pediatric Hematology, Emma Children's Hospital, Academic Medical Center, Amsterdam, The Netherlands.
J Inherit Metab Dis. 2018 Mar;41(2):249-255. doi: 10.1007/s10545-017-0113-8. Epub 2017 Nov 14.
Zellweger spectrum disorders (ZSDs) are caused by an impairment of peroxisome biogenesis, resulting in multiple metabolic abnormalities. This leads to a range of symptoms, including hepatic dysfunction and coagulopathy. This study evaluated the incidence and severity of coagulopathy and the effect of vitamin K supplementation orally and IV in ZSD.
Data were retrospectively retrieved from the medical records of 30 ZSD patients to study coagulopathy and the effect of vitamin K orally on proteins induced by vitamin K absence (PIVKA-II) levels. Five patients from the cohort with a prolonged prothrombin time, low factor VII, and elevated PIVKA-II levels received 10 mg of vitamin K IV. Laboratory results, including thrombin generation, at baseline and 72 h after vitamin K administration were examined.
In the retrospective cohort, four patients (13.3%) experienced intracranial bleedings and 14 (46.7%) reported minor bleeding. No thrombotic events occurred. PIVKA-II levels decreased 38% after start of vitamin K therapy orally. In the five patients with a coagulopathy, despite treatment with oral administration of vitamin K, vitamin K IV caused an additional decrease (23%) of PIVKA-II levels and increased thrombin generation.
Bleeding complications frequently occur in ZSD patients due to liver disease and vitamin K deficiency. Vitamin K deficiency is partly corrected by vitamin K supplementation orally, and vitamin K administered IV additionally improves vitamin K status, as shown by further decrease of PIVKA-II and improved thrombin generation.
Zellweger 谱障碍(ZSD)是由过氧化物酶体生物发生受损引起的,导致多种代谢异常。这导致一系列症状,包括肝功能障碍和凝血异常。本研究评估了 ZSD 患者凝血异常的发生率和严重程度,以及口服和静脉补充维生素 K 的效果。
从 30 名 ZSD 患者的病历中回顾性检索数据,以研究凝血异常以及口服维生素 K 对维生素 K 缺乏诱导蛋白(PIVKA-II)水平的影响。从队列中选择 5 名凝血酶原时间延长、VII 因子水平低和 PIVKA-II 水平升高的患者,给予 10mg 维生素 K IV。检查基线和维生素 K 给药后 72 小时的实验室结果,包括凝血酶生成。
在回顾性队列中,有 4 名患者(13.3%)发生颅内出血,14 名患者(46.7%)报告有轻微出血。无血栓事件发生。口服维生素 K 治疗开始后,PIVKA-II 水平下降了 38%。在 5 名有凝血异常的患者中,尽管口服给予维生素 K 治疗,但静脉给予维生素 K 导致 PIVKA-II 水平进一步下降(23%)和凝血酶生成增加。
由于肝脏疾病和维生素 K 缺乏,ZSD 患者经常发生出血并发症。口服补充维生素 K 部分纠正了维生素 K 缺乏,静脉给予维生素 K 进一步改善了维生素 K 状态,表现为 PIVKA-II 进一步下降和凝血酶生成改善。