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本文引用的文献

1
Janus kinase inhibitors for alopecia areata.治疗斑秃的 Janus 激酶抑制剂。
J Am Acad Dermatol. 2023 Aug;89(2S):S29-S32. doi: 10.1016/j.jaad.2023.05.049.
2
The evaluation of JAK inhibitors on effect and safety in alopecia areata: a systematic review and meta-analysis of 2018 patients.JAK 抑制剂治疗斑秃的疗效和安全性评价:2018 例患者的系统评价和荟萃分析。
Front Immunol. 2023 Jun 2;14:1195858. doi: 10.3389/fimmu.2023.1195858. eCollection 2023.
3
A Review on the Safety of Using JAK Inhibitors in Dermatology: Clinical and Laboratory Monitoring.JAK抑制剂在皮肤病学中应用的安全性综述:临床与实验室监测
Dermatol Ther (Heidelb). 2023 Mar;13(3):729-749. doi: 10.1007/s13555-023-00892-5. Epub 2023 Feb 15.
4
The safety of JAK-1 inhibitors.JAK-1 抑制剂的安全性。
Rheumatology (Oxford). 2021 May 5;60(Suppl 2):ii24-ii30. doi: 10.1093/rheumatology/keaa895.
5
JAK Inhibitors: What Is New?JAK 抑制剂:有何新进展?
Curr Rheumatol Rep. 2020 Jul 22;22(9):50. doi: 10.1007/s11926-020-00931-6.
6
Alopecia areata.斑秃。
Nat Rev Dis Primers. 2017 Mar 16;3:17011. doi: 10.1038/nrdp.2017.11.
7
Epidemiology and burden of alopecia areata: a systematic review.斑秃的流行病学与负担:一项系统综述
Clin Cosmet Investig Dermatol. 2015 Jul 24;8:397-403. doi: 10.2147/CCID.S53985. eCollection 2015.
8
Reversal of Alopecia Areata Following Treatment With the JAK1/2 Inhibitor Baricitinib.斑秃经 JAK1/2 抑制剂巴瑞替尼治疗后逆转。
EBioMedicine. 2015 Feb 26;2(4):351-5. doi: 10.1016/j.ebiom.2015.02.015. eCollection 2015 Apr.
9
Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci.斑秃的全基因组荟萃分析确定了 HLA 关联并揭示了两个新的易感基因座。
Nat Commun. 2015 Jan 22;6:5966. doi: 10.1038/ncomms6966.
10
Killing two birds with one stone: oral tofacitinib reverses alopecia universalis in a patient with plaque psoriasis.一石二鸟:口服托法替布使一名斑块状银屑病患者的全秃症得到逆转。
J Invest Dermatol. 2014 Dec;134(12):2988-2990. doi: 10.1038/jid.2014.260. Epub 2014 Jun 18.

斑秃患者对 Janus 激酶抑制剂实验室监测指南的依从性现状

The Current State of Patient Adherence to Lab Monitoring Guidelines for Janus Kinase Inhibitors in Patients with Alopecia Areata.

作者信息

Shanmugam Sujeeth Krishna, Palmer Victoria, McMichael Amy

机构信息

All authors are with the Department of Dermatology at the Wake Forest University School of Medicine in Winston-Salem, North Carolina.

出版信息

J Clin Aesthet Dermatol. 2025 Jun;18(6):26-28.

PMID:40575602
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12189223/
Abstract

BACKGROUND

While Janus kinase inhibitors (JAKi) show excellent outcomes in Phase2b/3 trials for alopecia areata (AA), they do have potential side effects due to their immunosuppressive nature and other effects on the JAK-STAT pathway. These side effects can be mitigated by adherence to lab monitoring.

OBJECTIVE

The authors sought to analyze patients, using JAKi, to manage symptoms of AA, to determine frequency of lab monitoring and check for adherence to the recommended rate of every three months.

METHODS

A retrospective chart review was conducted by first identifying all patients diagnosed with AA at a specialty hair clinic in an academic dermatology department between January 2021 and May 2024. Each patient chart was reviewed for past and current use of any known oral JAKi. Fifty-seven patients were identified to meet our inclusion criteria and all of their charts were reviewed. The primary outcome is the average time between lab monitoring dates for each patient. The hypothesis was formulated after the data collection in the form of whether patients were being adherent to lab monitoring protocol.

RESULTS

Most patients were non-adherent to the lab testing frequency standard. Significant differences were found in blood test times between adherent and non-adherent patients and between non-adherent and extremely non-adherent patients with -values less than 0.01 for both sets.

CONCLUSION

Patients with AA undergoing JAKi treatment are not adhering to the recommended lab monitoring frequency. New tactics to improve adherence need to be taken.

摘要

背景

虽然 Janus 激酶抑制剂(JAKi)在斑秃(AA)的 2b/3 期试验中显示出优异的疗效,但由于其免疫抑制特性以及对 JAK-STAT 通路的其他影响,它们确实存在潜在的副作用。通过坚持实验室监测可以减轻这些副作用。

目的

作者试图分析使用 JAKi 治疗 AA 症状的患者,以确定实验室监测的频率,并检查是否遵守每三个月一次的推荐频率。

方法

通过首先识别 2021 年 1 月至 2024 年 5 月期间在一所学术皮肤科的专科毛发诊所被诊断为 AA 的所有患者,进行回顾性病历审查。审查每个患者的病历,了解过去和当前使用任何已知口服 JAKi 的情况。确定 57 名患者符合纳入标准,并对他们所有的病历进行了审查。主要结果是每个患者两次实验室监测日期之间的平均时间。在数据收集之后,以患者是否遵守实验室监测方案的形式提出假设。

结果

大多数患者未遵守实验室检测频率标准。在坚持和不坚持的患者之间以及不坚持和极度不坚持的患者之间,血液检测时间存在显著差异,两组的 P 值均小于 0.01。

结论

接受 JAKi 治疗的 AA 患者未遵守推荐的实验室监测频率。需要采取新的策略来提高依从性。