使用光学相干断层血管造影术评估长期服用羟氯喹患者的早期视网膜变化。

IF 3.4 3区 医学 Q2 PHARMACOLOGY & PHARMACY Therapeutic Advances in Drug Safety Pub Date : 2024-01-27 eCollection Date: 2024-01-01 DOI:10.1177/20420986231225851
Huanhuan Zhao, Menglu Pan, Yaping Liu, Fangyue Cheng, Zongwen Shuai
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引用次数: 0

摘要

背景:结缔组织疾病(CTD),包括系统性红斑狼疮和类风湿性关节炎(RA),长期以来一直使用羟氯喹(HCQ)治疗。然而,长期使用 HCQ 会带来不良反应的风险,尤其是视网膜病变:通过光学相干断层血管造影术(OCTA)检测长期接受HCQ治疗的CTD患者视网膜的早期变化,并探讨OCTA参数与HCQ及其代谢物浓度之间的关系:设计:2020年3月至2021年10月在安徽医科大学第一附属医院进行的横断面研究:方法:对43例接受HCQ治疗6个月以上的CTD患者进行OCTA检查,测量黄斑部眼窝无血管区(FAZ)的面积和周长、眼窝和眼窝旁的厚度、浅层毛细血管丛(SCP)和深层毛细血管丛(DCP)的血管密度。同时,采用高效液相色谱-串联质谱法测定了血液中HCQ及其代谢物的浓度,并收集了所有43名患者的临床资料:结果:OCTA结果与患者的年龄、病程和体重依赖性剂量无明显相关性。HCQ累积持续时间与FAZ面积和周长呈正相关(分别为r = 0.419,p = 0.005和r = 0.407,p = 0.007),与DCP的眼窝血管密度呈负相关(r = -0.378,p = 0.012)。HCQ 累积剂量与 FAZ 面积和周长呈正相关(分别为 r = 0.445,p = 0.003 和 r = 0.434,p = 0.004),与 SCP 和 DCP 的眼窝血管密度呈负相关(分别为 r = -0.383,p = 0.011 和 r = -0.424,p = 0.005)。结论:OCTA结果与HCQ及其代谢物浓度无关:结论:OCTA 可用于检测长期接受 HCQ 治疗的 CTD 患者黄斑部微血管的变化。结论:OCTA可用于检测长期接受HCQ治疗的CTD患者黄斑部微血管的变化,但未发现HCQ及其代谢物的浓度与视网膜血管变化有关。
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Evaluation of early retinal changes in patients on long-term hydroxychloroquine using optical coherence tomography angiography.

Background: Connective tissue diseases (CTD), including systemic lupus erythematosus and rheumatoid arthritis (RA), have long been treated with hydroxychloroquine (HCQ). However, prolonged HCQ use poses a risk of adverse effects, particularly retinopathy.

Objective: To detect early retinal changes assessed by optical coherence tomography angiography (OCTA) in CTD patients with long-term HCQ treatment and to explore the relationship between OCTA parameters and the concentrations of HCQ and its metabolites.

Design: A cross-sectional study conducted from March 2020 to October 2021 at the First Affiliated Hospital of Anhui Medical University.

Methods: The area and perimeter of the foveal avascular zone (FAZ), the thickness of the fovea and parafovea, and the vascular density of the superficial capillary plexus (SCP) and deep capillary plexus (DCP) in each area of the macula were measured by OCTA in 43 CTD patients treated with HCQ for over 6 months. Meantime, blood concentrations of HCQ and its metabolites were determined by high-performance liquid chromatography-tandem mass spectrometry, and the clinical documents of all 43 involved patients were collected.

Results: There is no significant correlation between OCTA outcomes and the patient's age, disease duration, and weight-dependent dose. HCQ cumulative duration positively correlated with FAZ area and perimeter (r = 0.419, p = 0.005 and r = 0.407, p = 0.007, respectively) and negatively correlated with the foveal vessel density in DCP (r = -0.378, p = 0.012). HCQ cumulative dose had a positive correlation with FAZ area and perimeter (r = 0.445, p = 0.003 and r = 0.434, p = 0.004, respectively) and had a negative correlation with foveal vessel density in SCP and DCP (r = -0.383, p = 0.011 and r = -0.424, p = 0.005, respectively). OCTA outcomes did not correlate with HCQ and its metabolite concentrations.

Conclusion: OCTA could be used to detect microvascular changes in the macula of CTD patients with long-term HCQ therapy. It was not found the concentrations of HCQ and its metabolites were associated with retinal vascular changes.

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来源期刊
Therapeutic Advances in Drug Safety
Therapeutic Advances in Drug Safety Medicine-Pharmacology (medical)
CiteScore
6.70
自引率
4.50%
发文量
31
审稿时长
9 weeks
期刊介绍: Therapeutic Advances in Drug Safety delivers the highest quality peer-reviewed articles, reviews, and scholarly comment on pioneering efforts and innovative studies pertaining to the safe use of drugs in patients. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in drug safety, providing a forum in print and online for publishing the highest quality articles in this area. The editors welcome articles of current interest on research across all areas of drug safety, including therapeutic drug monitoring, pharmacoepidemiology, adverse drug reactions, drug interactions, pharmacokinetics, pharmacovigilance, medication/prescribing errors, risk management, ethics and regulation.
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