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新时代,新目标:囊性纤维化的心血管筛查与血脂管理

New era, new GOALs: cardiovascular screening and lipid management in cystic fibrosis.

作者信息

Despotes Katherine A, Ceppe Agathe S, Goralski Jennifer L, Donaldson Scott H

机构信息

Department of Pediatrics, School of Medicine, The University of North Carolina at Chapel Hill, 450 MacNider Building, Campus box #7217, 333 S. Columbia Street, Chapel Hill, NC 27599, USA.

Department of Medicine, School of Medicine, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27514-4309, USA.

出版信息

Ther Adv Respir Dis. 2025 Jan-Dec;19:17534666251317200. doi: 10.1177/17534666251317200.

Abstract

BACKGROUND

Cardiovascular disease (CVD) risks are increasing in people with cystic fibrosis (pwCF). While cholesterol levels were historically low in pwCF, higher levels after initiating highly effective modulator therapy (HEMT) have been reported. Mechanisms are unclear and there is little guidance on screening.

OBJECTIVES

To evaluate serum lipid changes at multiple timepoints after ivacaftor initiation, and to assess current screening practices for CVD risk factors among CF providers.

DESIGN

This was a post-hoc correlative analysis of prospectively collected clinical data and serum samples from the GOAL cohort study. Cross-sectional survey methodology was also employed.

METHODS

We evaluated serum lipids (total cholesterol (TC), low-density lipoprotein (LDL), and high-density lipoprotein (HDL)) at baseline, 3- and 18 months after ivacaftor initiation using samples from the GOAL study biorepository. We also surveyed CF providers across the United States on their CVD risk screening practices.

RESULTS

Fifty GOAL participants' samples were analyzed. Using the repeated measures model, TC significantly varied by visit ( = 0.004), driven by a significant increase from baseline at 3 months (mean difference 9.4 mg/dL). This difference diminished by 18 months. BMI was a significant covariate for TC. No significant differences by visit were detected in LDL or HDL. Seventy-five respondents participated in the survey (response rate 5.6%; 41 adult providers, 18 pediatric providers, and 10 providers caring for both) with 67% reporting no lipid screening policy existed in their center. In the past year, 29% of adult providers prescribed lipid-lowering therapy, 54% started anti-hypertensive medications, and 48% initiated ischemic cardiac evaluations for pwCF.

CONCLUSION

TC significantly increased within 3 months of initiating ivacaftor, but subsequently diminished toward baseline by 18 months. Lipid screening practices among CF providers were variable and providers are increasingly being confronted with managing CVD risk factors. Partnering with primary care providers is likely to become increasingly important in CF care models.

摘要

背景

囊性纤维化患者(pwCF)的心血管疾病(CVD)风险正在增加。虽然pwCF患者的胆固醇水平以往较低,但有报告称在开始高效调节剂治疗(HEMT)后胆固醇水平会升高。其机制尚不清楚,且关于筛查的指导意见很少。

目的

评估使用依伐卡托后多个时间点的血清脂质变化,并评估CF医疗服务提供者目前对CVD危险因素的筛查做法。

设计

这是一项对GOAL队列研究中前瞻性收集的临床数据和血清样本进行的事后相关性分析。还采用了横断面调查方法。

方法

我们使用GOAL研究生物样本库中的样本,在基线、使用依伐卡托后3个月和18个月时评估血清脂质(总胆固醇(TC)、低密度脂蛋白(LDL)和高密度脂蛋白(HDL))。我们还对美国各地的CF医疗服务提供者进行了关于他们CVD风险筛查做法的调查。

结果

分析了50名GOAL参与者的样本。使用重复测量模型,TC随就诊时间有显著变化(P = 0.004),这是由3个月时相对于基线的显著升高(平均差异9.4mg/dL)驱动的。这种差异在18个月时减小。BMI是TC的一个显著协变量。在LDL或HDL方面,未检测到随就诊时间的显著差异。75名受访者参与了调查(回复率5.6%;41名成人医疗服务提供者,18名儿科医疗服务提供者,10名同时照顾成人和儿童的医疗服务提供者),67%报告其所在中心没有脂质筛查政策。在过去一年中,29%的成人医疗服务提供者开具了降脂治疗药物,54%开始使用抗高血压药物,48%对pwCF患者进行了缺血性心脏评估。

结论

开始使用依伐卡托后3个月内TC显著升高,但随后在18个月时降至基线水平。CF医疗服务提供者的脂质筛查做法各不相同,且医疗服务提供者在管理CVD危险因素方面面临的情况越来越多。在CF护理模式中,与初级保健提供者合作可能会变得越来越重要。

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