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临床试验/NCT06833944
NCT06833944招募中不适用

Unraveling the Potential of Physical Activity in the Treatment of Familial Hypercholesterolemia: Impact of Exercise on Cardiorespiratory Fitness, Atherosclerosis Progression, and Underlying Mechanisms

Fundación Pública Andaluza para la Investigación Biomédica Andalucía Oriental1 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2025年2月20日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
75
试验地点
1
主要终点
Cardiorespiratory fitness

研究概览

简要总结

This study has one main objective:

a) To assess the impact of two different supervised exercise interventions on cardiorespiratory fitness and markers of subclinical atherosclerosis in patients with Familiar Hipercolesterolemia (FH), and to unravel the underlying mechanisms behind these effects.

The starting hypothesis of the UPPA-FH project anticipates that both exercise interventions will produce a large increase in cardiorespiratory fitness and will improve significant markers of atherosclerosis in patients with FH, with high-intensity interval training program (HIIT) being more efficient than the moderate-intensity continuous training (MICT) modality. The main effects will be mediated by a significant change in the metabolomic signature of the participants. In addition, higher physical activity will be associated with more favorable markers of atherosclerosis progression, as shown through blood and image technique

详细描述

Familial hypercholesterolemia (FH) is an inherited disorder characterized by high levels of LDL cholesterol and an increased risk of atherosclerosis and premature cardiovascular disease. From a clinical perspective, FH patients require lifelong management and monitoring of their cholesterol levels and may require multiple medications to control their cholesterol levels, leading to increased healthcare utilization and costs. From an economic perspective, the lifetime costs of managing FH can be significant and can include the cost of medications, diagnostic tests, and hospitalizations for cardiovascular events. In Spain, FH represents a heavy burden for the health care system, with direct costs of 37,299,000 €, indirect costs (due to loss of labor productivity) of 50,049,000 €, and an average of 25 years of life lost adjusted for labor productivity. From a public health perspective, FH affects around 25 million people worldwide that are at an increased risk of premature mortality, making FH a significant public health concern.

Hypercholesterolemia is one of the main vascular risk factors (VRF) related to the development of cardiovascular diseases (CVD), mainly myocardial infarction (MI) and stroke, the main causes of global mortality in the past decades. It is important to note that patients with FH present an increased prevalence of CVD at a very early age (44 years on average) and, in comparison to the general population, patients with FH have a 13.2 times higher risk of developing atherosclerotic CVD; specifically, up to 50% of men and 30% of women with FH will suffer an MI before the age of 60. Atherosclerosis is a complex process that involves endothelial dysfunction, inflammation, or oxidative stress. The presence of atherosclerosis can be assessed with positron emission tomography (PET), which has shown a high ability to predict the development of atherosclerotic plaque and cardiovascular events even after the consideration of classic VRF, so it is used as a method of early diagnosis of subclinical atherosclerosis in patients with chronic proinflammatory diseases. Therefore, the use of PET along with various plasma markers of inflammation in patients with FH (including C-reactive protein, [CRP], interleukin 10 [IL10], oxidized LDL [oxLDL], and the intracellular adhesion molecule 1 [ICAM1]), could allow the detection of atherosclerotic disease in the very early stages. Consequently, understanding novel markers that allow early identification of subclinical atherosclerosis, as well as strategies for reducing the VRF associated with FH, are key targets in these patients.

The treatment of hypercholesterolemia is primarily based on pharmacological therapies such as statins, ezetimibe, and monoclonal antibodies, which can decrease LDL cholesterol levels by up to 60%. However, the rate of achieving LDL cholesterol targets set by clinical practice guidelines is low (30-40%) due to poor tolerance to high doses of statins and other reasons. Importantly, new risk factors such as chronic vascular inflammation and oxidative stress are now considered in the etiology of atherosclerotic CVD beyond LDL cholesterol levels. Consequently, new treatment approaches are needed to address the treatment of FH as an important public health concern.

For all the above, unraveling the role of potential protective factors and interventions that might significantly improve the cardiometabolic profile and reduce the risk of morbi-mortality in this population, as well as the mechanisms involved, is of wide clinical and public health interest.

The UPPA-FH project will unravel the role of physical activity and different exercise interventions on critical health markers in men and women with FH and will study the mechanisms by which these effects are produced. For instance, whether the effects of exercise are mediated by changes in the metabolomic signature related to blood lipids will be explored. This will enable i) international institutions to develop clinical guidelines including exercise as a first-line treatment for the management of FH and ii) to unravel (for the first time) the potential mechanisms behind the effects of exercise in this population.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Individuals with a diagnosis of genetic FH.
  • •> 18 years old.
  • •Minimum follow-up of 1 year in the Vascular Risk Clinic of the Virgen de las Nieves University Hospital (HUVN).
  • •Clinical and treatment stability.
  • •Non-pathological angio-TAC of coronary arteries in the 2 years prior to the study (for participants >45 years old).

排除标准

  • •Inability to read, understand and sign the informed consent.
  • •Contraindications to exercise.
  • •History of clinical CVD (ischemic heart disease, stroke, and/or peripheral arterial disease).

研究组 & 干预措施

High Intensity Interval Training (HIIT) intervention program

Experimental

The HIIT protocol will involve 3 training sessions per week for 16 weeks (a total of 48 sessions lasting 36 minutes). The high-intensity intervals will follow the Norwegian 4 x 4-minute HIIT model: 4 bouts of 4 minutes of high intensity corresponding to a rating of perceived exertion (RPE) 15 to 18 on the Borg 6 to 20 Scale and an 85-95%HRmax, interspersed with 3-minute active recovery intervals (RPE of 11 to 13 and 54-69%HRmax).

干预措施: HIIT intervention program (Other)

Moderate Intensity Continous Training (MICT) intervention program

Experimental

The MICT protocol will involve 3 training sessions per week for 16 weeks (a total of 48 sessions lasting 44 minutes). The workout will be performed at RPE 11 to 13 (54-69%HRmax) to provide an isoenergetic workload (same energy expenditure) as the HIIT group

干预措施: MICT intervention program (Other)

Control group

No Intervention

The control group will follow a usual care regime during the intervention and will not participate in supervised exercise. However, the participants randomized to this group will be invited to participate in a similar intervention once the study is completed (waiting list control group).

结局指标

主要结局

Cardiorespiratory fitness

时间窗: Before and after the training intervention or control (16 weeks).

Cardiorespiratory fitness will be assessed using the Bruce Protocol Ramp, a variation of the widely used Bruce Protocol. The test will be performed on a treadmill, with speed and incline progressively increasing every 15 seconds until exhaustion. Because CRF is the primary study outcome, maximal oxygen uptake will be continuously measured using the Vyntus CPT.

次要结局

  • Low-Density Lipoprotein Cholesterol(Before and after the training intervention or control (16 weeks).)
  • High-Density Lipoprotein Cholesterol(Before and after the training intervention or control (16 weeks))
  • Apolipoprotein B(Before and after the training intervention or control (16 weeks).)
  • Lipoprotein(a)(Before and after the training intervention or control (16 weeks))
  • Carotid Doppler Ultrasound(Before and after the training intervention or control (16 weeks).)
  • Fat percentage(Before and after the training intervention or control (16 weeks).)
  • Visceral adipose tissue(Before and after the training intervention or control (16 weeks))
  • Lean tissue(Before and after the training intervention or control (16 weeks).)
  • Vascular inflammation(Before and after the training intervention or control (16 weeks).)
  • Arterial Stiffness(Before and after the training intervention or control (16 weeks).)
  • Ultrasensitive PCR(Before and after the training intervention or control (16 weeks).)
  • IL-6(Before and after the training intervention or control (16 weeks).)
  • Oxidized LDL(Before and after the training intervention or control (16 weeks).)
  • ICAM-1(Before and after the training intervention or control (16 weeks).)
  • Triglycerides(Before and after the training intervention or control (16 weeks).)
  • Fibrinogen(Before and after the training intervention or control (16 weeks).)
  • Lower body strength(Before and after the training intervention or control (16 weeks).)
  • Risk of suffering a cardiovascular event in 5 and 10 years(Before and after the training intervention or control (16 weeks).)

研究者

发起方
Fundación Pública Andaluza para la Investigación Biomédica Andalucía Oriental
申办方类型
Other
责任方
Principal Investigator
主要研究者

José Antonio Vargas Hitos

José A. Vargas-Hitos, MD, PhD

Fundación Pública Andaluza para la Investigación Biomédica Andalucía Oriental

研究点 (1)

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