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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04762472
Other study ID # 2020-398
Secondary ID
Status Not yet recruiting
Phase Phase 4
First received
Last updated
Start date September 2023
Est. completion date December 30, 2025

Study information

Verified date February 2023
Source Chinese University of Hong Kong
Contact Kam Sang Woo, MD, FACC
Phone 852-90230869
Email kamsangwoo@cuhk.edu.hk
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Background: Longterm exposure to air pollution has been associated with cardiovascular events and mortality on top of traditional risk factors. Pulmonary inflammation and oxidative stress have been implicated. Brachial (arm) vascular reactivity (flow-mediated dilation FMD) and carotid (neck) artery intima-media thickness (CIMT) are highly reproducible atherosclerosis surrogates, predictive of cardiovascular and stroke outcome. Montelukast is proven safe and effective in alleviating pulmonary inflammation and oxidative stress when used in prevention of asthma episode. Study objectives: 1. To test the hypothesis of pulmonary inflammation and oxidative stress-related vascular dysfunction in PM air pollution. 2. To evaluate the impact of Montelukast treatment as compared with placebo on predictive atherosclerosis surrogates (FMD and IMT). Design: Parallel placebo control, randomized comparative study. Subjects will be randomized to take Montelukast (10mg/daily) or image-matched placebo for 26 weeks. Measures will include PM2.5/PM10, indices of subclinical atherosclerosis (brachial FMD and CIMT), blood inflammatory biomarkers (platelet counts, hsCRP and fibrinogen) and potential confounders (lipids and glucose). Setting: 120 working adults aged 30-60 years in Hong Kong and 80 working adults in Chongqing (CREC Ref No: 2018.157, 2020.398) Main outcome measures: 1. Subclinical atherosclerosis: (a) Endothelial function (brachial FMD) and (b) carotid intima media thickness (CIMT). 2. PM2.5 & PM10 concentrations: real-time measurement by portable devices twice at home and work sites. 3. Blood inflammatory markers-platelet count, hsCRP and Fibrinogen 4. Potential confounders: we shall collect informations on a range of potential confounders, including other air pollutants and traditional risk factors of atherosclerosis, entrusted to be controlled (stable). Expected results: Adults after Montelukast treatment and exposed to high levels of PM2.5 or PM10 would have improved (increased) brachial FMD, and reduction of CIMT as compared with placebo. These will have great implication for comparative vascular epidemiology and development of preventive strategies.


Description:

2. Introduction Atherosclerosis related complications, in particular stroke and coronary artery disease, are the most important health issues in modernized societies, being the leading cause of death worldwide. In addition to traditional cardiovascular (CV) risk factors such as obesity, hypertension, dyslipidemia, diabetes mellitus, tobacco use and physical inactivity, particulate matter (PM) air pollution has been shown to be associated with cardiovascular morbidity and mortality in large epidemiological studies.[1-3] Long-term exposure to elevated PM levels can reduce life expectancy, especially particulate matter with an aerodynamic diameter <2.5um (PM2.5). Such PM has a causal relationship to cardiovascular morbidity and mortality.[1-4] An approximate 8-18% increase in cardiovascular mortality has been observed for every 10ug/m3 elevation in average PM2.5 exposure over the long term. [1. 3, 5] The biological mechanisms of atherogenic processes may involve direct effects of PM on cardiovascular system, and/or indirect effects mediated by oxidative stress and inflammation. [6-7] Far less research has been conducted so far on the contribution of PM to such long-term atherogenic processes in human populations. [1,2,8,9] We have previously studied 1656 Chinese adults in southern and northern China in 1996 to 2007 with PM2.5 concentration ranging from 34 to 94 ug/m3. PM2.5 were significantly related to prognostic atherosclerotic surrogates i.e. brachial flow-mediated dilatation (FMD) and carotid intima media thickness (IMT), independent of traditional-risk factors.[10] Our CATHAY study supports a hypothesis that PM2.5 air pollution is strongly correlated with early atherosclerotic process in modernizing China. Montelukast has been used successfully and proven safe for prevention of asthma episodes, supposed to be triggered by allergic-related inflammations of respiratory tract. Similar inflammatory process at lung and subsequently at blood vessels may be implicated in PM2.5-related accelerated atherosclerosis. [9] 3. Aims and Hypotheses to be Tested: PM2.5 air pollution has been proven accelerating atherosclerotic process in Hong Kong and mainland China (CATHAY study). To further test this initial hypothesis, this interventional substudy aims 1) To evaluate the impact of antiinflammatory agent Montelukast treatment on predictive atherosclerosis surrogates (FMD & IMT). 2) To evaluate the mechanism involved in PM2.5-related vascular dysfunction by monitoring changes in systemic inflammatory markers (platelet counts, HsCRP and fibrinogen). 4. Plan of Investigation 4.1 The impact of interventional agents on FMD and carotid IMT in working adults Subjects (120 adults in Hong Kong and 80 adults in Chongqing) Inclusion - asymptomatic adults - aged 30-60 years with - gender: male or female - concordance of home and workplace air pollution High exposure group: 60 adults, with PM2.5 concentration exposure >30ug/m3, both at residence and at work. Low exposure group: 60 sex and age-matched asymptomatic adults with PM2.5 exposure <30ug/m3 both at home and at work. Exclusion: - Those with family history of stroke, cardio-vascular disease - Hypertension with blood pressure >150/90 mmHg - Diabetes Mellitus - Overweight/ obesity (BMI >25kg/M2) - Cigarette smoking or ex-smoker <5 years - Known dyslipidemia defined as LDL-C >4.1mmol/l and triglyceride >3.0mmol/l. - Physical inactivity, with weekly leisure exercise less than 0.5 hour - Continuous usage of vitamins or herbal medicines in recent one year. Study design: A flowchart figure in Annex 1 illustrates the major procedures for the proposed study. Brachial flow-mediated dilation before and after Montelukast intervention will be compared between the control and intervention group. Methods After informed written consent, these participants (60 adults in Hong Kong, and 40 adults in Chongqing) will be randomized to take Montelukast 10mg/daily or image-matched placebo (60 adults in Hong Kong, and 40 adults in Chongqing) for 26 weeks. Week-0 Week-13 Week-26 Health Examination + 0 + Vascular Study + 0 + Blood Test + 0 + PM2.5 Evaluation + 0 + Medicine Dispatch + + 0 Compliance Assessment 0 + + - Collection of health data: 1. Questionnaire - All adult subjects will be interviewed and required to complete a detailed questionnaire regarding their individual and family history of cardiovascular diseases, hypertension, diabetes and current use of medications. Information on socio-economic status and lifestyle will be collected. Important factors associated with PM exposure, such as transportation between work and home, environmental tobacco use (ETS), duration of residence, home renovation, cooking/heating usage, and use of incense and mosquito coils will be recorded as well. 2. Health examination - Each participant will receive a health examination and their weight and height, blood pressures, body mass index (BMI) and wait-hip circumference ratio (WHR) will be measured when they are wearing light clothing and no shoes. 3. Blood test: 10ml of fasting blood will be taken for platelet, fasting glucose, low density cholesterol, hsC-reactive protein and fibrinogen. - Vascular Studies 1. Endothelial function, (flow mediated dilation, FMD) of the brachial artery will be studied by using high resolution ultrasound, as described previously. [11, 12] Using a linear array transducer (L10-5) with a median frequency of 7.5MHz and a standard Advanced Technology Laboratories 3000 or Sonosite systems, and forearm tourniquet cuff placement to induce reactive hyperemia on deflation. Scans will be acquired at rest, during reactive hyperemia (to induce flow-mediated endothelium-dependent dilation, FMD). FMD will be expressed as % of dilation from baseline vessel diameter normalized with vessel strain. 2. Carotid intima-media thickness (CIMT) measurement - B-mode ultrasound examinations will be performed using X12-3 probe with a 7 MHz scanning frequency linear array transducer. All carotid scans will be performed by standardized scanning protocol for the right and left carotid arteries as described by Salonen and Salonen [13] and Touboul et al [14], using images of the far wall of the distal 10 mm of the common carotid arteries, and a verified automatic edge-detecting and measurement software package as we described previously. [11-12, 15-16] The inter-observer variability of mean IMT is 0.003 to 0.011mm (CV 0.998%). - Collection of air pollution exposure data: Measurement of air pollutants at home and workplace will focus on PM2.5 and PM10. We shall measure PM2.5 and PM10 pollutant levels at homes and workplace twice (warm and cool seasons) by handy portable PM2.5 device. The micro-environment meteorological PM2.5 and PM10 data, at home and workplace, will be combined and compared with data using modeling techniques. Estimate of PM2.5/ PM10 exposure for each participant: Details of the methodology and its verification using PM2.5/ PM10 data from Hong Kong and China has already been published (17, 18). Change of residential address during follow-up will be taken into account. 5. Significance and Potential: The proposed study can serve as a baseline for cohort model study in near future, for comparison with other vascular epidemiological data and interventional strategies in mainland China. Investigating the relationship between particulate matter (PM) air pollution and atherosclerosis in working adulthood will enhance our abilities to elucidate the mechanisms underlying the effects of PM on atherosclerosis disease. Subsequently, it will help to develop appropriate strategies for both the control of PM air pollution (by legislation) and the prevention of atherosclerotic diseases, such as aerosol filters, facial masks, certain health food or nutrient (Aloe), statin or leukotriene modifiers (Montelukast) medicines. A huge number of Chinese exposed to PM air pollution throughout their life courses will be expected. 6. Compliance with Declaration of Helsinki The design, methodology and conduction of project are in compliance with Declaration of Helsinki. 7. Compliance will ICH-GCP. The medicines used are freely commercially available in Hong Kong Pharmacological Registry and compliant with ICH-GCP. 8. Data processing and analysis Power Calculation: The Proc Power in the STS 9.2 statistical packages (SAS institute Inc. Comy. NC, US) was used to calculate the sample size for FMD and carotid IMT. Data from our previous studies on adults in Hong Kong and mainland China, showed that the mean FMD is 6-8%+/-1.3% in otherwise healthy adults aged 30-60 years, and carotid IMT is 0.55-0.68mm+/-0.1mm. On the assumption of post Montelukast treatment, brachial FMD will improve to 6.7-8.7+/-1.4% in adults, and carotid IMT will reduce to 0.51-0.61mm+/-0.11mm, recruitment of 114 Chinese adults (57 in each group) will be adequately powered (80%) to detect a group difference in FMD of 1.2% and in CIMT of 0.1mm (12%) between the two treatment groups. In old adults, Kunzli reported a difference in CIMT of 12.1% in exposure of 20ug/m3 difference in PM2.5 pollution.[19] Data Analysis: Statistical Analysis System 9.2 will be used for all statistical analyses. The primary endpoints are brachial FMD and Carotid IMT, serological inflammatory biomarkers (Platelet hsCRP and Fibrinogen) are secondary endpoints. Students' T-tests will be used to detect group differences on FMD and CIMT. Multivariate linear and logistic regression will be used to calculate risk magnitude by Montelukast vs placebo, and to control for potential confounders such as various traditional cardiovascular risk factors.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 200
Est. completion date December 30, 2025
Est. primary completion date December 30, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 30 Years to 60 Years
Eligibility Inclusion Criteria: - asymptomatic Chinese adults - aged 30-60 years with - concordant ambient PM2.5 exposure, both at home and at workplace. Exclusion Criteria: - Those with family history of stroke, cardio-vascular disease - Hypertension with blood pressure >150/90 mmHg - Diabetics Mellitus - Overweight/ obesity (BMI >25kg/M2) - Cigarette smoking or ex-smoker <5 years - Known dyslipidemia defined as fasting LDL-C >4.1mmol/l and triglyceride >3.0 mmol/l. - Physical inactivity, with weekly leisure exercise less than 0.5 hour - Continuous usage of vitamins or herbal medicines in recent one year

Study Design


Intervention

Drug:
Montelukast Oral Tablet
i) Montelukast 10mg daily (tablet) orally x 26 weeks
Montelukast Placebo Oral Tablet
i) Placebo (Montelukast identical) tablet 1 daily orally x 26weeks

Locations

Country Name City State
Hong Kong The Chinese University of Hong Kong, Department of Medicine & Therapeutics Sha Tin

Sponsors (5)

Lead Sponsor Collaborator
Chinese University of Hong Kong Chongqing Medical University, Hong Kong University of Science and Technology, People's Hospital of Chongqing, University of Sydney

Country where clinical trial is conducted

Hong Kong, 

References & Publications (19)

[17] Lin CQ, Li Y, Yuan ZB, Lau AKH, Li, CC, and Fung JCH. Using satellite remote sensing data to estimate the high-resolution distribution of ground-level PM2.5. Remote Sens. Environ 2015;156:117-128.

[18] Lin CQ, Liu G, Lau AKH, Li Y, Li CC, Fung JCH, and Lao XQ. High-resolution satellite remote sensing of provincial PM2.5 trends in China from 2001 to 2015. Atmos. Environ 2018;180:110-116

Brook RD, Rajagopalan S, Pope CA 3rd, Brook JR, Bhatnagar A, Diez-Roux AV, Holguin F, Hong Y, Luepker RV, Mittleman MA, Peters A, Siscovick D, Smith SC Jr, Whitsel L, Kaufman JD; American Heart Association Council on Epidemiology and Prevention, Council o — View Citation

Franklin BA, Brook R, Arden Pope C 3rd. Air pollution and cardiovascular disease. Curr Probl Cardiol. 2015 May;40(5):207-38. doi: 10.1016/j.cpcardiol.2015.01.003. Epub 2015 Jan 3. — View Citation

Hajat A, Allison M, Diez-Roux AV, Jenny NS, Jorgensen NW, Szpiro AA, Vedal S, Kaufman JD. Long-term exposure to air pollution and markers of inflammation, coagulation, and endothelial activation: a repeat-measures analysis in the Multi-Ethnic Study of Ath — View Citation

Kunzli N, Jerrett M, Mack WJ, Beckerman B, LaBree L, Gilliland F, Thomas D, Peters J, Hodis HN. Ambient air pollution and atherosclerosis in Los Angeles. Environ Health Perspect. 2005 Feb;113(2):201-6. doi: 10.1289/ehp.7523. — View Citation

Kunzli N, Tager IB. Air pollution: from lung to heart. Swiss Med Wkly. 2005 Dec 10;135(47-48):697-702. doi: 10.4414/smw.2005.11025. — View Citation

Munzel T, Herzog J, Schmidt FP, Sorensen M. Environmental stressors and cardiovascular disease: the evidence is growing. Eur Heart J. 2017 Aug 1;38(29):2297-2299. doi: 10.1093/eurheartj/ehx306. No abstract available. — View Citation

Pope CA 3rd, Burnett RT, Thurston GD, Thun MJ, Calle EE, Krewski D, Godleski JJ. Cardiovascular mortality and long-term exposure to particulate air pollution: epidemiological evidence of general pathophysiological pathways of disease. Circulation. 2004 Ja — View Citation

Pun VC, Yu IT, Ho KF, Qiu H, Sun Z, Tian L. Differential effects of source-specific particulate matter on emergency hospitalizations for ischemic heart disease in Hong Kong. Environ Health Perspect. 2014 Apr;122(4):391-6. doi: 10.1289/ehp.1307213. Epub 20 — View Citation

Rajagopalan S, Al-Kindi SG, Brook RD. Air Pollution and Cardiovascular Disease: JACC State-of-the-Art Review. J Am Coll Cardiol. 2018 Oct 23;72(17):2054-2070. doi: 10.1016/j.jacc.2018.07.099. — View Citation

Salonen JT, Salonen R. Ultrasonographically assessed carotid morphology and the risk of coronary heart disease. Arterioscler Thromb. 1991 Sep-Oct;11(5):1245-9. doi: 10.1161/01.atv.11.5.1245. — View Citation

Thomas GN, Chook P, Qiao M, Huang XS, Leong HC, Celermajer DS, Woo KS. Deleterious impact of "high normal" glucose levels and other metabolic syndrome components on arterial endothelial function and intima-media thickness in apparently healthy Chinese sub — View Citation

Touboul PJ, Hennerici MG, Meairs S, Adams H, Amarenco P, Desvarieux M, Ebrahim S, Fatar M, Hernandez Hernandez R, Kownator S, Prati P, Rundek T, Taylor A, Bornstein N, Csiba L, Vicaut E, Woo KS, Zannad F; Advisory Board of the 3rd Watching the Risk Sympos — View Citation

Woo KS, Chook P, Hu YJ, Lao XQ, Lin CQ, Lee P, Kwok C, Wei AN, Guo DS, Yin YH, Lau K, Leung KS, Leung Y, Celermajer DS. The impact of particulate matter air pollution (PM2.5) on atherosclerosis in modernizing China: a report from the CATHAY study. Int J E — View Citation

Woo KS, Chook P, Raitakari OT, McQuillan B, Feng JZ, Celermajer DS. Westernization of Chinese adults and increased subclinical atherosclerosis. Arterioscler Thromb Vasc Biol. 1999 Oct;19(10):2487-93. doi: 10.1161/01.atv.19.10.2487. — View Citation

Woo KS, Chook P, Yu CW, Sung RY, Qiao M, Leung SS, Lam CW, Metreweli C, Celermajer DS. Effects of diet and exercise on obesity-related vascular dysfunction in children. Circulation. 2004 Apr 27;109(16):1981-6. doi: 10.1161/01.CIR.0000126599.47470.BE. Epub — View Citation

Woo KS, Robinson JT, Chook P, Adams MR, Yip G, Mai ZJ, Lam CW, Sorensen KE, Deanfield JE, Celermajer DS. Differences in the effect of cigarette smoking on endothelial function in chinese and white adults. Ann Intern Med. 1997 Sep 1;127(5):372-5. doi: 10.7 — View Citation

Yu ITS, hui Zhang Y, San Tam WW, Yan QH, Xu YJ, Xun XJ, Wu W, Ma WJ, Tian LW, Tse LA, Lao XQ. Effect of ambient air pollution on daily mortality rates in Guangzhou, China. Atmos Environ 2012;46:528-535.

* Note: There are 19 references in allClick here to view all references

Outcome

Type Measure Description Time frame Safety issue
Primary Brachial flow-mediated dilation (FMD) Changes in endothelial function (brachial FMD) in % At baseline and 26 weeks of interventional treatment
Primary Carotid intima media thickness (CIMT) Changes in carotid intima media thickness (CIMT) in mm At baseline and 26 weeks of interventional treatment
Secondary Changes of platelet count in k/uL Blood inflammatory markers At baseline and 26 weeks of interventional treatment
Secondary Changes of hsCRP in mg/ml Blood inflammatory markers At baseline and 26 weeks of interventional treatment
Secondary Changes of Fibrinogen in g/l Blood inflammatory markers At baseline and 26 weeks of interventional treatment
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