Cardiovascular Disease Biomarkers in Smokers and Moist Snuff Consumers

Cardiovascular Disease Clinical Trial

Official title:

Evaluation of Cardiovascular Disease Biomarkers in Exclusive Smokers and Exclusive Moist Snuff Consumers

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01692353
• Other study ID #: RJRT-CSD0806
• Status: Completed
• Phase: N/A
• First received: August 13, 2012
• Last updated: February 15, 2016
• Start date: September 2008
• Est. completion date: April 2009

Study information

• Verified date: February 2016
• Source: R.J. Reynolds Tobacco Company
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Observational

Clinical Trial Summary

This cross-sectional study was primarily a cardiovascular disease (CVD) study designed a) to compare selected CVD biomarker data between subjects who were long-term consumers of cigarettes or moist snuff and non-consumers of tobacco and b) to identify principal endpoints related to CVD risk that differed among the three tobacco-use cohorts. The following assessments provided the primary study endpoints for comparative analyses between the cohorts:

1. CVD-related physiological assessments: Flow-mediated dilation (FMD), carotid intima-media thickness (CIMT), ankle-brachial index (ABI), spirometry and expired carbon monoxide (ECO).

2. CVD-related biomarker assessments in blood and urine (biomarkers of tobacco effect).

3. Biomarkers of tobacco exposure in urine and blood.

Description:

This single site, observational study will provide an increased understanding of how consumption of different tobacco products (i.e., cigarettes and moist snuff compared to no tobacco use) affects 1) CVD-related physiological assessments and 2) CVD-related biomarkers of tobacco effect (i.e., proteins, lipids, and cellular components). A recent policy statement from the American Heart Association provides a review and analysis of the impact of smokeless (ST) use on cardiovascular disease (CVD) (Piano et al. 2010). The authors acknowledge that the evidence is consistent with the suggestion that the cardiovascular risks from ST products are markedly lower than those from cigarette smoking. Despite the potential risk reduction in transitioning from cigarettes to ST consumption, few studies have directly compared biomarkers of tobacco effect (BioEff) among smokers, moist snuff consumers (MSC) and non-tobacco consumers (NTC).

Furthermore, this study will measure biomarkers of tobacco exposure to assess their ability to differentiate the three tobacco consumer groups (smokers, moist snuff consumers, non-tobacco consumers) based on product use. Estimating exposures to combustion-related compounds found in tobacco smoke is best accomplished using biomarkers. A key advantage of human exposure biomarkers is that they are considered reliable metrics of the levels of exposure that consumers actually experience when using tobacco products (Hecht et al., 2010). Because combustion does not occur during ST use, ST products lack most of the combustion-related compounds found in tobacco smoke. Biomarker differences found between different tobacco use groups to harmful or potentially harmful constituents may indicate differences in subsequent health risks (Rodu and Godshall, 2006; Hatsukami et al., 2006).

Epidemiological data demonstrate that the health risks associated with cigarettes are significantly greater than those associated with the use of non-combustible tobacco and nicotine products (Surgeon General, 2010). On a relative risk continuum, cigarette smoking presents a significantly greater risk to tobacco users than use of non-combustible smokeless products. ST products, which are consumed orally, do no generate chemicals associated with the burning of tobacco, and thus, present a reduced toxicant profile compared to smoking.

To address the purpose and objectives of this study, the study was conducted as follows:

• Subjects were consented for the study prior to any procedures being performed and screened on study-specific inclusion/exclusion criteria to determine subject eligibility (within 28 days of study check-in).

• Eligible subjects were admitted to the clinical research unit between 12:00 noon and 5:00 p.m. on Day 1 and confined for one overnight stay (approximately 18-23 hours).

• After all study procedures were completed on Day 1 and Day 2, appropriate basic safety assessments were made and subjects were discharged approximately at 12:00 noon on Day 2.

A brief description of the study procedures performed is listed below.

• After check-in on Day 1, eligible subjects observed a 45-minute tobacco abstention period, followed by use of a single unit of their usual brand (UB) tobacco product, referred to as a "Challenge." For smokers, the "challenge" was smoking one UB cigarette in their usual manner; for moist snuff consumers, a 30-minute use of one typical pinch of their UB moist snuff.

• Fifteen minutes after the end of UB use, the following procedures were performed sequentially: ECO; blood samples for biomarkers of exposure (serum nicotine and cotinine, percent carboxyhemoglobin in whole blood); and ABI.

• At 30 minutes post-UB use, FMD was measured followed by administration of health-related questionnaires. The non-tobacco consumers had no product "Challenge". The completion of study questionnaires served as the reference point for collection of ECO, ABI and FMD.

• Blood biomarkers of tobacco exposure were collected on Day 1 following product "Challenge" and on Day 2 following an overnight tobacco abstention and fast.

• Urine biomarkers of tobacco exposure and effect were collected on both Day 1 post-"Challenge" and on Day 2 fasting.

• Blood biomarkers of tobacco effect were only collected on Day 2 fasting, followed by the re-assessment of the physiological measures (ECO, ABI, FMD) and assessment of CIMT.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 168
• Est. completion date: April 2009
• Est. primary completion date: February 2009
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 26 Years to 49 Years

Eligibility

Inclusion Criteria:

• Smokers: exclusive FF (full flavor; > 13.0 mg FTC "tar" ) or FFLT (full flavor, low "tar" [6.0 to 13.0 mg FTC "tar"]) smokers who reported smoking at least 15 cigarettes daily for at least three years prior to Day 1 and whose ECO was 10 to 100 ppm (ranges of 2 to 9 ppm and 101 to 125 ppm were allowed upon joint review by the Sponsor and Investigator).

• Moist Snuff Consumers: exclusive oral smokeless tobacco users of any brand (Copenhagen, Skoal, Grizzly, Kodiak, Timber Wolf, Longhorn, Red Man, Levi Garrett, Beech-Nut, Chattanooga Chew, Kayak, etc.), any style (snuff cut, long cut, fine cut, pouch, loose, or plug) and any flavor (natural, straight, mint, wintergreen, etc.) who reported using at least two cans or packages per week for at least three years prior to Day 1 and whose ECO was 0 to 5 ppm (a range of 6 to 10 ppm was allowed upon joint review by the Sponsor and Investigator).

• Non-tobacco Consumers: never-smokers/never-ST users whose ECO was 0 to 5 ppm (a range of 6 to 10 ppm was allowed upon joint review by the Sponsor and Investigator).

• Male, between 26 and 49 years of age, inclusive (on Day 1 check-in).

• Free of clinically significant health problems in the opinion of the Investigator.

• Forced expiratory volume exhaled in one second (FEV1) =70% of predicted at Screening.

• Willing to undergo all study procedures during confinement.

• Not taking medication on a daily basis for chronic medical disorders deemed clinically significant by the Investigator.

• Willing to suspend usage of daily aspirin or over-the-counter (OTC) medication seven days prior to Day 1.

• Not taking any creatine supplements.

• Negative tests for selected drugs of abuse and alcohol at Screening and at Day 1 check-in.

• Able to read and comprehend questionnaires in English.

• Able to comprehend and willing to sign an Informed Consent Form (ICF).

Exclusion Criteria:

• At Screening, a BP that exceeds 140/90.

• <70% predicted FEV1 from three acceptable maneuvers.

• Unwilling to have the FMD procedure performed two or more times during confinement.

• Unwilling to have the ABI procedure performed two times during confinement.

• For the FMD determination, poor brachial artery visualization due to extremely deep position or severe artifacts (noise) due to overlying muscle that, in the sonographer(s)' opinion, would result in an inferior, unreadable or unobtainable brachial artery image.

• A donation of blood from 30 days prior to Screening through Day 1, inclusive, or of plasma from two weeks prior to Screening through Day 1, inclusive.

• Receipt of blood products within two months prior to Day 1 check-in.

• Evidence of visible oral cancer, as found in an oral health examination at Screening or based on oral health questions at Day 1 check-in.

• Subject who is an employee of the clinical site.

• Subject who has participated in any other investigational study drug or product trial in which receipt of an investigational study drug or product occurred within 30 days prior to Day 1 check-in, inclusive.

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

• Cardiovascular Disease
• Cardiovascular Diseases
• Cigarette Smoking

Intervention

Other:
• Subject's usual brand (UB) tobacco product
For SMK: UB of cigarettes; For MSC: UB of moist snuff

Locations

Country	Name	City	State
United States	MDS Pharma Services (US), Inc. (Currently Celerion)	Lincoln	Nebraska

Sponsors (6)

Lead Sponsor	Collaborator
R.J. Reynolds Tobacco Company	Analytisch-biologisches Forschungslabor GmbH, BioClinica, Inc., MDS Pharma Services, Pacific Biomarkers, Rules-Based Medicine, Inc.

Country where clinical trial is conducted

United States, 

References & Publications (8)

Campbell LR, Brown BG, Jones BA, Marano KM, Borgerding MF. Study of cardiovascular disease biomarkers among tobacco consumers, part 1: biomarkers of exposure. Inhal Toxicol. 2015 Feb;27(3):149-56. doi: 10.3109/08958378.2015.1013228. Epub 2015 Mar 19. — View Citation

Centers for Disease Control and Prevention (US), National Center for Chronic Disease Prevention and Health Promotion (US), Office on Smoking and Health (US). How Tobacco Smoke Causes Disease: The Biology and Behavioral Basis for Smoking-Attributable Disease: A Report of the Surgeon General. Atlanta (GA): Centers for Disease Control and Prevention (US); 2010. — View Citation

Hatsukami DK, Benowitz NL, Rennard SI, Oncken C, Hecht SS. Biomarkers to assess the utility of potential reduced exposure tobacco products. Nicotine Tob Res. 2006 Aug;8(4):600-22. Review. — View Citation

Hecht SS, Yuan JM, Hatsukami D. Applying tobacco carcinogen and toxicant biomarkers in product regulation and cancer prevention. Chem Res Toxicol. 2010 Jun 21;23(6):1001-8. doi: 10.1021/tx100056m. — View Citation

Marano KM, Kathman SJ, Jones BA, Nordskog BK, Brown BG, Borgerding MF. Study of cardiovascular disease biomarkers among tobacco consumers. Part 3: evaluation and comparison with the US National Health and Nutrition Examination Survey. Inhal Toxicol. 2015 — View Citation

Nordskog BK, Brown BG, Marano KM, Campell LR, Jones BA, Borgerding MF. Study of cardiovascular disease biomarkers among tobacco consumers, part 2: biomarkers of biological effect. Inhal Toxicol. 2015 Feb;27(3):157-66. doi: 10.3109/08958378.2015.1013227. E — View Citation

Piano MR, Benowitz NL, Fitzgerald GA, Corbridge S, Heath J, Hahn E, Pechacek TF, Howard G; American Heart Association Council on Cardiovascular Nursing. Impact of smokeless tobacco products on cardiovascular disease: implications for policy, prevention, and treatment: a policy statement from the American Heart Association. Circulation. 2010 Oct 12;122(15):1520-44. doi: 10.1161/CIR.0b013e3181f432c3. Epub 2010 Sep 13. — View Citation

Rodu B, Godshall WT. Tobacco harm reduction: an alternative cessation strategy for inveterate smokers. Harm Reduct J. 2006 Dec 21;3:37. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Buccal cells	Determination of the feasibility and utility of using buccal cells to distinguish DNA methylation and gene expression differences (conducted as a post-hoc evaluation)	Day 2 (fasting)	No
Primary	Ankle-Brachial Index (ABI-C)	Non-invasive "functional" technique based on differential leg-arm blood pressure; aids in diagnosis of peripheral artery disease.; Comparison of ABI-C among the three cohorts.	Afternoon of Day 1, ~15 minutes after completion of a "tobacco product challenge"	No
Primary	Flow-mediated Dilation (FMD-C)	Non-invasive "functional" imaging technique to evaluate vascular tone of the brachial artery; indicator of individual's overall cardiovascular health.; Comparison of FMD-C among the three cohorts.	Afternoon of Day 1, ~30 minutes after completion of a "tobacco product challenge" and following ABI-C	No
Primary	Ankle-Brachial Index (ABI-F)	Non-invasive "functional" technique based on differential leg-arm blood pressure; aids in diagnosis of peripheral artery disease.; Comparison of ABI-F among the three cohorts.	Morning of Day 2 (fasting) measured immediately after vitals were obtained	No
Primary	Flow-mediated Dilation (FMD-F)	Non-invasive "functional" imaging technique to evaluate vascular tone of the brachial artery; indicator of individual's overall cardiovascular health.; Comparison of FMD-F among the three cohorts.	Morning of Day 2 (fasting) measured immediately after ABI was obtained	No
Primary	Carotid Intima-media Thickness (CIMT-F)	Non-invasive "morphological" imaging technique used to measure the thickness of the intima-media region of the carotid artery to detect presence/absence of atherosclerotic plaques.; Comparison of CIMT-F among the three cohorts.	Morning of Day 2 (fasting) immediately after FMD was obtained	No
Primary	Urine Biomarkers of Tobacco Effect (EffBio[U]-C)	Comparison of select CVD-related blood biomarkers among the three cohorts.	Afternoon of Day 1, ~15 minutes after completion of a "tobacco product challenge"	No
Primary	Urine Biomarkers of Tobacco Effect (EffBio[U]-F)	Comparison of select CVD-related urine biomarkers among the three cohorts.	Morning of Day 2 (fasting) from the first morning void collection	No
Primary	Blood Biomarkers of Tobacco Effect (EffBio[B]-F)	Comparison of select CVD-related urine biomarkers among the three cohorts.	Morning of Day 2 (fasting) after first morning void was obtained	No
Primary	Urine Biomarkers of Tobacco Exposure (ExpBio[U]-C)	Comparison of tobacco-specific and tobacco-related blood biomarkers among the three cohorts.	Afternoon of Day 1, ~15 minutes after completion of a "tobacco product challenge"	No
Primary	Blood Biomarkers of Tobacco Exposure (ExpBio[B]-C)	Comparison of tobacco-specific and tobacco-related blood biomarkers among the three cohorts.	Afternoon of Day 1, ~15 minutes after completion of a "tobacco product challenge" and following the urine collection	No
Primary	Urine Biomarkers of Tobacco Exposure (ExpBio[U]-F)	Comparison of tobacco-specific and tobacco-related blood biomarkers among the three cohorts.	Morning of Day 2 (fasting) from the first morning void collection	No
Primary	Blood Biomarkers of Tobacco Exposure (ExpBio[B]-F)	Comparison of tobacco-specific and tobacco-related blood biomarkers among the three cohorts.	Morning of Day 2 (fasting) after first morning void was obtained	No
Secondary	Health status scores from self-administered questionnaires on health, nicotine dependence and diet	Comparison of the self-reported health status measures between the three cohorts	All questionnaires: Administered once on evening of Day 1	No