PRESS RELEASE
01 JULY 2021
New research published today in the journal, Internal and Emergency Medicine, provides the first real-world evidence that people switching from cigarettes to exclusive use of glo, BAT’s flagship Tobacco Heating Product (THP), can significantly reduce their exposure to certain toxicants and indicators of potential harm related to several smoking-related diseases compared with continuing to smoke.
The results, recorded at 6-months of a 12-month study, showed that switching completely to glo resulted in statistically significant changes across a range of “biomarkers of exposure” (BoE)**, and indicators of potential harm, known as “biomarkers of potential harm” (BoPH)**, compared with continuing to smoke.
For most biomarkers measured, the reductions seen in people using glo were similar to those in participants who stopped smoking completely.
Based on the toxicants measured, glo users showed a:
Dr David O’Reilly, BAT’s Director of Scientific Research said: “These are exciting results as they allow us to understand the potential for reduction of risk that switching completely to glo can deliver. The study shows that smokers switching to glo can reduce their exposure to certain toxicants, which reduces their risk of developing certain smoking related diseases.* To have shown a significant reduction in measures of BOPH, some comparable to quitting completely, is very encouraging and provides further scientific substantiation of the harm reduction potential of glo and how it supports our ambition to build A Better Tomorrow by reducing the health impact of our business.”
Participants in this year-long randomised controlled study were UK-based smokers aged 23 to 55 in good general health who either did or did not want to quit. The smokers who did not intend to quit were randomised to either continue smoking cigarettes or switched to using only glo, while smokers who indicated they wanted to quit smoking received nicotine replacement therapy and access to a cessation counsellor. A group of “never smokers” was also included to act as a control group and continued not to use any tobacco or nicotine products.
This study was designed to explore the risk reduction potential of glo when used in a real world setting rather than in a controlled setting. The only intervention was a monthly clinic visit where samples of blood, urine and other measurements were taken. These samples were tested for “biomarkers of exposure” (to selected cigarette smoke toxicants) and “biomarkers of potential harm”. In addition, to ensure compliance, the glo and cessation groups were tested for the biomarker, CEVal, which indicated if they had recently smoked cigarettes.
Further results from the completed study are due by the end of 2021 and will determine whether the reduced exposure to toxicants and biomarkers of potential harm are maintained over the duration of the study.
* Based on the weight of evidence and assuming a complete switch from cigarette smoking. These products are not risk free and are addictive.
**
Biomarker of Exposure | Associated toxicant | Carcinogen | Respiratory Toxicant | CV Toxicant | Reproductive Toxicant |
---|---|---|---|---|---|
NNN | NNN | Y | |||
1-OHP | Pyrene | Y | |||
NNAL | NNK | Y | |||
o-Tol | o-toluidine | Y | |||
3-HPMA | Acrolein | Y | Y | ||
HMPMA | Crotonaldehyde | Y | |||
4-ABP | 4-aminobiphenyl | Y | |||
eCO | Carbon monoxide | Y | |||
HEMA | Ethylene oxide | Y | Y | Y | |
2-AN | 2-aminonaphthalene | Y | |||
MHBMA | 1,3-butadiene | Y | Y | Y | |
S-PMA | Benzene | Y | Y | Y | |
CEMA | Acrylonitrile | Y | Y | |
Biomarker of Potential Harm | Indicator | Association |
---|---|---|
HDL | Lipid metabolism | CVD |
WBC | General inflammation | CVD, COPD, cancers |
FEV1 | Lung health | Respiratory disease |
FeNO | Bronchodilation/vascular tone | Respiratory disease, CVD |
sICAM | Endothelial dysfunction | CVD |
11-dTx B2 | Platelet activation/coagulation | CVD |
8-epi-PGF2a | Oxidative stress | CVD, COPD, cancers |
NNAL | NNK exposure | Lung cancer |
i US Institute of Medicine: Scientific Standards for Studies on Modified Risk Tobacco Products 2012.
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