The DOI matches its Crossref record; 21 of the 21 references it cites were found in a registry or an index.
Comparison of tests used to distinguish smokers from nonsmokers
Abstract
Questionnaire and biochemical measures of smoking were studied in 211 hospital outpatients. Eleven different tests of smoke intake were compared for their ability to categorize smokers and nonsmokers correctly. The concentration of cotinine, whether measured in plasma, saliva, or urine, was the best indicator of smoking, with sensitivity of 96-97 per cent and specificity of 99-100 per cent. Thiocyanate provided the poorest discrimination. Carbon monoxide measured as blood carboxyhaemoglobin or in expired air gave sensitivity and specificity of about 90 per cent. Sensitivities of the tests were little affected by the presence among the claimed nonsmokers of a group of 21 "deceivers" who concealed their smoking. It is concluded that cotinine is the measure of choice, but for most clinical applications carbon monoxide provides an acceptable degree of discrimination and is considerably cheaper and simpler to apply.
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“Cotinine is a reliable biomarker for nicotine levels (sensitivity of 96–97%, specificity of 99–100%)19”
From Maternal Smoking during Pregnancy and Newborn Neurobehavior: Effects at 10 to 27 Days (2009) · cites this paper as [19]
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InfluentialCotinine Validation of Self-Reported Smoking During Pregnancy in the Swedish Medical Birth Register
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“2,4,17 Yet these measures vary in availability, cost, and ease of administration.”
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“Current smoking exposure was validated by cotinine assay of infant urine and maternal saliva obtained at the time of lung function testing ( 18 ).”
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“The increased blood concentration of carbon monoxide in smokers results in a decreased oxygen-carrying capacity of hemoglobin and this likely represents a further insult to the intervertebral disc’s nutritional pathway [40,41].”
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“Others have used 9 ppm[22,26,37,44]; 8 ppm[19]; 7 ppm[28]; 6.”
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“However, both in clinical and community settings, there is concern about the validity of self-reported information to define exposure to SHS.(33-36) This is because of a substantial overlap in the cotinine levels between the self-reported SHS unexposed nonsmokers and SHS-exposed nonsmokers.”
BackgroundCigarette Smoking in HIV Infection Induces a Suppressive Inflammatory Environment in the Lung
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“Eighteen of the 38 subjects’ samples contained cotinine at levels greater than 14 ng/ml, which represents the cutoff level that discriminates between smoking and nonsmoking status (27).”
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“0 ng/mL was considered the borderline, separating smokers from non-smokers [27,28].”
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“As far as we could determine, first mention of nonsmokers having 10 ng/mL of serum cotinine was also by Jarvis et al.18 However, since serum cotinine reflects exposure to tobacco smoke from all sources including main stream and second hand smoke, Benowitz et al.21 proposed a serum cotinine cut off of 2.99 ng/mL for ad…”
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“Research indicates that 8 ppm is an optimal cutoff score for reliably discriminating status as a daily smoker (Jarvis et al., 1987).”
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“CO has lower specificity than cotinine but is easy to obtain, is generally accurate among moderate to heavy smokers, and provides an acceptable degree of discrimination between smokers and nonsmokers (Jarvis et al., 1987) except with light smokers.”
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“Maternal blood cotinine level below 15.0 ng/L was considered the borderline value separating smokers from non-smokers (Jarvis et al., 1987; Peacock et al., 1998).”
InfluentialCigarette smoking and glaucoma in the United States population
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“This assay has been used widely in previous studies (Jarvis et al. 1987, Smith et al. 1998).”
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“Based on the saliva cotinine levels, a cut-off of 15 ng/ml [41, 42] was taken as confirmation of abstinence from smokeless tobacco use.”
MethodAccuracy of self-reported smoking status among participants in a chemoprevention trial
Martı́nez, M. E., Reid, M. E., Jiang, R., Einspahr, J. G., & Alberts, D. S. (2004) · Preventive Medicine · doi:10.1016/j.ypmed.2003.12.006 · Cited by 54
Hung, J., Lin, C., Wang, J., & Chan, C. (2006) · Journal of the Formosan Medical Association · doi:10.1016/s0929-6646(09)60307-7 · Cited by 54
Urinary levels of nicotine & cotinine in tobacco users.
Behera, D., Uppal, R., & Majumdar, S. (2003) · PubMed · Cited by 53
Genetic and Environmental Factors in Age-Related Hearing Impairment
Momi, S. K., Wolber, L. E., Fabiane, S. M., MacGregor, A. J., & Williams, F. M. K. (2015) · Twin Research and Human Genetics · doi:10.1017/thg.2015.35 · Cited by 52
“eral days (up to 1 week) with high sensitivity (96–97%) and specificity (99–100%; Jarvis et al., 1987; Pojer et al., 1984).”
BackgroundBlann, A. D., Steele, C., & McCollum, C. N. (1997) · Thrombosis and Haemostasis · doi:10.1055/s-0038-1657692 · Cited by 53
The relationship between thought suppression and smoking cessation
Toll, B. A., Sobell, M. B., Wagner, E. F., & Sobell, L. C. (2001) · Addictive Behaviors · doi:10.1016/s0306-4603(00)00140-4 · Cited by 52
Shuter, J., Morales, D. A., Considine-Dunn, S. E., An, L. C., & Stanton, C. A. (2014) · JAIDS Journal of Acquired Immune Deficiency Syndromes · doi:10.1097/qai.0000000000000226 · Cited by 51
McLeish, A. C., Zvolensky, M. J., & Bucossi, M. M. (2007) · Journal of Anxiety Disorders · doi:10.1016/j.janxdis.2006.11.003 · Cited by 51
“Research indicates that 8 ppm is an optimal cutoff score for reliably discriminating smoking status (Jarvis et al., 1987).”
BackgroundMurray, R. L., Coleman, T. J., Antoniak, M. D., Stocks, J., Fergus, A., Britton, J. R., & Lewis, S. (2008) · Addiction · doi:10.1111/j.1360-0443.2008.02206.x · Cited by 51
Earla, R., Ande, A., McArthur, C. P., Kumar, A., & Kumar, S. (2013) · Drug Metabolism and Disposition · doi:10.1124/dmd.113.055186 · Cited by 51
“Generally, the plasma concentration of nicotine and its metabolites is much lower than that in urine (Jarvis et al., 1987).”
BackgroundStroud, L. R., Papandonatos, G. D., Salisbury, A. L., PHIPPS, M. G., Huestis, M. A., NIAURA, R. S., Padbury, J. F., Marsit, C. J., & Lester, B. M. (2016) · Child Development · doi:10.1111/cdev.12482 · Cited by 51
Al‐Saleh, I., Coşkun, S., Al-Doush, I., Al-Rajudi, T., Abduljabbar, M., Al-Rouqi, R., Palawan, H., & Hassan, S. S. M. (2018) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2018.12.261 · Cited by 50
Slawecki, C. J., & Ehlers, C. L. (2002) · Developmental Brain Research · doi:10.1016/s0165-3806(02)00455-8 · Cited by 51
The effect of stopping smoking on cervical Langerhans'cells and lymphocytes
Szarewski, A., Maddox, P., Royston, P. J., Jarvis, M. J., Anderson, M., Guillebaud, J., & Cuzick, J. M. (2001) · BJOG An International Journal of Obstetrics & Gynaecology · doi:10.1111/j.1471-0528.2001.00074.x · Cited by 51
Phillips, K. (1997) · Environment International · doi:10.1016/s0160-4120(97)00004-4 · Cited by 51
Evaluation of tobacco use cessation (TUC) counselling in the dental office.
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Smoking cessation interventions among individuals in methadone maintenance: A brief review
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Response of choroidal blood flow to carbogen breathing in smokers and non-smokers
Wimpissinger, B. (2004) · British Journal of Ophthalmology · doi:10.1136/bjo.2003.031773 · Cited by 50
“The results of the Fagerstrom Tolerance Questionnaire were 0 (0) points for the non-smoking group and 4.0 (0.6) points for the smoking group, indicating nicotine dependence among the smokers. Cotinine levels in urine were 45.1 (11.5) ng/ml in non-smokers and 2025.7 (336.1) ng/ml in smokers. This again clearly indicate…”
BackgroundInfluentialPatterns of tobacco use in the United Arab Emirates Healthy Future (UAEHFS) pilot study
Al‐Houqani, M., Leinberger‐Jabari, A., Alnaeemi, A., AlJunaibi, A., Zaabi, E. A. A., Oumeziane, N., Kazim, M., Al‐Maskari, F., Dhaheri, A. S. A., Wareth, L. A., et al. (2018) · PLoS ONE · doi:10.1371/journal.pone.0198119 · Cited by 50
Objectively Measured Secondhand Smoke Exposure and Mental Health in Children
Hamer, M., Ford, T. J., Stamatakis, E. A., Dockray, S., & Batty, G. D. (2010) · Archives of Pediatrics and Adolescent Medicine · doi:10.1001/archpediatrics.2010.243 · Cited by 49
“In all children, objective exposure to SHS was assessed using salivary cotinine level, which is a reliable and valid circulating biochemical marker of nicotine exposure.(12,13) A dental roll saturated with the child’s saliva was placed in a tube and later analyzed with a rapid liquid chromatography technique using a H…”
Methodde Weerd, S., Thomas, C. M. G., Kuster, J. E. T. G., Cikot, R. J. L. M., & Steegers, E. A. P. (2002) · Environmental Research · doi:10.1006/enrs.2002.4395 · Cited by 49
Metadata
- Authors
- Jarvis, M. J., Tunstall-Pedoe, H., Feyerabend, C., Vesey, C., & Saloojee, Y.
- Venue
- American Journal of Public Health
- Publisher
- American Public Health Association
- Published
- 1987-11
- Volume
- 77
- Issue
- 11
- Pages
- 1435-1438
- ISSN
- 0090-0036 (ISSN-L)
- 1541-0048
- OpenAlex
- W2147528426
- Cited by
- 994
- References
- 21
- Citations by year
- 2026: 9 · 2025: 12 · 2024: 14 · 2023: 14 · 2022: 27 · 2021: 22 · 2020: 25 · 2019: 29 · 2018: 37 · 2017: 35 · 2016: 32 · 2015: 37 · 2014: 34 · 2013: 44 · 2012: 40
- FWCI
- 11.10
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- American Journal of Public Health (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Smoking Behavior and Cessation
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Chronic Obstructive Pulmonary Disease (COPD) Research
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Prenatal Substance Exposure Effects
- Keywords
- smoking detection, cotinine, carbon monoxide, carboxyhemoglobin, thiocyanate, salivary biomarkers, urinary biomarkers, plasma biomarkers, questionnaire-based screening, sensitivity and specificity
- MeSH terms
- Carbon Monoxide, Chromatography, Gas, Cotinine, Evaluation Studies as Topic, Female, Humans, Male, Middle Aged, Nicotine, Pyrrolidinones, Surveys and Questionnaires, Saliva, Smoking, Thiocyanates
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