Toxicological bases for the setting of health-related air pollution standards
The development of air pollution standards ideally involves the integration of data from the disciplines of epidemiology, controlled clinical studies, and animal toxicology. Epidemiological studies show statistical associations between health outcomes and exposure; they cannot establish a definite c...
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Veröffentlicht in: | Annual review of public health 2000, Vol.21 (1), p.309-333 |
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description | The development of air pollution standards ideally involves the integration of data from the disciplines of epidemiology, controlled clinical studies, and animal toxicology. Epidemiological studies show statistical associations between health outcomes and exposure; they cannot establish a definite cause-effect relationship. The utility of toxicological studies is to establish this relationship. Recently, there was simultaneous promulgation of a new National Ambient Air Quality Standard (NAAQS) for particulate matter < 2.5 microns in aerodynamic diameter (PM2.5) and a revised NAAQS for ozone (O3). The O3 NAAQS was based, in part, on a sound foundation of toxicological data from controlled exposure studies in humans and animals. It also relied on epidemiological studies of hospital admissions for respiratory diseases. Such studies also served as important bases for the new PM2.5 NAAQS. However, the most influential bases for the PM NAAQS were the numerous and generally consistent epidemiological studies that associated exposure with premature mortality in susceptible subpopulations and the inability of numerous hypothesized confounding factors to negate the associations. Using ozone and PM as examples, this paper discusses the scientific basis for NAAQS promulgations in situations in which the underlying database differed greatly in the extent of toxicological support. |
doi_str_mv | 10.1146/annurev.publhealth.21.1.309 |
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However, the most influential bases for the PM NAAQS were the numerous and generally consistent epidemiological studies that associated exposure with premature mortality in susceptible subpopulations and the inability of numerous hypothesized confounding factors to negate the associations. 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Epidemiological studies show statistical associations between health outcomes and exposure; they cannot establish a definite cause-effect relationship. The utility of toxicological studies is to establish this relationship. Recently, there was simultaneous promulgation of a new National Ambient Air Quality Standard (NAAQS) for particulate matter < 2.5 microns in aerodynamic diameter (PM2.5) and a revised NAAQS for ozone (O3). The O3 NAAQS was based, in part, on a sound foundation of toxicological data from controlled exposure studies in humans and animals. It also relied on epidemiological studies of hospital admissions for respiratory diseases. Such studies also served as important bases for the new PM2.5 NAAQS. However, the most influential bases for the PM NAAQS were the numerous and generally consistent epidemiological studies that associated exposure with premature mortality in susceptible subpopulations and the inability of numerous hypothesized confounding factors to negate the associations. Using ozone and PM as examples, this paper discusses the scientific basis for NAAQS promulgations in situations in which the underlying database differed greatly in the extent of toxicological support.</description><subject>Air Pollutants - adverse effects</subject><subject>Air Pollutants - analysis</subject><subject>Air pollution</subject><subject>Air Pollution - prevention & control</subject><subject>Air quality</subject><subject>Air quality standards</subject><subject>Asthma - epidemiology</subject><subject>Asthma - etiology</subject><subject>Cause-effect relationships</subject><subject>Confounding Factors (Epidemiology)</subject><subject>Data Interpretation, Statistical</subject><subject>Environmental Health - standards</subject><subject>Epidemiologic Studies</subject><subject>Epidemiology</subject><subject>Guidelines as Topic</subject><subject>Health Status</subject><subject>Humans</subject><subject>Maximum Allowable Concentration</subject><subject>Morbidity</subject><subject>Mortality</subject><subject>Ozone</subject><subject>Ozone - adverse effects</subject><subject>Ozone - analysis</subject><subject>Particle Size</subject><subject>Particulate matter</subject><subject>Patient Admission - statistics & numerical data</subject><subject>Respiratory diseases</subject><subject>Subpopulations</subject><subject>Threshold Limit Values</subject><subject>Toxicology</subject><subject>United States - epidemiology</subject><issn>0163-7525</issn><issn>1545-2093</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkEtLxDAUhYMoOj7-ggQFd625yaTT4ErEFyhudB3S5GamkmnGpBX993aYAcXV2Xz3nsNHyDmwEmBaXZquGxJ-lquhCQs0oV-UHEooBVM7ZAJyKgvOlNglEwaVKGaSywNymPM7Y0xxWe2TA2B1PVWympDn1_jV2hjivLUm0MZkzNTHRPsF0ox933ZzGj3dFBUJg-nRUdMmuoohDH0bO5p70zmTXD4me96EjCfbPCJvd7evNw_F08v94831U2HFVKjCK6fq9RRlTS1VpaCqvWxQujE91syCByEU4-C9FcIa54AhWl8765qZOCIXm7-rFD8GzL1ettliCKbDOGQNs0pwWasRPPsHvschdeM2zYXkYwdnI3S1gWyKOSf0epXapUnfGpheK9db5fpXueagQY_Kx-vTbcXQLNH9ud04Fj8ddYR8</recordid><startdate>2000</startdate><enddate>2000</enddate><creator>Lippmann, M</creator><creator>Schlesinger, R B</creator><general>Annual Reviews, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88C</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>LK8</scope><scope>M0R</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PATMY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PYCSY</scope><scope>Q9U</scope><scope>7T2</scope><scope>7TV</scope><scope>7U2</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>2000</creationdate><title>Toxicological bases for the setting of health-related air pollution standards</title><author>Lippmann, M ; Schlesinger, R B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3439-f9d9892569ca85969168f5be5d68ffe80c1f1339021ffc33cadd10eecf8dcdb73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Air Pollutants - adverse effects</topic><topic>Air Pollutants - analysis</topic><topic>Air pollution</topic><topic>Air Pollution - prevention & control</topic><topic>Air quality</topic><topic>Air quality standards</topic><topic>Asthma - epidemiology</topic><topic>Asthma - etiology</topic><topic>Cause-effect relationships</topic><topic>Confounding Factors (Epidemiology)</topic><topic>Data Interpretation, Statistical</topic><topic>Environmental Health - standards</topic><topic>Epidemiologic Studies</topic><topic>Epidemiology</topic><topic>Guidelines as Topic</topic><topic>Health Status</topic><topic>Humans</topic><topic>Maximum Allowable Concentration</topic><topic>Morbidity</topic><topic>Mortality</topic><topic>Ozone</topic><topic>Ozone - adverse effects</topic><topic>Ozone - analysis</topic><topic>Particle Size</topic><topic>Particulate matter</topic><topic>Patient Admission - statistics & numerical data</topic><topic>Respiratory diseases</topic><topic>Subpopulations</topic><topic>Threshold Limit Values</topic><topic>Toxicology</topic><topic>United States - 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However, the most influential bases for the PM NAAQS were the numerous and generally consistent epidemiological studies that associated exposure with premature mortality in susceptible subpopulations and the inability of numerous hypothesized confounding factors to negate the associations. Using ozone and PM as examples, this paper discusses the scientific basis for NAAQS promulgations in situations in which the underlying database differed greatly in the extent of toxicological support.</abstract><cop>United States</cop><pub>Annual Reviews, Inc</pub><pmid>10884956</pmid><doi>10.1146/annurev.publhealth.21.1.309</doi><tpages>25</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Air Pollutants - adverse effects Air Pollutants - analysis Air pollution Air Pollution - prevention & control Air quality Air quality standards Asthma - epidemiology Asthma - etiology Cause-effect relationships Confounding Factors (Epidemiology) Data Interpretation, Statistical Environmental Health - standards Epidemiologic Studies Epidemiology Guidelines as Topic Health Status Humans Maximum Allowable Concentration Morbidity Mortality Ozone Ozone - adverse effects Ozone - analysis Particle Size Particulate matter Patient Admission - statistics & numerical data Respiratory diseases Subpopulations Threshold Limit Values Toxicology United States - epidemiology |
title | Toxicological bases for the setting of health-related air pollution standards |
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