<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>25(1)</volume><submitter>Lehtomaki H</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Exposure to fine particles (PM&lt;sub>2.5&lt;/sub>) has been associated with adverse health outcomes, even at low exposure levels (&lt; 10 µg/m&lt;sup>3&lt;/sup>). Burden of disease assessments can quantify these associations; however, their sensitivity to methodological choices limits comparability between studies.&lt;h4>Methods&lt;/h4>This study aimed to quantify the impact of methodological choices on disease burden attributable to low levels of ambient PM&lt;sub>2.5&lt;/sub>, using Norway as a case study. Key methodological choices included (i) population exposure data, (ii) concentration-response curves, and (iii) population health data. Data from national and international sources were applied, including the global burden of disease (GBD) study. Attributable mortality and disability-adjusted life years (DALY) were estimated using burden of disease methodology. Additionally, the impact of choices related to concentration-response curves was assessed for higher exposure levels, using a scenario where exposure distributions were shifted to mean exposures up to 30 µg/m&lt;sup>3&lt;/sup>.&lt;h4>Results&lt;/h4>Methodological choices related to the concentration-response curves had the largest impacts on the estimated attributable deaths, ranging from - 91% to 104% change relative to the reference estimate (1,448 deaths, 95% CI 502-1497). These choices had a smaller impact on higher exposure levels, varying from - 46% to 53%. The choice of exposure and population health data led to 40% differences in attributable death estimates. DALYs attributable to PM&lt;sub>2.5&lt;/sub> were predominantly driven by years of life lost (YLL: 74%). The choice of relative risk (RR) for the concentration response curve caused around 30% variation in DALY estimates relative to the reference (11,730 DALYs; 5,980 - 16,790), with larger differences for ischemic heart disease (-44 to 79%).&lt;h4>Conclusion&lt;/h4>Attributable burden estimates for PM&lt;sub>2.5&lt;/sub> are highly sensitive to key methodological choices, particularly at low exposure levels. Consequently, transparent reporting of the methodological choices and data sources in PM&lt;sub>2.5&lt;/sub> health risk assessments are required to improve comparability and facilitate interpretations of the burden estimates.</pubmed_abstract><journal>Environmental health : a global access science source</journal><pagination>4</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12802007</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Burden of disease attributable to PM&amp;lt;sub&amp;gt;2.5&amp;lt;/sub&amp;gt; at low exposure levels: impact of methodological choices.</pubmed_title><pmcid>PMC12802007</pmcid><pubmed_authors>Bolling AK</pubmed_authors><pubmed_authors>Pereira G</pubmed_authors><pubmed_authors>Aasvang GM</pubmed_authors><pubmed_authors>Brauer M</pubmed_authors><pubmed_authors>Lehtomaki H</pubmed_authors><pubmed_authors>Sulo G</pubmed_authors><pubmed_authors>Dadras O</pubmed_authors><pubmed_authors>Denby BR</pubmed_authors><pubmed_authors>Hanninen OO</pubmed_authors></additional><is_claimable>false</is_claimable><name>Burden of disease attributable to PM&amp;lt;sub&amp;gt;2.5&amp;lt;/sub&amp;gt; at low exposure levels: impact of methodological choices.</name><description>&lt;h4>Background&lt;/h4>Exposure to fine particles (PM&lt;sub>2.5&lt;/sub>) has been associated with adverse health outcomes, even at low exposure levels (&lt; 10 µg/m&lt;sup>3&lt;/sup>). Burden of disease assessments can quantify these associations; however, their sensitivity to methodological choices limits comparability between studies.&lt;h4>Methods&lt;/h4>This study aimed to quantify the impact of methodological choices on disease burden attributable to low levels of ambient PM&lt;sub>2.5&lt;/sub>, using Norway as a case study. Key methodological choices included (i) population exposure data, (ii) concentration-response curves, and (iii) population health data. Data from national and international sources were applied, including the global burden of disease (GBD) study. Attributable mortality and disability-adjusted life years (DALY) were estimated using burden of disease methodology. Additionally, the impact of choices related to concentration-response curves was assessed for higher exposure levels, using a scenario where exposure distributions were shifted to mean exposures up to 30 µg/m&lt;sup>3&lt;/sup>.&lt;h4>Results&lt;/h4>Methodological choices related to the concentration-response curves had the largest impacts on the estimated attributable deaths, ranging from - 91% to 104% change relative to the reference estimate (1,448 deaths, 95% CI 502-1497). These choices had a smaller impact on higher exposure levels, varying from - 46% to 53%. The choice of exposure and population health data led to 40% differences in attributable death estimates. DALYs attributable to PM&lt;sub>2.5&lt;/sub> were predominantly driven by years of life lost (YLL: 74%). The choice of relative risk (RR) for the concentration response curve caused around 30% variation in DALY estimates relative to the reference (11,730 DALYs; 5,980 - 16,790), with larger differences for ischemic heart disease (-44 to 79%).&lt;h4>Conclusion&lt;/h4>Attributable burden estimates for PM&lt;sub>2.5&lt;/sub> are highly sensitive to key methodological choices, particularly at low exposure levels. Consequently, transparent reporting of the methodological choices and data sources in PM&lt;sub>2.5&lt;/sub> health risk assessments are required to improve comparability and facilitate interpretations of the burden estimates.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-06-06T14:55:11.119Z</modification><creation>2026-06-01T03:07:44.944Z</creation></dates><accession>S-EPMC12802007</accession><cross_references><pubmed>41382282</pubmed><doi>10.1186/s12940-025-01250-y</doi></cross_references></HashMap>