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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Singh, Siddharth | en_US |
| dc.date.accessioned | 2026-09-01T04:23:13Z | - |
| dc.date.available | 2026-09-01T04:23:13Z | - |
| dc.date.issued | 2026 | - |
| dc.identifier.citation | Razo, C., DeCleene, N. K., Johnson, C. O., Stark, B. A., LeGrand, K., Aalruz, H., Abaraogu, U. O., ElHafeez, S. A., Abdelmasseh, M., Abdelnabi, M., Abd-Elsalam, S., Elshenawy, R. A., Abdelwahab, S. I., Abdolizadeh, A., Abdollahi, A., Abdoun, M., Abdrabou, M. M., Abdulah, D. M., Abdullahi, A., … Roth, G. A. (2026). Global Burden of Elevated LDL-C Findings From the Global Burden of Disease Study 2023. JAMA. https://doi.org/10.1001/jama.2026.8628 | en_US |
| dc.identifier.issn | 0098-7484 | - |
| dc.identifier.other | EID(2-s2.0-105047028159) | - |
| dc.identifier.uri | https://dx.doi.org/10.1001/jama.2026.8628 | - |
| dc.identifier.uri | https://dspace.iiti.ac.in/handle/123456789/19011 | - |
| dc.description.abstract | IMPORTANCE Elevated low-density lipoprotein cholesterol (LDL-C) is a modifiable risk factor for cardiovascular disease, the leading cause of premature death worldwide. Assessing the LDL-C-related burden is critical for guiding prevention and treatment strategies. OBJECTIVES To estimate the global, regional, and national burden of ischemic heart disease and ischemic stroke attributable to elevated LDL-C (relative to 35-54 mg/dL) from 1990 to 2023 and to quantify the contributions of population growth, aging, risk-deleted burden, and exposure changes to burden trends. DESIGN, SETTING, AND POPULATION This comparative risk assessment, part of the Global Burden of Disease Study 2023, estimated population-level LDL-C exposure and associated health loss in 204 countries and territories. Mean LDL-C levels were estimated using spatiotemporal gaussian process regression based on 806 studies across 161 countries. Relative risks were derived from meta-analyses of 38 randomized clinical trials. Population-attributable fractions for deaths and disability-adjusted life-years (DALYs) were estimated by age and sex for adults aged 25 years or older from 1990 to 2023, with 95% uncertainty intervals. EXPOSURE Population-level LDL-C concentrations. MAIN OUTCOMES AND MEASURES Population-attributable fractions, counts, and rates (all ages and age standardized per 100 000) of LDL-C-attributable deaths and DALYs from ischemic heart disease and ischemic stroke, with uncertainty intervals. RESULTS In 2023, elevated LDL-C accounted for 3.6 million deaths (95% uncertainty interval, 2.2-5.4 million | en_US |
| dc.description.abstract | 6.0% of global mortality) and 90.7 million DALYs (95% uncertainty interval, 58.9-123.3 million | en_US |
| dc.description.abstract | 3.2% of DALYs). Although global all-ages rates remained stable, age-standardized death and DALY rates decreased by 45.6% and 39.5%, respectively, since 1990. In 2023, age-standardized LDL-C-attributable DALY rates were highest in Eastern Europe and lowest in high-income Asia-Pacific. One-third of the global LDL-C burden occurred in India and China. Population growth and aging drove the increasing burden, with notable regional disparities in LDL-C exposure and risk-deleted DALY rates shifting toward middle-sociodemographic settings. CONCLUSIONS AND RELEVANCE Despite declining age-standardized rates, the absolute LDL-C burden has increased since 1990 due to demographic changes and has shifted toward middle-sociodemographic countries. Measurement and surveillance gaps persist. Strengthened prevention, diagnosis, and treatment access strategies are essential to mitigate the health burden of LDL-C. © 2026 American Medical Association. All rights reserved, including those for text and data mining, AI training, and similar technologies. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | American Medical Association | en_US |
| dc.source | JAMA | en_US |
| dc.title | Global Burden of Elevated LDL-C Findings From the Global Burden of Disease Study 2023 | en_US |
| dc.type | Journal Article | en_US |
| dc.rights.license | All Open Access | - |
| dc.rights.license | Green Open Access | - |
| Appears in Collections: | Mehta Family School of Biosciences and Biomedical Engineering | |
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