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Original research
Low-density lipoprotein cholesterol levels and risk of incident dementia: a distributed network analysis using common data models
  1. Minwoo Lee1,
  2. Kyung Joo Lee2,
  3. Jinseob Kim3,
  4. Dong Yun Lee4,5,
  5. Rae Woong Park4,
  6. Sang Youl Rhee6,
  7. Jae Myung Cha7,
  8. Hyeon-Jong Yang8,
  9. Jae-Won Jang9,
  10. Seunguk Jung10,
  11. Jeeun Lee11,
  12. Sang-Hwa Lee12,
  13. Chulho Kim12,
  14. Jong-Seok Bae13,
  15. Yeo Jin Kim13,
  16. Ju-Hun Lee13,
  17. Hyoeun Bae13,
  18. Yerim Kim13
  1. 1 Department of Neurology, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, Anyang, Korea (the Republic of)
  2. 2 Department of Medical Informatics & Statistics, Kangdong Sacred Heart Hospital, Seoul, Korea (the Republic of)
  3. 3 Zarathu Co Ltd, Seoul, Korea (the Republic of)
  4. 4 Department of Biomedical Informatics, Ajou University School of Medicine, Suwon, Korea (the Republic of)
  5. 5 Bongdam forest mental health clinic, Hwaseong, Korea (the Republic of)
  6. 6 Department of Digital Health and Department of Endocrinology and Metabolism, Kyung Hee University College of Medicine, Seoul, Korea (the Republic of)
  7. 7 Department of Internal Medicine, Kyung Hee University Hospital at Gangdong, Kyung Hee University School of Medicine, Seoul, Korea (the Republic of)
  8. 8 Department of Pediatrics, Soonchunhyang University Seoul Hospital, Soonchunhyang University College of Medicine, Seoul, Korea (the Republic of)
  9. 9 Department of Neurology, Kangwon National University Hospital, Kangwon National University College of Medicine, Chuncheon, Korea (the Republic of)
  10. 10 Department of Neurology, Gyeongsang National University Changwon Hospital, Changwon, Korea (the Republic of)
  11. 11 Department of Neurology, Myongji Hospital, Hanyang University College of Medicine, Goyang, Korea (the Republic of)
  12. 12 Department of Neurology, Chuncheon Sacred Heart Hospital, Hallym University College of Medicine, Chuncheon, Korea (the Republic of)
  13. 13 Department of Neurology, Kangdong Sacred Heart Hospital, Hallym University College of Medicine, Seoul, Korea (the Republic of)
  1. Correspondence to Dr Yerim Kim; brainyrk{at}hallym.ac.kr

Abstract

Background The link between low-density lipoprotein cholesterol (LDL-C) levels and dementia risk is poorly understood, with conflicting evidence on the role of LDL-C and the impact of statin therapy on cognitive outcomes. Thus, we aimed to examine the association between low-density LDL-C levels and the risk of dementia and assess the influence of statin therapy.

Methods We retrospectively analysed data from 11 university hospitals participating in the Observational Medical Outcomes Partnership (OMOP) Common Data Model (CDM). Participants with a prior diagnosis of dementia or those with <180 days of observation before cohort inclusion, and those included in both cohorts were excluded. The primary outcome was all-cause dementia, with the secondary outcome being Alzheimer’s disease-related dementia (ADRD). The study utilised 1:1 propensity score matching to compare individuals with LDL-C levels below 70 mg/dL (1.8 mmol/L) against those with levels above 130 mg/dL (3.4 mmol/L), resulting in a primary analysis cohort of 108 980 matched patients. Secondary analyses further examined LDL-C thresholds below 55 mg/dL (1.4 mmol/L) and the influence of statin use.

Results The LDL-C levels below 70 mg/dL (1.8 mmol/L) were associated with a 26% reduction in the risk of all-cause dementia and a 28% reduction in the risk of ADRD, compared with levels above 130 mg/dL (3.4 mmol/L). For LDL-C levels below 55 mg/dL (1.4 mmol/L), there was an 18% risk reduction for both outcomes. Among those with LDL-C <70 mg/dL (<1.8 mmol/L), statin use was associated with a 13% reduction in all-cause dementia risk and a 12% decrease in ADRD risk compared with non-users.

Conclusion Low LDL-C levels (<70 mg/dL (<1.8 mmol/L)) are significantly associated with a reduced risk of dementia, including ADRD, with statin therapy providing additional protective effects. These findings support the necessity of targeted lipid management as a preventive strategy against dementia, indicating the importance of personalised treatment approaches.

  • DEMENTIA
  • CHOLESTEROL

Data availability statement

Data are available upon reasonable request. Due to existing embargoes on our datasets, the full data from this study cannot be publicly shared. However, anonymised data will be made available upon request to any qualified investigator.

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Data availability statement

Data are available upon reasonable request. Due to existing embargoes on our datasets, the full data from this study cannot be publicly shared. However, anonymised data will be made available upon request to any qualified investigator.

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Footnotes

  • Contributors YK: study concept and design, acquisition of data, analysis and interpretation of data, drafting of the manuscript, and revision of the manuscript, obtainment of funding, guarantor. ML: drafting of the manuscript, and revision of the manuscript. DYL, RWP, SYR, JMC, H-JY, J-WJ, SJ, JL, S-HL, CK, J-SB, YJK, J-HL, HB: critical revision of the manuscript for important intellectual content. JK and KJL: acquisition of data, analysis and interpretation of data. JK and KJL: statistical analysis. YK, KJL, DYL and JK: technical or material support.

  • Funding This research was supported by the Basic Science Research Program through the National Research Foundation of Korea funded by the Ministry of Science and ICT (NRF-2022R1F1A1074643). This study was supported by a grant from the Korean Neurological Association (KNA-22_SONGPA-1).

  • Competing interests None declared.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.