Association of remnant cholesterol with risk of dementia: a nationwide population-based cohort study in South Korea

IF 13.4 Q1 GERIATRICS & GERONTOLOGY Lancet Healthy Longevity Pub Date : 2024-08-01 DOI:10.1016/S2666-7568(24)00112-0
Prof Ji Hye Heo MD , Han Na Jung MD , Prof Eun Roh MD , Prof Kyung-do Han PhD , Prof Jun Goo Kang MD , Prof Seong Jin Lee MD , Prof Sung-Hee Ihm MD
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We excluded people who were younger than 40 years and those with a triglyceride concentration of 400 mg/dL or higher due to concerns regarding the accuracy of calculated low-density lipoprotein cholesterol concentration in individuals with extremely high triglyceride concentrations. People who were previously diagnosed with dementia before the index date, and those who had any missing variables were also excluded. To minimise the influence of possible reverse causation, we excluded individuals who had developed any type of dementia within 1 year of the baseline measurements. We calculated hazard ratios (HRs) for all-cause dementia, Alzheimer's disease, and vascular dementia in each quartile of remnant-C using the Cox proportional hazards model adjusted for age, sex, body-mass index, estimated glomerular filtration rate, income level, smoking status, alcohol consumption, regular exercise, diabetes, hypertension, statin and fibrate use, and total cholesterol concentrations. We also did subgroup analyses to investigate the association between remnant-C and the risk of dementia stratified by age, sex, obesity, glycaemic status (normoglycaemia, impaired fasting glucose, new-onset type 2 diabetes, type 2 diabetes with a duration of less than 5 years, and type 2 diabetes with a duration of 5 years or more), hypertension, chronic kidney disease, and dyslipidaemia, using likelihood ratio tests.</p></div><div><h3>Findings</h3><p>4 234 415 individuals who underwent the national health examination in 2009 were deemed eligible for inclusion. We excluded 1 612 819 individuals on the basis of age, triglyceride concentration, missing variables, or having dementia at baseline. We identified 2 621 596 participants aged 40 years and older (1 305 556 men and 1 316 040 women) who underwent the national health examination and followed them up until the date of any incident of dementia or the end of the study period of Dec 31, 2020. During a median follow-up of 10·3 years (IQR 10·1–10·6), 146 991 (5·6%) participants developed all-cause dementia, 117 739 (4·5%) developed Alzheimer's disease, and 14 536 (0·6%) developed vascular dementia. The risk of dementia increased progressively with higher remnant-C concentrations. Compared with the lowest quartile of remnant-C (quartile 1), HRs in the highest quartile (quartile 4) were 1·11 (95% CI 1·09–1·13) for all-cause dementia, 1·11 (1·08–1·13) for Alzheimer's disease, and 1·15 (1·09–1·21) for vascular dementia. Subgroup analyses revealed that the risk of dementia associated with high remnant-C concentrations was higher in middle-aged people aged 40–59 years than in older people. 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Abstract

Background

The association between remnant cholesterol (remnant-C) and cardiovascular disease risk is well established, but its association with dementia remains unclear. We aimed to examine this association using a large-scale population dataset.

Methods

We did a nationwide, population-based cohort study in which we identified participants aged 40 years and older who underwent the national health examination in 2009 from South Korea's National Health Insurance Service. We excluded people who were younger than 40 years and those with a triglyceride concentration of 400 mg/dL or higher due to concerns regarding the accuracy of calculated low-density lipoprotein cholesterol concentration in individuals with extremely high triglyceride concentrations. People who were previously diagnosed with dementia before the index date, and those who had any missing variables were also excluded. To minimise the influence of possible reverse causation, we excluded individuals who had developed any type of dementia within 1 year of the baseline measurements. We calculated hazard ratios (HRs) for all-cause dementia, Alzheimer's disease, and vascular dementia in each quartile of remnant-C using the Cox proportional hazards model adjusted for age, sex, body-mass index, estimated glomerular filtration rate, income level, smoking status, alcohol consumption, regular exercise, diabetes, hypertension, statin and fibrate use, and total cholesterol concentrations. We also did subgroup analyses to investigate the association between remnant-C and the risk of dementia stratified by age, sex, obesity, glycaemic status (normoglycaemia, impaired fasting glucose, new-onset type 2 diabetes, type 2 diabetes with a duration of less than 5 years, and type 2 diabetes with a duration of 5 years or more), hypertension, chronic kidney disease, and dyslipidaemia, using likelihood ratio tests.

Findings

4 234 415 individuals who underwent the national health examination in 2009 were deemed eligible for inclusion. We excluded 1 612 819 individuals on the basis of age, triglyceride concentration, missing variables, or having dementia at baseline. We identified 2 621 596 participants aged 40 years and older (1 305 556 men and 1 316 040 women) who underwent the national health examination and followed them up until the date of any incident of dementia or the end of the study period of Dec 31, 2020. During a median follow-up of 10·3 years (IQR 10·1–10·6), 146 991 (5·6%) participants developed all-cause dementia, 117 739 (4·5%) developed Alzheimer's disease, and 14 536 (0·6%) developed vascular dementia. The risk of dementia increased progressively with higher remnant-C concentrations. Compared with the lowest quartile of remnant-C (quartile 1), HRs in the highest quartile (quartile 4) were 1·11 (95% CI 1·09–1·13) for all-cause dementia, 1·11 (1·08–1·13) for Alzheimer's disease, and 1·15 (1·09–1·21) for vascular dementia. Subgroup analyses revealed that the risk of dementia associated with high remnant-C concentrations was higher in middle-aged people aged 40–59 years than in older people. The risk of dementia associated with high concentrations of remnant-C was notably more pronounced in individuals with diabetes compared with those without diabetes, and the risk increased steeply with a longer duration of diabetes.

Interpretation

Results showed that higher remnant-C concentrations were independently associated with increased risks of all-cause dementia, Alzheimer's disease, and vascular dementia. More research is needed to determine the mechanisms underlying this finding. Monitoring and managing higher concentrations of remnant-C might have important implications for reducing the risk of dementia.

Funding

None.

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残余胆固醇与痴呆症风险的关系:韩国一项全国性人群队列研究。
背景:残余胆固醇(remainant-C)与心血管疾病风险之间的关系已被证实,但其与痴呆症之间的关系仍不清楚。我们的目的是利用大规模人口数据集来研究这种关联:我们在全国范围内开展了一项基于人群的队列研究,从韩国国民健康保险服务机构中找到了在 2009 年接受国民健康检查的 40 岁及以上的参与者。由于担心计算甘油三酯浓度极高的人的低密度脂蛋白胆固醇浓度的准确性,我们排除了年龄小于 40 岁的人和甘油三酯浓度为 400 mg/dL 或更高的人。此外,还排除了在指数日期之前曾被诊断为痴呆症的患者以及变量缺失的患者。为了尽量减少可能的反向因果关系的影响,我们排除了在基线测量后 1 年内罹患任何类型痴呆症的人。我们使用 Cox 比例危险模型计算了残余 C 各四分位数中全因痴呆、阿尔茨海默病和血管性痴呆的危险比(HRs),并对年龄、性别、体重指数、估计肾小球滤过率、收入水平、吸烟状况、饮酒量、经常锻炼、糖尿病、高血压、他汀类药物和非贝特类药物的使用情况以及总胆固醇浓度进行了调整。我们还进行了亚组分析,利用似然比检验,按照年龄、性别、肥胖程度、血糖状况(正常血糖、空腹血糖受损、新发 2 型糖尿病、病程少于 5 年的 2 型糖尿病和病程 5 年或以上的 2 型糖尿病)、高血压、慢性肾病和血脂异常等分层,研究残余物-C 与痴呆症风险之间的关系:4 234 415 名在 2009 年接受了全国健康检查的人被认为符合纳入条件。由于年龄、甘油三酯浓度、变量缺失或基线时患有痴呆症,我们排除了 1 612 819 人。我们确定了 2 621 596 名 40 岁及以上的参与者(男性 1 305 556 人,女性 1 316 040 人)接受了全国健康检查,并对他们进行了随访,直至发生痴呆症或研究期于 2020 年 12 月 31 日结束。在中位 10-3 年(IQR 10-1-10-6)的随访期间,146 991 人(5-6%)患上了全因痴呆症,117 739 人(4-5%)患上了阿尔茨海默病,14 536 人(0-6%)患上了血管性痴呆症。患痴呆症的风险随着残余 C 浓度的升高而逐渐增加。与残余 C 最低四分位数(四分位数 1)相比,最高四分位数(四分位数 4)的全因痴呆 HR 值为 1-11 (95% CI 1-09-1-13),阿尔茨海默病为 1-11 (1-08-1-13),血管性痴呆为 1-15 (1-09-1-21)。亚组分析表明,40-59 岁的中年人患痴呆症的风险高于老年人。与没有糖尿病的人相比,患有糖尿病的人与高浓度残余物-C相关的痴呆风险明显更高,而且随着糖尿病持续时间的延长,痴呆风险急剧增加:结果显示,残余物-C浓度越高,患全因痴呆症、阿尔茨海默病和血管性痴呆症的风险越高。要确定这一发现的内在机制,还需要进行更多的研究。监测和管理较高浓度的残余 C 可能对降低痴呆症风险有重要意义:无。
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来源期刊
Lancet Healthy Longevity
Lancet Healthy Longevity GERIATRICS & GERONTOLOGY-
CiteScore
16.30
自引率
2.30%
发文量
192
审稿时长
12 weeks
期刊介绍: The Lancet Healthy Longevity, a gold open-access journal, focuses on clinically-relevant longevity and healthy aging research. It covers early-stage clinical research on aging mechanisms, epidemiological studies, and societal research on changing populations. The journal includes clinical trials across disciplines, particularly in gerontology and age-specific clinical guidelines. In line with the Lancet family tradition, it advocates for the rights of all to healthy lives, emphasizing original research likely to impact clinical practice or thinking. Clinical and policy reviews also contribute to shaping the discourse in this rapidly growing discipline.
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