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巴西健康评估项目中严重高胆固醇血症个体的胆固醇控制情况。

Uncontrolled Cholesterol in Individuals with Severe Hypercholesterolemia in a Health Evaluation Program in Brazil.

机构信息

Hospital Israelita Albert Einstein, São Paulo, SP - Brasil.

Instituto do Coração do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, SP - Brasil.

出版信息

Arq Bras Cardiol. 2024 Nov 22;121(11):e20240116. doi: 10.36660/abc.20240116. eCollection 2024.

DOI:10.36660/abc.20240116
PMID:39607222
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11634292/
Abstract

BACKGROUND

Individuals with severe hypercholesterolemia (SH) are considered at high atherosclerosis risk and should be intensively treated with lipid-lowering drugs aiming for an LDL-C reduction of≥50% and a goal of <70 mg/dL.

OBJECTIVES

This study aimed to evaluate cholesterol control in individuals with SH (LDL-C ≥ 190 mg/dL or 160-189 mg/dL using lipid-lowering drugs) followed in a health evaluation program.

METHODS

55,000 individuals were evaluated, of which 2,214 (4%) had SH, and 1,016 (45.8%) had repeated assessments. Achievement of recommended LDL-C goals was the primary study endpoint. A p-value < 0.05 was considered significant.

RESULTS

Mean age (± SD) was 44.9±8.8 years, 84.2% were men, and 0.5% reported previous myocardial infarction. Mean LDL-C was 203.0±22.0 mg/dL, and although 62.5% referred dyslipidemia, only 19% were using lipid-lowering drugs (5.9% in cases with LDL-C ≥ 190 mg/dL). During a 4.1±2.8-year follow-up, use of lipid-lowering drugs increased from 18.1% to 48.4% (p<0.00001), 5.9% to 45.4% in those with LDL-C ≥ 190 mg/dL (p< 0.00001) though 31% of cases with LDL-C 160-189 mg/dL stopped taking medications. Overall, there was a mean 26.7% reduction in LDL-C (p<0.0001), and LDL-C reductions ≥50% were attained in 19.2%, 19.1%, and 19.7 % of all individuals, and in those with LDL-C > 190 mg/dL and 160-189 mg/dL respectively. Only 3.1% reached LDL-C < 70 mg/dL (2.7% in those with LDL-C ≥ 190 and 5.3% in those with 160-189 mg/dL).

CONCLUSIONS

A serious gap was found between treatment recommendations and reality in individuals at high atherosclerosis risk due to SH.

摘要

背景

严重高胆固醇血症(SH)患者被认为具有较高的动脉粥样硬化风险,应采用降脂药物进行强化治疗,目标是 LDL-C 降低≥50%,并达到<70mg/dL。

目的

本研究旨在评估在健康评估计划中接受治疗的严重高胆固醇血症(LDL-C≥190mg/dL 或 160-189mg/dL 时使用降脂药物)患者的胆固醇控制情况。

方法

共评估了 55000 名个体,其中 2214 名(4%)患有 SH,1016 名(45.8%)有重复评估。推荐 LDL-C 目标的达标情况是主要的研究终点。p 值<0.05 被认为具有统计学意义。

结果

平均年龄(±标准差)为 44.9±8.8 岁,84.2%为男性,0.5%有心肌梗死病史。平均 LDL-C 为 203.0±22.0mg/dL,尽管 62.5%患者存在血脂异常,但仅 19%使用降脂药物(5.9% LDL-C≥190mg/dL)。在 4.1±2.8 年的随访期间,降脂药物的使用率从 18.1%增加到 48.4%(p<0.00001),LDL-C≥190mg/dL 患者从 5.9%增加到 45.4%(p<0.00001),但 31% LDL-C 为 160-189mg/dL 的患者停止了药物治疗。总体而言,LDL-C 平均降低了 26.7%(p<0.0001),所有患者中 LDL-C 降低≥50%的比例分别为 19.2%、19.1%和 19.7%,LDL-C>190mg/dL 和 160-189mg/dL 患者的比例分别为 19.2%、19.1%和 19.7%。仅有 3.1%的患者达到 LDL-C<70mg/dL(LDL-C≥190mg/dL 的患者为 2.7%,160-189mg/dL 的患者为 5.3%)。

结论

由于 SH,严重高胆固醇血症患者的治疗建议与实际情况之间存在严重差距,导致动脉粥样硬化风险较高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebd4/11634292/3418f24b7635/0066-782X-abc-121-11-e20240116-gf04-en.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebd4/11634292/98df35549022/0066-782X-abc-121-11-e20240116-gf01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebd4/11634292/9d303c9e2de7/0066-782X-abc-121-11-e20240116-gf02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebd4/11634292/c47ffd9b37fa/0066-782X-abc-121-11-e20240116-gf03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebd4/11634292/704f56af6a53/0066-782X-abc-121-11-e20240116-gf04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebd4/11634292/805fa445407f/0066-782X-abc-121-11-e20240116-gf01-en.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebd4/11634292/32e2a7b243ee/0066-782X-abc-121-11-e20240116-gf02-en.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebd4/11634292/cc6b17f3593d/0066-782X-abc-121-11-e20240116-gf03-en.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebd4/11634292/3418f24b7635/0066-782X-abc-121-11-e20240116-gf04-en.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebd4/11634292/98df35549022/0066-782X-abc-121-11-e20240116-gf01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebd4/11634292/9d303c9e2de7/0066-782X-abc-121-11-e20240116-gf02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebd4/11634292/c47ffd9b37fa/0066-782X-abc-121-11-e20240116-gf03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebd4/11634292/704f56af6a53/0066-782X-abc-121-11-e20240116-gf04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebd4/11634292/805fa445407f/0066-782X-abc-121-11-e20240116-gf01-en.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebd4/11634292/32e2a7b243ee/0066-782X-abc-121-11-e20240116-gf02-en.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebd4/11634292/cc6b17f3593d/0066-782X-abc-121-11-e20240116-gf03-en.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebd4/11634292/3418f24b7635/0066-782X-abc-121-11-e20240116-gf04-en.jpg

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