Your browser doesn't support javascript.
loading
Optimal target of LDL cholesterol level for statin treatment: challenges to monotonic relationship with cardiovascular events.
Sakuma, Masashi; Iimuro, Satoshi; Shinozaki, Tomohiro; Kimura, Takeshi; Nakagawa, Yoshihisa; Ozaki, Yukio; Iwata, Hiroshi; Miyauchi, Katsumi; Daida, Hiroyuki; Suwa, Satoru; Sakuma, Ichiro; Nishihata, Yosuke; Saito, Yasushi; Ogawa, Hisao; Matsuzaki, Masunori; Ohashi, Yasuo; Taguchi, Isao; Toyoda, Shigeru; Inoue, Teruo; Nagai, Ryozo.
Afiliação
  • Sakuma M; Department of Cardiovascular Medicine, Dokkyo Medical University School of Medicine, 880 Kitakobayashi, Mibu, Tochigi, 321-0293, Japan.
  • Iimuro S; Innovation and Research Support Center, International University of Health and Welfare, Tokyo, Japan.
  • Shinozaki T; Department of Information and Computer Technology, Faculty of Engineering, Tokyo University of Science, Tokyo, Japan.
  • Kimura T; Department of Cardiovascular Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan.
  • Nakagawa Y; Department of Cardiovascular Medicine, Shiga University of Medical Science, Otsu, Japan.
  • Ozaki Y; Department of Cardiology, Fujita Health University Okazaki Medical Center, Okazaki, Japan.
  • Iwata H; Department of Cardiovascular Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
  • Miyauchi K; Department of Cardiovascular Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
  • Daida H; Department of Cardiovascular Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
  • Suwa S; Department of Cardiovascular Medicine, Juntendo University Shizuoka Hospital, Izunokuni, Japan.
  • Sakuma I; Caress Sapporo Hokko Memorial Clinic, Sapporo, Japan.
  • Nishihata Y; Department of Cardiovascular Medicine, St. Lukes International Hospital, Tokyo, Japan.
  • Saito Y; Chiba University, Chiba, Japan.
  • Ogawa H; Kumamoto University, Kumamoto, Japan.
  • Matsuzaki M; St. Hill Hospital, Ube, Japan.
  • Ohashi Y; Department of Integrated Science and Technology for Sustainable Society, Chuo University, Tokyo, Japan.
  • Taguchi I; Department of Cardiology, Dokkyo Medical University Saitama Medical Center, Koshigaya, Japan.
  • Toyoda S; Department of Cardiovascular Medicine, Dokkyo Medical University School of Medicine, 880 Kitakobayashi, Mibu, Tochigi, 321-0293, Japan.
  • Inoue T; Department of Cardiovascular Medicine, Dokkyo Medical University School of Medicine, 880 Kitakobayashi, Mibu, Tochigi, 321-0293, Japan. inouet@dokkyomed.ac.jp.
  • Nagai R; Japan Red Cross Society, Nasu Red Cross Hospital, Otawara, Japan. inouet@dokkyomed.ac.jp.
BMC Med ; 20(1): 441, 2022 11 14.
Article em En | MEDLINE | ID: mdl-36372869
ABSTRACT

BACKGROUND:

Aggressive lipid lowering by high-dose statin treatment has been established for the secondary prevention of coronary artery disease (CAD). Regarding the low-density lipoprotein cholesterol (LDL-C) level, however, the "The lower is the better" concept has been controversial to date. We hypothesized that there is an optimal LDL-C level, i.e., a "threshold" value, below which the incidence of cardiovascular events is no longer reduced. We undertook a subanalysis of the REAL-CAD study to explore whether such an optimal target LDL-C level exists by a novel analysis procedure to verify the existence of a monotonic relationship.

METHODS:

For a total of 11,105 patients with CAD enrolled in the REAL-CAD study, the LDL-C level at 6 months after randomization and 5-year cardiovascular outcomes were assessed. We set the "threshold" value of the LDL-C level under which the hazards were assumed to be constant, by including an artificial covariate max (0, LDL-C - threshold) in the Cox model. The analysis was repeated with different LDL-C thresholds (every 10 mg/dl from 40 to 100 mg/dl) and the model fit was assessed by log-likelihood.

RESULTS:

For primary outcomes such as the composite of cardiovascular death, non-fatal myocardial infarction, non-fatal ischemic stroke, and unstable angina requiring emergency hospitalization, the model fit assessed by log-likelihood was best when a threshold LDL-C value of 70 mg/dl was assumed. And in the model with a threshold LDL-C ≥ 70 mg/dl, the hazard ratio was 1.07 (95% confidence interval 1.01-1.13) as the LDL-C increased by 10 mg/dl. Therefore, the risk of cardiovascular events decreased monotonically until the LDL-C level was lowered to 70 mg/dl, but when the level was further reduced, the risk was independent of LDL-C.

CONCLUSIONS:

Our analysis model suggests that a "threshold" value of LDL-C might exist for the secondary prevention of cardiovascular events in Japanese patients with CAD, and this threshold might be 70 mg/dl for primary composite outcomes. TRIAL REGISTRATION http//www. CLINICALTRIALS gov . Unique identifier NCT01042730.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença da Artéria Coronariana / Inibidores de Hidroximetilglutaril-CoA Redutases / Infarto do Miocárdio Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença da Artéria Coronariana / Inibidores de Hidroximetilglutaril-CoA Redutases / Infarto do Miocárdio Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article