Achieving LDL cholesterol target levels <1.81 mmol/L may provide extra cardiovascular protection in patients at high risk: Exploratory analysis of the Standard Versus Intensive Statin Therapy for Patients with Hypercholesterolaemia and Diabetic Retinopathy study.


Journal

Diabetes, obesity & metabolism
ISSN: 1463-1326
Titre abrégé: Diabetes Obes Metab
Pays: England
ID NLM: 100883645

Informations de publication

Date de publication:
04 2019
Historique:
received: 27 07 2018
revised: 19 10 2018
accepted: 31 10 2018
pubmed: 6 11 2018
medline: 8 9 2020
entrez: 6 11 2018
Statut: ppublish

Résumé

To assess the benefits of intensive statin therapy on reducing cardiovascular (CV) events in patients with type 2 diabetes complicated with hyperlipidaemia and retinopathy in a primary prevention setting in Japan. In the intension-to-treat population, intensive therapy [targeting LDL cholesterol <1.81 mmol/L (<70 mg/dL)] was no more effective than standard therapy [LDL cholesterol ≥2.59 to <3.10 mmol/L (≥100 to <120 mg/dL)]; however, after 3 years, the intergroup difference in LDL cholesterol was only 0.72 mmol/L (27.7 mg/dL), and targeted levels were achieved in <50% of patients. We hypothesized that the intergroup difference in CV events would have been statistically significant if more patients had been successfully treated to target. This exploratory post hoc analysis focused on intergroup data from patients who achieved their target LDL cholesterol levels. The primary endpoint was the composite incidence of CV events. A Cox proportional hazards model was used to estimate hazard ratios (HRs) for incidence of the primary endpoint in patients who achieved target LDL cholesterol levels in each group. Data were analysed from 1909 patients (intensive: 703; standard: 1206) who achieved target LDL cholesterol levels. LDL cholesterol at 36 months was 1.54 ± 0.30 mmol/L (59.7 ± 11.6 mg/dL) in the intensive group and 2.77 ± 0.46 mmol/L (107.1 ± 17.8 mg/dL) in the standard group (P < 0.05). After adjusting for baseline prognostic factors, the composite incidence of CV events or deaths associated with CV events was significantly lower in the intensive than the standard group (HR 0.48; 95% confidence interval 0.28-0.82; P = 0.007). This post hoc analysis suggests that achieving LDL cholesterol target levels <1.81 mmol/L may more effectively reduce CV events than achieving target levels ≥2.59 to <3.10 mmol/L in patients with hypercholesterolaemia and diabetic retinopathy.

Identifiants

pubmed: 30393955
doi: 10.1111/dom.13575
pmc: PMC6587486
doi:

Substances chimiques

Cholesterol, LDL 0
Glycated Hemoglobin A 0
Hydroxymethylglutaryl-CoA Reductase Inhibitors 0
hemoglobin A1c protein, human 0

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

791-800

Informations de copyright

© 2018 The Authors. Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd.

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Auteurs

Hiroshi Itoh (H)

Department of Endocrinology, Metabolism and Nephrology, Keio University School of Medicine, Tokyo, Japan.

Issei Komuro (I)

Department of Cardiovascular Medicine, University of Tokyo Graduate School of Medicine, Tokyo, Japan.

Masahiro Takeuchi (M)

Department of Clinical Medicine (Biostatistics and Pharmaceutical Medicine), School of Pharmacy, Kitasato University, Tokyo, Japan.

Takashi Akasaka (T)

Department of Cardiovascular Medicine, Wakayama Medical University, Wakayama, Japan.

Hiroyuki Daida (H)

Department of Cardiovascular Medicine, Graduate School of Medicine Juntendo University, Tokyo, Japan.

Yoshiki Egashira (Y)

Sakura Hospital, Fukuoka, Japan.

Hideo Fujita (H)

Department of Cardiology, Saitama Medical Centre, Jichi Medical University, Saitama, Japan.

Jitsuo Higaki (J)

Department of Integrated Medicine and Informatics, Ehime University Graduate School of Medicine, Toon, Japan.

Ken-Ichi Hirata (KI)

Division of Cardiovascular Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine, Kobe, Japan.

Shun Ishibashi (S)

Division of Endocrinology and Metabolism, Department of Internal Medicine, Jichi Medical University, Shimotsuke, Japan.

Takaaki Isshiki (T)

Division of Cardiology, Cardiovascular Centre, Ageo Central General Hospital, Ageo, Japan.

Sadayoshi Ito (S)

Division of Nephrology, Endocrinology and Vascular Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan.

Atsunori Kashiwagi (A)

Kusatsu General Hospital, Kusatsu, Japan.

Satoshi Kato (S)

Department of Ophthalmology, University of Tokyo Graduate School of Medicine, Tokyo, Japan.

Kazuo Kitagawa (K)

Department of Neurology, Tokyo Women's Medical University School of Medicine, Tokyo, Japan.

Masafumi Kitakaze (M)

Division of Cardiology, National Cerebral and Cardiovascular Centre, Suita, Japan.

Takanari Kitazono (T)

Department of Medicine and Clinical Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

Masahiko Kurabayashi (M)

Department of Medicine and Biological Science, Gunma University Graduate School of Medicine, Maebashi, Japan.

Katsumi Miyauchi (K)

Department of Cardiology, Graduate School of Medicine Juntendo University, Tokyo, Japan.

Tomoaki Murakami (T)

Department of Ophthalmology, Kyoto University Graduate School of Medicine, Kyoto, Japan.

Toyoaki Murohara (T)

Department of Cardiology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Koichi Node (K)

Department of Cardiovascular Medicine, Saga University, Saga, Japan.

Susumu Ogawa (S)

Division of Nephrology, Endocrinology and Vascular Medicine, Tohoku University Hospital, Sendai, Japan.

Yoshihiko Saito (Y)

First Department of Internal Medicine, Nara Medical University, Kashihara, Japan.

Yoshihiko Seino (Y)

Department of Cardiology, Nippon Medical School Chiba Hokusoh Hospital, Inzai, Japan.

Takashi Shigeeda (T)

Ideta Eye Clinic, Kumamoto, Japan.

Shunya Shindo (S)

Department of Cardiovascular Surgery, Tokyo Medical University Hachioji Medical Centre, Hachioji, Japan.

Masahiro Sugawara (M)

Sugawara Medical Clinic, Tokyo, Japan.

Seigo Sugiyama (S)

Department of Cardiology, Jinnouchi Hospital, Kumamoto, Japan.

Yasuo Terauchi (Y)

Department of Endocrinology and Metabolism, Yokohama City University School of Medicine, Yokohama, Japan.

Hiroyuki Tsutsui (H)

Department of Cardiovascular Medicine, Faculty of Medical Sciences, Kyushu University, Fukuoka, Japan.

Kenji Ueshima (K)

Department of EBM Research, Institute for Advancement of Clinical and Translational Science, Kyoto University Hospital, Kyoto, Japan.

Kazunori Utsunomiya (K)

Division of Diabetes, Metabolism and Endocrinology, Department of Internal Medicine, Jikei University School of Medicine, Tokyo, Japan.

Masakazu Yamagishi (M)

Department of Cardiovascular and Internal Medicine, Kanazawa University Graduate School of Medicine, Kanazawa, Japan.

Tsutomu Yamazaki (T)

Clinical Research Support Centre, University of Tokyo Hospital, Tokyo, Japan.

Shoei Yo (S)

Yo Clinic, Kyoto, Japan.

Koutaro Yokote (K)

Department of Clinical Cell Biology and Medicine, Chiba University Graduate School of Medicine, Chiba, Japan.

Kiyoshi Yoshida (K)

Sakakibara Heart Institute of Okayama, Okayama, Japan.

Michihiro Yoshimura (M)

Division of Cardiology, Department of Internal Medicine, Jikei University School of Medicine, Tokyo, Japan.

Nagahisa Yoshimura (N)

Kitano Hospital, Tazuke Kofukai Medical Research Institute, Osaka, Japan.

Kazuwa Nakao (K)

Medical Innovation Centre, Kyoto University Graduate School of Medicine, Kyoto, Japan.

Ryozo Nagai (R)

Jichi Medical University, Shimotsuke, Japan.

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