TY - JOUR
T1 - Achieving LDL cholesterol target levels <1.81 mmol/L may provide extra cardiovascular protection in patients at high risk
T2 - Exploratory analysis of the Standard Versus Intensive Statin Therapy for Patients with Hypercholesterolaemia and Diabetic Retinopathy study
AU - for the EMPATHY Investigators
AU - Itoh, Hiroshi
AU - Komuro, Issei
AU - Takeuchi, Masahiro
AU - Akasaka, Takashi
AU - Daida, Hiroyuki
AU - Egashira, Yoshiki
AU - Fujita, Hideo
AU - Higaki, Jitsuo
AU - Hirata, Ken ichi
AU - Ishibashi, Shun
AU - Isshiki, Takaaki
AU - Ito, Sadayoshi
AU - Kashiwagi, Atsunori
AU - Kato, Satoshi
AU - Kitagawa, Kazuo
AU - Kitakaze, Masafumi
AU - Kitazono, Takanari
AU - Kurabayashi, Masahiko
AU - Miyauchi, Katsumi
AU - Murakami, Tomoaki
AU - Murohara, Toyoaki
AU - Node, Koichi
AU - Ogawa, Susumu
AU - Saito, Yoshihiko
AU - Seino, Yoshihiko
AU - Shigeeda, Takashi
AU - Shindo, Shunya
AU - Sugawara, Masahiro
AU - Sugiyama, Seigo
AU - Terauchi, Yasuo
AU - Tsutsui, Hiroyuki
AU - Ueshima, Kenji
AU - Utsunomiya, Kazunori
AU - Yamagishi, Masakazu
AU - Yamazaki, Tsutomu
AU - Yo, Shoei
AU - Yokote, Koutaro
AU - Yoshida, Kiyoshi
AU - Yoshimura, Michihiro
AU - Yoshimura, Nagahisa
AU - Nakao, Kazuwa
AU - Nagai, Ryozo
N1 - Funding Information:
This study was funded by Shionogi & Co., Ltd EDIT, Inc. (Tokyo,
Publisher Copyright:
© 2018 The Authors. Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd.
PY - 2019/4
Y1 - 2019/4
N2 - Aims: 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. Materials and Methods: 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. Results: 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). Conclusions: 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.
AB - Aims: 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. Materials and Methods: 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. Results: 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). Conclusions: 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.
KW - cardiovascular disease
KW - clinical trial
KW - diabetic retinopathy
KW - dyslipidaemia
KW - lipid-lowering therapy
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U2 - 10.1111/dom.13575
DO - 10.1111/dom.13575
M3 - Article
C2 - 30393955
AN - SCOPUS:85057974713
SN - 1462-8902
VL - 21
SP - 791
EP - 800
JO - Diabetes, Obesity and Metabolism
JF - Diabetes, Obesity and Metabolism
IS - 4
ER -