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PCSK9 Inhibitor with Statin Therapy for Intracranial Artery Stenosis ( PISTIAS): Rationale and design of a multicenter randomized controlled trial.
Hu, Xinzhi; Zhang, Zongmuyu; Liu, Caiyan; Li, Mingli; Liu, Yiyang; Cheng, Anqi; Yu, Qiuyu; Guo, Haoyao; Zou, Yinxi; Zhou, Li; Wang, Hebo; Song, Bo; You, Yong; Xia, Jian; Zhang, Jingfen; Ai, Zhibing; Sun, Qinjian; Han, Ju; Liu, Jing; Lu, Baoquan; Deng, Qiwen; Li, Guanzeng; Wang, Peng-Fei; Li, Xiangqing; An, Yi; Wu, Bo; Yan, Zhongrui; Wang, Yining; Xu, Wei-Hai.
  • Hu X; Department of Neurology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
  • Zhang Z; Department of Neurology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
  • Liu C; Department of Neurology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
  • Li M; Department of Radiology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
  • Liu Y; Department of Neurology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
  • Cheng A; Department of Neurology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
  • Yu Q; Department of Neurology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
  • Guo H; Department of Neurology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
  • Zou Y; Department of Neurology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
  • Zhou L; Department of Neurology, Weifang People's Hospital, Weifang, China.
  • Wang H; Department of Neurology, Hebei General Hospital, Shijiazhuang, China.
  • Song B; Department of Neurology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
  • You Y; Department of Neurology, The Second Affiliated Hospital of Hainan Medical University, International Center for Aging and Cancer (ICAC), Hainan Medical University, Haikou, China.
  • Xia J; Key Laboratory of Brain Science Research & Transformation in Tropical Environment of Hainan Province, Haikou, China.
  • Zhang J; Department of Neurology, Xiangya Hospital, Central South University, Changsha, China.
  • Ai Z; Department of Neurology, Baotou City Central Hospital, Baotou, China.
  • Sun Q; Department of Neurology, Taihe Hospital, Hubei University of Medicine, Shiyan, China.
  • Han J; Department of Neurology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China.
  • Liu J; Department of Neurology, The First Affiliated Hospital of Shandong First Medical University and Shandong Provincial Qianfoshan Hospital, Jinan, China.
  • Lu B; Department of Neurology, Tangshan Gongren Hospital, Tangshan, China.
  • Deng Q; Department of Neurology, Tangshan Gongren Hospital, Tangshan, China.
  • Li G; Department of Neurology, Nanjing First Hospital, Nanjing, China.
  • Wang PF; Department of Neurology, Liaocheng People's Hospital, Liaocheng, China.
  • Li X; Department of Neurology, Weihai Municipal Hospital, Cheeloo College of Medicine, Shandong University, Weihai, China.
  • An Y; Department of Neurology, Zibo Central Hospital, Zibo, China.
  • Wu B; Department of Neurology, Chifeng Municipal Hospital, Chifeng, China.
  • Yan Z; Department of Neurology, West China Hospital, Sichuan University, Chengdu, China.
  • Wang Y; Department of Neurology, Jining No.1 People's Hospital, Jining, China.
  • Xu WH; Department of Radiology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Int J Stroke ; : 17474930241270447, 2024 Aug 15.
Article en En | MEDLINE | ID: mdl-39075747
ABSTRACT
RATIONALE Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors enable an additional 54-75% reduction in low-density lipoprotein cholesterol (LDL-C) in statin-treated patients, demonstrating plaque regression in coronary artery disease. However, the impact of achieving an extremely low level of LDL-C with PCSK9 inhibitors (e.g. Evolocumab) on symptomatic intracranial atherosclerosis remains unexplored. AIM AND

HYPOTHESIS:

To determine whether combining Evolocumab and statins achieves a more significant symptomatic intracranial plaque regression than statin therapy alone. SAMPLE SIZE ESTIMATES With a sample size of 1000 subjects, a two-sided α of 0.05, and 20% lost to follow-up, the study will have 83.3% power to detect the difference in intracranial plaque burden. METHODS AND

DESIGN:

This is an investigator-initiated multicenter, randomized, open-label, outcome assessor-blinded trial, evaluating the impact of combining Evolocumab and statins on intracranial plaque burden assessed by high-resolution magnetic resonance imaging at baseline in patients undergoing a clinically indicated acute stroke or transient ischemic attack due to intracranial artery stenosis, and after 24 weeks of treatment. Subjects (n = 1000) were randomized 11 into two groups to receive either Evolocumab 140 mg every 2 weeks with statin therapy or statin therapy alone. STUDY

OUTCOMES:

The primary endpoint is the change in intracranial plaque burden assessed by high-resolution magnetic resonance imaging, performed at baseline and at the end of the 24-week treatment period.

DISCUSSION:

This trial will explore whether more significant intracranial plaque regression is achievable with the treatment of combining Evolocumab and statins, providing information about efficacy and safety data. TRIAL REGISTRATION NUMBER ChiCTR2300068868; https//www.chictr.org.cn/.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2024 Tipo del documento: Article