TY - JOUR
T1 - Management of Dyslipidaemia for the Prevention of Stroke
T2 - Clinical Practice Recommendations from the Lipid Association of India
AU - Puri, Raman
AU - Mehta, Vimal
AU - Iyengar, Shamanna Seshadri
AU - Srivastava, Padma
AU - Yusuf, Jamal
AU - Pradhan, Akshaya
AU - Pandian, Jeyaraj Durai
AU - Sharma, Vijay K.
AU - Renjen, Pushpendra Nath
AU - Muruganathan, Arumugam
AU - Krishnan, Mugundhan
AU - Srinivasan, Avathvadi Venkatesan
AU - Shetty, Sadanand
AU - Narasingan, Sanjeevi Nathamuni
AU - Nair, Devaki R.
AU - Bansal, Manish
AU - Prabhakar, Dorairaj
AU - Varma, Mukul
AU - Paliwal, Vimal K.
AU - Kapoor, Aditya
AU - Mukhopadhyay, Saibal
AU - Mehrotra, Rahul
AU - Patanwala, Rashida Melinkari
AU - Aggarwal, Rajeev
AU - Mahajan, Kunal
AU - Kumar, Soumitra
AU - Bardoloi, Neil
AU - Pareek, Krishna Kumar
AU - Manoria, Prabhash Chand
AU - Pancholia, Arvind Kumar
AU - Nanda, Rashmi
AU - Wong, Nathan D.
AU - Duell, Paul Barton
N1 - Funding Information:
None. CONFLICT OF INTEREST Raman Puri: Boehringer Ingelheim, Novartis. Vimal Me-hta: Institutional research grant from Amgen, AstraZeneca, Boehringer Ingelheim, Eli Lilly, LIB Therapeutics, Torrent S S Iyengar: Reddy’s Lab, Amgen, Emcure, Glenmark, Boehringer Ingelheim, Pfizer, Novartis P Barton Duell: Espe-rion, Regeneron, Kaneka, Regenxbio, Retrophin/Travere, Regenxbio, Akcea, Amryt S N Narasingan: USV, Novo Nordisk, Eris, Glenmark, Torrent, Boehringer Ingelheim, J.B. Chemicals and Pharmaceuticals Devaki Nair: Abbott Diagnostics Nathan D Wong: Research support through his institution from Novartis and Esperion and is also a consultant for Novartis. The other authors have no conflict of interest.
Publisher Copyright:
© 2022 Bentham Science Publishers.
PY - 2022/3
Y1 - 2022/3
N2 - Stroke is the second most common cause of death worldwide. The rates of stroke are increasing in less affluent countries predominantly because of a high prevalence of modifiable risk factors. The Lipid Association of India (LAI) has provided a risk stratification algorithm for patients with ischaemic stroke and recommended low density lipoprotein cholesterol (LDL-C) goals for those in very high risk group and extreme risk group (category A) of <50 mg/dl (1.3 mmol/l) while the LDL-C goal for extreme risk group (category B) is <30 mg/dl (0.8 mmol/l). High intensity statins are the first-line lipid lowering therapy. Non¬statin therapy like ezetimibe and proprotein convertase subtilisin kexin type 9 (PCSK9) inhibitors may be added as an adjunct to statins in patients who do not achieve LDL-C goals with statins alone. In acute ischaemic stroke, high intensity statin therapy improves neurological and functional outcomes regardless of thrombolytic therapy. Although conflicting data exist regarding increased risk of intracerebral haemorrhage (ICH) with statin use, the overall benefit risk ratio favors long-term statin therapy necessitating detailed discussion with the patient. Patients who have statins withdrawn while being on prior statin therapy at the time of acute ischaemic stroke have worse functional outcomes and increased mortality. LAI recommends that statins be continued in such patients. In patients presenting with ICH, statins should not be started in the acute phase but should be continued in patients who are already taking statins. ICH patients, once sta¬ble, need risk stratification for atherosclerotic cardiovascular disease (ASCVD).
AB - Stroke is the second most common cause of death worldwide. The rates of stroke are increasing in less affluent countries predominantly because of a high prevalence of modifiable risk factors. The Lipid Association of India (LAI) has provided a risk stratification algorithm for patients with ischaemic stroke and recommended low density lipoprotein cholesterol (LDL-C) goals for those in very high risk group and extreme risk group (category A) of <50 mg/dl (1.3 mmol/l) while the LDL-C goal for extreme risk group (category B) is <30 mg/dl (0.8 mmol/l). High intensity statins are the first-line lipid lowering therapy. Non¬statin therapy like ezetimibe and proprotein convertase subtilisin kexin type 9 (PCSK9) inhibitors may be added as an adjunct to statins in patients who do not achieve LDL-C goals with statins alone. In acute ischaemic stroke, high intensity statin therapy improves neurological and functional outcomes regardless of thrombolytic therapy. Although conflicting data exist regarding increased risk of intracerebral haemorrhage (ICH) with statin use, the overall benefit risk ratio favors long-term statin therapy necessitating detailed discussion with the patient. Patients who have statins withdrawn while being on prior statin therapy at the time of acute ischaemic stroke have worse functional outcomes and increased mortality. LAI recommends that statins be continued in such patients. In patients presenting with ICH, statins should not be started in the acute phase but should be continued in patients who are already taking statins. ICH patients, once sta¬ble, need risk stratification for atherosclerotic cardiovascular disease (ASCVD).
KW - Carotid stenosis
KW - Intracerebral haemorrhage
KW - Ischaemic stroke
KW - Low density lipoprotein cholesterol
KW - Statin
KW - Stroke
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U2 - 10.2174/1570161119666211109122231
DO - 10.2174/1570161119666211109122231
M3 - Article
C2 - 34751121
AN - SCOPUS:85130634966
SN - 1570-1611
VL - 20
SP - 134
EP - 155
JO - Current Vascular Pharmacology
JF - Current Vascular Pharmacology
IS - 2
ER -