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The EffecTs of Amlodipine and other Blood PREssure Lowering Agents on Microvascular FuncTion in Small Vessel Diseases (TREAT-SVDs) trial: Study protocol for a randomised crossover trial.
Kopczak, Anna; S Stringer, Michael; van den Brink, Hilde; Kerkhofs, Danielle; W Blair, Gordon; van Dinther, Maud; Onkenhout, Laurien; A Wartolowska, Karolina; Thrippleton, Michael J; Duering, Marco; Staals, Julie; Middeke, Martin; André, Elisabeth; Norrving, Bo; Bousser, Marie-Germaine; Mansmann, Ulrich; Rothwell, Peter M; N Doubal, Fergus; van Oostenbrugge, Robert; Biessels, Geert Jan; Webb, Alastair Js; Wardlaw, Joanna M; Dichgans, Martin.
Afiliação
  • Kopczak A; Institute for Stroke and Dementia Research, University Hospital, LMU Munich, Munich, Germany.
  • S Stringer M; Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.
  • van den Brink H; Department of Neurology, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Kerkhofs D; Department of Neurology and School for cardiovascular diseases (CARIM), Maastricht University Medical Center+, Maastricht, The Netherlands.
  • W Blair G; Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.
  • van Dinther M; Department of Neurology and School for cardiovascular diseases (CARIM), Maastricht University Medical Center+, Maastricht, The Netherlands.
  • Onkenhout L; Department of Neurology, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht, The Netherlands.
  • A Wartolowska K; Wolfson Centre for Prevention of Stroke and Dementia, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.
  • Thrippleton MJ; Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.
  • Duering M; Institute for Stroke and Dementia Research, University Hospital, LMU Munich, Munich, Germany.
  • Staals J; Medical Image Analysis Center (MIAC AG) and Department of Biomedical Engineering, University of Basel, Basel, Switzerland.
  • Middeke M; Department of Neurology and School for cardiovascular diseases (CARIM), Maastricht University Medical Center+, Maastricht, The Netherlands.
  • André E; Hypertoniezentrum München, Excellence Centre of the European Society of Hypertension (ESH), Munich, Germany.
  • Norrving B; Münchner Studienzentrum, Faculty of Medicine, Technical University Munich (TUM), Munich, Germany.
  • Bousser MG; Neurology, Department of Clinical Sciences Lund, Lund University, and Neurology, Skåne University Hospital Lund/Malmö, Sweden.
  • Mansmann U; Hôpital Lariboisière, APHP, Université Paris-Cité, Paris, France.
  • Rothwell PM; Institute for Medical Information Processing, Biometry, and Epidemiology, LMU Munich, Munich, Germany.
  • N Doubal F; Wolfson Centre for Prevention of Stroke and Dementia, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.
  • van Oostenbrugge R; Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.
  • Biessels GJ; Department of Neurology and School for cardiovascular diseases (CARIM), Maastricht University Medical Center+, Maastricht, The Netherlands.
  • Webb AJ; Department of Neurology, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Wardlaw JM; Wolfson Centre for Prevention of Stroke and Dementia, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.
  • Dichgans M; Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.
Eur Stroke J ; 8(1): 387-397, 2023 03.
Article em En | MEDLINE | ID: mdl-37021189
ABSTRACT

Background:

Hypertension is the leading modifiable risk factor for cerebral small vessel diseases (SVDs). Yet, it is unknown whether antihypertensive drug classes differentially affect microvascular function in SVDs.

Aims:

To test whether amlodipine has a beneficial effect on microvascular function when compared to either losartan or atenolol, and whether losartan has a beneficial effect when compared to atenolol in patients with symptomatic SVDs.

Design:

TREAT-SVDs is an investigator-led, prospective, open-label, randomised crossover trial with blinded endpoint assessment (PROBE design) conducted at five study sites across Europe. Patients aged 18 years or older with symptomatic SVD who have an indication for antihypertensive treatment and are suffering from either sporadic SVD and a history of lacunar stroke or vascular cognitive impairment (group A) or CADASIL (group B) are randomly allocated 111 to one of three sequences of antihypertensive treatment. Patients stop their regular antihypertensive medication for a 2-week run-in period followed by 4-week periods of monotherapy with amlodipine, losartan and atenolol in random order as open-label medication in standard dose.

Outcomes:

The primary outcome measure is cerebrovascular reactivity (CVR) as determined by blood oxygen level dependent brain MRI signal response to hypercapnic challenge with change in CVR in normal appearing white matter as primary endpoint. Secondary outcome measures are mean systolic blood pressure (BP) and BP variability (BPv).

Discussion:

TREAT-SVDs will provide insights into the effects of different antihypertensive drugs on CVR, BP, and BPv in patients with symptomatic sporadic and hereditary SVDs.

Funding:

European Union's Horizon 2020 programme. Trial registration NCT03082014.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anlodipino / Anti-Hipertensivos Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anlodipino / Anti-Hipertensivos Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article