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Statins are underused in recent-onset Parkinson's disease with increased vascular risk: findings from the UK Tracking Parkinson's and Oxford Parkinson's Disease Centre (OPDC) discovery cohorts
BACKGROUND: Cardiovascular disease (CVD) influences phenotypic variation in Parkinson's disease (PD), and is usually an indication for statin therapy. It is less clear whether cardiovascular risk factors influence PD phenotype, and if statins are prescribed appropriately. OBJECTIVES: To quantif...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5116532/ https://www.ncbi.nlm.nih.gov/pubmed/27671901 http://dx.doi.org/10.1136/jnnp-2016-313642 |
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author | Swallow, Diane M A Lawton, Michael A Grosset, Katherine A Malek, Naveed Klein, Johannes Baig, Fahd Ruffmann, Claudio Bajaj, Nin P Barker, Roger A Ben-Shlomo, Yoav Burn, David J Foltynie, Thomas Morris, Huw R Williams, Nigel Wood, Nicholas W Hu, Michele T M Grosset, Donald G |
author_facet | Swallow, Diane M A Lawton, Michael A Grosset, Katherine A Malek, Naveed Klein, Johannes Baig, Fahd Ruffmann, Claudio Bajaj, Nin P Barker, Roger A Ben-Shlomo, Yoav Burn, David J Foltynie, Thomas Morris, Huw R Williams, Nigel Wood, Nicholas W Hu, Michele T M Grosset, Donald G |
author_sort | Swallow, Diane M A |
collection | PubMed |
description | BACKGROUND: Cardiovascular disease (CVD) influences phenotypic variation in Parkinson's disease (PD), and is usually an indication for statin therapy. It is less clear whether cardiovascular risk factors influence PD phenotype, and if statins are prescribed appropriately. OBJECTIVES: To quantify vascular risk and statin use in recent-onset PD, and examine the relationship between vascular risk, PD severity and phenotype. METHODS: Cardiovascular risk was quantified using the QRISK2 calculator (high ≥20%, medium ≥10 and <20%, low risk <10%). Motor severity and phenotype were assessed using the Movement Disorder Society Unified PD Rating Scale (UPDRS) and cognition by the Montreal cognitive assessment. RESULTS: In 2909 individuals with recent-onset PD, the mean age was 67.5 years (SD 9.3), 63.5% were men and the mean disease duration was 1.3 years (SD 0.9). 33.8% of cases had high vascular risk, 28.7% medium risk, and 22.3% low risk, while 15.2% of cases had established CVD. Increasing vascular risk and CVD were associated with older age (p<0.001), worse motor score (p<0.001), more cognitive impairment (p<0.001) and worse motor phenotype (p=0.021). Statins were prescribed in 37.2% with high vascular risk, 15.1% with medium vascular risk and 6.5% with low vascular risk, which compared with statin usage in 75.3% of those with CVD. CONCLUSIONS: Over 60% of recent-onset PD patients have high or medium cardiovascular risk (meriting statin usage), which is associated with a worse motor and cognitive phenotype. Statins are underused in these patients, compared with those with vascular disease, which is a missed opportunity for preventive treatment. TRIAL REGISTRATION NUMBER: GN11NE062, NCT02881099. |
format | Online Article Text |
id | pubmed-5116532 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51165322016-11-29 Statins are underused in recent-onset Parkinson's disease with increased vascular risk: findings from the UK Tracking Parkinson's and Oxford Parkinson's Disease Centre (OPDC) discovery cohorts Swallow, Diane M A Lawton, Michael A Grosset, Katherine A Malek, Naveed Klein, Johannes Baig, Fahd Ruffmann, Claudio Bajaj, Nin P Barker, Roger A Ben-Shlomo, Yoav Burn, David J Foltynie, Thomas Morris, Huw R Williams, Nigel Wood, Nicholas W Hu, Michele T M Grosset, Donald G J Neurol Neurosurg Psychiatry Movement Disorders BACKGROUND: Cardiovascular disease (CVD) influences phenotypic variation in Parkinson's disease (PD), and is usually an indication for statin therapy. It is less clear whether cardiovascular risk factors influence PD phenotype, and if statins are prescribed appropriately. OBJECTIVES: To quantify vascular risk and statin use in recent-onset PD, and examine the relationship between vascular risk, PD severity and phenotype. METHODS: Cardiovascular risk was quantified using the QRISK2 calculator (high ≥20%, medium ≥10 and <20%, low risk <10%). Motor severity and phenotype were assessed using the Movement Disorder Society Unified PD Rating Scale (UPDRS) and cognition by the Montreal cognitive assessment. RESULTS: In 2909 individuals with recent-onset PD, the mean age was 67.5 years (SD 9.3), 63.5% were men and the mean disease duration was 1.3 years (SD 0.9). 33.8% of cases had high vascular risk, 28.7% medium risk, and 22.3% low risk, while 15.2% of cases had established CVD. Increasing vascular risk and CVD were associated with older age (p<0.001), worse motor score (p<0.001), more cognitive impairment (p<0.001) and worse motor phenotype (p=0.021). Statins were prescribed in 37.2% with high vascular risk, 15.1% with medium vascular risk and 6.5% with low vascular risk, which compared with statin usage in 75.3% of those with CVD. CONCLUSIONS: Over 60% of recent-onset PD patients have high or medium cardiovascular risk (meriting statin usage), which is associated with a worse motor and cognitive phenotype. Statins are underused in these patients, compared with those with vascular disease, which is a missed opportunity for preventive treatment. TRIAL REGISTRATION NUMBER: GN11NE062, NCT02881099. BMJ Publishing Group 2016-11 /pmc/articles/PMC5116532/ /pubmed/27671901 http://dx.doi.org/10.1136/jnnp-2016-313642 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Movement Disorders Swallow, Diane M A Lawton, Michael A Grosset, Katherine A Malek, Naveed Klein, Johannes Baig, Fahd Ruffmann, Claudio Bajaj, Nin P Barker, Roger A Ben-Shlomo, Yoav Burn, David J Foltynie, Thomas Morris, Huw R Williams, Nigel Wood, Nicholas W Hu, Michele T M Grosset, Donald G Statins are underused in recent-onset Parkinson's disease with increased vascular risk: findings from the UK Tracking Parkinson's and Oxford Parkinson's Disease Centre (OPDC) discovery cohorts |
title | Statins are underused in recent-onset Parkinson's disease with increased vascular risk: findings from the UK Tracking Parkinson's and Oxford Parkinson's Disease Centre (OPDC) discovery cohorts |
title_full | Statins are underused in recent-onset Parkinson's disease with increased vascular risk: findings from the UK Tracking Parkinson's and Oxford Parkinson's Disease Centre (OPDC) discovery cohorts |
title_fullStr | Statins are underused in recent-onset Parkinson's disease with increased vascular risk: findings from the UK Tracking Parkinson's and Oxford Parkinson's Disease Centre (OPDC) discovery cohorts |
title_full_unstemmed | Statins are underused in recent-onset Parkinson's disease with increased vascular risk: findings from the UK Tracking Parkinson's and Oxford Parkinson's Disease Centre (OPDC) discovery cohorts |
title_short | Statins are underused in recent-onset Parkinson's disease with increased vascular risk: findings from the UK Tracking Parkinson's and Oxford Parkinson's Disease Centre (OPDC) discovery cohorts |
title_sort | statins are underused in recent-onset parkinson's disease with increased vascular risk: findings from the uk tracking parkinson's and oxford parkinson's disease centre (opdc) discovery cohorts |
topic | Movement Disorders |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5116532/ https://www.ncbi.nlm.nih.gov/pubmed/27671901 http://dx.doi.org/10.1136/jnnp-2016-313642 |
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