Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/27694
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dc.contributor.authorDobric, Aleksandar-
dc.contributor.authorDe Luca, Simone N-
dc.contributor.authorSpencer, Sarah J-
dc.contributor.authorBozinovski, Steven-
dc.contributor.authorSaling, Michael M-
dc.contributor.authorMcDonald, Christine F-
dc.contributor.authorVlahos, Ross-
dc.date2021-10-06-
dc.date.accessioned2021-10-11T04:12:30Z-
dc.date.available2021-10-11T04:12:30Z-
dc.date.issued2021-10-06-
dc.identifier.citationPharmacology & Therapeutics 2022; 233: 108017en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/27694-
dc.description.abstractChronic obstructive pulmonary disease (COPD) is a major incurable global health burden and currently, the 3rd largest cause of death in the world with approximately 3.23 million deaths per year. Globally, the financial burden of COPD is approximately €82 billion per year and causes substantial morbidity and mortality. Importantly, much of the disease burden and health care utilisation in COPD is associated with the management of its comorbidities and viral and bacterial-induced acute exacerbations (AECOPD). Recent clinical studies have shown that cognitive dysfunction is present in up to 60% of people with COPD, with impairments in executive function, memory, and attention, impacting on important outcomes such as quality of life, hospitalisation and survival. The high prevalence of cognitive dysfunction in COPD may also help explain the insufficient adherence to therapeutic plans and strategies, thus worsening disease progression in people with COPD. However, the mechanisms underlying the impaired neuropathology and cognition in COPD remain largely unknown. In this review, we propose that the observed pulmonary oxidative burden and inflammatory response of people with COPD 'spills over' into the systemic circulation, resulting in damage to the brain and leading to cognitive dysfunction. As such, drugs targeting the lungs and comorbidities concurrently represent an exciting and unique therapeutic opportunity to treat COPD and cognitive impairments, which may lead to the production of novel targets to prevent and reverse the debilitating and life-threatening effects of cognitive dysfunction in COPD.en
dc.language.isoeng-
dc.subjectChronic obstructive pulmonary diseaseen
dc.subjectCognitive dysfunctionen
dc.subjectMicrogliaen
dc.subjectNeuroinflammationen
dc.subjectOxidative stressen
dc.subjectSmokingen
dc.titleNovel pharmacological strategies to treat cognitive dysfunction in chronic obstructive pulmonary disease.en
dc.typeJournal Articleen
dc.identifier.journaltitlePharmacology & Therapeuticsen
dc.identifier.affiliationSchool of Health & Biomedical Sciences, RMIT University, Melbourne, VIC, Australiaen
dc.identifier.affiliationInstitute for Breathing and Sleepen
dc.identifier.affiliationRespiratory and Sleep Medicineen
dc.identifier.affiliationClinical Neuropsychologyen
dc.identifier.affiliationARC Centre of Excellence for Nanoscale Biophotonics, RMIT University, Melbourne, VIC, Australiaen
dc.identifier.affiliationThe University of Melbourne, Melbourne, VIC, Australiaen
dc.identifier.doi10.1016/j.pharmthera.2021.108017en
dc.type.contentTexten
dc.identifier.pubmedid34626675-
local.name.researcherMcDonald, Christine F
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
crisitem.author.deptClinical Neuropsychology-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptRespiratory and Sleep Medicine-
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