Early intervention and cumulative life course impairment in psoriasis: a review
- PMID: 39045914
- DOI: 10.1093/ced/llae282
Early intervention and cumulative life course impairment in psoriasis: a review
Abstract
Psoriasis is a chronic, systemic, inflammatory disease affecting the skin, joints and other organs. Psoriasis negatively affects patients' quality of life, causing social anxiety and negative coping, thus determining a cumulative life course impairment (CLCI). The concept of CLCI in psoriasis is reinforced by the understanding that psoriasis-associated comorbidities and stigma accumulate over a patient's life course, resulting from an interaction between the burden of stigmatization, physical and psychological comorbidities, coping strategies and external factors. The concept may help identify more vulnerable patients and facilitate more appropriate treatment decisions or earlier referrals. Although some potential risk factors for CLCI have been clarified, no all-encompassing screening tools are available. Patients at risk for CLCI should be identified by applying clinical, personal and psychosocial indicators and predictors individually. Early intervention in psoriasis treatment could improve long-term patient outcomes and modify the disease course. However, more research is needed to clearly define what constitutes 'early' intervention and to identify the most effective strategies for implementation. From a preventive point of view, it is helpful to identify early interventions aimed at reducing the risk of CLCI and establishing a new life course trajectory in patients with psoriasis. This review summarizes the latest developments in CLCI and psoriasis, highlighting knowledge gaps and future directions to make control of CLCI a possible goal for therapies.
© The Author(s) 2024. Published by Oxford University Press on behalf of British Association of Dermatologists.
Conflict of interest statement
Conflicts of interest L.M.H.A. has been a consultant and/or speaker for AbbVie, Almirall, Pfizer, Novartis and Janssen. D.D. has received fees from AbbVie, Janssen and Eli Lilly. S.D. has been a consultant or speaker for AbbVie, Almirall, Amgen, LEO Pharma and Novartis. G.M. has received fees from AbbVie, LEO Pharma, Sanofi and Eli Lilly. G.P. has received fees from AbbVie, Janssen and Pierre Fabre Pharma. S.P. has been a consultant and/or speaker for AbbVie, Almirall, Amgen, Eli Lilly, Janssen, LEO Pharma, Merck Sharp & Dohme, Novartis, Pfizer, Sandoz and UCB. C.S.F. and M.M. have no conflicts of interest to declare. A.L., S.D.F. and B.Z. are full-time employees of AbbVie and may hold AbbVie stock and/or stock options.
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