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Metabolic syndrome and psoriatic arthritis: the role of weight loss as a disease-modifying therapy.

Authors :
Williams, Jacob Corum
Hum, Ryan Malcolm
Rogers, Kira
Maglio, Cristina
Alam, Uazman
Zhao, Sizheng Steven
Source :
Therapeutic Advances in Musculoskeletal Disease; 8/19/2024, p1-15, 15p
Publication Year :
2024

Abstract

Psoriatic arthritis (PsA) is an inflammatory joint and entheseal disease associated with significant personal and public health burden. PsA has a prevalence of up to 1%, affecting ~20% of people suffering with psoriasis. PsA is frequently accompanied by metabolic syndrome (MetS), and both conditions are characterised by a chronic pro-inflammatory state, with several key cytokines in PsA (interleukin (IL)-17 and IL-23) also elevated in those with MetS. This narrative review aims to provide an update on MetS in PsA, focusing on its prevalence, pathogenesis, prognosis, treatment interactions and future therapeutic options. MetS is particularly prevalent in PsA compared to other inflammatory arthritides. Cohort studies indicate a higher risk of PsA in individuals with obesity, while Mendelian randomization studies link childhood obesity, insulin resistance, and dyslipidaemia to PsA. Weight loss interventions have been shown to reduce disease activity in PsA. Additionally, MetS negatively impacts the efficacy of tumour necrosis factor inhibitor (TNFi) drugs in treating PsA. Drugs given for PsA may also affect the conditions constituting MetS. Leflunomide has been shown to reduce body weight but also increase blood pressure. TNFi drugs lead to weight gain but reduce cardiovascular risk. Janus kinase inhibitors increase lipid levels and cardiovascular risk among high-risk groups. Anti-IL-17 and anti-IL-12/IL-23 drugs may cause a short-term increase in cardiovascular risk, although the long-term effects have yet to be established. Weight loss represents an unexplored avenue for disease modification in PsA, alongside a plethora of general health benefits. Dietary and exercise modifications are the cornerstone of weight management but vary substantially across individuals. Novel therapies to treat weight loss, such as glucagon-like peptide 1 agonists and sodium–glucose cotransporter 2 inhibitors, may prove useful alongside disease-modifying therapies for those with PsA and MetS and should be investigated as potential therapeutic adjuncts. Plain language summary: What effects do obesity and related health problems have on psoriatic arthritis? Psoriatic arthritis (PsA) is a condition that causes joint pain and swelling, which can lead to permanent damage to the joints over time. This condition affects 1 in 100 people and 1 in 5 people with psoriasis. Metabolic syndrome (MetS) is a condition where a person has a combination of high body fat, high blood pressure, high blood sugar and/or high cholesterol. MetS is more common in someone with PsA. If a person has MetS, they are more likely to get PsA. If a person with PsA has MetS, they have worse joint problems and their joint problems do not improve as much with certain treatments. Many of the drugs given for PsA can affect MetS. This can include increasing or decreasing body weight, increasing blood pressure and increasing or decreasing the risk of having a heart attack or stroke. Different medications affect these risks in different ways. Weight loss helps people with PsA improve their joint problems. However, some people find losing weight harder than others. Medications that can help people lose weight, could be useful to improve joint problems in PsA. Future studies should see if these medications can be useful in people with PsA and MetS. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1759720X
Database :
Complementary Index
Journal :
Therapeutic Advances in Musculoskeletal Disease
Publication Type :
Academic Journal
Accession number :
179084563
Full Text :
https://doi.org/10.1177/1759720X241271886