Psoriatic arthritis and obesity: the role of anti-IL-12/IL-23 treatment

被引:16
作者
Costa, Luisa [1 ]
Ramonda, Roberta [2 ]
Ortolan, Augusta [2 ]
Favero, Marta [2 ]
Foti, Rosario [3 ]
Visalli, Elisa [3 ]
Rossato, Marco [4 ]
Cacciapaglia, Fabio [5 ]
Lapadula, Giovanni [5 ]
Scarpa, Raffaele [1 ]
机构
[1] Univ Federico II Naples, Dept Clin Med & Surg, Rheumatol Unit, Naples, Italy
[2] Univ Padua, Dept Med DIMED, Rheumatol Unit, Padua, Italy
[3] AOU Policlin Vittorio Emanuele, Rheumatol Unit, Catania, Italy
[4] Padova Univ Hosp, Ctr Study & Integrated Management Obes, Dept Med DIMED, Clin Med 3, Padua, Italy
[5] Univ Bari, Dept Emergency & Organs Transplantat DETO, Rheumatol Unit, Bari, Italy
关键词
Biological therapy; Interleukin inhibitor; MDA in PsA; Obesity; Psoriatic arthritis; Therapeutic response; NECROSIS-FACTOR-ALPHA; BODY-MASS INDEX; MINIMAL DISEASE-ACTIVITY; CHRONIC PLAQUE PSORIASIS; METABOLIC SYNDROME; USTEKINUMAB; WEIGHT; THERAPY; INFLAMMATION; RISK;
D O I
10.1007/s10067-019-04663-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Patients with psoriatic arthritis (PsA) have an increased prevalence of obesity, but mechanisms underlying this association remain unknown and it is unclear if obesity is the cause or effect of PsA. For PsA patients, comorbid obesity may influence their clinical response to systemic treatment, and especially targeted immunomodulators such as anti-tumor necrosis factor (TNF)alpha. Weight gain has also been associated with anti-TNF alpha treatment. Consequently, modification of the therapeutic approach may be needed for patients with an inadequate response to TNF alpha inhibitors. In recent years, interleukin (IL)-12/IL-23 inhibitors have entered clinical practice as a new class of drug for the treatment of PsA, with some data suggesting a lower effect of body weight on their effectiveness. Recent findings demonstrate effective and sustained responses in patients with PsA to ustekinumab, an IL-12/IL-23 inhibitor. This narrative review critically discusses the link between PsA, obesity, and response to therapy. The current role of ustekinumab in this setting is also discussed.
引用
收藏
页码:2355 / 2362
页数:8
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