Reduced dementia risk in middle-aged and older atopic dermatitis patients treated with dupilumab: A target trial emulation.

IF 7.6 2区 医学 Q1 IMMUNOLOGY
Yi-Hsuan Fan, Kuo-Sheng Fan, Teng-Li Lin
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引用次数: 0

Abstract

Background: Middle-aged and older adults with atopic dermatitis (AD) are at increased risk of dementia, possibly driven by chronic inflammation and involving IL-4 and IL-13 pathways. Whether treatment with dupilumab, an IL-4/IL-13 inhibitor, influences subsequent dementia risk in this population remains unclear.

Methods: This target trial emulation study utilized the TriNetX database. Patients aged ≥ 50 years with AD were identified and divided into two groups: those newly prescribed dupilumab and those newly prescribed conventional systemic agents without dupilumab exposure. Propensity score matching (1:1) was performed based on age, sex, race, and comorbidities. Dementia risk was assessed using Cox regression.

Results: After matching, each group included 10,039 patients (∼52% female; mean age, 63 years; 63% White). The 5-year cumulative incidence of dementia was lower among dupilumab users than controls (2.37% vs 3.33%; P = 0.001). Dupilumab use was associated with a reduced risk of all-cause dementia (HR 0.68; 95% CI, 0.54-0.86), with similar reductions observed across dementia subtypes, including secondary (HR 0.69; 95% CI, 0.48-0.99), unspecified (HR 0.70; 95% CI, 0.53-0.93), and Alzheimer's dementia (HR 0.61; 95% CI, 0.40-0.93). Subgroup and sensitivity analyses showed consistent results, with control outcome analyses supporting the robustness of the findings. In a validation analysis of middle-aged and older asthma patients, dupilumab users likewise had a lower dementia risk than omalizumab users (HR 0.68; 95% CI, 0.47-0.98).

Conclusions: Dupilumab use was associated with a reduced risk of dementia in middle-aged and older adults with AD compared with conventional systemic agents.

dupilumab治疗中老年特应性皮炎患者痴呆风险降低:一项目标试验模拟
背景:中老年特应性皮炎(AD)患者痴呆风险增加,可能由慢性炎症驱动,并涉及IL-4和IL-13途径。使用IL-4/IL-13抑制剂dupilumab治疗是否会影响该人群随后的痴呆风险仍不清楚。方法:利用TriNetX数据库进行目标试验仿真研究。年龄 ≥ 50岁的AD患者被确定并分为两组:新开dupilumab的患者和新开常规全身性药物的患者。根据年龄、性别、种族和合并症进行倾向评分匹配(1:1)。采用Cox回归评估痴呆风险。结果:匹配后,每组纳入10039例患者(52%为女性,平均年龄63 岁,63%为白人)。dupilumab使用者的5年累积痴呆发病率低于对照组(2.37% vs 3.33%; P = 0.001)。Dupilumab的使用与全因痴呆的风险降低相关(HR 0.68; 95% CI, 0.54-0.86),在痴呆亚型中也观察到类似的降低,包括继发性(HR 0.69; 95% CI, 0.48-0.99),未明确(HR 0.70; 95% CI, 0.53-0.93)和阿尔茨海默氏痴呆(HR 0.61; 95% CI, 0.40-0.93)。亚组分析和敏感性分析显示了一致的结果,对照结果分析支持研究结果的稳健性。在中老年哮喘患者的验证分析中,dupilumab使用者的痴呆风险同样低于omalizumab使用者(HR 0.68; 95% CI, 0.47-0.98)。结论:与传统全身药物相比,Dupilumab的使用与中老年AD患者痴呆风险降低相关。
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来源期刊
CiteScore
29.60
自引率
2.00%
发文量
290
审稿时长
28 days
期刊介绍: Established in 1987, Brain, Behavior, and Immunity proudly serves as the official journal of the Psychoneuroimmunology Research Society (PNIRS). This pioneering journal is dedicated to publishing peer-reviewed basic, experimental, and clinical studies that explore the intricate interactions among behavioral, neural, endocrine, and immune systems in both humans and animals. As an international and interdisciplinary platform, Brain, Behavior, and Immunity focuses on original research spanning neuroscience, immunology, integrative physiology, behavioral biology, psychiatry, psychology, and clinical medicine. The journal is inclusive of research conducted at various levels, including molecular, cellular, social, and whole organism perspectives. With a commitment to efficiency, the journal facilitates online submission and review, ensuring timely publication of experimental results. Manuscripts typically undergo peer review and are returned to authors within 30 days of submission. It's worth noting that Brain, Behavior, and Immunity, published eight times a year, does not impose submission fees or page charges, fostering an open and accessible platform for scientific discourse.
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