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Journal of Nippon Medical School

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Real-World 52-Week Effectiveness of Tildrakizumab for Psoriasis: Analysis Stratified by Age, Disease Duration, and Body Mass Index

Yuriko Okabe1, Teppei Hagino1, Hidehisa Saeki2 and Naoko Kanda1

1Department of Dermatology, Nippon Medical School Chiba Hokusoh Hospital, Chiba, Japan
2Department of Dermatology, Nippon Medical School, Tokyo, Japan


Background: Age, disease duration, and body mass index (BMI) influence the real-world effectiveness of tildrakizumab for psoriasis. We evaluated the 52-week real-world effectiveness of tildrakizumab for psoriasis patients stratified by age (<65 versus ≥65 years), disease duration (≤2 vs >2 years), and BMI (<25 versus ≥25 kg/m2).
Methods: This study included 55 patients with psoriasis who were treated with tildrakizumab 100 mg. Clinical outcomes and laboratory indices were assessed during the 52-week treatment period.
Results: Psoriasis area and severity index (PASI) decreased throughout the 52-week treatment period in all patients. At week 52, PASI 90 and PASI 100 rates were higher in patients aged <65 years, those with a disease duration of ≤2 years, and those with a BMI of <25 kg/m2 than in their respective comparison groups. PASI 90 rates were 62.5% versus 35.7%, 100% versus 36.8%, and 60.0% versus 33.3%, respectively. At week 52, the rate of an absolute PASI ≤1 was higher in patients aged <65 years, those with a disease duration ≤2 years, and those with a BMI ≥25 kg/m2. The systemic immune-inflammation index, calculated as neutrophil × platelet/lymphocyte count, was significantly lower at week 52 than at baseline. Metabolic laboratory indices did not change significantly during the 52-week treatment period.
Conclusions: Tildrakizumab showed sustained real-world effectiveness for psoriasis for 52 weeks across patient subgroups stratified by age, disease duration, and BMI.

J Nippon Med Sch 2026; 93: 384-393

Keywords
psoriasis, tildrakizumab, interleukin-23, age, disease duration

Correspondence to
Teppei Hagino
teppei-hagino@nms.ac.jp

Received, June 19, 2026
Accepted, July 16, 2026