Evidence map›Paper›PMID 42292810›Full record

ArticleFrontiers in pharmacology2026

The efficacy and safety of telitacicept and its combination with glucocorticoids in IgA nephropathy: a retrospective cohort study.

Yiyang Li, Lijuan Zhao, Meijing Pan, Yan Wang, Xin Gou, Xinrong Yang, Qian Zhang, Chenchen Ma, Jiaoyang Zhang, Guoshuang Xu

Abstract read
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Article in Frontiers in pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Yiyang Li *Department of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Lijuan Zhao *Department of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Meijing PanDepartment of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Yan WangDepartment of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Xin GouDepartment of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Xinrong YangDepartment of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Qian ZhangDepartment of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Chenchen MaDepartment of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Jiaoyang ZhangDepartment of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Guoshuang XuDepartment of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Immunoglobulin A nephropathy (IgAN) has a high incidence rate and a poor prognosis. Currently, no ideal treatment is available for this disease. Despite some reports on the use of telitacicept in IgAN, studies with a treatment duration of 24 weeks or longer remain limited, and data on its combination with glucocorticoids are currently lacking. Methods: This retrospective cohort study enrolled 136 individuals diagnosed with IgAN via renal biopsy who exhibited 24-h urinary protein excretion (UPE) ≥ 1 g and an estimated glomerular filtration rate (eGFR) ≥ 30 ml/min/1.73 m Results: At 24 weeks, compared with baseline, median UPE decreased by 0.70 g (41.75%) in the RAS inhibitor group, by 0.92 g (62.85%) in the glucocorticoid ± immunosuppressant group, by 1.14 g (73.68%) in the telitacicept group, and by 1.34 g (81.18%) in the telitacicept + glucocorticoid group. The reduction in UPE was significantly greater in the latter three groups than in the RAS inhibitor group (p < 0.05). Moreover, the telitacicept + glucocorticoid group demonstrated a significantly greater reduction in UPE than the other groups. The eGFR decreased by 3.22 ml/min/1.73 m Conclusion: These findings indicate that in IgAN patients with a high risk of progression, telitacicept effectively reduces proteinuria and confers kidney protective effects. Furthermore, in individuals with UPE ≥2.5 g or impaired renal function, the combination of telitacicept and glucocorticoids is associated with improved rates of UPE remission.

Indexed as

efficacyIgA nephropathyproteinuriasafetytelitacicept

Identifiers

PMID42292810
PMCPMC13260495

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