Evidence map›Paper›PMID 42835100›Full record

ArticleKidney international reports2026

Clinical and Pathologic Characteristics of Patients With ANCA-Associated Vasculitis With Renal Arteritis.

Yan-Jie Li, Shu-Juan Zhao, Fan Zhang, Shu-Hong Bi, Zhi-Ying Li, Xiao-Juan Yu, Su-Xia Wang, Jin-Wei Wang, Xiao-Tao Ma, Jing Wang and 7 more

Abstract read
In one paragraph

Article in Kidney international reports, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Yan-Jie LiRenal Division, Department of Medicine, Peking University First Hospital; Institute of Nephrology, Peking University; Key Laboratory of Renal Disease, Ministry of Health of China; Key Laboratory of Chronic Kidney Disease Prevention and Treatment (Peking University), Ministry of Education; Research Units of Diagnosis and Treatment of Immune-mediated Kidney Diseases, Chinese Academy of Medical Sciences; Beijing Key Laboratory of Precision Medicine and New-drug/Equipment Development for Severe Kidney Disease; Beijing, China.
Shu-Juan ZhaoDepartment of Nephrology, Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Fan ZhangRenal Division, Department of Medicine, Peking University Shenzhen Hospital, Shenzhen, China.
Shu-Hong BiDivision of Nephrology, Peking University Third Hospital, Beijing, China.
Zhi-Ying LiRenal Division, Department of Medicine, Peking University First Hospital; Institute of Nephrology, Peking University; Key Laboratory of Renal Disease, Ministry of Health of China; Key Laboratory of Chronic Kidney Disease Prevention and Treatment (Peking University), Ministry of Education; Research Units of Diagnosis and Treatment of Immune-mediated Kidney Diseases, Chinese Academy of Medical Sciences; Beijing Key Laboratory of Precision Medicine and New-drug/Equipment Development for Severe Kidney Disease; Beijing, China.
Xiao-Juan YuRenal Division, Department of Medicine, Peking University First Hospital; Institute of Nephrology, Peking University; Key Laboratory of Renal Disease, Ministry of Health of China; Key Laboratory of Chronic Kidney Disease Prevention and Treatment (Peking University), Ministry of Education; Research Units of Diagnosis and Treatment of Immune-mediated Kidney Diseases, Chinese Academy of Medical Sciences; Beijing Key Laboratory of Precision Medicine and New-drug/Equipment Development for Severe Kidney Disease; Beijing, China.
Su-Xia WangRenal Division, Department of Medicine, Peking University First Hospital; Institute of Nephrology, Peking University; Key Laboratory of Renal Disease, Ministry of Health of China; Key Laboratory of Chronic Kidney Disease Prevention and Treatment (Peking University), Ministry of Education; Research Units of Diagnosis and Treatment of Immune-mediated Kidney Diseases, Chinese Academy of Medical Sciences; Beijing Key Laboratory of Precision Medicine and New-drug/Equipment Development for Severe Kidney Disease; Beijing, China.
Jin-Wei WangRenal Division, Department of Medicine, Peking University First Hospital; Institute of Nephrology, Peking University; Key Laboratory of Renal Disease, Ministry of Health of China; Key Laboratory of Chronic Kidney Disease Prevention and Treatment (Peking University), Ministry of Education; Research Units of Diagnosis and Treatment of Immune-mediated Kidney Diseases, Chinese Academy of Medical Sciences; Beijing Key Laboratory of Precision Medicine and New-drug/Equipment Development for Severe Kidney Disease; Beijing, China.
Xiao-Tao MaDepartment of Nephrology, Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Jing WangDepartment of Nephrology, Hanzhong Central Hospital, Hanzhong, China.
Yi LiDepartment of Nephrology, 3201 Hospital, Hanzhong, China.
Zu-Ying XiongRenal Division, Department of Medicine, Peking University Shenzhen Hospital, Shenzhen, China.
Yue WangDivision of Nephrology, Peking University Third Hospital, Beijing, China.
Rong-Guo FuDepartment of Nephrology, Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Su-Fang ChenRenal Division, Department of Medicine, Peking University First Hospital; Institute of Nephrology, Peking University; Key Laboratory of Renal Disease, Ministry of Health of China; Key Laboratory of Chronic Kidney Disease Prevention and Treatment (Peking University), Ministry of Education; Research Units of Diagnosis and Treatment of Immune-mediated Kidney Diseases, Chinese Academy of Medical Sciences; Beijing Key Laboratory of Precision Medicine and New-drug/Equipment Development for Severe Kidney Disease; Beijing, China.
Ming-Hui ZhaoRenal Division, Department of Medicine, Peking University First Hospital; Institute of Nephrology, Peking University; Key Laboratory of Renal Disease, Ministry of Health of China; Key Laboratory of Chronic Kidney Disease Prevention and Treatment (Peking University), Ministry of Education; Research Units of Diagnosis and Treatment of Immune-mediated Kidney Diseases, Chinese Academy of Medical Sciences; Beijing Key Laboratory of Precision Medicine and New-drug/Equipment Development for Severe Kidney Disease; Beijing, China.
Min ChenRenal Division, Department of Medicine, Peking University First Hospital; Institute of Nephrology, Peking University; Key Laboratory of Renal Disease, Ministry of Health of China; Key Laboratory of Chronic Kidney Disease Prevention and Treatment (Peking University), Ministry of Education; Research Units of Diagnosis and Treatment of Immune-mediated Kidney Diseases, Chinese Academy of Medical Sciences; Beijing Key Laboratory of Precision Medicine and New-drug/Equipment Development for Severe Kidney Disease; Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is characterized by necrotizing inflammation of small vessels, typically affecting glomerular capillaries. However, small arteries can also be affected. The clinical significance of this subgroup of patients remains unclear. This study aimed to analyze the clinicopathologic features and prognostic significance of renal arteritis in Chinese patients with AAV. Methods: A large multicenter cohort of 511 patients with renal biopsy-proven AAV, diagnosed between 2002 and 2023, was retrospectively enrolled. Clinicopathologic parameters were compared between those with and without renal arteritis (termed AAV_A+ and AAV_A-, respectively). The prognostic value of renal arteritis was further analyzed. Results: Among the 511 patients with AAV, 73 (14.3%) had renal arteritis. Compared with patients with AAV_A-, patients with AAV_A+ were significantly older at diagnosis, with more pronounced systemic inflammation and more frequent extrarenal involvement. Although baseline renal function was comparable, patients with AAV_A+ exhibited a distinct histopathologic phenotype, with fewer crescentic lesions but more inflammatory and necrotizing injuries. Despite patients with AAV_A+ showed a better response to immunosuppressive therapy, renal survival was similar between the 2 groups. However, among patients classified as low or moderate risk by the ANCA kidney risk score (AKRiS), renal survival was significantly worse in patients with AAV_A+. For this subgroup, renal arteritis was independently associated with an increased risk of end-stage kidney disease (ESKD). Conclusion: AAV with renal arteritis represents a distinct clinical and pathologic phenotype in the Chinese population. In patients classified as low or moderate risk by the AKRiS, renal arteritis was independently associated with an increased risk of ESKD.

Indexed as

ANCArenal arteritisvasculitis

Identifiers

PMID42835100
PMCPMC13634887

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