Evidence map›Paper›PMID 42577505›Full record

ArticleBioengineering & translational medicine2026

Monitoring vascular changes in renal fibrosis in mice using multimodal optical and ultrasonic imaging.

Ruijing Zhang, Yuhang Zhang, Chuanlong Lu, Keyi Fan, Heng Wang, Qian Wang, Yijie Ning, Yaling Li, Zeyu Zhang, Xiaohua Jia and 1 more

Abstract read
In one paragraph

Article in Bioengineering & translational medicine, 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

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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Ruijing ZhangVascular Institute of Shanxi Medical University, Shanxi Medical University Taiyuan Shanxi People's Republic of China.
Yuhang ZhangVascular Institute of Shanxi Medical University, Shanxi Medical University Taiyuan Shanxi People's Republic of China.
Chuanlong LuVascular Institute of Shanxi Medical University, Shanxi Medical University Taiyuan Shanxi People's Republic of China.ORCID https://orcid.org/0009-0005-2137-6853
Keyi FanVascular Institute of Shanxi Medical University, Shanxi Medical University Taiyuan Shanxi People's Republic of China.ORCID https://orcid.org/0000-0002-1820-9107
Heng WangVascular Institute of Shanxi Medical University, Shanxi Medical University Taiyuan Shanxi People's Republic of China.ORCID https://orcid.org/0000-0001-7408-0398
Qian WangVascular Institute of Shanxi Medical University, Shanxi Medical University Taiyuan Shanxi People's Republic of China.
Yijie NingVascular Institute of Shanxi Medical University, Shanxi Medical University Taiyuan Shanxi People's Republic of China.
Yaling LiDepartment of Vascular Surgery The Second Hospital of Shanxi Medical University Taiyuan Shanxi People's Republic of China.ORCID https://orcid.org/0009-0001-7932-9313
Zeyu ZhangKey Laboratory of Molecular Imaging of Chinese Academy of Sciences Institute of Automation, Chinese Academy of Sciences Beijing People's Republic of China.ORCID https://orcid.org/0000-0002-4035-4028
Xiaohua JiaKey Laboratory of Molecular Imaging of Chinese Academy of Sciences Institute of Automation, Chinese Academy of Sciences Beijing People's Republic of China.
Honglin DongVascular Institute of Shanxi Medical University, Shanxi Medical University Taiyuan Shanxi People's Republic of China.ORCID https://orcid.org/0000-0002-5924-7003

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic kidney disease (CKD) has become one of the major diseases threatening global health, with its increasing incidence and mortality rates. Early identification of chronic kidney disease is crucial for accurate disease staging, timely intervention, and improved prognosis. However, the commonly used clinical diagnostic indicators, such as creatinine, albumin level and glomerular filtration rate, can only identify advanced CKD. Imaging examinations, such as computed tomography and magnetic resonance imaging, have limitations such as high costs and high risk of complications, and are not suitable for large-scale screening of high-risk populations. Renal biopsy is the gold standard for diagnosing renal fibrosis, but it is invasive. Previous studies have shown that capillary rarefaction is an early event of renal fibrosis, occurring earlier than tubular atrophy and interstitial collagen deposition. However, there is a lack of a minimally invasive, low-cost, high-resolution, dynamic and real-time monitoring method for renal microcirculation that is suitable for large-scale screening. There is an urgent need for reliable methods to screen early-stage CKD patients. In this study, we have for the first time combined real-time and wide-field laser speckle imaging (RFLSI), near-infrared II imaging (NIR-II), duplex ultrasound (DUS) and Contrast-Enhanced Ultrasound (CEUS) to monitor vascular changes and evaluate the progression of renal fibrosis. The combination of four imaging methods enabled the early monitoring of CKD progression by monitoring microcirculation. Among them, CEUS can detect changes in the renal microcirculation at the early stage of renal fibrosis, even earlier than the pathological damage of the kidneys. Through visualization and quantification of the progression of renal fibrosis and validation through histopathology, this study utilizes preclinical imaging to supplement clinical imaging of renal fibrosis, providing a more comprehensive method for monitoring microcirculation, which is helpful for guiding clinical decisions and providing insights into disease progression.

Indexed as

chronic kidney diseasecontinuous microcirculation monitoringcontrast‐enhanced ultrasounddiabetic kidney diseaseduplex ultrasoundnear‐infrared II imagingreal‐time and wide‐field laser speckle imaging

Identifiers

PMID42577505
PMCPMC13454415

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.