Evidence map›Paper›PMID 41601399›Full record

ArticleAdvanced healthcare materials2026

Preliminary Study of a Ninj1-Loaded Bimodal Ultrasound/NIR Fluorescence Targeted Molecular Probe for Diagnosing Early-Stage Inflammation in Coronary Microvascular Dysfunction.

Xiaohui Xu, Lina Guan, Baihetiya Tayier, Chen Yuan, Shangke Chen, Qi Shi, Yuming Mu

Abstract read
In one paragraph

Article in Advanced healthcare materials, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
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

7 authors.

Xiaohui XuDepartment of Echocardiography, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang, China.
Lina GuanDepartment of Echocardiography, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang, China.
Baihetiya TayierDepartment of Echocardiography, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang, China.
Chen YuanDepartment of Echocardiography, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang, China.
Shangke ChenXinjiang Key Laboratory of Ultrasound Medicine, Urumqi, Xinjiang, China.
Qi ShiDepartment of Echocardiography, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang, China.
Yuming MuDepartment of Echocardiography, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang, China.ORCID https://orcid.org/0000-0002-4097-5502

Funding

National Natural Science Foundation of China 32071459、82572221、82560344Scientific Research Cultivation Project of Xinjiang Medical University XYD2024ZX07
6 · The paper itself

Abstract

Coronary microvascular dysfunction (CMD) exhibits a high prevalence and is associated with adverse clinical outcomes, underscoring the critical importance of early detection. Early identification of CMD can significantly improve patient prognosis. This study aims to provide a novel strategy for the precise diagnosis of CMD during its early inflammatory phase. Focusing on this key inflammatory stage in the pathological progression, we sought to identify stage-specific molecular biomarkers. Through proteomic screening, we identified Nerve Injury-Induced Protein 1 (Ninj1). During the inflammatory response, Ninj1 promotes leukocyte migration and macrophage transendothelial migration, thereby influencing the trafficking and distribution of inflammatory cells. IR780 is a novel near-infrared (NIR) fluorescent agent characterized by excellent photostability and low toxicity. Loading IR780 onto nanoparticles enhances its in vivo biocompatibility and photostability while prolonging its circulation time. This project proposes a dual-modal molecular imaging probe targeting Ninj1 and loaded with IR780, which integrates NIR fluorescence and ultrasound imaging capabilities. This probe is designed to enable the early screening of CMD.

Indexed as

Cell Adhesion Molecules, NeuronalCoronary VesselsFluorescent DyesInflammationMolecular ProbesNerve Growth FactorsAnimalsFluorescent Chemosensor CompoundsHumansMaleMiceSpectroscopy, Near-InfraredUltrasonographyCell Adhesion Molecules, NeuronalFluorescent Chemosensor CompoundsFluorescent DyesMolecular ProbesNerve Growth FactorsNINJ1 protein, humanNinj1 protein, mousecoronary microvascular dysfunctiondual modalinflammatorymolecular imaging probe

Identifiers

PMID41601399
PMCPMC13088751

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.