Evidence map›Paper›PMID 40060765›Full record

ArticleBioengineering & translational medicine2025

A CRISPR mediated point-of-care assay for the detection of mucosal calprotectin in an animal model of ulcerative colitis.

Selena Chia, Tianruo Guo, Ewa M Goldys, Sophie C Payne, Wenlu Duan, Nigel H Lovell, Mohit N Shivdasani, Fei Deng

Abstract read
In one paragraph

Article in Bioengineering & translational medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

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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

8 authors.

Selena ChiaGraduate School of Biomedical Engineering UNSW Sydney Sydney New South Wales Australia.
Tianruo GuoGraduate School of Biomedical Engineering UNSW Sydney Sydney New South Wales Australia.
Ewa M GoldysGraduate School of Biomedical Engineering UNSW Sydney Sydney New South Wales Australia.
Sophie C PayneBionics Institute Melbourne Victoria Australia.
Wenlu DuanGraduate School of Biomedical Engineering UNSW Sydney Sydney New South Wales Australia.
Nigel H LovellGraduate School of Biomedical Engineering UNSW Sydney Sydney New South Wales Australia.
Mohit N ShivdasaniGraduate School of Biomedical Engineering UNSW Sydney Sydney New South Wales Australia.
Fei DengGraduate School of Biomedical Engineering UNSW Sydney Sydney New South Wales Australia.ORCID https://orcid.org/0000-0002-5606-0278

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammatory bowel disease (IBD) is a chronic disorder associated with inflammation in the gastrointestinal tract, leading to a range of debilitating symptoms. Fecal calprotectin is an established biomarker for ulcerative colitis (UC), one of the main IBD diseases, which provides indications of the presence and severity of inflammation in the digestive tract. Enzyme-Linked Immunosorbent Assay (ELISA) as a gold standard approach for fecal calprotectin detection is time-consuming and impractical in point-of-care settings. Moreover, obtaining fecal samples from patients is challenging and inhibits longitudinal monitoring. To address these specific problems, we have developed a novel approach for detecting calprotectin which leverages clustered regularly interspaced short palindromic repeats (CRISPR)/Cas technology. We successfully developed a portable tube-based CRISPR/Cas assay for point-of-care testing of calprotectin. This assay showed a detection range from 1 to 10,000 ng/ml (over 4 log units), using both fluorescent and colorimetric analytical techniques. The established assay was further validated through measurements in mucosal samples obtained in an anesthetised preclinical rodent model of UC, with 2-3 times higher calprotectin concentration detected in UC rat samples compared to that of healthy control animals. This point-of-care test may provide a rapid, precise, and user-friendly approach for the diagnosis and monitoring of IBD through mucosal sample testing.

Indexed as

calprotectinCRISPR sensorIBDPOCT

Identifiers

PMID40060765
PMCPMC11883116

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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.