Evidence map›Paper›PMID 31073168›Full record

ArticleScientific reports2019

Towards minimally-invasive, quantitative assessment of chronic kidney disease using optical spectroscopy.

Mostafa E Belghasem, Ousama A'amar, Daniel Roth, Joshua Walker, Nkiruka Arinze, Sean M Richards, Jean M Francis, David J Salant, Vipul C Chitalia, Irving J Bigio

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 16% of its field
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

6 citing papers in PubMed, 6 citations in OpenAlex.

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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

10 authors at 1 institution in 1 country.

Mostafa E BelghasemDepartment of Pathology and Laboratory Medicine, Boston University School of Medicine, Boston, MA, USA.ORCID http://orcid.org/0000-0002-2097-6882
Ousama A'amarDepartment of Biomedical Engineering, Boston University, Boston, MA, USA.
Daniel RothDepartment of Pathology and Laboratory Medicine, Boston University School of Medicine, Boston, MA, USA.
Joshua WalkerRenal Section, Department of Medicine, Boston University School of Medicine, Boston, MA, USA.
Nkiruka ArinzeDepartment of Pathology and Laboratory Medicine, Boston University School of Medicine, Boston, MA, USA.
Sean M RichardsRenal Section, Department of Medicine, Boston University School of Medicine, Boston, MA, USA.
Jean M FrancisRenal Section, Department of Medicine, Boston University School of Medicine, Boston, MA, USA.
David J SalantRenal Section, Department of Medicine, Boston University School of Medicine, Boston, MA, USA.ORCID http://orcid.org/0000-0002-3866-3120
Vipul C ChitaliaDepartment of Pathology and Laboratory Medicine, Boston University School of Medicine, Boston, MA, USA.
Irving J BigioDepartment of Biomedical Engineering, Boston University, Boston, MA, USA. bigio@bu.edu.
Boston University · US

Funding

Project-005UL1TR001430 · NCATS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BAIR-MERRITT, MEGAN H, CENTER, DAVID M. · 2015 to 2024
$52.3M
Multidisciplinary Training in Cardiovascular ResearchT32HL007224 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI HAMBURG, NAOMI MIRIAM, WAINFORD, RICHARD DAVID · 1985 to 2020
$12.3M
Impact of Biological, Clinical, and Social Determinants on Trauma and Trauma OutcomesT32GM086308 · NIGMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI Alik Farber, Daniel G. Remick · 2010 to 2026
$3.5M
Role of c-Cbl in Colon cancerR01CA175382 · NCI · BOSTON MEDICAL CENTER · PI CHITALIA, VIPUL C · 2014 to 2018
$1.8M
Thrombotic complication of uremia: role of prothrombotic uremic solutesR01HL132325 · NHLBI · BOSTON MEDICAL CENTER · PI CHITALIA, VIPUL C · 2016 to 2019
$1.7M
NCATS NIH HHS UL1 TR001430NCI NIH HHS R01 CA175382NHLBI NIH HHS R01 HL132325NHLBI NIH HHS T32 HL007224NIGMS NIH HHS T32 GM086308
6 · The paper itself

Abstract

The universal pathologic features implicated in the progression of chronic kidney disease (CKD) are interstitial fibrosis and tubular atrophy (IFTA). Current methods of estimating IFTA are slow, labor-intensive and fraught with variability and sampling error, and are not quantitative. As such, there is pressing clinical need for a less-invasive and faster method that can quantitatively assess the degree of IFTA. We propose a minimally-invasive optical method to assess the macro-architecture of kidney tissue, as an objective, quantitative assessment of IFTA, as an indicator of the degree of kidney disease. The method of elastic-scattering spectroscopy (ESS) measures backscattered light over the spectral range 320-900 nm and is highly sensitive to micromorphological changes in tissues. Using two discrete mouse models of CKD, we observed spectral trends of increased scattering intensity in the near-UV to short-visible region (350-450 nm), relative to longer wavelengths, for fibrotic kidneys compared to normal kidney, with a quasi-linear correlation between the ESS changes and the histopathology-determined degree of IFTA. These results suggest the potential of ESS as an objective, quantitative and faster assessment of IFTA for the management of CKD patients and in the allocation of organs for kidney transplantation.

Indexed as

AdenineAnimalsAtrophyBlood Urea NitrogenDietDisease Models, AnimalFemaleFibrosisKidneyMaleMiceMice, Inbred C57BLRenal Insufficiency, ChronicSpectrophotometryAdenine

Identifiers

PMID31073168
PMCPMC6509114
OpenAlexW2944056388

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.