Evidence map›Paper›PMID 39383112›Full record

ArticleClinical chemistry2024

Deconvolution of Human Urine across the Transcriptome and Metabolome.

Sevahn K Vorperian, Brian C DeFelice, Joseph A Buonomo, Hagop J Chinchinian, Ira J Gray, Jia Yan, Kathleen E Mach, Vinh La, Timothy J Lee, Joseph C Liao and 4 more

Abstract read
In one paragraph

Article in Clinical chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Sevahn K VorperianDepartment of Chemical Engineering, Stanford University, Stanford, CA, United States.
Brian C DeFeliceChan Zuckerberg Biohub, San Francisco, CA, United States.
Joseph A BuonomoSarafan ChEM-H, Stanford University, Stanford, CA, United States.
Hagop J ChinchinianDepartment of Electrical Engineering, Stanford University, Stanford, CA, United States.
Ira J GrayChan Zuckerberg Biohub, San Francisco, CA, United States.
Jia YanChan Zuckerberg Biohub, San Francisco, CA, United States.
Kathleen E MachDepartment of Urology, Stanford University, Stanford, CA, United States.
Vinh LaDepartment of Urology, Stanford University, Stanford, CA, United States.
Timothy J LeeDepartment of Urology, Stanford University, Stanford, CA, United States.
Joseph C LiaoDepartment of Urology, Stanford University, Stanford, CA, United States.
Richard LafayetteDivision of Nephrology, Stanford School of Medicine, Stanford, CA, United States.
Gabriel B LoebDepartment of Medicine and Cardiovascular Research Institute, University of California, San Francisco, San Francisco, CA, United States.
Carolyn R BertozziSarafan ChEM-H, Stanford University, Stanford, CA, United States.
Stephen R QuakeDepartment of Bioengineering, Stanford University, Stanford, CA, United States.

Funding

Mycobacterial Sulfation PathwaysR01AI051622 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI BERTOZZI, CAROLYN · 2002 to 2015
$6.0M
Chemical MycobateriologyR37AI051622 · NIAID · STANFORD UNIVERSITY · PI BERTOZZI, CAROLYN · 2016 to 2025
$4.7M
Investigating the Surface GlycoproteomeR01CA200423 · NCI · STANFORD UNIVERSITY · PI Carolyn Bertozzi · 2015 to 2026
$3.8M
Analysis of urine tumor nucleic acids for detection and personalized surveillance of bladder cancerR01CA244526 · NCI · STANFORD UNIVERSITY · PI ALIZADEH, ASH ARASH, DIEHN, MAXIMILIAN · 2020 to 2024
$3.0M
Characterization and Modulation of Caspase 4-Mediated PyroptosisF32GM134689 · NIGMS · STANFORD UNIVERSITY · PI BUONOMO, JOSEPH ANTHONY · 2019 to 2021
$195k
BLRD VA I01 BX004962NCI NIH HHS R01 CA200423NCI NIH HHS R01 CA244526NIAID NIH HHS R01 AI051622NIAID NIH HHS R37 AI051622NIGMS NIH HHS F32 GM134689
6 · The paper itself

Abstract

backgroundEarly detection of the cell type changes underlying several genitourinary tract diseases largely remains an unmet clinical need, where existing assays, if available, lack the cellular resolution afforded by an invasive biopsy. While messenger RNA in urine could reflect the dynamic signal that facilitates early detection, current measurements primarily detect single genes and thus do not reflect the entire transcriptome and the underlying contributions of cell type-specific RNA.

methodsWe isolated and sequenced the cell-free RNA (cfRNA) and sediment RNA from human urine samples (n = 6 healthy controls and n = 12 kidney stone patients) and measured the urine metabolome. We analyzed the resulting urine transcriptomes by deconvolving the noninvasively measurable cell type contributions and comparing to plasma cfRNA and the measured urine metabolome.

resultsUrine transcriptome cell type deconvolution primarily yielded relative fractional contributions from genitourinary tract cell types in addition to cell types from high-turnover solid tissues beyond the genitourinary tract. Comparison to plasma cfRNA yielded enrichment of metabolic pathways and a distinct cell type spectrum. Integration of urine transcriptomic and metabolomic measurements yielded enrichment for metabolic pathways involved in amino acid metabolism and overlapped with metabolic subsystems associated with proximal tubule function.

conclusionsNoninvasive whole transcriptome measurements of human urine cfRNA and sediment RNA reflects signal from hard-to-biopsy tissues exhibiting low representation in blood plasma cfRNA liquid biopsy at cell type resolution and are enriched in signal from metabolic pathways measurable in the urine metabolome.

Indexed as

MetabolomeTranscriptomeAdultCell-Free Nucleic AcidsFemaleHumansKidney CalculiMaleMiddle AgedUrineCell-Free Nucleic Acids

Identifiers

PMID39383112
PMCPMC11927302

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Registered trials

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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.