Evidence map›Paper›PMID 26447222›Full record

ArticleAmerican journal of physiology. Renal physiology2016

Dynamic contrast-enhanced quantitative susceptibility mapping with ultrashort echo time MRI for evaluating renal function.

Luke Xie, Anita T Layton, Nian Wang, Peder E Z Larson, Jeff L Zhang, Vivian S Lee, Chunlei Liu, G Allan Johnson

Abstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Nephron number and its determinants: a 2020 update.Pediatric nephrology (Berlin, Germany) · 2021
    Article
  4. Feasibility of QSM in the human placenta.Magnetic resonance in medicine · 2021
    Article
  5. Hardware Considerations for Preclinical Magnetic Resonance of the Kidney.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. MRI tools for assessment of microstructure and nephron function of the kidney.American journal of physiology. Renal physiology · 2016
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 1 country.

Luke XieCenter for In Vivo Microscopy, Department of Radiology, Duke University Medical Center, Durham, North Carolina; Utah Center for Advanced Imaging Research, Department of Radiology, University of Utah, Salt Lake City, Utah lukenxie@gmail.com.ORCID http://orcid.org/0000-0002-3712-5558
Anita T LaytonDepartment of Mathematics, Duke University, Durham, North Carolina;
Nian WangBrain Imaging and Analysis Center, Duke University Medical Center, Durham, North Carolina;
Peder E Z LarsonDepartment of Radiology and Biomedical Engineering, University of California, San Francisco, California; and.
Jeff L ZhangUtah Center for Advanced Imaging Research, Department of Radiology, University of Utah, Salt Lake City, Utah.
Vivian S LeeUtah Center for Advanced Imaging Research, Department of Radiology, University of Utah, Salt Lake City, Utah.
Chunlei LiuCenter for In Vivo Microscopy, Department of Radiology, Duke University Medical Center, Durham, North Carolina; Brain Imaging and Analysis Center, Duke University Medical Center, Durham, North Carolina;
G Allan JohnsonCenter for In Vivo Microscopy, Department of Radiology, Duke University Medical Center, Durham, North Carolina;
Duke Medical Center · USUniversity of Utah · USDuke University · USUniversity of California, San Francisco · US

Funding

INTEGRATED CENTER FOR IN VIVO MICROSCOPYP41EB015897 · NIBIB · DUKE UNIVERSITY · PI JOHNSON, GEORGE ALLAN · 2012 to 2017
$7.4M
MR Angiography and Renography for Renovascular DiseaseR01DK063183 · NIDDK · UNIVERSITY OF UTAH · PI LEE, VIVIAN S. · 2003 to 2014
$5.5M
Accurate Measurement of Renal Function in CirrhosisR01DK088375 · NIDDK · UNIVERSITY OF UTAH · PI LEE, VIVIAN S. · 2010 to 2014
$2.4M
Ultra-Resolution Imaging of Brain Circuitry and its Development in Mental HealthR01MH096979 · NIMH · UNIVERSITY OF CALIFORNIA BERKELEY · PI LIU, CHUNLEI · 2013 to 2017
$1.8M
Modeling Solute Transport and Urine Concentrating Mechanism in the Rat KidneyR01DK089066 · NIDDK · DUKE UNIVERSITY · PI LAYTON, ANITA · 2010 to 2014
$1.2M
Agilent Direct Drive 9.4T MRS/MRI ConsoleS10OD010683 · OD · DUKE UNIVERSITY · PI JOHNSON, GEORGE ALLAN · 2012 to 2012
$597k
NIBIB NIH HHS P41 EB015897NIDDK NIH HHS R01 DK063183NIDDK NIH HHS R01 DK088375NIDDK NIH HHS R01 DK089066NIH HHS S10 OD010683NIMH NIH HHS R01 MH096979
6 · The paper itself

Abstract

Dynamic contrast-enhanced (DCE) MRI can provide key insight into renal function. DCE MRI is typically achieved through an injection of a gadolinium (Gd)-based contrast agent, which has desirable T1 quenching and tracer kinetics. However, significant T2* blooming effects and signal voids can arise when Gd becomes very concentrated, especially in the renal medulla and pelvis. One MRI sequence designed to alleviate T2* effects is the ultrashort echo time (UTE) sequence. In the present study, we observed T2* blooming in the inner medulla of the mouse kidney, despite using UTE at an echo time of 20 microseconds and a low dose of 0.03 mmol/kg Gd. We applied quantitative susceptibility mapping (QSM) and resolved the signal void into a positive susceptibility signal. The susceptibility values [in parts per million (ppm)] were converted into molar concentrations of Gd using a calibration curve. We determined the concentrating mechanism (referred to as the concentrating index) as a ratio of maximum Gd concentration in the inner medulla to the renal artery. The concentrating index was assessed longitudinally over a 17-wk course (3, 5, 7, 9, 13, 17 wk of age). We conclude that the UTE-based DCE method is limited in resolving extreme T2* content caused by the kidney's strong concentrating mechanism. QSM was able to resolve and confirm the source of the blooming effect to be the large positive susceptibility of concentrated Gd. UTE with QSM can complement traditional magnitude UTE and offer a powerful tool to study renal pathophysiology.

Indexed as

AnimalsContrast MediaKidneyMagnetic Resonance ImagingMiceContrast Media3D dynamic contrast-enhancedgadolinium-based contrast agentkidney concentrating mechanismmagnetic resonance imagingMR renographyquantitative susceptibility mappingsmall animal preclinical imagingultrashort echo time

Identifiers

PMID26447222
PMCPMC4719043
OpenAlexW2224251089

What OpenQuestion holds

Textmetadata
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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.