1.Urine metabolomic analysis to detect metabolites associated with the development of contrast induced nephropathy.
Deborah B DIERCKS ; Kelly P OWEN ; Jeffrey A KLINE ; Mark E SUTTER
Clinical and Experimental Emergency Medicine 2016;3(4):204-212
OBJECTIVE: Contrast induced nephropathy (CIN) is a result of injury to the proximal tubules. The incidence of CIN is around 11% for imaging done in the acute care setting. We aim to analyze the metabolic patterns in the urine, before and after dosing with intravenous contrast for computed tomography (CT) imaging of the chest, to determine if metabolomic changes exist in patients who develop CIN. METHODS: A convenience sample of high risk patients undergoing a chest CT with intravenous contrast were eligible for enrollment. Urine samples were collected prior to imaging and 4 to 6 hours post imaging. Samples underwent gas chromatography/mass spectrometry profiling. Peak metabolite values were measured and data was log transformed. Significance analysis of microarrays and partial least squares was used to determine the most significant metabolites prior to CT imaging and within subject. Analysis of variance was used to rank metabolites associated with temporal change and CIN. CIN was defined as an increase in serum creatinine level of ≥ 0.5 mg/dL or ≥ 25% above baseline within 48 hours after contrast administration. RESULTS: We sampled paired urine samples from 63 subjects. The incidence of CIN was 6/63 (9.5%). Patients without CIN had elevated urinary citric acid and taurine concentrations in the pre-CT urine. Xylulose increased in the post CT sample in patients who developed CIN. CONCLUSION: Differences in metabolomics patterns in patients who do and do not develop CIN exist. Metabolites may be potential early identifiers of CIN and identify patients at high-risk for developing this condition prior to imaging.
Citric Acid
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Creatinine
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Humans
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Incidence
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Least-Squares Analysis
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Metabolomics*
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Spectrum Analysis
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Taurine
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Thorax
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Tomography, X-Ray Computed
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Xylulose
2.Prenatal MRI Findings of Fetuses with Congenital High Airway Obstruction Sequence.
Carolina V GUIMARAES ; Leann E LINAM ; Beth M KLINE-FATH ; Lane F DONNELLY ; Maria A CALVO-GARCIA ; Eva I RUBIO ; Jeffrey C LIVINGSTON ; Robert J HOPKIN ; Elizabeth PEACH ; Foong Yen LIM ; Timothy M CROMBLEHOLME
Korean Journal of Radiology 2009;10(2):129-134
OBJECTIVE: To define the MRI findings of congenital high airway obstruction sequence (CHAOS) in a series of fetuses. MATERIALS AND METHODS: Prenatal fetal MR images were reviewed in seven fetuses with CHAOS at 21 to 27 weeks of gestation. The MRI findings were reviewed. The MRI parameters evaluated included the appearance of the lungs and diaphragm, presence or absence of hydrops, amount of amniotic fluid, airway appearance, predicted level of airway obstruction, and any additional findings or suspected genetic syndromes. RESULTS: All the fetuses viewed (7 of 7) demonstrated the following MRI findings: dilated airway below the level of obstruction, increased lung signal, markedly increased lung volumes with flattened or inverted hemidiaphragms, massive ascites, centrally positioned and compressed heart, as well as placentomegaly. Other frequent findings were anasarca (6 of 7) and polyhydramnios (3 of 7). MRI identified the level of obstruction as laryngeal in five cases and tracheal in two cases. In four of the patients, surgery or autopsy confirmed the MRI predicted level of obstruction. Associated abnormalities were found in 4 of 7 (genetic syndromes in 2). Postnatal radiography (n = 3) showed markedly hyperinflated lungs with inverted or flattened hemidiaphragms, strandy perihilar opacities, pneumothoraces and tracheotomy. Two fetuses were terminated and one fetus demised in utero. Four fetuses were delivered via ex utero intrapartum treatment procedure. CONCLUSION: MRI shows a consistent pattern of abnormalities in fetuses with CHAOS, accurately identifies the level of airway obstruction, and helps differentiate from other lung abnormalities such as bilateral congenital pulmonary airway malformation by demonstrating an abnormally dilated airway distal to the obstruction.
Abnormalities, Multiple
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Airway Obstruction/congenital/*pathology
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Ascites/pathology
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Diaphragm/abnormalities
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Female
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Fetal Diseases/*pathology
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Humans
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Lung/pathology
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*Magnetic Resonance Imaging
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Placenta Diseases/pathology
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Pregnancy
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*Prenatal Diagnosis
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Retrospective Studies