Increased arterial inflammation in individuals with stage 3 chronic kidney disease
Creators
- 1. University Medical Center Utrecht, Department of Radiology, Utrecht (Netherlands)
- 2. Massachusetts General Hospital and Harvard Medical School, Cardiac MR PET CT Program, Boston, MA (United States)
- 3. New York Presbyterian Hospital, Weill Cornell Medical College, Division of Cardiology, New York, NY (United States)
- 4. Brigham and Women's Hospital and Harvard Medical School, Division of Radiology, Department of Medicine, Boston, MA (United States)
- 5. F. Hoffmann-La Roche Ltd., Basel (Switzerland)
- 6. Massachusetts General Hospital, Boston, MA (United States)
- 7. Massachusetts General Hospital and Harvard Medical School, Cardiology Division, Boston, MA (United States)
Description
While it is well known that patients with chronic kidney disease (CKD) are at increased risk for the development and progression of atherosclerosis, it is not known whether arterial inflammation is increased in mild CKD. The aim of this study was to compare arterial inflammation using 18F-FDG PET/CT in patients with CKD and in matched controls. This retrospective study included 128 patients undergoing FDG PET/CT imaging for clinical indications, comprising 64 patients with stage 3 CKD and 64 control patients matched by age, gender, and cancer history. CKD was defined according to guidelines using a calculated glomerular filtration rate (eGFR). Arterial inflammation was measured in the ascending aorta as FDG uptake on PET. Background FDG uptake (venous, subcutaneous fat and muscle) were recorded. Coronary artery calcification (CAC) was assessed using the CT images. The impact of CKD on arterial inflammation and CAC was then assessed. Arterial inflammation was higher in patients with CKD than in matched controls (standardized uptake value, SUV: 2.41 ± 0.49 vs. 2.16 ± 0.43; p = 0.002). Arterial SUV correlated inversely with eGFR (r = -0.299, p = 0.001). Venous SUV was also significantly elevated in patients with CKD, while subcutaneous fat and muscle tissue SUVs did not differ between groups. Moreover, arterial SUV remained significantly elevated in patients with CKD compared to controls after correcting for muscle and fat background, and also remained significant after adjusting for clinical risk factors. Further, CKD was associated with arterial inflammation (SUV) independent of the presence of subclinical atherosclerosis (CAC). Moderate CKD is associated with increased arterial inflammation beyond that of controls. Further, the increased arterial inflammation is independent of presence of subclinical atherosclerosis. Current risk stratification tools may underestimate the presence of atherosclerosis in patients with CKD and thereby the risk of cardiovascular events. (orig.)
Availability note (English)
Available from: http://dx.doi.org/10.1007/s00259-015-3203-6Additional details
Identifiers
Publishing Information
- Journal Title
- European Journal of Nuclear Medicine and Molecular Imaging
- Journal Volume
- 43
- Journal Issue
- 2
- Journal Page Range
- p. 333-339
- ISSN
- 1619-7070
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- INIS RN
- 47040416
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- AGE DEPENDENCE; AORTA; ARTERIOSCLEROSIS; COMPUTERIZED TOMOGRAPHY; CORONARIES; FLUORINE 18; FLUORODEOXYGLUCOSE; INFLAMMATION; KIDNEYS; POSITRON COMPUTED TOMOGRAPHY; RADIOPHARMACEUTICALS; SEX DEPENDENCE; UPTAKE; UROGENITAL SYSTEM DISEASES
- Descriptors DEC
- ANTIMETABOLITES; ARTERIES; BETA DECAY RADIOISOTOPES; BETA-PLUS DECAY RADIOISOTOPES; BLOOD VESSELS; BODY; CARDIOVASCULAR DISEASES; CARDIOVASCULAR SYSTEM; COMPUTERIZED TOMOGRAPHY; DIAGNOSTIC TECHNIQUES; DISEASES; DRUGS; EMISSION COMPUTED TOMOGRAPHY; FLUORINE ISOTOPES; HOURS LIVING RADIOISOTOPES; ISOMERIC TRANSITION ISOTOPES; ISOTOPES; LABELLED COMPOUNDS; LIGHT NUCLEI; MATERIALS; NANOSECONDS LIVING RADIOISOTOPES; NUCLEI; ODD-ODD NUCLEI; ORGANS; PATHOLOGICAL CHANGES; RADIOACTIVE MATERIALS; RADIOISOTOPES; SYMPTOMS; TOMOGRAPHY; VASCULAR DISEASES