Associations between liver 18F fluoro-2-deoxy-d-glucose accumulation and various clinical parameters in a Japanese population: influence of the metabolic syndrome

被引:43
作者
Kamimura, Kiyohisa [1 ]
Nagamachi, Shigeki [1 ]
Wakamatsu, Hideyuki [1 ]
Higashi, Ryutaro [1 ]
Ogita, Mikio [1 ]
Ueno, Shin-ichiro [1 ]
Fujita, Seigo [1 ]
Umemura, Yoshiro [1 ]
Fujimoto, Toshiro [2 ]
Nakajo, Masayuki [3 ]
机构
[1] Fujimoto Hayasuzu Hosp, Dept Radiol, Miyazaki 8850055, Japan
[2] Fujimoto Hosp, Dept Psychiat, Miyazaki, Japan
[3] Kagoshima Univ, Grad Sch Med & Dent Sci, Dept Radiol, Kagoshima 890, Japan
关键词
F-18-FDG PET; Liver; Body mass index; Metabolic syndrome; POSITRON-EMISSION-TOMOGRAPHY; FLUORINE-18-FLUORODEOXYGLUCOSE; TISSUES; DISEASE; PET;
D O I
10.1007/s12149-009-0338-1
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Liver demonstrates a heterogeneous F-18 fluoro-2-deoxy-d-glucose (F-18-FDG) uptake pattern and sometimes shows an abnormally increased uptake even when there is no malignant tissue. The aim of this study was to evaluate the relationships of liver F-18-FDG uptake as related to physical factors, fatty liver, blood glucose (BG), and other biochemical data. F-18-FDG positron emission tomography (PET) imaging was performed in 101 consecutive subjects for cancer screening. Multiple stepwise regression analysis was used to define the best predictors of the liver standardized uptake value (SUV) among height, weight, waist circumference, body mass index (BMI), systolic and diastolic blood pressure, BG and other biochemical data, i.e., aspartate aminotransferase, alanine aminotransferase, gamma-glutamyl transpeptidase, total cholesterol, high-density lipoprotein cholesterol, triglycerides, total protein, total bilirubin, and alkaline phosphatase. Furthermore, we evaluated the association between liver F-18-FDG uptake and the metabolic syndrome. The independent factors for increased liver F-18-FDG uptake (mean SUV >= 2) were BMI (P < 0.0001), triglycerides (P = 0.0007), and high-density lipoprotein cholesterol (P = 0.0013). Other factors were not significantly associated with liver F-18-FDG uptake. In addition, the liver F-18-FDG uptake of metabolic syndrome subjects was significantly higher than that of a non-metabolic syndrome subjects. BMI was the strongest determinant of liver F-18-FDG uptake, and the liver F-18-FDG uptake of metabolic syndrome subjects was significantly higher than that of non-metabolic syndrome subjects. This result suggests that a subject with a high liver F-18-FDG uptake should be screened for the metabolic syndrome.
引用
收藏
页码:157 / 161
页数:5
相关论文
共 16 条
  • [1] [Anonymous], 2005, Nihon Naika Gakkai Zasshi, V94, P794
  • [2] INTERLEUKIN-6, BUT NOT TUMOR-NECROSIS-FACTOR-ALPHA, INCREASES LIPOGENESIS IN RAT HEPATOCYTE PRIMARY CULTURES
    BRASS, EP
    VETTER, WH
    [J]. BIOCHEMICAL JOURNAL, 1994, 301 : 193 - 197
  • [3] Normal physiological and benign pathological variants of 18-fluoro-2-deoxyglucose positron-emission tomography scanning: Potential for error in interpretation
    Cook, GJR
    Fogelman, I
    Maisey, MN
    [J]. SEMINARS IN NUCLEAR MEDICINE, 1996, 26 (04) : 308 - 314
  • [4] Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III) Final Report
    Grundy, SM
    Becker, D
    Clark, LT
    Cooper, RS
    Denke, MA
    Howard, WJ
    Hunninghake, DB
    Illingworth, R
    Luepker, RV
    McBride, P
    McKenney, JM
    Pasternak, RC
    Stone, NJ
    Van Horn, L
    Brewer, HB
    Cleeman, JI
    Ernst, ND
    Gordon, D
    Levy, D
    Rifkind, B
    Rossouw, JE
    Savage, P
    Haffner, SM
    Orloff, DG
    Proschan, MA
    Schwartz, JS
    Sempos, CT
    Shero, ST
    Murray, EZ
    Keller, SA
    Jehle, AJ
    [J]. CIRCULATION, 2002, 106 (25) : 3143 - 3421
  • [5] Ichiya Y, 1996, Ann Nucl Med, V10, P185
  • [6] Clinical usefulness of positron emission tomography with fluorine-18-fluorodeoxyglucose in the diagnosis of liver tumors
    Iwata, Y
    Shiomi, S
    Sasaki, N
    Jomura, H
    Nishiguchi, S
    Seki, S
    Kawabe, J
    Ochi, H
    [J]. ANNALS OF NUCLEAR MEDICINE, 2000, 14 (02) : 121 - 126
  • [7] KUBOTA R, 1992, J NUCL MED, V33, P1972
  • [8] WHO and ATPIII proposals for the definition of the metabolic syndrome in patients with Type 2 diabetes
    Marchesini, G
    Forlani, G
    Cerrelli, F
    Manini, R
    Natale, S
    Baraldi, L
    Ermini, G
    Savorani, G
    Zocchi, D
    Melchionda, N
    [J]. DIABETIC MEDICINE, 2004, 21 (04) : 383 - 387
  • [9] Non-alcoholic fatty liver disease and the metabolic syndrome: An update
    Rector, R. Scott
    Thyfault, John P.
    Wei, Yongzhong
    Ibdah, Jamal A.
    [J]. WORLD JOURNAL OF GASTROENTEROLOGY, 2008, 14 (02) : 185 - 192
  • [10] Emerging paradigms for understanding fatness and diabetes risk.
    Smith S.R.
    Ravussin E.
    [J]. Current Diabetes Reports, 2002, 2 (3) : 223 - 230