Serum selenoprotein-P levels in patients with inflammatory bowel disease

被引:76
作者
Andoh, A [1 ]
Hirashima, M
Maeda, H
Hata, K
Inatomi, O
Tsujikawa, T
Sasaki, M
Takahashi, K
Fujiyama, Y
机构
[1] Shiga Univ Med Sci, Dept Internal Med, Otsu, Shiga 52021, Japan
[2] Chemo Sero Therapeut Res Inst, Kumamoto, Japan
[3] Hokkaido Univ, Grad Sch Pharmaceut Sci, Dept Hyg Chem, Sapporo, Hokkaido, Japan
关键词
inflammatory bowel disease; antioxidant; selenium; enzyme-linked immunosorbent assay;
D O I
10.1016/j.nut.2004.08.025
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Objective: Selenoprotein-P is a selenium-rich serum protein that carries more than 50% of serum selenium. We evaluated changes in serum selenoprotein-P levels in patients with inflammatory bowel disease. Methods: Serum selenoprotein-P levels were measured by enzyme-linked immunosorbent assay. Twenty healthy individuals (controls), 34 patients with ulcerative colitis, and 37 patients with Crohn's disease (CD) were studied. Results: A highly significant correlation was found between the serum selenium and selenoprotein-P levels. There was no significant difference in serum selenoprotein-P levels between healthy controls (average 3.4 ± 0.8 μ g/mL, n = 20) and patients with ulcerative colitis (3.0 ± 1.0 μ g/mL, n = 34). Serum selenoprotein-P levels were significantly lower in patients with CD (average 1.8 ± 0.5 μ g/mL, it = 37). Serum selenoprotein-P levels were significantly lower in the elemental diet group of patients who had CD (average 1.4 ± 0.4 μ g/mL, n = 17) than in the non-elemental diet group of patients who had CD (average 2.1 ± 0.3 Ag/mL, n 20). Conclusion: We found that the serum selenoprotein-P level is decreased in patients with CID. It may be a useful marker to monitor the systemic selenium status in various disorders. © 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:574 / 579
页数:6
相关论文
共 31 条
[1]   Responsiveness of selenoproteins to dietary selenium [J].
Allan, CB ;
Lacourciere, GM ;
Stadtman, TC .
ANNUAL REVIEW OF NUTRITION, 1999, 19 :1-16
[2]  
Arteel GE, 1998, BIOL CHEM, V379, P1201
[3]  
BEST WR, 1976, GASTROENTEROLOGY, V70, P439
[4]  
Brown K M, 2001, Public Health Nutr, V4, P593
[5]   PROXIMAL MUSCLE WEAKNESS AND SELENIUM DEFICIENCY ASSOCIATED WITH LONG-TERM PARENTERAL-NUTRITION [J].
BROWN, MR ;
COHEN, HJ ;
LYONS, JM ;
CURTIS, TW ;
THUNBERG, B ;
COCHRAN, WJ ;
KLISH, WJ .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1986, 43 (04) :549-554
[6]  
FLEMING CR, 1982, GASTROENTEROLOGY, V83, P689
[7]   Selenium kinetics and changes in glutathione peroxidase activities in patients receiving long-term parenteral nutrition and effects of supplementation with selenite [J].
Hatanaka, N ;
Nakaden, H ;
Yamamoto, Y ;
Matsuo, S ;
Fujikawa, T ;
Matsusue, S .
NUTRITION, 2000, 16 (01) :22-26
[8]   CONSERVED NUCLEOTIDE-SEQUENCES IN THE OPEN READING FRAME AND 3' UNTRANSLATED REGION OF SELENOPROTEIN-P MESSENGER-RNA [J].
HILL, KE ;
LLOYD, RS ;
BURK, RF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (02) :537-541
[9]  
HILL KE, 1991, J BIOL CHEM, V266, P10050
[10]  
Hirashima M, 2003, BIOL PHARM BULL, V26, P794