TY - JOUR
T1 - Establishment of chemiluminescence enzyme immunoassay for apolipoprotein B-48 and its clinical applications for evaluation of impaired chylomicron remnant metabolism
AU - Hanada, Hiroyuki
AU - Mugii, Satomi
AU - Okubo, Manabu
AU - Maeda, Ikuhiro
AU - Kuwayama, Kazuya
AU - Hidaka, Yoh
AU - Kitazume-Taneike, Rika
AU - Yamashita, Taiji
AU - Kawase, Ryota
AU - Nakaoka, Hajime
AU - Inagaki, Miwako
AU - Yuasa-Kawase, Miyako
AU - Nakatani, Kazuhiro
AU - Tsubakio-Yamamoto, Kazumi
AU - Masuda, Daisaku
AU - Ohama, Tohru
AU - Matsuyama, Akifumi
AU - Ishigami, Masato
AU - Nishida, Makoto
AU - Komuro, Issei
AU - Yamashita, Shizuya
N1 - Funding Information:
The authors acknowledge Kaori Hizu, Miki Kato and Risa Wada for their excellent clerical and technical assistance. The authors also appreciate Fujirebio Inc. for their apoB-48 measurements. This work was supported by the following grants: a grant-in-aid for Scientific Research (No. 18659267 ) to Yamashita S from the Ministry of Education, Science, Sports and Culture in Japan ; a grant from the National Institute of Biomedical Innovation to Yamashita S, Tsubakio-Yamamoto K and Masuda D; a grant from Mitsui Life Social Welfare Foundation to Yamashita S; a Takeda Medical Research Foundation Grant to Yamashita S; and in part by the Program for Promotion of Fundamental Studies in Health Sciences of the National Institute of Biomedical Innovation (NIBIO) to Yamashita S and Matsuyama A.
PY - 2012/1/18
Y1 - 2012/1/18
N2 - Background: Apolipoprotein B-48 (apoB-48) is a constituent of chylomicron remnants synthesized in the small intestines. The serum concentration of apoB-48 at fasting has been reported to be a marker of postprandial hyperlipidemia, a presumed risk factor for atherosclerosis. Methods: We evaluated the basal performance of a recently developed chemiluminescent enzyme immunoassay (CLEIA). We also examined the correlations between serum apoB-48 concentrations and other lipid concentrations or life style patterns, including smoking and drinking. We analyzed the data of 273 clinical samples by multiple regression analysis to examine the influence of other serum lipid values, age, sex, smoking, drinking status and BMI on serum apoB-48 values. Results: Within-run and between-run precision was obtained with 1.7-2.7% and 1.2-7.3%, respectively. The correlativity of enzyme-linked immunosorbent assay was correlation coefficient r = 0.953, and regression y = 1.02 × -1.59. Serum apoB-48 concentrations were higher in males than in females, and were correlated with the status of smoking as well as with remnant-like particle-cholesterol (RLP-C) concentrations. Patients with the metabolic syndrome showed higher values of serum apoB-48 compared with control subjects. Conclusion: Serum apoB-48 measurement by CLEIA was satisfactory for clinical use to assess abnormalities in the chylomicron remnant metabolism.
AB - Background: Apolipoprotein B-48 (apoB-48) is a constituent of chylomicron remnants synthesized in the small intestines. The serum concentration of apoB-48 at fasting has been reported to be a marker of postprandial hyperlipidemia, a presumed risk factor for atherosclerosis. Methods: We evaluated the basal performance of a recently developed chemiluminescent enzyme immunoassay (CLEIA). We also examined the correlations between serum apoB-48 concentrations and other lipid concentrations or life style patterns, including smoking and drinking. We analyzed the data of 273 clinical samples by multiple regression analysis to examine the influence of other serum lipid values, age, sex, smoking, drinking status and BMI on serum apoB-48 values. Results: Within-run and between-run precision was obtained with 1.7-2.7% and 1.2-7.3%, respectively. The correlativity of enzyme-linked immunosorbent assay was correlation coefficient r = 0.953, and regression y = 1.02 × -1.59. Serum apoB-48 concentrations were higher in males than in females, and were correlated with the status of smoking as well as with remnant-like particle-cholesterol (RLP-C) concentrations. Patients with the metabolic syndrome showed higher values of serum apoB-48 compared with control subjects. Conclusion: Serum apoB-48 measurement by CLEIA was satisfactory for clinical use to assess abnormalities in the chylomicron remnant metabolism.
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U2 - 10.1016/j.cca.2011.09.013
DO - 10.1016/j.cca.2011.09.013
M3 - Article
C2 - 21958700
AN - SCOPUS:82955212918
SN - 0009-8981
VL - 413
SP - 160
EP - 165
JO - Clinica Chimica Acta
JF - Clinica Chimica Acta
IS - 1-2
ER -