Cross-sectional analysis of BioBank Japan clinical data: A large cohort of 200,000 patients with 47 common diseases

被引:121
作者
Hirata, Makoto [1 ]
Kamatani, Yoichiro [2 ]
Nagai, Akiko [3 ]
Kiyohara, Yutaka [4 ]
Ninomiya, Toshiharu [5 ]
Tamakoshi, Akiko [6 ]
Yamagata, Zentaro [7 ]
Kubo, Michiaki [8 ]
Muto, Kaori [3 ]
Mushiroda, Taisei [9 ]
Murakami, Yoshinori [10 ,12 ]
Yuji, Koichiro [11 ]
Furukawa, Yoichi
Zembutsu, Hitoshi [13 ,14 ]
Tanaka, Toshihiro [15 ,16 ,17 ]
Ohnishi, Yozo [15 ,18 ]
Nakamura, Yusuke [13 ,19 ]
Matsuda, Koichi [13 ,20 ]
机构
[1] Univ Tokyo, Inst Med Sci, Lab Genome Technol, Tokyo, Japan
[2] RIKEN, Ctr Integrat Med Sci, Lab Stat Anal, Yokohama, Kanagawa, Japan
[3] Univ Tokyo, Inst Med Sci, Dept Publ Policy, Tokyo, Japan
[4] Hisayama Res Inst Lifestyle Dis, Fukuoka, Japan
[5] Kyushu Univ, Grad Sch Med Sci, Dept Epidemiol & Publ Hlth, Fukuoka, Japan
[6] Hokkaido Univ, Grad Sch Med, Dept Publ Hlth, Sapporo, Hokkaido, Japan
[7] Univ Yamanashi, Dept Hlth Sci, Yamanashi, Japan
[8] RIKEN, Ctr Integrat Med Sci, Yokohama, Kanagawa, Japan
[9] RIKEN, Ctr Integrat Med Sci, Lab Pharmacogen, Yokohama, Kanagawa, Japan
[10] Univ Tokyo, Inst Med Sci, Div Mol Pathol, Tokyo, Japan
[11] Univ Tokyo, Inst Med Sci, Project Div Int Adv Med Res, Tokyo, Japan
[12] Univ Tokyo, Inst Med Sci, Div Clin Genome Res, Tokyo, Japan
[13] Univ Tokyo, Inst Med Sci, Mol Med Lab, Tokyo, Japan
[14] Res Inst, Natl Canc Ctr, Div Genet, Tokyo, Japan
[15] RIKEN, Yokohama Inst, SNP Res Ctr, Yokohama, Kanagawa, Japan
[16] Tokyo Med & Dent Univ, Grad Sch Med & Dent Sci, Dept Human Genet & Dis Divers, Tokyo, Japan
[17] Tokyo Med & Dent Univ, Bioresource Res Ctr, Tokyo, Japan
[18] Med Corp Shinkokai, Shinko Clin, Tokyo, Japan
[19] Univ Chicago, Dept Med, Sect Hematol Oncol, 5841 S Maryland Ave, Chicago, IL 60637 USA
[20] Univ Tokyo, Grad Sch Frontier Sci, Lab Clin Genome Sequencing, Tokyo, Japan
关键词
BioBank Japan Project; Biobank; Common disease; Clinical information; Family history; GENOME-WIDE ASSOCIATION; CHRONIC HEPATITIS-B; GRAVES-DISEASE; FAMILY-HISTORY; POLYMORPHISM; GENE; SUSCEPTIBILITY; RECEPTOR; REGION; RISK;
D O I
10.1016/j.je.2016.12.003
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: To implement personalized medicine, we established a large-scale patient cohort, BioBank Japan, in 2003. BioBank Japan contains DNA, serum, and clinical information derived from approximately 200,000 patients with 47 diseases. Serum and clinical information were collected annually until 2012. Methods: We analyzed clinical information of participants at enrollment, including age, sex, body mass index, hypertension, and smoking and drinking status, across 47 diseases, and compared the results with the Japanese database on Patient Survey and National Health and Nutrition Survey. We conducted multivariate logistic regression analysis, adjusting for sex and age, to assess the association between family history and disease development. Results: Distribution of age at enrollment reflected the typical age of disease onset. Analysis of the clinical information revealed strong associations between smoking and chronic obstructive pulmonary disease, drinking and esophageal cancer, high body mass index and metabolic disease, and hypertension and cardiovascular disease. Logistic regression analysis showed that individuals with a family history of keloid exhibited a higher odds ratio than those without a family history, highlighting the strong impact of host genetic factor(s) on disease onset. Conclusions: Cross-sectional analysis of the clinical information of participants at enrollment revealed characteristics of the present cohort. Analysis of family history revealed the impact of host genetic factors on each disease. BioBank Japan, by publicly distributing DNA, serum, and clinical information, could be a fundamental infrastructure for the implementation of personalized medicine. (C) 2017 The Authors. Publishing services by Elsevier B. V. on behalf of The Japan Epidemiological Association.
引用
收藏
页码:S9 / S21
页数:13
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