Skip to main content
Erschienen in: BMC Gastroenterology 1/2013

Open Access 01.12.2013 | Research article

A nationwide population-based study of the inflammatory bowel diseases between 1998 and 2008 in Taiwan

verfasst von: Shu-Chen Wei, Meng-Hung Lin, Chien-Chih Tung, Meng-Tzu Weng, Jen-Shin Kuo, Ming-Jium Shieh, Cheng-Yi Wang, Wen-Chao Ho, Jau-Min Wong, Pau-Chung Chen

Erschienen in: BMC Gastroenterology | Ausgabe 1/2013

Abstract

Background

The incidence of the inflammatory bowel diseases (IBD), ulcerative colitis (UC) and Crohn’s disease (CD), has been increasing in Asia. We probed the nationwide registered database to assess the incidence, prevalence, gender distribution, age of diagnosis and the survival status of IBD patients in Taiwan.

Methods

A retrospective study was conducted to analyze the registered database compiled by the National Health Insurance provided by the Department of Health, Taiwan, from January 1998 through December 2008.

Results

A total of 1591 IBD patients were registered from 1998 to 2008 in Taiwan (CD: 385; UC: 1206). The incidence of CD increased from 0.19/100,000 in 1998 to 0.24/100,000 in 2008. The incidence of UC increased from 0.61/100,000 in 1998 to 0.94/100,000 in 2008. The prevalence of CD increased from 0.19/100,000 in 1998 to 1.78/100,000 in 2008. The prevalence of UC increased from 0.61/100,000 in 1998 to 7.62/100,000 in 2008. Male to female ratio for CD was 2.22 and 1.64 for UC. Age of registered for CD was predominantly between 20 to 39, and for UC between 30 to 49 years of age. The standardized mortality ratio (95% CI) was 4.97 (3.72–6.63) for CD and 1.78 (1.46–2.17) for UC, from 1998 to 2008 in Taiwan.

Conclusions

Using the Taiwan nationwide database for IBD, the incidence and prevalence of IBD in Taiwan significantly increased from 1998 to 2008. The mortality rate was higher for CD patients than UC patients, and both were higher than the general population.
Hinweise

Electronic supplementary material

The online version of this article (doi:10.​1186/​1471-230X-13-166) contains supplementary material, which is available to authorized users.

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

SCW, CCT, MTW, JSK, MJS, CYW, JMW: study desing, data collection, manuscript preparation. MHL, WCH, PCC: statistics analysis and manucript preparation. All authors read and approved the final manuscript.

Background

The inflammatory bowel diseases (IBDs) Crohn’s disease (CD) and ulcerative colitis (UC) are common causes of chronic gastrointestinal disease in the developed world. Initially regarded as a Western lifestyle disease, inflammatory bowel disease (IBD) is increasing in both incidence and prevalence in many parts of the Asia Pacific area [18]. The reason for this increasing trend has not been established but is most likely related to environment factors, including improved hygiene and “Westernization” of diet [9].
Based on a hospital (National Taiwan University Hospital)-based analysis, we previously showed that CD as well as UC has increased in both incidence and prevalence in Taiwan [1012]. The National Taiwan University Hospital is a tertiary referral center in Taiwan; with the first case of ulcerative colitis being diagnosed in 1969. The previous reports offered a detailed disease phenotypic analysis with a long follow-up period (from 1989 to 2008). However, the exact condition of the general incidence and prevalence of CD and UC in Taiwan still needs a nationwide-based collection of data for a more representative and comprehensive analysis.
In Taiwan, the National Health Insurance provided by the Department of Health, Executive Yuan of Taiwan government was launched in 1995. Almost 99% of the residents of Taiwan subscribe to this program for their health insurance. Since 1997, CD and UC, due to their potential for repetitive admissions and the need for chronic, careful caring, are registered as catastrophic illnesses. When a patient’s ailment is diagnosed by a physician as a “catastrophic illness” under Department of Health guidelines, the patient can submit related information and apply for a catastrophic illness certificate/registration. For IBD, the application includes the clinical diagnosis, pathological report as well as the possible image studies to be formally reviewed to validate and register the patient’s diagnosis of CD or UC, as well as for excluding intestinal tuberculosis. In this study, we used this nationwide-based data set to reveal the incidence, prevalence, age/gender distribution and the mortality rate of IBD patients in Taiwan.

Methods

Data source and ethical considerations

The nationwide population-based Taiwanese study of IBD was compiled between January 1998 and December 2008. Data was obtained from the Taiwan National Health Insurance (NHI) research database, which has been routinely collected by the National Health Research Institute (NHRI). These high quality databases have previously been used for epidemiologic research, information on prescription use, diagnoses, and hospitalizations [1315]. With strict confidentiality guidelines being closely followed in accordance with personal electronic data protection regulations; the NHRI anonymized and maintained the NHI reimbursement data as files suitable for research. In addition, this study was approved by the Ethics Review Board at the National Taiwan University Hospital.

Patient identification

We used the diagnostic code (The International Classification of Diseases, Ninth Revision, Clinical Modification 2001 edition) to retrieve the IBD patients (UC: 556.XX; CD: 555.XX) from the catastrophic illness registration database. For each patient, medical records were collected in the NHI claim database, including date of admission, date of discharge, dates of visits, clinical diagnosis, prescription and total expenditure. The databases also contained patient information, including sex, date of birth and date of death.

Statistical analyses

The characteristics of IBD patients, including the year of diagnosis, sex ratio and age distribution, were described in this study. The annual incidence and prevalence were defined as the number of newly diagnosed patients and the number of patients with IBD per 100,000 persons per year, respectively, namely, the crude incidence and prevalence. We used the Kaplan-Meier method to estimate IBD cumulative survival rate over an eleven year follow-up period. To compare with the general population of Taiwan, the standardized mortality ratio and 95% confidence interval were calculated based on the Poisson assumption. Furthermore, the direct mortality rate was also standardized to the WHO 2000 standard population using 5-year age groups per 1,000 person-years. All statistical analyses were performed with the SAS version 9.3 (SAS Institute, Cary, NC, USA). A P value of less than 0.05 was set to declare statistical significance.

Results

A total of 1,591 IBD patients were registered from 1998 to 2008 in Taiwan. Among them, 385 were diagnosed with CD and 1,206 with UC. As shown in Figure 1, the incidence of CD increased from 0.19/100,000 in 1998 to 0.24/100,000 in 2008. The incidence of UC increased from 0.61/100,000 in 1998 to 0.94/100,000 in 2008. When this period was arbitrarily divided into the first stage as 1998 to 2003 and second stage from 2004 to 2008, the mean incidence for CD in the first stage was 0.16/100,000 and 0.22/100,000 for the second stage; the incidence of CD increased significantly from the first stage to the second stage (p = 0.005). For UC, the mean incidence in the first stage was 0.70/100,000 and 0.88/100,000 for the second stage; the incidence of UC increased also significantly from the first stage to the second stage (p = 0.047).
As shown in Figure 2, the prevalence of CD increased from 0.19/100,000 in 1998 to 1.78/100,000 in 2008. The prevalence of UC increased from 0.62/100,000 in 1998 to 7.62/100,000 in 2008. The mean prevalence for CD in the first stage was 0.51/100,000 and 1.42/100,000 for the second stage; the prevalence of CD increased significantly from the first stage to the second stage (p = 0.0003). For UC, the mean prevalence in the first stage was 2.2/100,000 and 6.12/100,000 for the second stage; the prevalence of UC increased also significantly from the first stage to the second stage (p = 0.0005).
The year of diagnosis and sex-specific number of patients with CD and UC in Taiwan from 1998 to 2008 are summarized in Table 1. Sex- and age-specific number of patients registered with CD are summarized in Table 2, and for UC in Table 3. The age of registration for CD patients was primarily between 20 to 39 (Figure 3), with the mean and standard deviation of 37.8 and 18.8 years of age, respectively. The age of registration for UC was mostly between 30 to 49 years old (Figure 4), with the mean and standard deviation of 44.5 and 15.8 years old, respectively. Male to female ratios for CD was 2.22 and 1.64 for UC. These ratios reflect a male predominant pattern in Taiwan for CD over UC (p = 0.01) (Figure 5).
Table 1
Year of diagnosis and sex-specific number of patients with Crohn’s disease and ulcerative colitis in Taiwan, 1998-2008
Year of diagnosis
Male
Female
Total
Male to female ratio
Crohn’s disease
    
1998
25
13
38
1.9
1999
18
10
28
1.8
2000
22
10
32
2.2
2001
28
12
40
2.3
2002
27
9
36
3
2003
26
17
43
1.5
2004
37
15
52
2.5
2005
33
15
48
2.2
2006
32
16
48
2
2007
31
14
45
2.2
2008
41
15
56
2.7
Ulcerative colitis
    
1998
69
49
118
1.4
1999
91
44
135
2.1
2000
78
42
120
1.9
2001
82
37
119
2.2
2002
113
76
189
1.5
2003
123
72
195
1.7
2004
100
69
169
1.4
2005
136
85
221
1.6
2006
116
85
201
1.4
2007
119
74
193
1.6
2008
123
95
218
1.3
Table 2
Sex- and age-specific number of patients registered as Crohn’s disease in Taiwan, 1998-2008
Age group
Male
Female
Total
0–9
18
8
26
10–19
30
16
46
20–29
77
17
94
30–39
72
30
102
40–49
56
26
82
50–59
26
23
49
60–69
22
14
36
70–79
18
7
25
≥80
1
5
6
Table 3
Sex- and age-specific number of patients registered as ulcerative colitis in Taiwan, 1998-2008
Age group
Male
Female
Total
0–9
8
3
11
10–19
34
26
60
20–29
175
76
251
30–39
290
164
454
40–49
264
162
426
50–59
193
138
331
60–69
109
92
201
70–79
61
58
119
≥80
16
9
25
As shown in Figure 6, the survival status of CD patients after registration for one year, 5 years and 10 years were: 96%, 90% and 82%, respectively. For UC patients, the survival status after registration for one year, 5 years and 10 years were: 99%, 95% and 90%, respectively. There was a statistical difference between the survival status of UC and CD patients from 1998 to 2008 in Taiwan (p = 0.001). The standardized mortality ratio (95% CI) was 4.97 (3.72–6.63) and the standardized mortality rate (per 1,000 person-years) was 29.7 for CD; and the standardized mortality ratio (95% CI) was 1.78 (1.46–2.17) with the standardized mortality rate (per 1,000 person-years) of 9.62 for UC from 1998 to 2008 in Taiwan.

Discussion

Increased incidence and prevalence of IBD in Asia have been reported [1, 312]. This information is mostly based on hospital-based data except for a report from Japan where there is a nationwide registration system [16]. By using a nationwide registration system in Taiwan, we confirmed this phenomenon by adding a second nationwide-based data analysis in Asia, which confirmed that the incidence and prevalence of IBD increased from 1998 to 2008 in Taiwan. From our experience, the true IBD patient number should be more than the registered number as there are always IBD patients who have not yet registered or who have not passed the registration process, therefore, there is no way to know the real number. The bottom line is that we have at least the number of cases reported in this study with a confirmed diagnosis of IBD and the number of cases increased significantly over the past years in Taiwan. Although the incidence (CD: 0.24/100,000; UC: 0.94/100,000, in 2008) and prevalence (CD: 1.78/100,000; UC: 7.62/100,000, in 2008) increased in Taiwan, they were still lower than the reports from Japan (prevalence: approximately 21/100,000 for CD and 63.6/100,000 for UC), Korea (prevalence: approximately 11/100,000 for CD and 30.9/100,000 for UC), and much lower than those from Western Countries (prevalence: approximately 200/100,000 for CD and 400/100,000 for UC) [1, 9, 16]. And according to the recently pusblised large scale population-based epidemiologic study across nine countries in Asia-Pacific showing geographic variability in disease incidence even within Asia [17]. Taiwan appeared to have disease incidence that is lower than Hong Kong, some parts of mainland China, and Macau, and relatively similar to that of Malaysia and Sri Lanka, but higher than those of Thailand and Indonesia. One may speculate that different degrees of urbanization/socioeconomic status may play a part in the variation.
The mean age of patients registered with CD was 37.8 and for UC was 44.5 years of age. We previously have shown that, based on a referral center in Taiwan, the mean age of diagnosis for CD was 30.5 and for UC was 36 in the National Taiwan University Hospital [11, 12]. This difference might be related to the lag between diagnosis and registration, as well as the possible gap between the IBD diagnosis efficiency between an experienced center and the other general hospitals. Nonetheless, the mean age for CD and UC registered patients was still within the range reported from other countries in Asia [16].
Considering the male to female ratio, in the current study we found the ratio for CD was 2.22 and for UC was 1.64, which was consistent with our previous results which showed 1.82 for CD and 1.35 for UC [11, 12]. Both diseases showed a male predominant pattern, especially significant for CD. This observation was consistent with the reports from the other Asian countries, most of them revealed a male predominant prevalence. Interestingly, this differed from reports from Western countries [16, 18].
The survival status, or vice versa, the mortality rate from this report was quite different from previous reports, even when compared to our previous results based on a referral center follow-up study which showed the accumulated mortality rate for CD to be 2.7% (3 of 110) and 1.72% for UC (7 of 406) from 1988 to 2008. In this study, the survival rate of CD patients after the registration for one year, 5 years and 10 years were: 96%, 90% and 82%, respectively. For UC patients, the survival status after the registration for one year, 5 years and 10 years were: 99%, 95% and 90%, respectively. There was a statistical difference of the survival status between UC and CD patients from 1998 to 2008 in Taiwan (p = 0.001). When compared with the general population, the standardized mortality ratio (95% CI) was 4.97 (3.72–6.63) and the standardized mortality rate (per 1,000 person-years) was 29.7 for CD; the standardized mortality ratio (95% CI) was 1.78 (1.46–2.17) with the standardized mortality rate (per 1,000 person-years) as 9.62 for UC from 1998 to 2008 in Taiwan. Both were higher than the reports from Japan as well as from most Western countries, with the standardized mortality ratio for CD around 1.5 fold the general population. The mortality rate of CD patients was slightly higher than the general population and the mortality rates for UC patients, either from Japan or from Western countries were mostly the same as the general population [1931].
The higher mortality shown in this study was unexpected. However, as the data was anonymized, only the date of death but not the cause of death nor comorbidity could be traced from this data set. The registered data only provided the diagnosis, no phenotypic information was included. Therefore, we were not able to know whether the higher mortality resulted from the severity of the disease or not. The ages of diagnosis in this cohort were comparable to the reports from other Asian countries [1, 17, 30], age did not seem to be able to explain the higher mortality. However, when comparing the results from a referral center (National Taiwan University Hospital, for example) with the nationwide population-base, patients tended to be diagnosed at earlier ages and with less mortality when seen in a referral center. This result might reflect the low awareness of IBD in the general practice, since previously in Taiwan,IBD was a relatively low prevalence disease. Experience diagnosing and treating IBD patients when they presented outside the referral center (NTUH, for example) was lagging. Therefore, since 2010, we have started to emphasize the increasing trend of IBD as well as an IBD awareness education program. Hopefully in the future, we can improve the awareness, the quality of care, and the outcome of IBD patients in Taiwan. Our experience might also afford other countries where IBD is low in prevalence, to modify their quality of care in treating IBD patients which should translate into improving the prognosis of IBD patients.

Conclusion

Using the Taiwan nationwide database for IBD, the incidence and prevalence of IBD in Taiwan significantly increased from 1998 to 2008.
The mortality rate was higher for CD patients than UC patients, and both were higher than the general population. After our promotion of the disease awareness, we hope the outcome of IBD patients in Taiwan could be improved in the future.
Open Access This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution License ( https://​creativecommons.​org/​licenses/​by/​2.​0 ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

SCW, CCT, MTW, JSK, MJS, CYW, JMW: study desing, data collection, manuscript preparation. MHL, WCH, PCC: statistics analysis and manucript preparation. All authors read and approved the final manuscript.
Literatur
1.
Zurück zum Zitat Yang SK, Yun S, Kim JH, Park JY, Kim HY, Kim YH, Chang DK, Kim JS, Song IS, Park JB, et al: Epidemiology of inflammatory bowel disease in the Songpa-Kangdong district, Seoul, Korea, 1986–2005: a KASID study. Inflamm Bowel Dis. 2008, 14 (4): 542-549. 10.1002/ibd.20310.CrossRefPubMed Yang SK, Yun S, Kim JH, Park JY, Kim HY, Kim YH, Chang DK, Kim JS, Song IS, Park JB, et al: Epidemiology of inflammatory bowel disease in the Songpa-Kangdong district, Seoul, Korea, 1986–2005: a KASID study. Inflamm Bowel Dis. 2008, 14 (4): 542-549. 10.1002/ibd.20310.CrossRefPubMed
2.
Zurück zum Zitat Yang SK, Hong WS, Min YI, Kim HY, Yoo JY, Rhee PL, Rhee JC, Chang DK, Song IS, Jung SA, et al: Incidence and prevalence of ulcerative colitis in the Songpa-Kangdong District, Seoul, Korea, 1986–1997. J Gastroenterol Hepatol. 2000, 15 (9): 1037-1042. 10.1046/j.1440-1746.2000.02252.x.CrossRefPubMed Yang SK, Hong WS, Min YI, Kim HY, Yoo JY, Rhee PL, Rhee JC, Chang DK, Song IS, Jung SA, et al: Incidence and prevalence of ulcerative colitis in the Songpa-Kangdong District, Seoul, Korea, 1986–1997. J Gastroenterol Hepatol. 2000, 15 (9): 1037-1042. 10.1046/j.1440-1746.2000.02252.x.CrossRefPubMed
3.
Zurück zum Zitat Yoshida Y, Murata Y: Inflammatory bowel disease in Japan: studies of epidemiology and etiopathogenesis. Med Clin North Am. 1990, 74 (1): 67-90.CrossRefPubMed Yoshida Y, Murata Y: Inflammatory bowel disease in Japan: studies of epidemiology and etiopathogenesis. Med Clin North Am. 1990, 74 (1): 67-90.CrossRefPubMed
4.
Zurück zum Zitat Chow DK, Leong RW, Tsoi KK, Ng SS, Leung WK, Wu JC, Wong VW, Chan FK, Sung JJ: Long-term follow-up of ulcerative colitis in the Chinese population. Am J Gastroenterol. 2009, 104 (3): 647-654. 10.1038/ajg.2008.74.CrossRefPubMed Chow DK, Leong RW, Tsoi KK, Ng SS, Leung WK, Wu JC, Wong VW, Chan FK, Sung JJ: Long-term follow-up of ulcerative colitis in the Chinese population. Am J Gastroenterol. 2009, 104 (3): 647-654. 10.1038/ajg.2008.74.CrossRefPubMed
5.
Zurück zum Zitat Ling KL, Ooi CJ, Luman W, Cheong WK, Choen FS, Ng HS: Clinical characteristics of ulcerative colitis in Singapore, a multiracial city-state. J Clin Gastroenterol. 2002, 35 (2): 144-148. 10.1097/00004836-200208000-00005.CrossRefPubMed Ling KL, Ooi CJ, Luman W, Cheong WK, Choen FS, Ng HS: Clinical characteristics of ulcerative colitis in Singapore, a multiracial city-state. J Clin Gastroenterol. 2002, 35 (2): 144-148. 10.1097/00004836-200208000-00005.CrossRefPubMed
6.
Zurück zum Zitat Asakura K, Nishiwaki Y, Inoue N, Hibi T, Watanabe M, Takebayashi T: Prevalence of ulcerative colitis and Crohn’s disease in Japan. J Gastroenterol. 2009, 44 (7): 659-665. 10.1007/s00535-009-0057-3.CrossRefPubMed Asakura K, Nishiwaki Y, Inoue N, Hibi T, Watanabe M, Takebayashi T: Prevalence of ulcerative colitis and Crohn’s disease in Japan. J Gastroenterol. 2009, 44 (7): 659-665. 10.1007/s00535-009-0057-3.CrossRefPubMed
7.
Zurück zum Zitat Ouyang Q, Tandon R, Goh KL, Ooi CJ, Ogata H, Fiocchi C: The emergence of inflammatory bowel disease in the Asian Pacific region. Curr Opin Gastroenterol. 2005, 21 (4): 408-413.PubMed Ouyang Q, Tandon R, Goh KL, Ooi CJ, Ogata H, Fiocchi C: The emergence of inflammatory bowel disease in the Asian Pacific region. Curr Opin Gastroenterol. 2005, 21 (4): 408-413.PubMed
8.
Zurück zum Zitat Ooi CJ, Fock KM, Makharia GK, Goh KL, Ling KL, Hilmi I, Lim WC, Kelvin T, Gibson PR, Gearry RB, et al: The Asia-Pacific consensus on ulcerative colitis. J Gastroenterol Hepatol. 2010, 25 (3): 453-468. 10.1111/j.1440-1746.2010.06241.x.CrossRefPubMed Ooi CJ, Fock KM, Makharia GK, Goh KL, Ling KL, Hilmi I, Lim WC, Kelvin T, Gibson PR, Gearry RB, et al: The Asia-Pacific consensus on ulcerative colitis. J Gastroenterol Hepatol. 2010, 25 (3): 453-468. 10.1111/j.1440-1746.2010.06241.x.CrossRefPubMed
9.
Zurück zum Zitat Yao T, Matsui T, Hiwatashi N: Crohn’s disease in Japan: diagnostic criteria and epidemiology. Dis Colon Rectum. 2000, 43 (10 Suppl): S85-S93.CrossRefPubMed Yao T, Matsui T, Hiwatashi N: Crohn’s disease in Japan: diagnostic criteria and epidemiology. Dis Colon Rectum. 2000, 43 (10 Suppl): S85-S93.CrossRefPubMed
10.
Zurück zum Zitat Hsiao CH, Wei SC, Wong JM, Lai HS, Chang MH, Ni YH: Pediatric Crohn disease: clinical and genetic characteristics in Taiwan. J Pediatr Gastroenterol Nutr. 2007, 44 (3): 342-346. 10.1097/MPG.0b013e31802c6997.CrossRefPubMed Hsiao CH, Wei SC, Wong JM, Lai HS, Chang MH, Ni YH: Pediatric Crohn disease: clinical and genetic characteristics in Taiwan. J Pediatr Gastroenterol Nutr. 2007, 44 (3): 342-346. 10.1097/MPG.0b013e31802c6997.CrossRefPubMed
11.
Zurück zum Zitat Wei SC, Ni YH, Yang HI, Su YN, Chang MC, Chang YT, Shieh MJ, Wang CY, Wong JM: A hospital-based study of clinical and genetic features of Crohn’s disease. J Formos Med Assoc. 2011, 110 (9): 600-606. 10.1016/j.jfma.2011.07.009.CrossRefPubMed Wei SC, Ni YH, Yang HI, Su YN, Chang MC, Chang YT, Shieh MJ, Wang CY, Wong JM: A hospital-based study of clinical and genetic features of Crohn’s disease. J Formos Med Assoc. 2011, 110 (9): 600-606. 10.1016/j.jfma.2011.07.009.CrossRefPubMed
12.
Zurück zum Zitat Wei SC, Shieh MJ, Chang MC, Chang YT, Wang CY, Wong JM: Long-term follow-up of ulcerative colitis in Taiwan. J Chin Med Assoc. 2012, 75 (4): 151-155. 10.1016/j.jcma.2012.02.017.CrossRefPubMed Wei SC, Shieh MJ, Chang MC, Chang YT, Wang CY, Wong JM: Long-term follow-up of ulcerative colitis in Taiwan. J Chin Med Assoc. 2012, 75 (4): 151-155. 10.1016/j.jcma.2012.02.017.CrossRefPubMed
13.
Zurück zum Zitat Chiu HF, Ho SC, Chen CC, Yang CY: Statin use and the risk of liver cancer: a population-based case–control study. Am J Gastroenterol. 2011, 106 (5): 894-898. 10.1038/ajg.2010.475.CrossRefPubMed Chiu HF, Ho SC, Chen CC, Yang CY: Statin use and the risk of liver cancer: a population-based case–control study. Am J Gastroenterol. 2011, 106 (5): 894-898. 10.1038/ajg.2010.475.CrossRefPubMed
14.
Zurück zum Zitat Lai MN, Wang SM, Chen PC, Chen YY, Wang JD: Population-based case–control study of Chinese herbal products containing aristolochic acid and urinary tract cancer risk. J Natl Cancer Inst. 2010, 102 (3): 179-186. 10.1093/jnci/djp467.CrossRefPubMedPubMedCentral Lai MN, Wang SM, Chen PC, Chen YY, Wang JD: Population-based case–control study of Chinese herbal products containing aristolochic acid and urinary tract cancer risk. J Natl Cancer Inst. 2010, 102 (3): 179-186. 10.1093/jnci/djp467.CrossRefPubMedPubMedCentral
15.
Zurück zum Zitat Tsan YT, Lee CH, Wang JD, Chen PC: Statins and the risk of hepatocellular carcinoma in patients with hepatitis B virus infection. J Clin Oncol. 2012, 30 (6): 623-630. 10.1200/JCO.2011.36.0917.CrossRefPubMed Tsan YT, Lee CH, Wang JD, Chen PC: Statins and the risk of hepatocellular carcinoma in patients with hepatitis B virus infection. J Clin Oncol. 2012, 30 (6): 623-630. 10.1200/JCO.2011.36.0917.CrossRefPubMed
16.
Zurück zum Zitat Prideaux L, Kamm MA, De Cruz PP, Chan FK, Ng SC: Inflammatory bowel disease in Asia: a systematic review. J Gastroenterol Hepatol. 2012, 27 (8): 1266-1280. 10.1111/j.1440-1746.2012.07150.x.CrossRefPubMed Prideaux L, Kamm MA, De Cruz PP, Chan FK, Ng SC: Inflammatory bowel disease in Asia: a systematic review. J Gastroenterol Hepatol. 2012, 27 (8): 1266-1280. 10.1111/j.1440-1746.2012.07150.x.CrossRefPubMed
17.
Zurück zum Zitat Ng SC, Tang W, Ching JY, Wong M, Chow CM, Hui AJ, Wong TC, Leung VK, Tsang SW, Yu HH, et al: Incidence and phenotype of inflammatory bowel disease based on results from the Asia-pacific Crohn’s and colitis epidemiology study. Gastroenterology. 2013, 145 (1): 158-165. 10.1053/j.gastro.2013.04.007. e152CrossRefPubMed Ng SC, Tang W, Ching JY, Wong M, Chow CM, Hui AJ, Wong TC, Leung VK, Tsang SW, Yu HH, et al: Incidence and phenotype of inflammatory bowel disease based on results from the Asia-pacific Crohn’s and colitis epidemiology study. Gastroenterology. 2013, 145 (1): 158-165. 10.1053/j.gastro.2013.04.007. e152CrossRefPubMed
18.
Zurück zum Zitat Tragnone A, Corrao G, Miglio F, Caprilli R, Lanfranchi GA: Incidence of inflammatory bowel disease in Italy: a nationwide population-based study. Gruppo Italiano per lo Studio del Colon e del Retto (GISC). Int J Epidemiol. 1996, 25 (5): 1044-1052. 10.1093/ije/25.5.1044.CrossRefPubMed Tragnone A, Corrao G, Miglio F, Caprilli R, Lanfranchi GA: Incidence of inflammatory bowel disease in Italy: a nationwide population-based study. Gruppo Italiano per lo Studio del Colon e del Retto (GISC). Int J Epidemiol. 1996, 25 (5): 1044-1052. 10.1093/ije/25.5.1044.CrossRefPubMed
19.
Zurück zum Zitat Button LA, Roberts SE, Goldacre MJ, Akbari A, Rodgers SE, Williams JG: Hospitalized prevalence and 5-year mortality for IBD: record linkage study. World J Gastroenterol. 2010, 16 (4): 431-438. 10.3748/wjg.v16.i4.431.CrossRefPubMedPubMedCentral Button LA, Roberts SE, Goldacre MJ, Akbari A, Rodgers SE, Williams JG: Hospitalized prevalence and 5-year mortality for IBD: record linkage study. World J Gastroenterol. 2010, 16 (4): 431-438. 10.3748/wjg.v16.i4.431.CrossRefPubMedPubMedCentral
20.
Zurück zum Zitat Canavan C, Abrams KR, Mayberry JF: Meta-analysis: mortality in Crohn’s disease. Aliment Pharm Ther. 2007, 25 (8): 861-870. 10.1111/j.1365-2036.2007.03276.x.CrossRef Canavan C, Abrams KR, Mayberry JF: Meta-analysis: mortality in Crohn’s disease. Aliment Pharm Ther. 2007, 25 (8): 861-870. 10.1111/j.1365-2036.2007.03276.x.CrossRef
21.
Zurück zum Zitat Doi Y, Yokoyama T, Sakai M: [Trends in mortality from intractable diseases in Japan, 1972–2004]. [Nihon koshu eisei zasshi] Japanese. J Public Health. 2007, 54 (10): 684-694. Doi Y, Yokoyama T, Sakai M: [Trends in mortality from intractable diseases in Japan, 1972–2004]. [Nihon koshu eisei zasshi] Japanese. J Public Health. 2007, 54 (10): 684-694.
22.
Zurück zum Zitat Duricova D, Pedersen N, Elkjaer M, Gamborg M, Munkholm P, Jess T: Overall and cause-specific mortality in Crohn’s disease: a meta-analysis of population-based studies. Inflamm Bowel Dis. 2010, 16 (2): 347-353. 10.1002/ibd.21007.CrossRefPubMed Duricova D, Pedersen N, Elkjaer M, Gamborg M, Munkholm P, Jess T: Overall and cause-specific mortality in Crohn’s disease: a meta-analysis of population-based studies. Inflamm Bowel Dis. 2010, 16 (2): 347-353. 10.1002/ibd.21007.CrossRefPubMed
23.
Zurück zum Zitat Hutfless SM, Weng X, Liu L, Allison J, Herrinton LJ: Mortality by medication use among patients with inflammatory bowel disease, 1996–2003. Gastroenterology. 2007, 133 (6): 1779-1786. 10.1053/j.gastro.2007.09.022.CrossRefPubMed Hutfless SM, Weng X, Liu L, Allison J, Herrinton LJ: Mortality by medication use among patients with inflammatory bowel disease, 1996–2003. Gastroenterology. 2007, 133 (6): 1779-1786. 10.1053/j.gastro.2007.09.022.CrossRefPubMed
24.
Zurück zum Zitat Jess T, Riis L, Vind I, Winther KV, Borg S, Binder V, Langholz E, Thomsen OO, Munkholm P: Changes in clinical characteristics, course, and prognosis of inflammatory bowel disease during the last 5 decades: a population-based study from Copenhagen, Denmark. Inflamm Bowel Dis. 2007, 13 (4): 481-489. 10.1002/ibd.20036.CrossRefPubMed Jess T, Riis L, Vind I, Winther KV, Borg S, Binder V, Langholz E, Thomsen OO, Munkholm P: Changes in clinical characteristics, course, and prognosis of inflammatory bowel disease during the last 5 decades: a population-based study from Copenhagen, Denmark. Inflamm Bowel Dis. 2007, 13 (4): 481-489. 10.1002/ibd.20036.CrossRefPubMed
25.
Zurück zum Zitat Persson PG, Bernell O, Leijonmarck CE, Farahmand BY, Hellers G, Ahlbom A: Survival and cause-specific mortality in inflammatory bowel disease: a population-based cohort study. Gastroenterology. 1996, 110 (5): 1339-1345. 10.1053/gast.1996.v110.pm8613037.CrossRefPubMed Persson PG, Bernell O, Leijonmarck CE, Farahmand BY, Hellers G, Ahlbom A: Survival and cause-specific mortality in inflammatory bowel disease: a population-based cohort study. Gastroenterology. 1996, 110 (5): 1339-1345. 10.1053/gast.1996.v110.pm8613037.CrossRefPubMed
26.
Zurück zum Zitat Peyrin-Biroulet L, Loftus EV, Colombel JF, Sandborn WJ: Long-term complications, extraintestinal manifestations, and mortality in adult Crohn’s disease in population-based cohorts. Inflamm Bowel Dis. 2011, 17 (1): 471-478. 10.1002/ibd.21417.CrossRefPubMed Peyrin-Biroulet L, Loftus EV, Colombel JF, Sandborn WJ: Long-term complications, extraintestinal manifestations, and mortality in adult Crohn’s disease in population-based cohorts. Inflamm Bowel Dis. 2011, 17 (1): 471-478. 10.1002/ibd.21417.CrossRefPubMed
27.
Zurück zum Zitat Romberg-Camps M, Kuiper E, Schouten L, Kester A, Hesselink-van de Kruijs M, Limonard C, Bos R, Goedhard J, Hameeteman W, Wolters F, et al: Mortality in inflammatory bowel disease in the Netherlands 1991–2002: results of a population-based study: the IBD South-Limburg cohort. Inflamm Bowel Dis. 2010, 16 (8): 1397-1410. 10.1002/ibd.21189.CrossRefPubMed Romberg-Camps M, Kuiper E, Schouten L, Kester A, Hesselink-van de Kruijs M, Limonard C, Bos R, Goedhard J, Hameeteman W, Wolters F, et al: Mortality in inflammatory bowel disease in the Netherlands 1991–2002: results of a population-based study: the IBD South-Limburg cohort. Inflamm Bowel Dis. 2010, 16 (8): 1397-1410. 10.1002/ibd.21189.CrossRefPubMed
28.
Zurück zum Zitat Selinger CP, Leong RW: Mortality from inflammatory bowel diseases. Inflamm Bowel Dis. 2012, 18 (8): 1566-1572. 10.1002/ibd.22871.CrossRefPubMed Selinger CP, Leong RW: Mortality from inflammatory bowel diseases. Inflamm Bowel Dis. 2012, 18 (8): 1566-1572. 10.1002/ibd.22871.CrossRefPubMed
29.
Zurück zum Zitat Travis SP: Review article: insurance risks for patients with ulcerative colitis or Crohn’s disease. Aliment Pharm Ther. 1997, 11 (1): 51-59. 10.1046/j.1365-2036.1997.119290000.x.CrossRef Travis SP: Review article: insurance risks for patients with ulcerative colitis or Crohn’s disease. Aliment Pharm Ther. 1997, 11 (1): 51-59. 10.1046/j.1365-2036.1997.119290000.x.CrossRef
30.
Zurück zum Zitat Uno H, Yao T, Matsui T, Sakurai T, Iida M, Matsumoto T, Aoyagi K, Fuchigami T: Mortality and cause of death in Japanese patients with Crohn’s disease. Dis Colon Rectum. 2003, 46 (10 Suppl): S15-S21.PubMed Uno H, Yao T, Matsui T, Sakurai T, Iida M, Matsumoto T, Aoyagi K, Fuchigami T: Mortality and cause of death in Japanese patients with Crohn’s disease. Dis Colon Rectum. 2003, 46 (10 Suppl): S15-S21.PubMed
31.
Zurück zum Zitat Winther KV, Jess T, Langholz E, Munkholm P, Binder V: Survival and cause-specific mortality in ulcerative colitis: follow-up of a population-based cohort in Copenhagen County. Gastroenterology. 2003, 125 (6): 1576-1582. 10.1053/j.gastro.2003.09.036.CrossRefPubMed Winther KV, Jess T, Langholz E, Munkholm P, Binder V: Survival and cause-specific mortality in ulcerative colitis: follow-up of a population-based cohort in Copenhagen County. Gastroenterology. 2003, 125 (6): 1576-1582. 10.1053/j.gastro.2003.09.036.CrossRefPubMed
Metadaten
Titel
A nationwide population-based study of the inflammatory bowel diseases between 1998 and 2008 in Taiwan
verfasst von
Shu-Chen Wei
Meng-Hung Lin
Chien-Chih Tung
Meng-Tzu Weng
Jen-Shin Kuo
Ming-Jium Shieh
Cheng-Yi Wang
Wen-Chao Ho
Jau-Min Wong
Pau-Chung Chen
Publikationsdatum
01.12.2013
Verlag
BioMed Central
Erschienen in
BMC Gastroenterology / Ausgabe 1/2013
Elektronische ISSN: 1471-230X
DOI
https://doi.org/10.1186/1471-230X-13-166

Weitere Artikel der Ausgabe 1/2013

BMC Gastroenterology 1/2013 Zur Ausgabe

Leitlinien kompakt für die Innere Medizin

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Bei seelischem Stress sind Checkpoint-Hemmer weniger wirksam

03.06.2024 NSCLC Nachrichten

Wie stark Menschen mit fortgeschrittenem NSCLC von einer Therapie mit Immun-Checkpoint-Hemmern profitieren, hängt offenbar auch davon ab, wie sehr die Diagnose ihre psychische Verfassung erschüttert

Antikörper mobilisiert Neutrophile gegen Krebs

03.06.2024 Onkologische Immuntherapie Nachrichten

Ein bispezifischer Antikörper formiert gezielt eine Armee neutrophiler Granulozyten gegen Krebszellen. An den Antikörper gekoppeltes TNF-alpha soll die Zellen zudem tief in solide Tumoren hineinführen.

Erhebliches Risiko für Kehlkopfkrebs bei mäßiger Dysplasie

29.05.2024 Larynxkarzinom Nachrichten

Fast ein Viertel der Personen mit mäßig dysplastischen Stimmlippenläsionen entwickelt einen Kehlkopftumor. Solche Personen benötigen daher eine besonders enge ärztliche Überwachung.

Nach Herzinfarkt mit Typ-1-Diabetes schlechtere Karten als mit Typ 2?

29.05.2024 Herzinfarkt Nachrichten

Bei Menschen mit Typ-2-Diabetes sind die Chancen, einen Myokardinfarkt zu überleben, in den letzten 15 Jahren deutlich gestiegen – nicht jedoch bei Betroffenen mit Typ 1.

Update Innere Medizin

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.