| Literature DB >> 29914399 |
Adalberta Lima Martins1,2, Rhaisa Almeida Volpato3, Maria da Penha Zago-Gomes4.
Abstract
BACKGROUND: The epidemiology of inflammatory bowel disease (IBD) varies in different countries. This study aimed to assess phenotype, medications, prevalence and incidence of IBD in the State of Espírito Santo, Brazil.Entities:
Keywords: Brazil; Crohn’s disease; Inflammatory bowel disease; Phenotype; Prevalence; Ulcerative colitis
Mesh:
Substances:
Year: 2018 PMID: 29914399 PMCID: PMC6006948 DOI: 10.1186/s12876-018-0822-y
Source DB: PubMed Journal: BMC Gastroenterol ISSN: 1471-230X Impact factor: 3.067
Fig. 1Map of Espírito Santo, Brazil, South America
Fig. 2Flowchart for the analysis of medication dispensing requests for IBD in Espírito Santo, Brazil
Distribution of ulcerative colitis and Crohn’s disease
| Demographic variables | IBD | |||||
|---|---|---|---|---|---|---|
| UC | CD |
| ||||
|
| % |
| % | |||
| Year (Yr) | 2013 | 339 | 62.8% | 207 | 37.92% | 0.043 |
| 2014 | 330 | 68.75% | 150 | 31.25% | ||
| Age at diagnosis (A)a | A1: ≤ 16 | 23 | 3.40% | 25 | 7.00% | |
| A2: 17–40 | 318 | 47.50% | 208 | 58.30% | 0.001 | |
| A3: > 40 | 328 | 49.00% | 124 | 34.70% | ||
| Gender | Female | 407 | 60.80% | 195 | 54.60% | 0.156 |
| Male | 262 | 39.20% | 162 | 45.40% | ||
| New cases | 2013 | 215 | 51.3% | 117 | 55.7% | 0.346 |
| 2014 | 204 | 48.7% | 94 | 44.3% | ||
| Old Cases | 2013 | 124 | 49.6% | 90 | 61.6% | 0.058 |
| 2014 | 126 | 50.4% | 56 | 38.4% | ||
aAge at diagnosis is not a phenotypic element of the Montreal classification for ulcerative colitis; UC ulcerative colitis, CD, Crohn’s disease
Clinical characteristics of ulcerative colitis (n = 654)
| Phenotypic elements | Extension | |||||||
|---|---|---|---|---|---|---|---|---|
| E1 | E2 | E3 |
| |||||
| Proctitis | Left-sided colitis | Pancolitis | ||||||
| n | % | n | % | n | % | |||
| Age at diagnosis (A)a | A1: ≤ 16 | 3 | 13.0 | 6 | 26.1 | 14 | 60.9 | 0.007 |
| A2: 17–40 | 89 | 28.4 | 116 | 37.1 | 108 | 34.5 | ||
| A3: > 40 | 106 | 30.5 | 125 | 39.3 | 87 | 26.8 | ||
| Gender | Female | 126 | 31.5 | 153 | 38.2 | 121 | 30.2 | 0.469 |
| Male | 72 | 28.3 | 94 | 37.0 | 88 | 32.0 | ||
aAge at diagnosis is not a phenotypic element of the Montreal classification for ulcerative colitis
Clinical characteristics of Crohn’s disease (n = 357)
| Phenotypic elements | Total DC | ||
|---|---|---|---|
|
|
| ||
| Location (L) | L1: terminal ileum | 111 | 31.4 |
| L2: colonic | 102 | 28.9 | |
| L3: ileocolonic | 109 | 30.9 | |
| L4: isolated upper disease | 11 | 3.2 | |
| L1 + L4 | 8 | 2.3 | |
| L3 + L4 | 12 | 3.4 | |
| Behavior (B) | B1: nonstricturing/non-fistulizing | 176 | 50.0 |
| B2: stricturing | 56 | 15.9 | |
| B3: fistulizing | 29 | 8.2 | |
| B1pa | 27 | 7.7 | |
| B2pa | 18 | 5.1 | |
| B3pa | 46 | 13.1 | |
| Gender | Female | 195 | 54.6 |
| Male | 162 | 45.4 | |
ap perianal disease modifier
Crohn disease ‘s behavior in relation to age and gender
| Phenotypic elements | Behavior (B) | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| B1 | B2 | B3 | B1p | B2p | B3p |
| ||||||||
| n | % | n | % | n | % | n | % | n | % | n | % | |||
| Age at diagnosis (A) | A1: ≤ 16 | 10 | 5.6 | 0 | 0.0 | 2 | 6.9 | 3 | 11.1 | 1 | 5.6 | 9 | 19.6 | 0.001 |
| A2: 17–40 | 90 | 50.9 | 30 | 53.6 | 20 | 69.0 | 20 | 74.1 | 16 | 88.8 | 29 | 63.0 | ||
| A3: > 40 | 77 | 43.5 | 26 | 46.4 | 7 | 24.1 | 4 | 14.8 | 1 | 5.6 | 8 | 17.4 | ||
| Gender | Female | 110 | 62.1 | 26 | 46.4 | 16 | 55.2 | 10 | 37.0 | 11 | 61.1 | 22 | 47.8 | 0.042 |
| Male | 67 | 37.9 | 30 | 53.6 | 13 | 44.8 | 17 | 63.0 | 7 | 38.9 | 24 | 52.2 | ||
B1 nonstricturing/non-fistulizing, B2 stricturing, B3 fistulizing, p-perianal disease modifier
Fig. 3Distribution of medications used for ulcerative colitis and Crohn’s disease UC: ulcerative colitis; CD: Crohn’s disease;5-ASA: mesalazine, SSZ: sulfasalazine, IMN: immunomodulators (azathioprine and methotrexate)