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P045:巴西一家公共医疗诊所中炎症性肠病(IBD)患者的非酒精性脂肪性肝病(NAFLD)患病率

P045 Prevalence of non-alcoholic fatty liver disease (NAFLD) in patients with inflammatory bowel disease (IBD) in a Brazilian public healthcare clinic.

作者信息

Lopes Marina, Shintaku Daniel, de Oliveira Ana Carolina, Beraldo Rodrigo, Godoi Giovana, Castelhano Natalia, Vulcano Daniela, Pereira Jessica, de Oliveira Ellen Cristina, Herrerias Giedre, Saad-Hossne Rogerio, Baima Julio, Barbosa Walnei, Silva Giovanni, Sassaki Ligia

机构信息

Botucatu Medical School (São Paulo State University ), Botucatu, Brazil.

出版信息

Am J Gastroenterol. 2021 Dec 1;116(Suppl 1):S11-S12. doi: 10.14309/01.ajg.0000798780.14901.4e.

DOI:10.14309/01.ajg.0000798780.14901.4e
PMID:37461963
Abstract

BACKGROUND

Inflammatory Bowel Disease (IBD) is an inflammatory and chronic disease, as well as non-alcoholic fatty liver disease (NAFLD). Current literature has shown that IBD patients are at high risk for NAFLD. In those patients, the pathogenesis of NAFLD may be more complex and related to multifactor causes, such as gut dysbiosis, unhealthy nutritional behavior, body composition and systemic inflammation. There is an increase in NAFLD's incidence in the general population, otherwise, there are few studies evaluating NAFLD prevalence in IBD patients. So, this study aimed to evaluate prevalence of NAFLD and identify the clinical factors associated with the presence of NAFLD in patients with IBD.

METHODS

This cross-sectional, descriptive, observational study included 71 IBD patients from an IBD public outpatient in São Paulo State, Brazil. Laboratory evaluation and clinical data were collected. The presence of NAFLD was evaluated by ultrasonography. The exclusion criteria were as follows: pre-existing liver disease, history of alcohol intake >20g/day for women and >30g/day for men, and glucocorticoids treatment >20mg/day. Statistical analysis: descriptive statistics and association tests.

RESULTS

71 patients were included, of which 34 (47.89%) were Crohn´s disease (CD) and 37 (52.11%) ulcerative colitis (UC). Median age was 45.32±13.59 years, 63.38% were female, 69.1% Caucasian, 7.04% smokers. The time from diagnosis was 12.55 ± 8.01 years. Regarding the characteristics of the diseases, 42.42% of patients with CD have ileocolonic involvement, 50% penetrating disease and 39.4% perianal involvement. In relation to patients with UC, most patients have pancolitis (72.22%). Mostly, the patients were in clinical (63.89%) and endoscopic (52.86%) remission. Regarding medical treatment, the most used drugs were biological therapy (79.41%) and azathioprine (52.94%) in CD, and mesalazine (45.95%), azathioprine (40.54%) and biological therapy (40.54%) in UC. The NAFLD group consists of 32 (45.07%) patients: 40.63% had mild steatosis; 40.63% moderate and 18.65% intense NAFLD. Development of NAFLD vs no NAFLD was associated with body mass index (29.49 ± 3.93 vs 24.32 ± 3.85, p < 0.0001), and laboratory biomarkers, such as C-reactive protein (1.99 ± 4.39 vs 0.87 ± 0.52, p = 0.0061), AST (29.72 ± 16.64 vs 23.46 ± 5.31, p = 0.0226), ALT (24.92 ± 14.22 vs 17.92 ± 6.57, p = 0.0099), albumin (4.1 ± 0.37 vs 4.36 ± 0.32, p = 0.0415), fasting glucose (95.5 ± 14.01 vs 84.36 ± 13.01, p = 0.0251) and blood insulin (18.41 ± 11.88 vs 6.4 ± 4.26, p = 0.0054). Also, the NAFLD group had higher prevalence of systemic arterial hypertension (31.25% vs 10.26%, p = 0.0369). When comparing patients with the presence or absence of NAFLD, there was no difference between the groups regarding time since diagnosis (p = 0.9684), previous surgery (p = 0.5908), Montreal classification, clinical activity assessed by CDAI (p = 0.2258), clinical activity assessed by the Mayo score (p = 0.4935), endoscopic activity (p = 0.0599), histological activity (p = 1.0), or medical treatment.

CONCLUSION

Development of NAFLD is a frequent occurrence in patients with IBD. NAFLD group had higher levels of body mass index, C-reactive protein, AST, ALT, fasting glucose and blood insulin, which are also associated with metabolic syndrome. Early diagnosis and appropriate nutritional orientation are necessary to prevent NAFLD related complications.

摘要

背景

炎症性肠病(IBD)是一种炎症性慢性病,非酒精性脂肪性肝病(NAFLD)亦是如此。当前文献表明,IBD患者患NAFLD的风险很高。在这些患者中,NAFLD的发病机制可能更为复杂,与多种因素有关,如肠道菌群失调、不健康的营养行为、身体组成和全身炎症。一般人群中NAFLD的发病率在上升,然而,评估IBD患者中NAFLD患病率的研究较少。因此,本研究旨在评估IBD患者中NAFLD的患病率,并确定与NAFLD存在相关的临床因素。

方法

这项横断面、描述性、观察性研究纳入了来自巴西圣保罗州一家IBD公立门诊的71例IBD患者。收集了实验室评估和临床数据。通过超声检查评估NAFLD的存在。排除标准如下:既往存在肝脏疾病、女性每日酒精摄入量>20g且男性每日酒精摄入量>30g,以及糖皮质激素治疗>20mg/天。统计分析:描述性统计和关联检验。

结果

纳入71例患者,其中34例(47.89%)为克罗恩病(CD),37例(52.11%)为溃疡性结肠炎(UC)。中位年龄为45.32±13.59岁,63.38%为女性,69.1%为白种人,7.04%为吸烟者。自诊断以来的时间为12.55±8.01年。关于疾病特征,42.42%的CD患者有回结肠受累,50%有穿透性疾病,39.4%有肛周受累。对于UC患者,大多数患者有全结肠炎(72.22%)。大多数患者处于临床缓解(63.89%)和内镜缓解(52.86%)。关于药物治疗,CD患者最常用的药物是生物疗法(79.41%)和硫唑嘌呤(52.94%),UC患者最常用的药物是美沙拉嗪(45.95%)、硫唑嘌呤(40.54%)和生物疗法(40.54%)。NAFLD组由32例(45.07%)患者组成:40.63%有轻度脂肪变性;40.63%有中度脂肪变性,18.65%有重度NAFLD。NAFLD的发生与无NAFLD与体重指数(29.49±3.93 vs 24.32±3.85,p<0.0001)以及实验室生物标志物有关,如C反应蛋白(1.99±4.39 vs 0.87±0.52,p = 0.0061)、谷草转氨酶(29.72±16.64 vs 23.46±5.31,p = 0.0226)、谷丙转氨酶(24.92±14.22 vs 17.92±6.57,p = 0.0099)、白蛋白(4.1±0.37 vs 4.36±0.32,p = 0.0415)、空腹血糖(95.5±14.01 vs 84.36±13.01,p = 0.0251)和血胰岛素(18.41±11.88 vs 6.4±4.26,p = 0.0054)。此外,NAFLD组系统性动脉高血压的患病率更高(31.25% vs 10.26%,p = 0.0369)。比较有或无NAFLD的患者时,两组在自诊断以来的时间(p = 0.9684)、既往手术(p = 0.5908)、蒙特利尔分类、通过CDAI评估的临床活动(p = 0.2258)、通过梅奥评分评估的临床活动(p = 0.4935)、内镜活动(p = 0.0599)、组织学活动(p = 1.0)或药物治疗方面无差异。

结论

NAFLD在IBD患者中经常发生。NAFLD组的体重指数、C反应蛋白、谷草转氨酶、谷丙转氨酶、空腹血糖和血胰岛素水平较高,这些也与代谢综合征相关。早期诊断和适当的营养指导对于预防NAFLD相关并发症是必要的。

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