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肝硬化住院患者常见精神疾病中基于种族和性别的差异及趋势:一项为期十年的美国研究。

Racial and gender-based disparities and trends in common psychiatric conditions in liver cirrhosis hospitalizations: A ten-year United States study.

作者信息

Patel Pratik, Ali Hassam, Inayat Faisal, Pamarthy Rahul, Giammarino Alexa, Ilyas Fariha, Smith-Martinez Lucia Angela, Satapathy Sanjaya K

机构信息

Department of Gastroenterology, Mather Hospital and Hofstra University Zucker School of Medicine, Port Jefferson, NY 11777, United States.

Department of Internal Medicine, East Carolina University Brody School of Medicine, Greenville, NC 27834, United States.

出版信息

World J Hepatol. 2023 Feb 27;15(2):289-302. doi: 10.4254/wjh.v15.i2.289.

Abstract

BACKGROUND

Chronic liver disease is associated with various neuropsychiatric conditions. There are currently no large studies assessing and comparing the prevalence of psychiatric illnesses based on patient profiles and the etiology of cirrhosis.

AIM

To examine the trends of hospitalizations among psychiatric conditions in cirrhosis.

METHODS

We used the National Inpatient Sample database 2016-2019 for the primary diagnosis of liver cirrhosis. The outcomes included the prevalence, trends, and associations of psychiatric diagnoses in these hospitalizations. Chi-square for categorical variables and the Wilcoxon rank test for continuous variables were utilized.

RESULTS

The prevalence of generalized anxiety disorder (GAD) in liver cirrhosis hospitalizations increased from 0.17% in 2009 to 0.92% in 2019 ( < 0.001). The prevalence of depression increased from 7% in 2009 to 12% in 2019 ( < 0.001). Attention deficit hyperactivity disorder (ADHD) prevalence increased from 0.06% to 0.24%. The prevalence of schizophrenia increased from 0.59% to 0.87% ( < 0.001). Schizoaffective disorder prevalence increased from 0.10% to 0.35% ( < 0.001). Post-traumatic stress disorder (PTSD) prevalence displayed increasing trends from 0.36% in 2009 to 0.93% in 2019 ( < 0.001). The prevalence of suicidal ideation increased from 0.23% to 0.56% in 2019. Cirrhosis related to alcoholic liver disease [adjusted odds ratios (aOR) 1.18, 95%CI 1.08-1.29, < 0.001] and non-alcoholic fatty liver disease (NAFLD) (aOR 1.14, 95%CI 1.01-1.28, = 0.025) was associated with depression more than other causes. Alcohol- and NAFLD-associated cirrhosis had a stronger link to psychiatric disorders. Females had a higher association with GAD (aOR 2.56, 95%CI 2.14-3.06, < 0.001), depression (aOR 1.78, 95%CI 1.71-1.84, < 0.001), bipolar disorder (aOR 1.64, 95%CI 1.52-1.77, < 0.001] and chronic fatigue (aOR 2.31, 95%CI 1.31-4.07, < 0.001) when compared to males. Blacks, Hispanics, and Asian/Native Americans had a significantly lower association with GAD, depression, bipolar disorder, PTSD, and ADHD when compared to the white race.

CONCLUSION

The prevalence of psychiatric comorbidities in liver cirrhosis hospitalizations has increased over the last decade. Females had a higher association with psychiatric disorders compared to males. Blacks, Hispanics, and Asian/Native Americans had lower associations with psychiatric comorbidities compared to the white race.

摘要

背景

慢性肝病与多种神经精神疾病相关。目前尚无大型研究基于患者特征和肝硬化病因评估及比较精神疾病的患病率。

目的

研究肝硬化患者精神疾病住院治疗的趋势。

方法

我们使用2016 - 2019年全国住院患者样本数据库进行肝硬化的初步诊断。结果包括这些住院患者中精神疾病诊断的患病率、趋势及相关性。分类变量采用卡方检验,连续变量采用Wilcoxon秩和检验。

结果

肝硬化住院患者中广泛性焦虑障碍(GAD)的患病率从2009年的0.17%增至2019年的0.92%(<0.001)。抑郁症患病率从2009年的7%增至2019年的12%(<0.001)。注意缺陷多动障碍(ADHD)患病率从0.06%增至0.24%。精神分裂症患病率从0.59%增至0.87%(<0.001)。分裂情感性障碍患病率从0.10%增至0.35%(<0.001)。创伤后应激障碍(PTSD)患病率呈上升趋势,从2009年的0.36%增至2019年的0.93%(<0.001)。自杀意念患病率在2019年从0.23%增至0.56%。与酒精性肝病相关的肝硬化[调整优势比(aOR)1.18,95%置信区间(CI)1.08 - 1.29,<0.001]和非酒精性脂肪性肝病(NAFLD)(aOR 1.14,95%CI 1.01 - 1.28,=0.025)比其他病因更易引发抑郁症。酒精性和NAFLD相关的肝硬化与精神障碍的关联更强。与男性相比,女性与GAD(aOR 2.56,95%CI 2.14 - 3.06,<0.001)、抑郁症(aOR 1.78,95%CI 1.71 - 1.84,<0.001)、双相情感障碍(aOR 1.64,95%CI 1.52 - 1.77,<0.001]和慢性疲劳(aOR 2.31,95%CI 1.31 - 4.07,<0.001)的关联更高。与白人相比,黑人、西班牙裔和亚洲/美洲原住民与GAD、抑郁症、双相情感障碍、PTSD和ADHD的关联显著更低。

结论

过去十年中,肝硬化住院患者精神疾病共病的患病率有所上升。与男性相比,女性与精神障碍的关联更高。与白人相比,黑人、西班牙裔和亚洲/美洲原住民与精神疾病共病的关联更低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/535a/10011900/d9f000d73bd0/WJH-15-289-g001.jpg

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