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本文引用的文献

1
Psoriatic Arthritis and Diabetes Mellitus: A Narrative Review.银屑病关节炎与糖尿病:一篇叙述性综述
Rheumatol Ther. 2020 Jun;7(2):271-285. doi: 10.1007/s40744-020-00206-7. Epub 2020 Apr 18.
2
Assessment of liver marker enzymes and its association with type 2 diabetes mellitus in Northwest Ethiopia.埃塞俄比亚西北部肝脏标记酶的评估及其与2型糖尿病的关联。
BMC Res Notes. 2019 Oct 29;12(1):707. doi: 10.1186/s13104-019-4742-x.
3
Liver Abnormalities in Patients with Psoriatic Arthritis.银屑病关节炎患者的肝脏异常
J Rheumatol. 2020 Jun 1;47(6):847-853. doi: 10.3899/jrheum.181312. Epub 2019 Oct 15.
4
Real-world burden of comorbidities in US patients with psoriatic arthritis.美国银屑病关节炎患者并存疾病的实际负担
RMD Open. 2017 Dec 28;3(2):e000588. doi: 10.1136/rmdopen-2017-000588. eCollection 2017.
5
Risk of liver disease in methotrexate treated patients.甲氨蝶呤治疗患者的肝脏疾病风险。
World J Hepatol. 2017 Sep 18;9(26):1092-1100. doi: 10.4254/wjh.v9.i26.1092.
6
Comorbidities in Psoriatic Arthritis.银屑病关节炎的合并症
Rheum Dis Clin North Am. 2015 Nov;41(4):677-98. doi: 10.1016/j.rdc.2015.07.008. Epub 2015 Sep 5.
7
IL-17 Axis Driven Inflammation in Non-Alcoholic Fatty Liver Disease Progression.白细胞介素-17轴驱动非酒精性脂肪性肝病进展中的炎症反应。
Curr Drug Targets. 2015;16(12):1315-23. doi: 10.2174/1389450116666150531153627.
8
IL-17A plays a critical role in the pathogenesis of liver fibrosis through hepatic stellate cell activation.白细胞介素-17A 通过激活肝星状细胞在肝纤维化发病机制中起关键作用。
J Immunol. 2013 Aug 15;191(4):1835-44. doi: 10.4049/jimmunol.1203013. Epub 2013 Jul 10.
9
Liver injury from tumor necrosis factor-α antagonists: analysis of thirty-four cases.肿瘤坏死因子-α拮抗剂致肝损伤:34 例分析。
Clin Gastroenterol Hepatol. 2013 May;11(5):558-564.e3. doi: 10.1016/j.cgh.2012.12.025. Epub 2013 Jan 17.
10
Efficacy and safety of adalimumab for the treatment of peripheral arthritis in spondyloarthritis patients without ankylosing spondylitis or psoriatic arthritis.阿达木单抗治疗非强直性脊柱炎或银屑病关节炎的脊柱关节炎患者外周关节炎的疗效和安全性。
Ann Rheum Dis. 2013 Nov;72(11):1793-9. doi: 10.1136/annrheumdis-2012-202245. Epub 2012 Nov 8.

银屑病关节炎患者肝脏异常的影响因素:一项综合研究。

Factors Influencing Liver Abnormalities in Psoriatic Arthritis Patients: A Comprehensive Study.

作者信息

Ong Ping Seung, Tan Lay Kim, Mat Hasnah, Tohar Najjah, Fathi Abdul Muhaimin, Kosenin Nia Maslia Atiera, Naim Muhammad Najmi Budiman, Redzuan Rafiqah Farhanah, Rani Nur Iffah Ab, Norhisham Najiha Arrissa, Sulaiman Wahinuddin

机构信息

Rheumatology Unit, Department of Medicine, Hospital Raja Permaisuri Bainun, Jalan Raja Ashman Shah, Ipoh, Perak, Malaysia.

Sector for Biostatistics & Data Repository, Office of NIH Manager, National Institutes of Health, Ministry of Health Malaysia, Selangor, Malaysia.

出版信息

Mediterr J Rheumatol. 2023 Aug 27;35(2):234-240. doi: 10.31138/mjr.050723.fla. eCollection 2024 Jun.

DOI:10.31138/mjr.050723.fla
PMID:39211017
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11350418/
Abstract

OBJECTIVE

The aim of this study was to establish the incidence of liver abnormalities in psoriatic arthritis patients and identify the factors that contributed to this condition.

METHODS

This is a longitudinal cohort study. Psoriatic arthritis (PsA) patients with liver enzymes abnormalities were identified. Our control group consisted of PsA patient from the same cohort who had no history of liver abnormalities. Factors associated with liver abnormalities were identified using univariate and multivariate analysis.

RESULTS

A total of 247 of PsA patients were included and out of those, 99 developed liver enzymes abnormalities. The mean age of the patients was 56 years old (±13.5) with 56.1% female and 39.4% Indian descendants. The univariate logistic regression demonstrated that disease duration of PsA (OR=1.06, 95% CI=1.01 - 1.10, p=0.012), diabetes mellitus (OR=2.16, 95% CI=1.26 - 3.70, 0.005) and non-alcoholic fatty liver disease (NAFLD) (OR=3.90, 95% CI = 1.44 - 10.53, p=0.007) were associated with abnormal liver function in PsA patients. No association was found with both conventional synthetic disease-modifying antirheumatic drugs or biologics.

CONCLUSION

Liver enzymes abnormalities in PsA patients were linked to disease duration, diabetes mellitus and NAFLD. For these high-risk populations, vigilant monitoring of liver function tests is vital for early detection and intervention.

摘要

目的

本研究旨在确定银屑病关节炎患者肝脏异常的发生率,并找出导致这种情况的因素。

方法

这是一项纵向队列研究。识别出肝功能酶异常的银屑病关节炎(PsA)患者。我们的对照组由同一队列中无肝脏异常病史的PsA患者组成。使用单因素和多因素分析来确定与肝脏异常相关的因素。

结果

共纳入247例PsA患者,其中99例出现肝功能酶异常。患者的平均年龄为56岁(±13.5),女性占56.1%,印度裔占39.4%。单因素逻辑回归显示,PsA的病程(OR=1.06,95%CI=1.01 - 1.10,p=0.012)、糖尿病(OR=2.16,95%CI=1.26 - 3.70,p=0.005)和非酒精性脂肪性肝病(NAFLD)(OR=3.90,95%CI = 1.44 - 10.53,p=0.007)与PsA患者的肝功能异常有关。未发现与传统合成抗风湿药物或生物制剂有相关性。

结论

PsA患者的肝功能酶异常与病程、糖尿病和NAFLD有关。对于这些高危人群,密切监测肝功能检查对于早期发现和干预至关重要。