Clinical characteristics and risk factors of primary Sjögren's syndrome with liver function damage
-
摘要:
目的 分析原发性干燥综合征(pSS)合并肝功能及多系统损害患者的临床特征,以探究pSS肝功能损害的危险因素,为临床诊治提供新依据。 方法 选取2020年1月—2023年10月就诊于中国人民解放军联勤保障部队第920医院的92例确诊为pSS合并肝功能损害的患者为肝损组,另选取92例无肝功能损害的pSS患者作为非肝损组,分别收集2组患者的临床资料、辅助检查结果并行对比分析。 结果 pSS肝损组合并血液系统受累(56.5%, 52/92)、骨关节受累(54.3%, 50/92)及甲状腺受累(23.9%, 22/92)者均显著多于pSS非肝损组[34.8%(32/92)、32.6%(30/92)、8.7%(8/92), P < 0.05];肝损组合并2个以上系统受累(73.9%, 68/92)者亦显著多于非肝损组[55.4%(51/92), P < 0.05]。pSS肝损组CRP[6.45(2.83, 17.10)mg/L]、WBC[6.28(4.37, 9.51)×109/L]水平均显著高于非肝损组[2.45(0.80, 8.40)mg/L、5.31(4.14, 6.74)×109/L, P<0.05]。pSS肝损组ANA阳性率(84.8%,78/92)、抗SSB阳性率(50.0%, 46/92)均显著高于pSS非肝损组[65.2%(60/92)、28.3%(26/92), P < 0.05]。Logistic回归分析显示,高CRP(OR=1.037,95% CI: 1.003~1.071,P<0.05)、高WBC(OR=1.325,95% CI: 1.139~1.542,P<0.01)、多系统受累(OR=2.262,95% CI: 1.039~4.925,P<0.05)均为pSS患者合并肝功能损害的危险因素。 结论 肝功能损害的pSS患者常伴有多个系统损害,高CRP、WBC水平以及多系统受累均为pSS肝功能损害的危险因素。 Abstract:Objective To analyze the clinical characteristics of patients with primary Sjögren's syndrome (pSS) complicated with liver function and multi-system damage, and to explore the risk factors of liver function damage in pSS, so as to provide new basis for clinical diagnosis and treatment. Methods A total of 92 patients diagnosed with PSS and liver function damage admitted to the 920th Hospital of the Joint Logistics Support Force of PLA from January 2020 to October 2023 were selected as liver injury groups, and 92 patients with PSS patients who has no liver damage were selected as non-liver injury groups. The clinical data and auxiliary examination results of the two groups of patients were collated for comparison and analysis. Results The combination of liver damage and blood system involvement (56.5%, 52/92), joint and bone involvement (54.3%, 50/92), and thyroid involvement (23.9%, 22/92) in patients with pSS is significantly higher than in patients with pSS, however, without liver damage [34.8% (32/92), 32.6% (30/92), 8.7% (8/92), P < 0.05]. The proportion of patients with involvement of two or more systems in the liver injury group (73.9%, 68/92) is also significantly higher than that in the non-liver injury group (55.4%, 51/92, P < 0.05). The levels of CRP [6.45 (2.83, 17.10) mg/L] and WBC [6.28 (4.37, 9.51)×109/L] in the pSS liver lesion group were found to be significantly higher than those in the non-liver injury group [2.45 (0.80, 8.40) mg/L, 5.31 (4.14, 6.74)×109/L, P < 0.05]. The positive rates of ANA (84.8%, 78/92) and anti-SSB (50.0%, 46/92) in the pSS liver injury group were significantly higher than those in the pSS non-liver injury group [65.2% (60/92) and 28.3% (26/92), respectively, P < 0.05]. The logistic regression analysis demonstrated that elevated CRP (OR=1.037, 95% CI: 1.003-1.071, P < 0.05) and elevated WBC (OR=1.325, 95% CI: 1.139-1.542, P < 0.01), multi-system involvement (OR=2.262, 95% CI: 1.039-4.925, P < 0.05) were risk factors for liver function damage in pSS patients. Conclusion Patients with pSS who also have impaired liver function are frequently accompanied by multiple system impairment. Elevated CRP and WBC levels, in conjunction with multi-system involvement, constitute risk factors for pSS-related liver dysfunction. -
Key words:
- Sjögren's syndrome /
- Liver function impairment /
- Multisystem damage
-
表 1 2组pSS患者基本特征比较
Table 1. Comparison of basic characteristics between two groups of pSS patients
组别 例数 性别(男/女, 例) 年龄(x ±s,岁) 肝损组 92 22/70 58.02±15.81 非肝损组 92 16/76 57.02±13.71 统计量 1.194a 0.458b P值 0.275 0.647 注:a为χ2值,b为t值。 表 2 2组pSS患者系统受累方面比较[例(%)]
Table 2. Comparison of systemic involvement between the two groups of pSS patients [case(%)]
组别 例数 口干、眼干 胃肠道受累 血液系统三系受累 肺部受累 心血管系统受累 甲状腺受累 骨关节受累 皮肤受累 肝损组 92 78(84.8) 48(52.2) 52(56.5) 22(23.9) 18(19.6) 22(23.9) 50(54.3) 10(10.9) 非肝损组 92 72(78.3) 44(47.8) 32(34.8) 14(15.2) 12(13.0) 8(8.7) 30(32.6) 6(6.5) χ2值 1.299 0.348 8.762 2.210 1.434 7.806 8.846 1.095 P值 0.254 0.555 0.003 0.137 0.231 0.005 0.003 0.295 表 3 2组pSS患者合并2个与2个以上(>2个)系统受累情况比较[例(%)]
Table 3. Comparison of two or more systemic involvement between the two groups of pSS patients [cases (%)]
组别 例数 2个系统受累 2个以上系统受累 肝损组 92 24(26.1) 68(73.9) 非肝损组 92 41(44.6) 51(55.4) χ2值 6.875 P值 0.009 表 4 2组pSS患者实验室指标比较
Table 4. Comparison of laboratory indexes between the two groups of pSS patients
组别 例数 CRP [M(P25, P75),mg/L] ESR [M(P25, P75),mm/h] WBC [M(P25, P75),×109/L] HB (x ±s,g/L) PLT [M(P25, P75),×109/L] 肝损组 92 6.45(2.83, 17.10) 23.00(14.00, 48.75) 6.28(4.37, 9.51) 125.35±22.74 202.00(149.00, 244.00) 非肝损组 92 2.45(0.80, 8.40) 21.00(10.50, 36.50) 5.31(4.14, 6.74) 123.26±25.50 178.50(117.00, 264.00) 统计量 -4.126a -1.236a -2.514a 0.586b -0.476a P值 < 0.001 0.217 0.012 0.559 0.634 注:a为Z值,b为t值。 表 5 2组pSS患者自身抗体谱比较[例(%)]
Table 5. Comparison of autoantibody spectrum between the two groups of pSS patients [cases (%)]
组别 例数 ANA (+) RF (+) 抗dsDNA (+) 抗SSA (+) 抗SSB (+) 抗AMA (+) 肝损组 92 78(84.8) 36(39.1) 12(13.0) 74(80.4) 46(50.0) 10(10.9) 非肝损组 92 60(65.2) 40(43.5) 10(10.9) 68(73.9) 26(28.3) 8(8.7) χ2值 9.391 0.359 0.207 1.111 9.127 0.246 P值 0.002 0.594 0.650 0.292 0.003 0.620 表 6 pSS合并肝功能损害影响因素的多因素logistic回归分析
Table 6. Multivariate Logistic regression analysis of influencing factors of pSS combined with liver function damage
变量 B SE Waldχ2 P值 OR值 95% CI CRP 0.036 0.017 4.675 0.031 1.037 1.003~1.071 WBC 0.282 0.077 13.230 < 0.001 1.325 1.139~1.542 ESR 0.011 0.007 2.402 0.121 1.011 0.997~1.026 ANA(+) -1.264 0.457 7.647 0.006 0.282 0.115~0.692 抗SSB(+) -0.846 0.379 4.995 0.025 0.429 0.204~0.901 血液系统受累 -0.592 0.378 2.455 0.117 0.553 0.264~1.160 骨关节受累 -1.131 0.375 9.086 0.003 0.323 0.155~0.673 甲状腺受累 0.613 0.524 1.372 0.242 1.847 0.662~5.156 多系统受累 0.816 0.397 4.225 0.040 2.262 1.039~4.925 -
[1] QIN B, WANG J, YANG Z, et al. Epidemiology of primary Sjögren's syndrome: a systematic review and meta-analysis[J]. Ann Rheum Dis, 2015, 74(11): 1983-1989. doi: 10.1136/annrheumdis-2014-205375 [2] 段维佳, 李淑香, 吕婷婷, 等. 结缔组织病与肝损伤[J]. 中华肝脏病杂志, 2022, 30(4): 357-361. doi: 10.3760/cma.j.cn501113-20220317-00116DUAN W J, LI S X, LYU T T, et al. Connective tissue diseases and the liver injury[J]. Chinese Journal of Hepatology, 2022, 30(4): 357-361. doi: 10.3760/cma.j.cn501113-20220317-00116 [3] 梅永君, 李志军. 干燥综合征的诊断与治疗[J]. 中华全科医学, 2020, 18(6): 890-891. http://www.zhqkyx.net/article/id/7789ea4e-535d-4c41-9dac-467ceb3d00a2MEI Y J, LI Z J. Diagnosis and treatment of Sjogren's syndrome[J]. Chinese Journal of General Practice, 2020, 18(6): 890-891. http://www.zhqkyx.net/article/id/7789ea4e-535d-4c41-9dac-467ceb3d00a2 [4] BOTH T, DALM V A, VAN HAGEN P M, et al. Reviewing primary Sjögren's syndrome: beyond the dryness-from pathophysiology to diagnosis and treatment[J]. Int J Med Sci, 2017, 14(3): 191-200. doi: 10.7150/ijms.17718 [5] 林磊. 原发性干燥综合征肝脏损害临床特点及转归[D]. 合肥: 安徽医科大学, 2018.LIN L. Clinical characteristics and prognosis of liver damage in primary Sjogren's syndrome[D]. Hefei: Anhui Med Univ, 2018. [6] CORNEC D, JOUSSE-JOULIN S, PERS J O, et al. Contribution of salivary gland ultrasonography to the diagnosis of Sjögren's syndrome: toward new diagnostic criteria?[J]. Arthritis Rheum, 2013, 65(1): 216-225. doi: 10.1002/art.37698 [7] MARIETTE X, CRISWELL L A. Primary Sjögren's syndrome[J]. N Engl J Med, 2018, 378(10): 931-939. doi: 10.1056/NEJMcp1702514 [8] CHOUDHRY H S, HOSSEINI S, CHOUDHRY H S, et al. Updates in diagnostics, treatments, and correlations between oral and ocular manifestations of Sjögren's syndrome[J]. Ocul Surf, 2022, 26: 75-87. doi: 10.1016/j.jtos.2022.08.001 [9] BALDINI C, PEPE P, QUARTUCCIO L, et al. Primary Sjögren's syndrome as a multi-organ disease: impact of the serological profile on the clinical presentation of the disease in a large cohort of Italian patients[J]. Rheumatology(Oxford), 2014, 53(5): 839-844. doi: 10.1093/rheumatology/ket427 [10] BRITO-ZERON P, ACAR-DENIZLI N, NG W F, et al. Epidemiological profile and north-south gradient driving baseline systemic involvement of primary Sjögren's syndrome[J]. Rheumatology(Oxford), 2020, 59(9): 2350-2359. doi: 10.1093/rheumatology/kez578 [11] 陈树, 陈洁, 常新, 等. 原发性干燥综合征合并血液系统受累的危险因素分析[J]. 实用临床医药杂志, 2023, 27(3): 91-96, 102.CHEN S, CHEN J, CHANG X, et al. Analysis of risk factors for primary Sjogren's syndrome with hematological involvement[J]. J Pract Clin Med, 2023, 27(3): 91-96, 102. [12] BRITO-ZERON P, THEANDER E, BALDINI C, et al. Early diagnosis of primary Sjögren's syndrome: EULAR-SS task force clinical recommendations[J]. Expert Rev Clin Immunol, 2016, 12(2): 137-156. doi: 10.1586/1744666X.2016.1109449 [13] JARA L J, NAVARRO C, BRITO-ZERON MDEL P, et al. Thyroid disease in Sjögren's syndrome[J]. Clin Rheumatol, 2007, 26(10): 1601-1606. doi: 10.1007/s10067-007-0638-6 [14] 颜淑敏, 张文, 李梦涛, 等. 原发性干燥综合征573例临床分析[J]. 中华风湿病学杂志, 2010, 14(4): 223-227. doi: 10.3760/cma.j.issn.1007-7480.2010.04.003YAN S M, ZHANG W, LI M T, et al. Clinical analysis of 573 cases of primary Sjogren's syndrome[J]. Chin J Rheumat, 2010, 14(4): 223-227. doi: 10.3760/cma.j.issn.1007-7480.2010.04.003 [15] SAMBATARO D, SAMBATARO G, DAL BOSCO Y, et al. Present and future of biologic drugs in primary Sjögren's syndrome[J]. Expert Opin Biol Ther, 2017, 17(1): 63-75. doi: 10.1080/14712598.2017.1235698 [16] ZHANG K, YU X, ZHANG Y, et al. Identification of key genes in salivary gland in Sjögren's syndrome complicated with Hashimoto thyroiditis: common pathogenesis and potential diagnostic markers[J]. Medicine(Baltimore), 2023, 102(39): e35188. DOI: 10.1097/MD.0000000000035188. [17] ANAYA J M, RESTREPO-JIMÉNEZ P, RODRÍGUEZ Y, et al. Sjögren's syndrome and autoimmune thyroid disease: two sides of the same coin[J]. Clin Rev Allergy Immunol, 2019, 56(3): 362-374. doi: 10.1007/s12016-018-8709-9 [18] POPOV Y, SALOMON-ESCOTO K. Gastrointestinal and hepatic disease in Sjögren syndrome[J]. Rheum Dis Clin North Am, 2018, 44(1): 143-151. doi: 10.1016/j.rdc.2017.09.010 [19] EBERT E C. Gastrointestinal and hepatic manifestations of Sjögren syndrome[J]. J Clin Gastroenterol, 2012, 46(1): 25-30. doi: 10.1097/MCG.0b013e3182329d9c [20] NEGRINI S, EMMI G, GRECO M, et al. Sjögren's syndrome: a systemic autoimmune disease[J]. Clin Exp Med, 2022, 22(1): 9-25. doi: 10.1007/s10238-021-00728-6 [21] KIM Y J, CHOE J, KIM H J, et al. Long-term clinical course and outcome in patients with primary Sjögren syndrome-associated interstitial lung disease[J]. Sci Rep, 2021, 11(1): 12827. DOI: 10.1038/s41598-021-92024-2. [22] 王建军, 吕群, 龚玲, 等. 原发性干燥综合征合并间质性肺病患者临床与影像特点分析[J]. 中华全科医学, 2019, 17(8): 1275-1278. doi: 10.16766/j.cnki.issn.1674-4152.000920WANG J J, LYU Q, GONG L, et al. Analysis of clinical and imaging characteristics of patients with primary Sjogren's syndrome complicated with interstitial lung disease[J]. Chin Gen Med, 2019, 17(8): 1275-1278. doi: 10.16766/j.cnki.issn.1674-4152.000920 [23] 冯大莺, 陈华英, 潘虹英, 等. 血浆proBDNF水平与原发性干燥综合征伴抑郁症状的相关性研究[J]. 昆明医科大学学报, 2023, 44(6): 54-58.FENG D Y, CHEN H Y, PAN H Y, et al. The correlation between plasma proBDNF level and primary Sjogren's syndrome with depressive symptoms[J]. Academic J Kun Ming Med Univ, 2023, 44(6): 54-58.
计量
- 文章访问数: 9
- HTML全文浏览量: 7
- PDF下载量: 2
- 被引次数: 0