Correlation analysis of pepsinogen and gastrin in secondary gastrointestinal involvement in systemic sclerosis
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摘要: 目的 分析系统性硬化症(SSc)继发胃肠道受累与胃蛋白酶原(PG)、胃泌素(GAS)的相关性。方法 选取2020年12月-2021年12月在上海市中西医结合医院风湿科住院诊治的102例SSc患者,其中继发胃肠道受累者64例,未继发胃肠道受累者38例,比较2组间患者性别、年龄、病程、SSc分型及胃蛋白酶原Ⅰ(PGⅠ)、胃蛋白酶原Ⅱ(PGⅡ)及胃蛋白酶原比值(PGR)等差异。结果 102例SSc患者中,男13例(12.75%),女89例(87.25%);年龄20~70岁,平均(48.63±11.35)岁;病程6~444个月,平均(116.11±91.06)个月;胃肠道分级中0级38例,1级12例,2级49例,3级3例。不同胃肠道受累评分级间的性别、年龄及病程分布差异无统计学意义(P>0.05)。同时不同组别中PGⅠ、PGⅡ差异有统计学意义(P< 0.05),可见随胃肠道受累程度加重,PGⅠ及PGⅡ呈上升趋势。而GAS、PGR在各组中差异无统计学意义(P>0.05)。结论 血清PGⅠ、PGⅡ测定可作为评估SSc胃肠道受累程度的一种无创、可重复性高的辅助手段。Abstract: Objective To analyze the correlation between pepsinogen(PG), gastrin(GAS) and gastrointestinal involvement in systemic sclerosis(SSc).Methods The data of 102 patients with SSc who were hospitalized in the Department of Rheumatology, Shanghai Integrated Traditional Chinese and Western Medicine Hospital from December 2020 to December 2021 were selected for retrospective analysis. Among them, 64 patients had secondary gastrointestinal tract involvement, and 38 patients had no gastrointestinal tract involvement. The gender, age, disease duration, SSc type, pepsinogen Ⅰ(PGⅠ), pepsinogen Ⅱ(PGⅡ), and pepsinogen ratio(PGR) were compared between the two groups.Results Among the 102 SSc patients, there were 13 males(12.75%) and 89 females(87.25%). In the gastrointestinal tract classification, 38 patients were grade 0, 12 patients were grade 1, 49 patients were grade 2, and only 3 patients were grade 3. The age ranged from 20 to 70(48.63±11.35) years old; the disease duration was 6 to 444(116.11±91.06) months. There was no difference in gender distribution, age distribution and disease course distribution among different gastrointestinal involvement scores(P>0.05). At the same time, the differences in PGⅠ and PGⅡ in different groups were statistically significant(P< 0.05). It can be seen that with the severity of gastrointestinal involvement, PGⅠ and PGⅡ showed an upward trend. However, there were no significant differences in GAS and PGR among the groups(P>0.05).Conclusion The determination of serum PGⅠ and PGⅡ can be used as a non-invasive and highly reproducible auxiliary method for evaluating the degree of gastrointestinal involvement in SSc.
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Key words:
- systemic sclerosis /
- gastrointestinal involvement /
- pepsin Ⅰ /
- pepsin Ⅱ /
- gastrin
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表 1 不同组别患者基本临床资料比较
胃肠道受累评分/分 性别/例(%) 年龄/岁 病程/月 男 女 0 4(3.92) 34(33.33) 49.00(41.00,57.00) 90.00(48.00,144.00) 1 2(1.96) 10(9.80) 49.50(45.50,52.50) 72.00(53.00,216.00) 2 7(6.86) 42(41.17) 48.00(41.00,59.00) 96.00(54.00,168.00) 3 0 3(2.94) 57.00(49.50,57.00) 125.00(92.50,266.50) χ2 0.877 0.458 1.132 P 0.831 0.928 0.769 表 2 不同组别血清GAS、PGⅠ、PGⅡ及PGR比较
M(Q1,Q3) 胃肠道评分/分 例数 GAS/(pg·mL-1) PGⅠ/(pg·L-1) PGⅡ/(pg·L-1) PGR 0 38 58.04(49.06,70.89) 164.70(148.00,170.10) 11.50(9.70,16.60) 13.20(9.25,17.00) 1 12 51.40(46.19,84.77) 161.90(151.90,168.00) 16.10(14.00,23.20) 11.50(6.40,12.25) 2 49 52.81(44.88,63.90) 171.80(156.50,182.00) 17.90(11.50,20.80) 10.20(8.40,14.70) 3 3 45.90(45.81,58.78) 194.80(180.80,197.20) 32.80(24.80,39.15) 5.90(5.15,7.90) χ2 1.609 8.737 9.452 7.472 P 0.657 0.033 0.024 0.058 表 3 SSc-GERD与SSc-非GERD的一般资料分析
组别 例数 性别/例(%) 年龄/岁 病程/月 男 女 SSc-GERD 33 0 33(32.35) 48.76±10.15 96.00(60.00, 126.00) SSc-非GERD 69 13(12.75) 56(54.90) 48.57±11.96 84.00(48.00, 156.00) χ2/t/Z 7.126 -0.08 -0.988 P 0.008 0.937 0.323 表 4 SSc-GERD诊断与血清胃肠激素相关性分析
M(Q1,Q3) 组别 例数 GAS/(pg·mL-1) PGⅠ/(pg·L-1) PGⅡ/(pg·L-1) PGR SSc-GERD 33 52.81(45.14,66.89) 166.8(152.10,180.40) 16.40(11.10,19.50) 10.30(8.10,15.20) 非SSc-GERD 69 55.71(48.42,67.58) 167.7(54.90,177.25) 14.30(9.85,20.50) 12.00(8.45,16.35) Z -0.400 -0.174 -0.799 -0.766 P 0.690 0.862 0.424 0.444 表 5 lcSSc和dcSSc的抗体分布比较
例 组别 ATA ACA nRNP SSA PM-Scl χ2 P 弥漫型 43 4 9 18 1 5.536 0.237 肢端型 28 9 9 23 1 -
[1] Mayes MD. Scleroderma epidemiology[J]. Rheum Dis Clin North Am, 2003, 29(2): 239-254. doi: 10.1016/S0889-857X(03)00022-X
[2] Sjogren RW. Gastrointestinal motility disor ders in scleroderma[J]. Arthritis Rheum, 1994, 37: 1265-1282. doi: 10.1002/art.1780370902
[3] Voulgaris TA, Karamanolis GP. Esophageal manifestation in patients with scleroderma[J]. World J Clin Cases, 2021, 9(20): 5408-5419. doi: 10.12998/wjcc.v9.i20.5408
[4] Alastal Y, Hammad TA, Renno A, et al. Gastrointestinal manifestations associated with systemic sclerosis: results from the nationwide inpatient sample[J]. Ann Gastroenterol, 2017, 30(5): 498-503. http://www.annalsgastro.gr/files/journals/1/earlyview/2017/ev-07-2017-01-AG3095-0171.pdf
[5] 林慧玲, 庄云英, 陈玲红. 血清胃蛋白酶原三项检测在上消化道疾病中的诊断价值[J]. 人民军医, 2015, 58(7): 808-809. https://www.cnki.com.cn/Article/CJFDTOTAL-RMJZ201507050.htm
[6] 顾红. 老年胃食管反流病患者血清胃蛋白酶原的变化及其与反流症状评分的关系[J]. 中国老年学杂志, 2016, 36(6): 1390-1391. doi: 10.3969/j.issn.1005-9202.2016.06.050
[7] Medsger TA Jr, Silman AJ, Steen VD, et al. A disease severity scale for systemic sclerosis: development and testing[J]. J Rheumatol, 1999, 26(10): 2159-2167. https://www.ndorms.ox.ac.uk/publications/545413
[8] Schmeiser T, Saar P, Jin D, et al. Profile of gastrointestinal involvement in patients with systemic sclerosis[J]. Rheumatol Int, 2012, 32(8): 2471-2478. doi: 10.1007/s00296-011-1988-6
[9] Ebert EC. Esophageal disease in progressive systemic sclerosis[J]. Curr Treat Options Gastroenterol, 2008, 11(1): 64-69. doi: 10.1007/s11938-008-0008-8
[10] Christmann RB, Wells AU, Capelozzi VL, et al. Gastroesophageal reflux incites interstitial lung disease in systemic sclerosis: clinical, radiologic, histopathologic, and treatment evidence[J]. Semin Arthritis Rheum, 2010, 40(3): 241-249. doi: 10.1016/j.semarthrit.2010.03.002
[11] Zhang XJ, Bonner A, Hudson M, et al. Association of gastroesophageal factors and worsening of forced vital capacity in systemic sclerosis[J]. J Rheumatol, 2013, 40(6): 850-858. doi: 10.3899/jrheum.120705
[12] Gyger G, Baron M. Gastrointestinal manifestations of scleroderma: recent progress in evaluation, pathogenesis, and management[J]. Curr Rheumatol Rep, 2012, 14(1): 22-29. doi: 10.1007/s11926-011-0217-3
[13] Emmanuel A. Current management of the gastrointestinal complications of systemic sclerosis[J]. Nat Rev Gastroenterol Hepatol, 2016, 13(8): 461-472. doi: 10.1038/nrgastro.2016.99
[14] 黄争艳. 血清胃蛋白酶原及血清胃泌素17联合检测在诊断胃部疾病中的应用价值[J]. 当代医药论丛, 2019, 17(21): 169-170. doi: 10.3969/j.issn.2095-7629.2019.21.128
[15] Pimanov SI, Makarenko EV, Voropaeva AV, et al. Helicobacter pylori eradication improves gastric histology and decreases serum gastrin, pepsinogen Ⅰ and pepsinogen Ⅱ levels in patients with duodenal ulcer[J]. J Gastroenterol Hepatol, 2008, 23(11): 1666-1671. doi: 10.1111/j.1440-1746.2007.04983.x
[16] Sun LP, Guo XL, Zhang Y, et al. Impact of pepsinogen C polymorphism on individual susceptibility to gastric cancer and its precancerous conditions in a Northeast Chinese population[J]. J Cancer Res Clin Oncol, 2009, 135(8): 1033-1039. doi: 10.1007/s00432-008-0539-3
[17] 高文琴, 张改连, 杨艳丽, 等. 系统性硬化病甲襞微循环特点及其临床意义[J]. 中华风湿病学杂志, 2021, 25(11): 739-746. doi: 10.3760/cma.j.cn141217-20201216-00479
[18] Di MF, Crafa P, Barchi A, et al. Pepsinogen Ⅱ in gastritis and Helicobacter pylori infection[J]. Helicobacter, 2022, 27(2): e12872.
[19] 刘惠武, 严红梅, 许丹, 等. 消胀颗粒对功能性消化不良大鼠胃排空及胃肠激素的影响[J]. 中国中西医结合消化杂志, 2021, 29(4): 231-233, 239. doi: 10.3969/j.issn.1671-038X.2021.04.01 http://zxpw.cbpt.cnki.net/WKD2/WebPublication/paperDigest.aspx?paperID=06e35979-0f17-421e-a650-6f5a5d3caaae
[20] Ebert EC. Gastric and enteric involvement in progressive systemic sclerosis[J]. J Clin Gastroenterol, 2008, 42(1): 5-12. doi: 10.1097/MCG.0b013e318042d625
[21] Roberts CG, Hummers LK, Ravich WJ, et al. A case-control study of the pathology of oesophageal disease in systemic sclerosis(scleroderma)[J]. Gut, 2006, 55(12): 1697-1703. doi: 10.1136/gut.2005.086074
[22] Tiev KP, Cabane J. Digestive tract involvement in systemic sclerosis[J]. Autoimmun Rev, 2011, 11(1): 68-73. doi: 10.1016/j.autrev.2010.06.002
[23] 李红艳, 杨林, 何晶晶, 等. 系统性硬化症消化道受累诊疗进展[J]. 中华全科医师杂志, 2017, 16(9): 725-728. doi: 10.3760/cma.j.issn.1671-7368.2017.09.020
[24] 杨森, 陈琛, 姜智星, 等. 系统性硬化病自身抗体研究进展[J]. 中华风湿病学杂志, 2019, 23(11): 773-776. doi: 10.3760/cma.j.issn.1007-7480.2019.11.013
[25] 张巧云, 欧红玲, 王岩, 等. 血清胃蛋白酶原水平在胃食管反流病诊断中的应用价值[J]. 标记免疫分析与临床, 2019, 26(7): 1093-1096. https://www.cnki.com.cn/Article/CJFDTOTAL-BJMY201907003.htm
[26] 毛笑非, 孙秋宁. 系统性硬化症90例生活质量的评估与分析[J]. 中华医学杂志, 2014, 94(44): 3471-3474. doi: 10.3760/cma.j.issn.0376-2491.2014.44.005
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