留言板

尊敬的读者、作者、审稿人, 关于本刊的投稿、审稿、编辑和出版的任何问题, 您可以本页添加留言。我们将尽快给您答复。谢谢您的支持!

姓名
邮箱
手机号码
标题
留言内容
验证码

慢性肾脏病非透析患者脑钠肽前体异常的危险因素分析

金德伟 陶敏 马晓燕 王奕 盛丽莉 刘娜

金德伟, 陶敏, 马晓燕, 王奕, 盛丽莉, 刘娜. 慢性肾脏病非透析患者脑钠肽前体异常的危险因素分析[J]. 中华全科医学, 2021, 19(8): 1314-1317. doi: 10.16766/j.cnki.issn.1674-4152.002049
引用本文: 金德伟, 陶敏, 马晓燕, 王奕, 盛丽莉, 刘娜. 慢性肾脏病非透析患者脑钠肽前体异常的危险因素分析[J]. 中华全科医学, 2021, 19(8): 1314-1317. doi: 10.16766/j.cnki.issn.1674-4152.002049
JIN De-wei, TAO Min, MA Xiao-yan, WANG Yi, SHENG Li-li, LIU Na. Study on risk factors of N-terminal pro-brain natriuretic peptide abnormalities in non-dialysis patients with chronic kidney disease[J]. Chinese Journal of General Practice, 2021, 19(8): 1314-1317. doi: 10.16766/j.cnki.issn.1674-4152.002049
Citation: JIN De-wei, TAO Min, MA Xiao-yan, WANG Yi, SHENG Li-li, LIU Na. Study on risk factors of N-terminal pro-brain natriuretic peptide abnormalities in non-dialysis patients with chronic kidney disease[J]. Chinese Journal of General Practice, 2021, 19(8): 1314-1317. doi: 10.16766/j.cnki.issn.1674-4152.002049

慢性肾脏病非透析患者脑钠肽前体异常的危险因素分析

doi: 10.16766/j.cnki.issn.1674-4152.002049
基金项目: 

国家自然科学基金项目 81670690

国家自然科学基金项目 81470991

国家自然科学基金项目 81200492

上海市自然基金项目 20ZR1445800

浦东新区重点学科附带课题 PWZxk2017-05

详细信息
    通讯作者:

    刘娜,E-mail:naliubrown@163.com

  • 中图分类号: R692

Study on risk factors of N-terminal pro-brain natriuretic peptide abnormalities in non-dialysis patients with chronic kidney disease

  • 摘要:   目的   研究慢性肾脏病(chronic kidney disease, CKD)非透析患者氨基末端脑钠肽前体(N-terminal pro-brain natriuretic peptide, NT-proBNP)异常的危险因素。   方法   选取2018年1月1日—2019年12月31日在东方医院肾内科入院治疗的259例CKD非透析患者。根据患者NT-proBNP水平将患者分为NT-proBNP正常组(Ⅰ组:NT-proBNP<125 ng/L)和NT-proBNP异常组(Ⅱ组:NT-proBNP≥125 ng/L),其中Ⅰ组患者129例,Ⅱ组患者130例。采用多因素logistic回归、ROC曲线分析患者NT-proBNP异常的影响因素。   结果   Logistic回归分析显示高龄(P=0.008)为NT-proBNP异常的独立危险因素,高血红蛋白(P=0.014)、eGFR(P < 0.001)水平为患者NT-proBNP异常的保护因素。ROC分析显示, 当患者年龄>75.5岁(AUC=0.658, P < 0.001), 血红蛋白 < 124.5 g/L(AUC=0.769, P < 0.001), eGFR < 47.53 mL/(min·1.73 m2)(AUC=0.810, P < 0.001)时, 患者发生NT-proBNP增高的风险将显著增加。   结论   高龄为NT-proBNP异常的独立危险因素,高水平血红蛋白、eGFR是患者NT-proBNP异常的保护因素。

     

  • 表  1  2组CKD非透析患者基本临床资料比较

    组别 例数 性别[例(%)] 年龄(x ±s,岁) BMI (x ±s) 吸烟[例(%)] 饮酒[例(%)] 收缩压(x ±s,mm Hg) 舒张压(x ±s,mm Hg) 心率(x ±s,次/min) UACR [M(P25, P75), mg/g]
    男性 女性
    Ⅰ组 129 82(63.6) 47(36.4) 54.8±15.4 25.0±3.4 24(18.6) 16(12.4) 144.5±91.4 84.5±12.8 80.65±14.2 307.5(91.1, 1 277.6)
    Ⅱ组 130 72(55.4) 58(44.6) 63.8±14.8 24.5±4.4 27(20.8) 21(16.2) 144.8±23.5 85.3±13.2 80.3±13.2 1 218.8(161.6, 3 560.3)
    统计量 1.798a -4.829b 1.062b 0.192a 0.744a -0.038b -0.527b 0.206b 10 510.000c
    P 0.180 < 0.001 0.289 0.661 0.388 0.970 0.599 0.837 < 0.001
    组别 例数 24小时尿蛋白定量[M(P25, P75), g] 血红蛋白(x ±s,g/L) 白蛋白[M(P25, P75), g/L] ALT [M(P25, P75), U/L] AST [M(P25, P75), U/L] SUA (x ±s,μmol/L) eGFR[x ±s,mL/(min·1.73 m2)]
    Ⅰ组 129 0.7(0.3, 2.2) 131.3±22.2 40.7(35.5, 44.2) 18.0(13.5, 25.0) 18.0(15.0, 23.0) 378.6±104.5 73.2±26.0
    Ⅱ组 130 1.8(0.3, 3.7) 108.3±26.2 36.7(30.6, 40.1) 13.5(10.0, 20.0) 17.0(14.0, 24.0) 410.4±112.5 40.6±26.4
    统计量 9 651.500c 7.632b 5 764.000c 5 924.500c 7 647.500c -2.354b 10.001b
    P 0.036 < 0.001 < 0.001 < 0.001 0.220 0.019 < 0.001
    组别 例数 空腹血糖[M(P25, P75), mmol/L] 糖化血红蛋白[M(P25, P75), %] 疾病史[例(%)] 用药史[例(%)]
    高血压 糖尿病 冠心病 钙离子拮抗剂 ACEI/ARB 降糖药
    Ⅰ组 129 5.3(4.9, 6.5) 5.8(5.4, 6.6) 87(67.4) 38(29.5) 10(7.8) 51(39.5) 77(59.7) 33(25.6)
    Ⅱ组 130 5.1(4.6, 5.9) 5.8(5.3, 6.5) 108(83.1) 46(35.4) 19(14.6) 75(57.7) 76(58.5) 42(32.3)
    统计量 6 632.000c 8 254.000c 8.508a 1.038a 3.068a 8.545a 0.040a 1.424a
    P 0.004 0.828 0.004 0.308 0.080 0.003 0.841 0.233
        注:a为χ2值;bt值;cU值。
    下载: 导出CSV

    表  2  NT-proBNP异常升高的多因素logistic回归分析

    因素 B SE Wald χ2 P OR(95% CI)
    年龄(岁) 0.032 0.012 7.135 0.008 1.033(1.009~1.057)
    UACR(mg/g) < 0.001 < 0.001 0.420 0.517 1.000(1.000~1.000)
    24小时尿蛋白定量(g) 0.092 0.080 1.309 0.253 1.096(0.937~1.282)
    血红蛋白(g/L) 0.021 0.009 6.005 0.014 0.979(0.963~0.996)
    白蛋白(g/L) 0.032 0.027 1.344 0.246 0.969(0.918~1.022)
    ALT(U/L) 0.003 0.010 0.072 0.789 1.003(0.983~1.023)
    SUA (μmol/L) 0.001 0.002 0.091 0.763 1.001(0.997~1.004)
    eGFR[mL/(min·1.73 m2)] 0.034 0.008 19.272 < 0.001 0.966(0.952~0.981)
    空腹血糖(mmol/L) 0.131 0.072 3.263 0.071 0.877(0.761~1.011)
    高血压 0.218 0.451 0.232 0.630 1.243(0.513~3.011)
    钙离子拮抗剂 0.206 0.382 0.289 0.591 1.228(0.581~2.600)
    下载: 导出CSV
  • [1] ROMAGNANI P, REMUZZI G, GLASSOCK R, et al. Chronic kidney disease[J]. Nat Rev Dis Primers, 2017, 3: 17088. doi: 10.1038/nrdp.2017.88
    [2] SONG Y, LOBENE A J, WANG Y, et al. The dash diet and cardiometabolic health and chronic kidney disease: A narrative review of the evidence in east asian countries[J]. Nutrients, 2021, 13(3): 984. doi: 10.3390/nu13030984
    [3] 陈建峰, 李莹. 上海市浦东城乡老年人估算肾小球滤过率及危险因素分析[J]. 中华全科医学, 2017, 15(5): 823-826. https://www.cnki.com.cn/Article/CJFDTOTAL-SYQY201705030.htm
    [4] GREGG L P, HEDAYATI S S. Management of traditional cardiovascular risk factors in ckd: What are the data?[J]. Am J Kidney Dis, 2018, 72(5): 728-744. doi: 10.1053/j.ajkd.2017.12.007
    [5] SUN B, MENG M, WEI J, et al. Long noncoding RNA PVT1 contributes to vascular endothelial cell proliferation via inhibition of miR-190a-5p in diagnostic biomarker evaluation of chronic heart failure[J]. Exp Ther Med, 2020, 19(5): 3348-3354.
    [6] 刘俊生, 刘莉, 杨丽娟, 等. 血清iPTH、血浆BNP、NT-proBNP水平在CKD 5期患者心功能评价中的应用价值分析[J]. 中华全科医学, 2018, 16(9): 1427-1430. https://www.cnki.com.cn/Article/CJFDTOTAL-SYQY201809006.htm
    [7] 中华医学会心血管病学分会心力衰竭学组, 中国医师协会心力衰竭专业委员会, 中华心血管病杂志编辑委员会. 中国心力衰竭诊断和治疗指南2018[J]. 中华心血管病杂志, 2018, 10(46): 760-789. https://www.cnki.com.cn/Article/CJFDTOTAL-ZLYS201904009.htm
    [8] UNGER T, BORGHI C, CHARCHAR F, et al. 2020 international society of hypertension global hypertension practice guidelines[J]. Hypertension, 2020, 75(6): 1334-1357. doi: 10.1161/HYPERTENSIONAHA.120.15026
    [9] 中华医学会糖尿病学分会. 中国2型糖尿病防治指南(2017年版)[J]. 中国实用内科杂志, 2018, 38(4): 292-344. https://www.cnki.com.cn/Article/CJFDTOTAL-SYNK201804009.htm
    [10] LEI L, HE Y, GUO Z, et al. A simple nomogram to predict contrast-induced acute kidney injury in patients with congestive heart failure undergoing coronary angiography[J]. Cardiol Res Pract, 2021. DOI: 10.1155/2021/9614953.
    [11] RANGASWAMI J, BHALLA V, BLAIR J E A, et al. Cardiorenal syndrome: classification, pathophysiology, diagnosis, and treatment strategies: A scientific statement from the American Heart Association[J]. Circulation, 2019, 139(16): e840-e878. http://www.ncbi.nlm.nih.gov/pubmed/30852913
    [12] HOUSE A A, WANNER C, SARNAK M J, et al. Heart failure in chronic kidney disease: conclusions from a kidney disease: Improving Global Outcomes (KDIGO) controversies conference[J]. Kidney Int, 2019, 95(6): 1304-1317. doi: 10.1016/j.kint.2019.02.022
    [13] TSUJIMOTO T, KAJIO H. Efficacy of renin-angiotensin system inhibitors for patients with heart failure with preserved ejection fraction and mild to moderate chronic kidney disease[J]. Eur J Prev Cardiol, 2018, 25(12): 1268-1277. doi: 10.1177/2047487318780035
    [14] 郝黎明, 李莹, 陈建峰, 等. 托伐普坦对左室射血分数降低心衰患者预后的影响[J]. 中国临床医学, 2018, 25(6): 872-878. https://www.cnki.com.cn/Article/CJFDTOTAL-LCYX201806003.htm
    [15] TANAKA A, HIRAMATSU E, WATANABE Y, et al. Efficacy of long-term treatment with tolvaptan to prolong the time until dialysis initiation in patients with chronic kidney disease and heart failure[J]. Ther Apher Dial, 2019, 23(4): 319-327. doi: 10.1111/1744-9987.12789
    [16] CHANG D R, YEH H C, TING I W, et al. The ratio and difference of urine protein-to-creatinine ratio and albumin-to-creatinine ratio facilitate risk prediction of all-cause mortality[J]. Sci Rep, 2021, 11(1): 7851. doi: 10.1038/s41598-021-86541-3
    [17] HE J, SHLIPAK M, ANDERSON A, et al. Risk factors for heart failure in patients with chronic kidney disease: The cric (chronic renal insufficiency cohort) study[J]. J Am Heart Assoc, 2017, 6(5): e005336. http://www.onacademic.com/detail/journal_1000039907823510_3eb9.html
    [18] LAWSON C A, TESTANI J M, MAMAS M, et al. Chronic kidney disease, worsening renal function and outcomes in a heart failure community setting: A UK national study[J]. Int J Cardiol, 2018, 267: 120-127. doi: 10.1016/j.ijcard.2018.04.090
    [19] KIM C J, CHOI I J, PARK H J, et al. Impact of cardiorenal anemia syndrome on short- and long-term clinical outcomes in patients hospitalized with heart failure[J]. Cardiorenal Med, 2016, 6(4): 269-278. doi: 10.1159/000443339
    [20] PORTOLÉS J, MARTÍN L, BROSETA J J, et al. Anemia in chronic kidney disease: From pathophysiology and current treatments, to future agents[J]. Front Med (Lausanne), 2021, 8: 642296. http://www.researchgate.net/publication/350404338_Anemia_in_Chronic_Kidney_Disease_From_Pathophysiology_and_Current_Treatments_to_Future_Agents
    [21] EISENGA M F, EMANS M E, VAN DER PUTTEN K, et al. Epoetin beta and c-terminal fibroblast growth factor 23 in patients with chronic heart failure and chronic kidney disease[J]. J Am Heart Assoc, 2019, 8(16): e011130. http://www.researchgate.net/publication/335273832_Epoetin_Beta_and_C-Terminal_Fibroblast_Growth_Factor_23_in_Patients_With_Chronic_Heart_Failure_and_Chronic_Kidney_Disease
    [22] MELAMED M L, RAPHAEL K L. Metabolic acidosis in ckd: A review of recent findings[J]. Kidney Med, 2021, 3(2): 267-277. doi: 10.1016/j.xkme.2020.12.006
    [23] SELVARAJ S, SHAH S J, OMMERBORN M J, et al. Pulmonary hypertension is associated with a higher risk of heart failure hospitalization and mortality in patients with chronic kidney disease: The jackson heart study[J]. Circ Heart Fail, 2017, 10(6): e003940. http://www.ncbi.nlm.nih.gov/pubmed/28611127
    [24] BANSAL N, ZELNICK L, GO A, et al. Cardiac biomarkers and risk of incident heart failure in chronic kidney disease: The cric (chronic renal insufficiency cohort) study[J]. J Am Heart Assoc, 2019, 8(21): e012336. http://www.ncbi.nlm.nih.gov/pubmed/31645163
  • 加载中
表(2)
计量
  • 文章访问数:  228
  • HTML全文浏览量:  44
  • PDF下载量:  12
  • 被引次数: 0
出版历程
  • 收稿日期:  2021-02-08
  • 网络出版日期:  2022-02-16

目录

    /

    返回文章
    返回