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-  2018 

先天性脊柱畸形合并泌尿系畸形患者的肾功能评估
Evaluation of renal function in congenital spinal deformities patients with urinary malformations

DOI: 10.7652/jdyxb201802018

Keywords: 先天性脊柱畸形,泌尿系畸形,肾脏早期损伤
congenital spinal deformities
,congenital urinary malformation,early renal function impairment

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Abstract:

摘要:目的 评估先天性脊柱畸形合并泌尿系畸形患者的肾功能。方法 前瞻性收集先天性脊柱畸形合并泌尿系畸形的患者和年龄、体质量相近的健康人,并分成肾脏畸形组、尿路畸形组和健康对照组。检测血肌酐、尿素、胱抑素C、估计肾小球滤过率(eGFR)用于评估患者的一般肾功能;检测尿微量白蛋白(mALB)、α1-微球蛋白(α1-MG)、β2-微球蛋白(β2-MG)和N-乙酰-β-D-葡萄糖苷酶(NAG)用于评价患者的早期肾功能。结果 共募集到肾脏畸形患者16例、尿路畸形患者14例、健康对照组20例,3组之间的血肌酐、尿素、胱抑素C以及eGFR均在正常范围内,且各指标无统计学差异(P>0.05);3组之间的mALB、α1-MG以及NAG浓度存在统计学差异(P<0.05),而β2-MG浓度未见统计学差异(P>0.05);肾脏畸形组的mALB以及NAG浓度显著高于尿路畸形组,且差异有统计学意义(P<0.05),而α1-MG浓度在两组间未见明显差异(P>0.05)。结论 先天性脊柱畸形合并泌尿系畸形患者存在肾功能早期损害,且相较于尿路畸形患者,肾脏畸形患者的肾损害程度更严重。
ABSTRACT: Objective To evaluate renal function in congenital spinal deformities patients with urinary malformations. Methods We prospectively enrolled patients diagnosed with congenital spinal deformities combined with urinary malformation as well as age- and weight-matched healthy individuals and divided them into three groups: renal malformations group, urinary tract malformations group, and healthy control group. Serum creatinine, blood urea, blood uric acid, serum cystatin C, and estimate glomerular filtration rate (eGFR) level were used to evaluate general renal function. Urinary microalbumin (mALB), urinary alpha-1-microglobulin (α1-MG), beta-2-microglobulin (β2-MG), and N-acetyl-beta-D-glucosaminidase (NAG) level were determined to evaluate early renal function. Results We enrolled totally 16 patients with renal malformations, 14 patients with urinary tract malformations group, and 20 healthy individuals as controls. The concentration of serum creatinine, blood urea, blood uric acid, serum cystatin C, and the value of eGFR in the three groups were within normal reference values, with no significant difference (P>0.05). There were significant differences in the urinary levels of mALB, α1-MG and NAG in the three groups (P<0.05), but not for the concentration of β2-MG (P>0.05). Urinary levels of mALB and NAG were significantly higher in renal malformations group than in urinary tract malformations group (P<0.05), but not for the concentration of α1-MG (P>0.05). Conclusion Early renal function impairment occurs in congenital spinal deformities children with urinary malformation. Moreover, it appears more severe in patients with renal malformations than in those with urinary tract malformations

References

[1]  BEAUREGARD-LACROIX E, TARDIF J, CAMURRI MV, et al. Retrospectiveanalysis of congenital scoliosis: Associated anomalies and genetic diagnoses[J]. Spine, 2017, 42(14):E841.
[2]  彭纪临,刘莉,曹文富. 胱抑素C与慢性肾功能衰竭的相关研究进展[J]. 内蒙古中医药, 2016, 35(6):113-114.
[3]  OLVERA-POSADA D, DAYARATHNA T, DION M, et al. KIM-1 is a potential urinary biomarker of obstruction: Results from a prospective cohort study[J]. J Endourol, 2016, 31(2).
[4]  刘莉娟,袁清茹,赵明中. 血清胱抑素C与肌酐在评估75岁以上老年慢性心衰患者预后中的价值[J]. 西安交通大学学报(医学版), 2017, 38(1):58-61.
[5]  NICOLAOU N, RENKEMA KY, BONGERS EM, et al. Genetic, environmental, and epigenetic factors involved in CAKUT[J]. Nat Rev Nephrol, 2015, 11(12):720.
[6]  Arch Environ Contam Toxicol, 2017, 73(3):401-409.
[7]  黄琼莲,覃西,李浩,等. 尿α1-MG 检测对肾损害早期诊断的应用价值[J]. 临床误诊误治, 2014(7):87-89.
[8]  SCHAUB S, WILKINS JA, ANTONOVICI M, et al. Proteomic-based identification of cleaved urinary beta2-microglobulin as a potential marker for acute tubular injury in renal allografts[J]. Am J Transplant, 2005, 5(4 Pt 1):729-738.
[9]  DOS SJA, DE MIRANDA DM, SIMOES ESA. Congenitalanomalies of the kidney and urinary tract: An embryogenetic review[J]. Birth Defects Res C Embryo Today, 2014, 4:374-381.
[10]  NEPHROLOGY JSO. Evidence-Based Clinical Practice Guideline for CKD 2013[J]. Clini Exp Nephrol, 2014, 3:346-423.
[11]  HARAMBAT J, VAN STRALEN KJ, KIM JJ, et al. Epidemiology of chronic kidney disease in children[J]. Pediatr Nephrol, 2012, 3:363-373.
[12]  PAHYS JM, GUILLE JT. What??s New incongenital scoliosis? [J]. J Pediatr Orthop, 2016.
[13]  孙保胜,谢向辉,孙琳,等. 儿童先天性脊柱侧凸合并泌尿系畸形临床分析[J]. 临床小儿外科杂志, 2016, 15(6):562-565.
[14]  SHEN J, WANG Z, LIU J, et al. Abnormalitiesassociated with congenital scoliosis: A retrospective study of 226 Chinese surgical cases[J]. Spine (Phila Pa 1976), 2013, 10:814-818.
[15]  TIAN YL, LU H, LIN CY, et al. Incidence and risks of congenital anomalies of kidney and urinary tract in newborns: A population-based case-control study in Taiwan[J]. Medicine (Baltimore), 2016, 5: e2659.
[16]  HEDEQUIST D, EMANS J. Congenital scoliosis[J]. J Am Acad Orthop Surg, 2004, 4:266-275.
[17]  SUPPLEMENTS KI. Chapter 1: Definition and Classification of CKD[J]. Kidney Int Suppl, 2013, 3(1):19-62.
[18]  DEVARAJAN P. Proteomics for the investigation of acute kidney injury[J]. Contrib Nephrol, 2008, 160:1-16.
[19]  RUANGYUTTIKAM W, PANYAMOON A, NAMBUMEE K, et al. Use of the kidney injury molecule-1 as a biomarker for early detection of renal tubular dysfunction in a population chronically exposed to cadmium in the environment[J]. Springerplus, 2013, 2(1):1-8.
[20]  ZHENG J, YAO Y, HAN L, et al. Renal function and injury in infants and young children with congenital heart disease[J]. Pediat Nephrol, 2013, 28(1):99-104.
[21]  EOM SY, SEO MN, LEE YS, et al. Low-Level Environmentalcadmium exposure induces kidney tubule damage in the general population of Korean adults[J].

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