The clinical characteristics of posterior reversible encephalopathy syndrome in patients with chronic renal failure

被引:6
作者
Hu, Hongtao [1 ]
Xu, Shen [1 ]
Hu, Shuang [1 ]
Xu, Weijia [1 ,2 ]
Shui, Hua [1 ]
机构
[1] Wuhan Univ, Zhongnan Hosp, Dept Nephrol, 169 Rd Donghu, Wuhan 430071, Hubei, Peoples R China
[2] Taihe Hosp, Dept Nephrol, Shiyan 442000, Hubei, Peoples R China
关键词
chronic renal failure; posterior reversible encephalopathy syndrome; imageology; biochemical tests; clinical manifestations; SERUM LACTATE-DEHYDROGENASE; LEUKOENCEPHALOPATHY SYNDROME; KIDNEY-DISEASE; HEMODIALYSIS; PATHOPHYSIOLOGY; FEATURES; EDEMA;
D O I
10.3892/etm.2017.4570
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Few studies have investigated posterior reversible encephalopathy syndrome (PRES) in patients with chronic renal failure (CRF). The present study analyzed the clinical manifestations, laboratory examinations and imaging features of PRES in patients with CRF. A total of 42 patients with CRF with or without PRES were recruited in the current retrospective case-control study. Patient data taken prior to the onset of PRES in patients with CRF and PRES (n=21) were collected and analyzed. At the same time, data from patients with CRF but without PRES (n=21) were also analyzed. Brain magnetic resonance imaging (MRI) scans were collected from patients in the PRES group. The mean blood pressure of patients in the PRES group was significantly higher than that of the control group (systolic blood pressure: 172 +/- 15 mmHg vs. 135 +/- 14 mmHg, P<0.01; diastolic blood pressure: 95 +/- 16 mmHg vs. 64 +/- 13 mmHg, P<0.01). Furthermore, compared with the control group, mean serum albumin (Alb) and hemoglobin (Hb) concentrations in the PRES group were significantly lower (Alb: 29.1 +/- 5.3 g/l vs. 34.6 +/- 6.1 g/l, P=0.001; Hb: 74 +/- 16 g/l vs. 89 +/- 28 g/l, P=0.037). By contrast, mean LDH concentration was significantly higher in the PRES group (LDH: 336 +/- 141 U/l vs. 235 +/- 89 U/l, P=0.004). In the PRES group, 24 h urine volume was significantly lower in the PRES group than in the control group (24 h urine volume: 651 +/- 520 ml vs. 982 +/- 518 ml, P=0.046). No significant differences in levels of serum potassium (4.5 +/- 0.6 mmol/l vs. 4.4 +/- 0.5 mmol/l, P=0.377), sodium (138.3 +/- 4.9 mmol/l vs. 139.0 +/- 6.8 mmol/l, P=0.325), calcium (2.0 0 +/- 24 mmol/l vs. 1.9 +/- 0.24 mmol/l, P=0.673), alanine aminotransferase; (24 +/- 14 U/l vs. 18 +/- 8 U/l, P=0.975); aspartate aminotransferase (29 +/- 11 U/l vs. 24 +/- 9 U/I, P=0.619) and uric acid (448 +/- 148 mu mol/l vs. 378 +/- 116 mu mol/l, P=0.599) were found between the two groups. PRES is a relatively common nervous system complication arising in patients with CRF. Certain biochemical markers, including Hb and Alb, may be associated with PRES. Diagnosing PRES is difficult as computed tomography (CT) brain scans may be normal and MRI scans, which are more sensitive than CT scans at diagnosing PRES, are not always performed in patients with CRF. Thus, brain MRI scans should be taken first in such patients when PRES is suspected.
引用
收藏
页码:881 / 887
页数:7
相关论文
共 34 条
  • [1] Stimulation of HIF-1α, HIF-2α, and VEGF by prolyl 4-hydroxylase inhibition in human lung endothelial and epithelial cells
    Asikainen, TM
    Ahmad, A
    Schneider, BK
    Ho, WB
    Arend, M
    Brenner, M
    Günzler, V
    White, CW
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 2005, 38 (08) : 1002 - 1013
  • [2] Posterior reversible encephalopathy syndrome, part 2: Controversies surrounding pathophysiology of vasogenic edema
    Bartynski, W. S.
    [J]. AMERICAN JOURNAL OF NEURORADIOLOGY, 2008, 29 (06) : 1043 - 1049
  • [3] Heme Degradation and Vascular Injury
    Belcher, John D.
    Beckman, Joan D.
    Balla, Gyorgy
    Balla, Jozsef
    Vercellotti, Gregory
    [J]. ANTIOXIDANTS & REDOX SIGNALING, 2010, 12 (02) : 233 - 248
  • [4] Burrus TM, 2010, ARCH NEUROL-CHICAGO, V67, P831, DOI 10.1001/archneurol.2010.119
  • [5] Defining, Treating, and Understanding Chronic Kidney DiseaseA Complex Disorder
    Campbell, Dean
    Weir, Matthew R.
    [J]. JOURNAL OF CLINICAL HYPERTENSION, 2015, 17 (07) : 514 - 527
  • [6] Posterior Reversible Encephalopathy Syndrome in End-Stage Kidney Disease: Not Strictly Posterior or Reversible
    Canney, Mark
    Kelly, Dearbhla
    Clarkson, Michael
    [J]. AMERICAN JOURNAL OF NEPHROLOGY, 2015, 41 (03) : 177 - 182
  • [7] Erythropoietin-associated hypertensive posterior leukoencephalopathy
    Delanty, N
    Vaughan, C
    Frucht, S
    Stubgen, P
    [J]. NEUROLOGY, 1997, 49 (03) : 686 - 689
  • [8] Posterior reversible encephalopathy syndrome in a patient with ANCA-associated vasculitis
    Fuentes, Alexandra Gonzalez
    Komarla, Ashwini
    Gomez, John I.
    [J]. RHEUMATOLOGY INTERNATIONAL, 2012, 32 (08) : 2529 - 2530
  • [9] Clinical features of reversible posterior leukoencephalopathy syndrome in patients with systemic lupus erythematosus
    Fujieda, Yuichiro
    Kataoka, Hiroshi
    Odani, Toshio
    Otomo, Kotaro
    Kato, Masaru
    Fukaya, Shinji
    Oku, Kenji
    Horita, Tetsuya
    Yasuda, Shinsuke
    Atsumi, Tatsuya
    Koike, Takao
    [J]. MODERN RHEUMATOLOGY, 2011, 21 (03) : 276 - 281
  • [10] Association of degree and type of edema in posterior reversible encephalopathy syndrome with serum lactate dehydrogenase level: Initial experience
    Gao Bo
    Liu Feng-li
    Zhao Bin
    [J]. EUROPEAN JOURNAL OF RADIOLOGY, 2012, 81 (10) : 2844 - 2847