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  • 2013 Volue 29 Issue 11      Published: 15 November 2013
      

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    Objective    To evaluate if KDIGO (kidney disease: improving global outcomes) criteria for short?term prognosis of cardiorenal syndrome type I was superior to RIFLE (risk, injury, failure, loss of kidney function, end?stage kidney disease) and AKIN (the acute kidney injury network) criteria.    Methods    Data was retrospectively collected from patients with acute heart failure in Guangdong General Hospital between July 2005 and July 2012. The in?hospital mortality was regarded as outcome measures. Baseline serum creatinine was defined as first serum creatinine on admission. Kaplan?Meier curve was used to evaluate in?hospital survival by three AKI criteria and AKI by KDIGO but not RIFLE or AKIN in patients with cardiorenal syndrome type I. Cox regression was used for multivariate analysis of in?hospital mortality.    Results    Among 732 patients, 154 cases (21%) were diagnosed as AKI by KDIGO instead of RIFLE or AKIN. Incidence for the cardiorenal syndrome type I by KDIGO, RIFLE and AKIN were significantly different (54.7% vs. 38.6%, 54.7% vs 50.1%, P<0.001). Kaplan?Meier curve showed that in?hospital survival rates of patients with AKI diagnosed by KDIGO but not RIFLE or AKIN are lower than those without AKI (Log rank P=0.011). Cox regression indicated that AKI by KDIGO but not RIFLE or AKIN was an independent risk factor of in?hospital mortality (P=0.008).    Conclusion    KDIGO criteria is superior to RIFLE and AKIN criteria on predicting in?hospital mortality of cardiorenal syndrome type I.

     
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    Objective    To enhance the understanding of mercury poisoning related minimal change disease (MP?MCD).    Methods    A retrospective analysis about the clinical, laboratory and pathological manifestations, diagnosis, treatment and outcome of 7 patients with MP?MCD caused by skin?lightening cosmetics were conducted.    Results    All of the 7 patients were female with mean age 37.2 years. One patient had intermittently used skin?lightening cosmetics for 15 years and the other 6 patients continuously used the cosmetics for 2~6 months. Urine mercury levels of the 7 patients were significantly increased, reaching to 2.2~59.1 times of the normal value. The mercury content of 2 cosmetics used by patients was 1200 to 1560 times the mercury limit in cosmetics set by the government in 1987. Seven patients all presented as nephrotic syndrome, and all had MCD on renal biopsy. After the diagnosis of MP?MCD was confirmed, all the patients stopped using the mercury?contain cosmetics and accepted corticosteroid and chelation therapy. The nephrotic syndrome underwent complete remission after 1~2 months of therapy. Urine mercury levels in the 5 patients who repeated test returned to normal levels after 1~3 courses of chelation therapy.    Conclusion    MP?MCD caused by skin?lightening cosmetics should be considered as one of the differential diagnosis in the patients, especially in adult females who present with nephrotic syndrome in China.   

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    Objective    To analyze the clinical outcome of PD related peritonitis in our center.   Methods    All patients who developed PD related peritonitis between January 2004 and December 2010 in Renji Hospital of Shanghai Jiao Tong University School of Medicine were included. Outcomes of PD related peritonitis were analyzed.    Results    A total of 220 patients developed 371 episodes of PD related peritonitis during the study period in our center, and the average peritonitis rate was one episode per every 54.4 patient-months. Among the 371 episodes of peritonitis, 285 (76.8%) episodes had been cured, 17 (4.6%) episodes had needed temporary hemodialysis (HD), 46 (12.4%) episodes had led to switch to permanent HD and 21 (5.7%) episodes had caused death. After refractory peritonitis, there was a significant reduction of 4 h ultrafiltration (330 vs 270 ml, P=0.036) and an increase tendency of 4h D/Pcr (0.55±0.08 vs 0.58±0.10, P=0.086).    Conclusions    Peritoneal dialysis related peritonitis is an important contributor to technique failure and death in Chinese PD patients. Refractory peritonitis might injure peritoneal membrane function. 

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    Objective    To explore possible associations between osteopontin(OPN) and intact parathyroid hormone(iPTH), to investigate effects of them on the progression of carotid artery calcification in patients receiving long-term hemodialysis.    Methods    Forty-eight maintenance hemodialysis (MHD) patients and 28 age- and sex-matched healthy volunteers were recruited. The concentration of OPN in peripheral blood was determined by enzyme linked immunosorbent assay (ELISA). Levels of iPTH and presence of plaques in the common carotid arteries were also measured. The demographics were recorded.    Results    Compared with controls, levels of OPN[(137.4±80.8) ng/L vs (31.6±6.7) ng/L, P<0.01] and iPTH[(456.4±326.4) ng/L vs (66.9±19.3) ng/L, P<0.01] were higher in MHD patients before hemodialysis, the numbers of calcific plaques in the common carotid arteries were increased in MHD patients (P<0.01). There was a positive correlation between pre-dialysis OPN levels and iPTH levels (r=0.620, P<0.01) in MHD patients. Higher levels of OPN and iPTH correlated with greater numbers of calcific plaques in the common carotid arteries after division into three subgroups of MHD patients based on calcific plaques. In multiple linear regression analysis, the correlation between the pre-dialysis OPN and iPTH levels remained the same even if adjusting for confounding effects[β=0.468, 95%CI (0.036, 0.195), t=2.936, P=0.005].    Conclusion    OPN level is positively correlated with iPTH level in hemodialysis patients, which suggesting that both of them play important roles in the progression of carotid artery calcification.
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    Objective    To evaluate fluid distribution in patients on maintenance hemodialysis(HD) by bioimpedance analysis and on the effect of adjusting the dry weight in hemodialysis patients. Methods    Forty maintenance HD patients from the dialysis center of the Second Affiliated Hospital of Dalian Medical University were enrolled as study group. One hundred and two individuals who were tested of physical examination in the same hospital were enrolled as the control group. Sex and age of the two groups were recorded. Body weight, body high, blood pressure, bioimpedance of HD patients (pre-dialysis and post-dialysis) and controls were measured. Bioimpedance was measured by multi-frequency segmental bioimpedance analysis, including right arm (RA) bioimpedance, trunk (TR)bioimpedance and right leg (RL) bioimpedance. Bioimpedance ratio (BIR) of three parts was calculated as of 100kHz and 20kHz including RA-BIR, TR-BIR and RL-BIR. Then eight HD patients who had high RA-BIA or TR-BIA according to the reference range which were obtained from 102 controls were chosen for dry weight adjustment. Post-dialysis body weight, blood pressure, and bioimpedance of the eight HD patients were measured again after adjusting the dry weight.    Results     ⑴ BIR of three parts in pre-dialysis HD patients were all significantly higher than that in the control group (P<0.05). BIR of three parts of the post-dialysis HD patients were still higher than that of the control group, but RL-BIR was not significantly (P>0.05). BIR of three parts of the post-dialysis HD patients were lower than BIR of three parts of the pre-dialysis HD patients, and there was significant different (P<0.05) with RA-BIR and RL-BIR. ⑵ After adjusting the dry weight, BIR of three parts of the post-dialysis HD patients were still higher than that of the control group, but none of them was significantly (P>0.05). BIR of three parts of the HD patients after adjusting the dry weight were lower than BIR of three parts of the HD patients before adjusting the dry weight, but there was no significant different with TR-BIR(P>0.05). After adjusting the dry weight, systolic blood pressure of the post-dialysis HD patients were significantly decrease[(150.00±29.28) vs (140.63±20.78) mm Hg,P<0.05].    Conclusions     Bioimpedance analysis may be an effective method for adjusting dry weight in hemodialysis patients, and the bioimpedance of arms is the most effective method. The bioimpedance reference range of hemodialysis patients can be according to the reference range of normal individuals

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    Objective    To observe the mitochondrial damage associated with protein-energy wasting of skeletal muscle in diabetic kidney disease (DKD) model of Goto-Kakizaki(GK) rats and evaluate the effects of low-protein diet supplemented with α-keto acids on muscle wasting.    Methods    Forty-five male 24-week-age GK rats were randomly divided into three groups, normal protein diet group (NPD), low-protein diet group (LPD) and LPD +α-keto group (Keto). Fifteen gender and age matched Wistar rats were served as control group (CTL). The living condition of GK rats was observed and the weight was measured once a week. Urine albumin, serum glucose, creatinine and urea nitrogen were measured at 24, 32, 40, 48 week age. Soleus muscle was observed to calculate the muscle size and the percentage of I and Ⅱ type muscle fiber with software after SDH and NADH staining at 48-week-age. Tissue ultrastructure was observed under the transmission electron microscopy. The activity of citrate synthase was detected by spectrophotometer. Expression of mitochondrial DNA was examined by Q-PCR. Results    Compared with the CTL group, NPD, LPD and Keto groups had lower body weight, higher urine albumin, higher serum creatinine and urea nitrogen (P <0.05). The cross-sectional area of muscle fibers was larger in CTL group. Compared with CTL group, the muscle fiber was partly broken, the mitochondrial morphology was obviously changed, the percentage of type Ⅱ muscle fiber was increased significantly (P<0.05), and the activity of citrate synthase and the number of mitochondrial DNA were decreased significantly in NPD, LPD and Keto groups (P<0.05). In Keto group, muscle wasting was improved compared with NPD and LPD group (P<0.05), the cross-sectional area of soleus muscle increased and the percentage of type Ⅱ muscle fiber decreased, levels of urine albumin, serum creatinine and urea nitrogen decreased (P<0.05). Under transmission electron microscopy, the muscle fiber of keto group was intact and mitochondiral morphology was close to that of CTL group. The activity of citrate synthase and number of mitochondiral DNA were higher as compared to CTL group (P<0.05). There were no significant differences between NPD and LPD group. Conclusions    In DKD condition, protein degradation in the skeletal muscle is accelerated, mitochondrion is swelling, the number of mitochondrial DNA is decreased and mitochondrial function is impaired. Low-protein diet supplemented with α-keto acids can improve mitochondrial damage and muscle wasting induced by DKD.

     

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    Objective    CXCR4-overexpressing bone marrow-derived mesenchymal stem cells (CXCR4-BMSC) were constructed and co-cultured with hypoxia/re-oxygenation pretreated renal tubular epithelial cells (HR-RTEC). Repair of HR-RTEC was detected and the possible mechanism was also discussed.   Methods   CXCR4-BMSC (CXCR4-BMSC/eGFP, eGFP as the tracer gene) and null-BMSC (BMSC/eGFP) were obtained by gene transfection technique, and the level of CXCR4 in the transfected cells was detected. RTEC was cultured under hypoxia/re-oxygenation condition for 12 h, respectively, to obtain HR-RTEC, which was used to simulate AKI in vitro. BMSC and HR-RTEC were co-cultured for 12 h, and the proportion of apoptotic cells among the HR-RTEC was assayed by immunofluorescence technique. Western blot was used to test the protein levels of cleaved Caspase-3 and Bcl-2. The number of migrating BMSC was also assayed. After culturing with the HR-RTEC culture supernatant, the expression of cytokeratin 18 (CK18) in BMSC was tested by immunofluorescence staining. Cytokines including bone morphogenetic protein-7 (BMP-7), hepatic growth factor (HGF) and interleukin-10 (IL-10) in the BMSC culture supernatant were detected by ELISA method.    Results    Expression of CXCR4 was enhanced in CXCR4-BMSC. Proportions of the apoptotic cells among HR-RTEC after being co-cultured with BMSC, CXCR4-BMSC and null-BMSC were all decreased, especially in the C/H group. The decreased cleaved Caspase-3 and enhanced Bcl-2 were also observed in HR-RTEC. The number of migrating CXCR4-BMSC was the highest. Proportions of CK18+ cells in BMSC, CXCR4-BMSC and null-BMSC were all low and showed no difference. However, CXCR4 overexpression in BMSC stimulated secretions of BMP-7, HGF and IL-10.    Conclusions    CXCR4-overexpressing BMSC has more repair effect on the co-cultured HR-RTEC, the enhanced migration ability and secretion ability of CXCR4-BMSC are the possible mechanisms.
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    Objective    To observe the expression of toll like receptor 4(TLR4) Signaling and the release of inflammation factors in rat tubular epithelial cell(NRK-52E) under high glucose condition after TLR4-siRNA transfection.    Methods    Three TLR4-siRNA sequences were designed and synthesized. The transfection efficiency was observed by fluorescence microscope after transfection, and the expression of TLR4 mRNA was detected by real time PCR. The most effective siRNA was selected to be used for forward experiments. After transfection for 24 h, cells were stimulated with 25 mmol/L glucose and/or 10-7 mmol/L Angiotension Ⅱ(AngⅡ) for 12 h, 24 h; cells without stimulation were as normal control. Real-time PCR was used to analyze TLR4 and myeloid differentiation factor 88 (MyD88) mRNA expression; Western blot was used to observe TLR4/MyD88 and NF-κB protein expression. ELISA assay was used to detect the concentration of monocyte chemoattractant protein-1(MCP-1), interleukin-6(IL-6) in cell supernatant after cells were stimulated for 24 h.    Results    TLR4/MyD88 mRNA and TLR4/MyD88/NF-κB protein were highly expressed under high glucose or AngⅡ co-incubated NRK-52E(P<0.01), the MCP-1 and IL-6 levels were also increased markedly compared with normal control group (P<0.01). TLR4/MyD88 mRNA and TLR4/MyD88/NF-kB protein expressions were obviously inhibited in cells that were transfected with TLR4-siRNA compared with high glucose group(P<0.01), MCP-1 and IL-6 production decreased remarkably compared with high glucose or   AngⅡ co-stimulated group(P<0.01).    Conclusions    High glucose can lead to the activation of TLR4/MyD88/NF-kB signaling and the secretion of inflammation factors in NRK-52E,      AngⅡ further augments these effects. The effect can be blocked efficiently by specific siRNA gene silence. TLR4 signaling plays a pivotal role in the innate-immune inflammatory reaction in NRK-52E.
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    Objective    To analyse the relationship and mechanism between chronic periodontitis (CP) and IgA nephropathy (IgAN) by establishing animal model of chronic periodontitis and IgA nephropathy in SD rats.    Methods    Eighty health male SD rats were divided into four groups, control group (A, n=20), IgAN group (B, n=20), CP group (C, n=20), CP accompanied with IgAN group (D, n=20). CP model was established by ligating silk suture and besmeared pathogenic bacterium in rats dental cervix. Experimental IgAN model was established by lavage of bovine serum albumin (BSA) and injection of lipopolysaccharide (LPS) and carbon tetrachloride (CCl4). Ten rats were sacrificed in every group at the end of week 8 and 12. The blood, urine, kidney tissue samples were examined. The observation index included proteinuria, kidney and liver function, renal tissue pathology and periodontal tissue pathology. The data were statistically analysed.    Results    Animal models were established successfully. The levels of Scr and BUN in group A, B, C were not obvious difference, but that in group D was higher than the other third groups at 8 weeks (P<0.05). The levels of Scr and BUN in group D and group B were significantly higher than that in group A, meanwhile that in group D was significantly higher than that in group B at 12 weeks(P<0.05). The levels of 24 h urine protein in B, C, D groups were higher than that in group A at 8 weeks(P<0.05), but at 12 week, that in group D was higher than that in group B and C (P<0.05). At 8 weeks, glomeruli had little mesangial broadening and renal interstitium had mild hyperplasia of fibrous tissue in group B and D, and that in the group D significantly was heavier than that in group B. The focal varying degrees were glomerular mesangial proliferation hardening, glomerular mesangial broadening, focal segmental sclerosis, and diffuse or focal inflammatory cell infiltration in D group at the end of week 12. The score of PAS between group A and group C had no statistical significance. The scores of PAS in group B and D were higher than that in group A (P<0.01), and that in group D was higher than that in group B (P<0.01). Obvious inflammation of periodontal tissue was observed in group C and D, and modified sulcus bleeding index (MBI) were higher than that in group A and B, and MBI in group D was significantly higher than that in group C (P<0.01).    Conclusions    The model can be used to research the change of biochemistry and pathology and observe the relationship between chronic periodontitis and IgAN. This study shows that there is relationship between chronic periodontitis and IgAN. Chronic periodontitis maybe make more serious pathology damage in kidney by inflammation mechanism.