新医学
新醫學
신의학
NEW CHINESE MEDICINE
2015年
4期
262-267
,共6页
张莉%朱翠颜%王筱菁%邢晓欢%黎雅清%林健才
張莉%硃翠顏%王篠菁%邢曉歡%黎雅清%林健纔
장리%주취안%왕소정%형효환%려아청%림건재
2型糖尿病%糖尿病肾病%血清尿酸%肾小球滤过率
2型糖尿病%糖尿病腎病%血清尿痠%腎小毬濾過率
2형당뇨병%당뇨병신병%혈청뇨산%신소구려과솔
Type 2 diabetes mellitus%Diabetic kidney disease%Serum uric acid%eGFR
目的:分析糖尿病肾病(DKD)1~3期血清尿酸水平与肾小球滤过率估计值(eG-FR)的关系,探讨血清尿酸在诊断早期 DKD 的应用价值。方法纳入2型糖尿病患者中已确诊合并DKD 的239例患者(A 组)、正常健康人228名(B 组),2组受检者的 eGFR 均≥30 ml/(min·1.73 m2),并按 DKD 分期将 A 组分为 A1组(DKD 1期)96例、A2组(DKD 2期)101例、A3组(DKD 3期)42例。比较各组及各亚组间血清尿酸水平,分析 A、B 组各自血清尿酸水平与 eGFR 的相关性。结果A、B 组间 eGFR 比较差异无统计学意义(P >0.05),A 组血清尿酸水平高于 B 组(P <0.01);A1~3组间血清尿酸比较差异有统计学意义(P <0.05),并且随 DKD 分期呈上升趋势(P <0.05)。A、B 组中,血清尿酸与 eGFR 均有良好相关性(P <0.01),多重线性回归显示,血清尿酸是DKD 患者 eGFR 下降的危险因素(P <0.01)。结论高血清尿酸与早期 DKD 的 eGFR 异常相关,是其危险因素之一,提示尿酸可能参与 DKD 早期肾损害的发生、发展。
目的:分析糖尿病腎病(DKD)1~3期血清尿痠水平與腎小毬濾過率估計值(eG-FR)的關繫,探討血清尿痠在診斷早期 DKD 的應用價值。方法納入2型糖尿病患者中已確診閤併DKD 的239例患者(A 組)、正常健康人228名(B 組),2組受檢者的 eGFR 均≥30 ml/(min·1.73 m2),併按 DKD 分期將 A 組分為 A1組(DKD 1期)96例、A2組(DKD 2期)101例、A3組(DKD 3期)42例。比較各組及各亞組間血清尿痠水平,分析 A、B 組各自血清尿痠水平與 eGFR 的相關性。結果A、B 組間 eGFR 比較差異無統計學意義(P >0.05),A 組血清尿痠水平高于 B 組(P <0.01);A1~3組間血清尿痠比較差異有統計學意義(P <0.05),併且隨 DKD 分期呈上升趨勢(P <0.05)。A、B 組中,血清尿痠與 eGFR 均有良好相關性(P <0.01),多重線性迴歸顯示,血清尿痠是DKD 患者 eGFR 下降的危險因素(P <0.01)。結論高血清尿痠與早期 DKD 的 eGFR 異常相關,是其危險因素之一,提示尿痠可能參與 DKD 早期腎損害的髮生、髮展。
목적:분석당뇨병신병(DKD)1~3기혈청뇨산수평여신소구려과솔고계치(eG-FR)적관계,탐토혈청뇨산재진단조기 DKD 적응용개치。방법납입2형당뇨병환자중이학진합병DKD 적239례환자(A 조)、정상건강인228명(B 조),2조수검자적 eGFR 균≥30 ml/(min·1.73 m2),병안 DKD 분기장 A 조분위 A1조(DKD 1기)96례、A2조(DKD 2기)101례、A3조(DKD 3기)42례。비교각조급각아조간혈청뇨산수평,분석 A、B 조각자혈청뇨산수평여 eGFR 적상관성。결과A、B 조간 eGFR 비교차이무통계학의의(P >0.05),A 조혈청뇨산수평고우 B 조(P <0.01);A1~3조간혈청뇨산비교차이유통계학의의(P <0.05),병차수 DKD 분기정상승추세(P <0.05)。A、B 조중,혈청뇨산여 eGFR 균유량호상관성(P <0.01),다중선성회귀현시,혈청뇨산시DKD 환자 eGFR 하강적위험인소(P <0.01)。결론고혈청뇨산여조기 DKD 적 eGFR 이상상관,시기위험인소지일,제시뇨산가능삼여 DKD 조기신손해적발생、발전。
Objective To analyze the relationship between serum uric acid (SUA)and estimated glomerular filtration rate (eGFR)in type 2 diabetes mellitus (T2DM)patients with stages 1-3 of diabetic kid-ney disease (DKD)and evaluate the diagnostic value of SUA in early DKD.Methods In total,231 T2DM patients complicated with DKD were assigned into group A and 228 healthy controls in group B.All participants presented with eGFR ≥ 30 ml/(min·1.73 m2 ).Patients in group A were sub-grouped into A1 (stage DKD-1,n =96),A2 (stage DKD-2,n =101)and A3 (stage DKD-3,n =42)groups according to DKD stag-ing.The SUA levels were statistically compared and the correlation between SUA and eGFR was analyzed among different groups and sub-groups.Results eGFR did not significantly differ between groups A and B (P>0.05),whereas SUA level in group A was significantly higher compared with that in group B (P <0.01).The SUA levels significantly differed among subgroups A1,A2 and A3 (P <0.05)and were elevated along with DKD staging (P <0.05).In both groups A and B,SUA level was significantly correlated with eGFR (both P <0.01).Multiple linear regression analysis revealed that SUA was a risk factor for eGFR impairment in DKD patients (P <0.01).Conclusions SUA is related to the abnormity of eGFR during early DKD and acts as one of the independent risk factors,prompting that SUA probably participates in the incidence and de-velopment of renal damage during early stage of DKD.