中华医学杂志
中華醫學雜誌
중화의학잡지
National Medical Journal of China
2009年
10期
669-672
,共4页
康怡%陆菊明%孙敬芳%李春霖%王先令%张小群%吕朝晖%窦京涛%母义明
康怡%陸菊明%孫敬芳%李春霖%王先令%張小群%呂朝暉%竇京濤%母義明
강이%륙국명%손경방%리춘림%왕선령%장소군%려조휘%두경도%모의명
糖尿病%动态血糖监测%血糖波动
糖尿病%動態血糖鑑測%血糖波動
당뇨병%동태혈당감측%혈당파동
Diabetes mellitus%Continuous glucose monitoring%Glucose excurtion
目的 研究不同糖调节受损人群的动态血糖波动特征.方法 采用动态血糖监测系统(CGMS)根据连续2次口服葡萄糖耐量试验结果,选取稳定人群中单纯空腹血糖受损(IFG)组12例,单纯餐后血糖受损(IGT)组19例,空腹血糖受损合并糖耐量低减(IFG/IGT)组11例,新诊断2型糖尿病(T2DM)组21例,正常对照(NGT)组18例,分析其各项临床指标和CGMS动态血糖数据.结果 (1)日内血糖波动:NGT、IFG、IGT、IFG/IGT至T2DM组的最大血糖波动幅度(LAGE)、平均血糖(MBG)和血糖水平标准差(SDBG)依次升高.IGT组的平均血糖波动幅度(MAGE)(3.2±1.2)mmol/L较NGT组(1.6±0.5)mmol/L高,较T2DM组(5.2±1.9)mmol/L低(P<0.05);IFG/IGT的有效血糖波动频率(FGE)(5.5±2.5)次/d较NGT组(6.1±3.4)次/d低,较T2DM组(4.8±1.8)高.糖尿病前期3组间IGT组MAGE(3.2±1.2)mmol/L最高,FGE(4.9±1.8)最低.(2)日间血糖波动:与NGT组(0.8±0.3)mmo/L相比,IGT组(1.1±0.4)mmol/L、IFG/IGT组(1.2±0.4)mmol/L和T2DM组(2.0±1.0)mmol/L的日间血糖平均绝对差依次升高(P<0.05).(3)不同糖调节受损人群血糖波动特征:IFG组空腹血糖受损程度最重,餐后高峰以IFG/IGT组为著.血糖水平曲线由低至高依次为NGT、IGT、IFG/IGT、IFG、T2DM组.(4)不同HbAlc水平的血糖波动:受试者HbAlc<7%时,空腹血糖曲线几乎重合,餐后血糖曲线略微分开;HbAlc7.0%~7.9%时,餐后高峰明显上升;HbAlc≥8%时,空腹曲线明显上移,餐后波动继续升高.结论 (1)随着糖调节受损程度的加重,日内血糖波动及日间血糖波动逐渐增加.(2)正常人血糖波动幅度小,频率高;T2DM餐后血糖波动幅度大,有效波动频率低;(3)IFG组的血糖波动特征最接近于NGT,而IGT组最接近于T2DM;(4)在糖尿病前期阶段餐后血糖受损明显早于空腹.
目的 研究不同糖調節受損人群的動態血糖波動特徵.方法 採用動態血糖鑑測繫統(CGMS)根據連續2次口服葡萄糖耐量試驗結果,選取穩定人群中單純空腹血糖受損(IFG)組12例,單純餐後血糖受損(IGT)組19例,空腹血糖受損閤併糖耐量低減(IFG/IGT)組11例,新診斷2型糖尿病(T2DM)組21例,正常對照(NGT)組18例,分析其各項臨床指標和CGMS動態血糖數據.結果 (1)日內血糖波動:NGT、IFG、IGT、IFG/IGT至T2DM組的最大血糖波動幅度(LAGE)、平均血糖(MBG)和血糖水平標準差(SDBG)依次升高.IGT組的平均血糖波動幅度(MAGE)(3.2±1.2)mmol/L較NGT組(1.6±0.5)mmol/L高,較T2DM組(5.2±1.9)mmol/L低(P<0.05);IFG/IGT的有效血糖波動頻率(FGE)(5.5±2.5)次/d較NGT組(6.1±3.4)次/d低,較T2DM組(4.8±1.8)高.糖尿病前期3組間IGT組MAGE(3.2±1.2)mmol/L最高,FGE(4.9±1.8)最低.(2)日間血糖波動:與NGT組(0.8±0.3)mmo/L相比,IGT組(1.1±0.4)mmol/L、IFG/IGT組(1.2±0.4)mmol/L和T2DM組(2.0±1.0)mmol/L的日間血糖平均絕對差依次升高(P<0.05).(3)不同糖調節受損人群血糖波動特徵:IFG組空腹血糖受損程度最重,餐後高峰以IFG/IGT組為著.血糖水平麯線由低至高依次為NGT、IGT、IFG/IGT、IFG、T2DM組.(4)不同HbAlc水平的血糖波動:受試者HbAlc<7%時,空腹血糖麯線幾乎重閤,餐後血糖麯線略微分開;HbAlc7.0%~7.9%時,餐後高峰明顯上升;HbAlc≥8%時,空腹麯線明顯上移,餐後波動繼續升高.結論 (1)隨著糖調節受損程度的加重,日內血糖波動及日間血糖波動逐漸增加.(2)正常人血糖波動幅度小,頻率高;T2DM餐後血糖波動幅度大,有效波動頻率低;(3)IFG組的血糖波動特徵最接近于NGT,而IGT組最接近于T2DM;(4)在糖尿病前期階段餐後血糖受損明顯早于空腹.
목적 연구불동당조절수손인군적동태혈당파동특정.방법 채용동태혈당감측계통(CGMS)근거련속2차구복포도당내량시험결과,선취은정인군중단순공복혈당수손(IFG)조12례,단순찬후혈당수손(IGT)조19례,공복혈당수손합병당내량저감(IFG/IGT)조11례,신진단2형당뇨병(T2DM)조21례,정상대조(NGT)조18례,분석기각항림상지표화CGMS동태혈당수거.결과 (1)일내혈당파동:NGT、IFG、IGT、IFG/IGT지T2DM조적최대혈당파동폭도(LAGE)、평균혈당(MBG)화혈당수평표준차(SDBG)의차승고.IGT조적평균혈당파동폭도(MAGE)(3.2±1.2)mmol/L교NGT조(1.6±0.5)mmol/L고,교T2DM조(5.2±1.9)mmol/L저(P<0.05);IFG/IGT적유효혈당파동빈솔(FGE)(5.5±2.5)차/d교NGT조(6.1±3.4)차/d저,교T2DM조(4.8±1.8)고.당뇨병전기3조간IGT조MAGE(3.2±1.2)mmol/L최고,FGE(4.9±1.8)최저.(2)일간혈당파동:여NGT조(0.8±0.3)mmo/L상비,IGT조(1.1±0.4)mmol/L、IFG/IGT조(1.2±0.4)mmol/L화T2DM조(2.0±1.0)mmol/L적일간혈당평균절대차의차승고(P<0.05).(3)불동당조절수손인군혈당파동특정:IFG조공복혈당수손정도최중,찬후고봉이IFG/IGT조위저.혈당수평곡선유저지고의차위NGT、IGT、IFG/IGT、IFG、T2DM조.(4)불동HbAlc수평적혈당파동:수시자HbAlc<7%시,공복혈당곡선궤호중합,찬후혈당곡선략미분개;HbAlc7.0%~7.9%시,찬후고봉명현상승;HbAlc≥8%시,공복곡선명현상이,찬후파동계속승고.결론 (1)수착당조절수손정도적가중,일내혈당파동급일간혈당파동축점증가.(2)정상인혈당파동폭도소,빈솔고;T2DM찬후혈당파동폭도대,유효파동빈솔저;(3)IFG조적혈당파동특정최접근우NGT,이IGT조최접근우T2DM;(4)재당뇨병전기계단찬후혈당수손명현조우공복.
Objective To investigate the characteristics of glycemic excursion of different subtypes of glucose tolerance. Methods Assessed by oral glucose tolerance test (OGTT) repeated twice, 81 individuals were divided into 4 groups: normal glucose tolerance (NGT, n=18), isolated impaired fasting glycemia (IFG, n=12), isolated impaired glucose tolerance (IGT, n=19), combined IFG/IGT (n=11), and newly diagnosed type 2 diabetes mellitus (T2DM, n=21). And then continuous glucose monitoring system (CGMS) was used for 72 hours to monitor the blood glucose (BG) level before drug intervention. Results (1) The levels of largest amplitude of glycemic excursions (LAGE), mean blood glucose (MBG), and standard deviation of mean level of blood glucose fluctuation (SDBG) increased gradually with the deterioration of glucose tolerance. The mean amplitude of glucose excursion (MAGE) readout of the IGT group was (3.2±1.2) mmol/L , significantly higher than that of the NGT group [(1.6±0.5) mmol/L, P<0.05], and significantly lower than that of the T2DM group [(5.2±1.9) mmol/L, P<0.05]. The level of frequency of glucose excursion (FGE) decreased along with the decrease of glucose tolerance: NGT group [(6.1±3.4)] > IGT/IFG group [(5.5±2.5)] > T2DM group [(4. 8±1.8)]. Among the three components of IGR, the IGT group showed highest MAGE (3.2±1.2) mmol/L and lowest FGE level (4.9±1.8). (2) The level of absolute mean of daily difference (MODD) increased in the following order: NGT group [(0.8±0.3) mmol/L], IGT group [(1.1±0.4) mmol/L], IFG/IGT group [(1.2±0.4) mmol/L], and T2DM group [(2.0±1.0) mmol/L] (all P<0.05). (3) The fasting glucose level deteriorated the most rapidly in the IFG group, while it reached the highest postprandial peak in the IFG/IGT group. The blood glucose curve increased along the order of NGT, I-IGT, IFG/IGT, IFG, and T2DM. (4) When the level of glycosylated hemoglobin (HbAlc) level was less than 7%, the fasting phase of curve virtually coincided with each other among individual groups with different HbAlc levels; however, the postprandial peak separated slightly. When the HbAlC level was between 7. 0% and 7.9% , the postprandial peaks of individual groups with different HbAlc levels dispersed markedly. When the HbAlc level was higher than 8% , the fasting blood glucose curve moved upwards significantly with increasing postprandial excursion. Conclusion (1) With the deterioration of glucose regulation, the intraday and day-to-day blood glucose excursions become increasingly fluctuant. (2) The amplitude of glycemic excursion is lower in the NGT group than in the T2DM group, however, the frequency of glycemic excursion is higher in the NGT subject than in the T2DM subjects. The glucose excursion profile of the IGR subjects is between the NGR and T2DM subjects. (3) The characteristics of glucose excursion of the IGT group are similar to those of the T2DM group, and the characteristics of the IFG group are similar to those of the NGT group. (4)The loss of postprandial glycemie control precedes evident deterioration in fasting phase of IGR.