中华内分泌代谢杂志
中華內分泌代謝雜誌
중화내분비대사잡지
CHINESE JOURNAL OF ENDOCRINOLOGY AND METABOLISM
2014年
8期
678-681
,共4页
瞿华%刘强%胡振平%王行%邓敏%魏慧丽%邓华聪
瞿華%劉彊%鬍振平%王行%鄧敏%魏慧麗%鄧華聰
구화%류강%호진평%왕행%산민%위혜려%산화총
分泌型卷曲相关蛋白5%肥胖症%糖尿病,2型%炎症
分泌型捲麯相關蛋白5%肥胖癥%糖尿病,2型%炎癥
분비형권곡상관단백5%비반증%당뇨병,2형%염증
Secreted frizzled-related protein5%Obesity%Diabetes mellitus,type 2%Inflammation
本研究旨在探讨脂肪因子分泌型卷曲相关蛋白5(sfrp5)与体脂参数、糖脂代谢、胰岛素抵抗及炎症的关系。89例正常糖耐量者及87例新诊断2型糖尿病患者,根据2000年世界卫生组织推荐的亚洲成年人肥胖诊断标准,各分为非肥胖和肥胖亚组。测量体脂参数,计算体重指数、腰臀比。检测血糖、血脂指标及空腹胰岛素水平,计算稳态模型评估的胰岛素抵抗指数( HOMA-IR)。用酶联免疫吸附测定血浆sfrp5和白细胞介素6的含量。结果显示血浆sfrp5含量在2型糖尿病组中低于正常糖耐量组[(8.35±3.38对11.35±3.69)ng/ml, P<0.01],正常糖耐量组和2型糖尿病组内肥胖者均低于非肥胖者[(9.46±2.70对13.12±3.62)ng/ml和(6.70±2.34对10.12±3.45)ng/ml,均P<0.01],且2型糖尿病-肥胖组明显低于正常糖耐量-肥胖组(P<0.01)。(2)相关分析显示血浆sfrp5水平与腰臀比、HbA1C、空腹胰岛素、甘油三酯、腰围、空腹血糖、白细胞介素6、ln(HOMA-IR)及体重指数均呈负相关(P<0.01或P<0.05)。(3)多元逐步回归分析发现血浆 sfrp5水平与 ln(HOMA-IR)、体重指数、甘油三酯独立相关(r2=0.216、0.177、0.113,均P<0.05)。 sfrp5在肥胖及2型糖尿病者中表达明显降低,且与体脂分布、糖脂代谢、胰岛素抵抗及炎症相关;sfrp5可能参与了肥胖及2型糖尿病的病理生理过程。
本研究旨在探討脂肪因子分泌型捲麯相關蛋白5(sfrp5)與體脂參數、糖脂代謝、胰島素牴抗及炎癥的關繫。89例正常糖耐量者及87例新診斷2型糖尿病患者,根據2000年世界衛生組織推薦的亞洲成年人肥胖診斷標準,各分為非肥胖和肥胖亞組。測量體脂參數,計算體重指數、腰臀比。檢測血糖、血脂指標及空腹胰島素水平,計算穩態模型評估的胰島素牴抗指數( HOMA-IR)。用酶聯免疫吸附測定血漿sfrp5和白細胞介素6的含量。結果顯示血漿sfrp5含量在2型糖尿病組中低于正常糖耐量組[(8.35±3.38對11.35±3.69)ng/ml, P<0.01],正常糖耐量組和2型糖尿病組內肥胖者均低于非肥胖者[(9.46±2.70對13.12±3.62)ng/ml和(6.70±2.34對10.12±3.45)ng/ml,均P<0.01],且2型糖尿病-肥胖組明顯低于正常糖耐量-肥胖組(P<0.01)。(2)相關分析顯示血漿sfrp5水平與腰臀比、HbA1C、空腹胰島素、甘油三酯、腰圍、空腹血糖、白細胞介素6、ln(HOMA-IR)及體重指數均呈負相關(P<0.01或P<0.05)。(3)多元逐步迴歸分析髮現血漿 sfrp5水平與 ln(HOMA-IR)、體重指數、甘油三酯獨立相關(r2=0.216、0.177、0.113,均P<0.05)。 sfrp5在肥胖及2型糖尿病者中錶達明顯降低,且與體脂分佈、糖脂代謝、胰島素牴抗及炎癥相關;sfrp5可能參與瞭肥胖及2型糖尿病的病理生理過程。
본연구지재탐토지방인자분비형권곡상관단백5(sfrp5)여체지삼수、당지대사、이도소저항급염증적관계。89례정상당내량자급87례신진단2형당뇨병환자,근거2000년세계위생조직추천적아주성년인비반진단표준,각분위비비반화비반아조。측량체지삼수,계산체중지수、요둔비。검측혈당、혈지지표급공복이도소수평,계산은태모형평고적이도소저항지수( HOMA-IR)。용매련면역흡부측정혈장sfrp5화백세포개소6적함량。결과현시혈장sfrp5함량재2형당뇨병조중저우정상당내량조[(8.35±3.38대11.35±3.69)ng/ml, P<0.01],정상당내량조화2형당뇨병조내비반자균저우비비반자[(9.46±2.70대13.12±3.62)ng/ml화(6.70±2.34대10.12±3.45)ng/ml,균P<0.01],차2형당뇨병-비반조명현저우정상당내량-비반조(P<0.01)。(2)상관분석현시혈장sfrp5수평여요둔비、HbA1C、공복이도소、감유삼지、요위、공복혈당、백세포개소6、ln(HOMA-IR)급체중지수균정부상관(P<0.01혹P<0.05)。(3)다원축보회귀분석발현혈장 sfrp5수평여 ln(HOMA-IR)、체중지수、감유삼지독립상관(r2=0.216、0.177、0.113,균P<0.05)。 sfrp5재비반급2형당뇨병자중표체명현강저,차여체지분포、당지대사、이도소저항급염증상관;sfrp5가능삼여료비반급2형당뇨병적병리생리과정。
To investigate the relationships among plasma secreted frizzled-related protein ( sfrp) 5 level and body fat parameters, glucolipid metabolism, insulin resistance index, and inflammation. 89 subjects with normal glucose tolerance(NGT) and 87 patients with type 2 diabetes mellitus (T2DM) were enrolled and each group was divided into no-obese and obese subgroups. Obesity was defined as body mass index ( BMI)≥25 kg/m2 according to the World Health Organization -Western Pacific Region diagnostic criteria ( 2000 ) . Body fat parameters were measured and BMI, waist-hip ratio were evaluated, meanwhile, the levels of blood glucose-lipid parameters and fasting insulin were also determined. Insulin resistance index ( IR) was assessed by homeostasis model assessment ( HOMA) . The concentrations of plasma sfrp5 and interleukin 6 were detected by enzyme-linked immunosorbent assay. Plasma sfrp5 level in T2DM group was significantly lower than that in NGT group [(8. 35±3. 38 vs 11. 35±3. 69)ng/ml, P<0. 01]. The levels of plasma sfrp5 in subjects with obesity were also lower than those in subjects with no-obesity in both NGT and T2DM groups [(9. 46±2. 70 vs 13. 12±3. 62)ng/ml and(6. 70±2. 34 vs 10. 12±3. 45) ng/ml, both P<0. 01]. Plasma concentrations of sfrp5 in T2DM-obese group were significantly lower than that in NGT-obese group(P<0. 01). Correlation analysis showed that plasma sfrp5 levels were negatively correlated with waist-hip ratio, HbA1C, fasting insulin, triglycerides, waist circumference, fasting plasma glucose, interleukin 6, natural logarithm of HOMA-IR [ln(HOMA-IR)], and BMI(P<0. 01 or P<0. 05). Multiple linear regression showed that ln(HOMA-IR), BMI, triglycerides were independent related factors in influencing the levels of plasma sfrp5 (r2=0. 216, 0. 177, 0. 113, all P<0. 05). Plasma sfrp5 levels were decreased in obesity and T2DM subjects and were correlated with body fat disposition, glucose-lipid metabolism, insulin resistance and inflammation. Lack of sfrp5 may contribute to the pathophysiology of obesity and T2DM.