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Section 2 Pancreatic   -Cells and Insulin Secretion in Type 2 Diabetes
 -Cell Adaptation and Failure: Opportunities for Prevention and Treatment of Type 2 Diabetes
Disclosure ,[object Object],[object Object],[object Object]
Hypothetical Relationships Determine Categories of Glucose Tolerance Adapted from Kahn SE et al.  Diabetes . 1993;42:1663-1672. Type 2 Diabetes Insulin sensitivity index (x10 -5  min -1 /pmol/L) AIRglucose  (pmol/L) IGT Normal 0 500 1,000 1,500 95th 75th 50th 25th 5th 0 2 4 6 8 10
Hypothetical Outcomes of Interventions to Treat Type 2 Diabetes Adapted from Kahn SE et al.  Diabetes . 1993;42:1663-1672. Type 2 Diabetes IGT Insulin sensitivity index (x10 -5  min -1 /pmol/L) Increased Insulin Secretion Normal Increased Insulin Sensitivity 0 500 1,000 1,500 95th 75th 50th 25th 5th 0 2 4 6 8 10 AIRglucose  (pmol/L)
Hypothetical Outcomes of Interventions to Prevent Type 2 Diabetes Adapted from Kahn SE et al.  Diabetes . 1993;42:1663-1672. 0 0 2 4 6 8 10 Type 2 Diabetes 95th 75th 50th 25th 5th 500 1,000 1,500 IGT Insulin sensitivity index (x10 -5  min -1 /pmol/L) Increased Insulin Sensitivity Increased Insulin Secretion Normal AIRglucose  (pmol/L)
Type 2 Diabetes:  Pathogenesis in a Nutshell ,[object Object],[object Object],[object Object],[object Object],Buchanan TA.  Clin Ther . 2003;25(suppl B):B32-B46. DeFronzo RA.  Med Clin North Am . 2004;88:787-835.  Kahn SE.  J Clin Endocrinol Metab . 2001;86:4047-4058.
Type 2 Diabetes: Pathogenesis in a Nutshell (cont.) ,[object Object],[object Object],[object Object],[object Object],Buchanan TA.  Clin Ther . 2003;25(suppl B):B32-B46. DeFronzo RA.  Med Clin North Am . 2004;88:787-835.  Kahn SE.  J Clin Endocrinol Metab . 2001;86:4047-4058.
Decreased   -Cell Function in Groups With Diabetes and at High Risk Insulin sensitivity index ( S i ; x10 -5  min -1 /pmol/L) Vidal J, Kahn SE. In: Lowe WL Jr, ed.  Genetics of Diabetes Mellitus . 2001:109-131. 0 1 2 3 4 5 6 7 0 100 200 300 400 500 600 700 50th 25th 75th 5th Relatives of  Patients With  Type 2 Diabetes PCOS  Women Former GDMs IGT Type 2 Diabetes Older Subjects AIRglucose  (pmol/L)
Short-term   -Cell Adaptation: Response to Pregnancy Insulin sensitivity index  (  mol/kg/min per pmol/L) Insulin  secretion  rate (pmol/min) Buchanan TA.  J Clin Endocrinol Metab . 2001;86:989-993. 0.3 400 800 600 200 0 0 0.2 0.1 0.4 3rd trimester Nonpregnant postpartum Gestational  Diabetes 1,000 Normal
Pathogenesis of Type 2 Diabetes:   -Cell Dysfunction vs Insulin Resistance  ,[object Object],[object Object],[object Object],Weyer C et al.  J Clin Invest . 1999;104:787-794.
Declining   -Cell Function:  Best Correlation of Progression Acute insulin  response (  U/mL) Weyer C et al.  J Clin Invest . 1999;104:787-794. EMBS=estimated metabolic body size 500 400 300 200 100 0 0 1 2 3 4 5 Measure of insulin resistance (mg/kg EMBS/min) Nonprogressors Progressors DIA IGT NGT NGT NGT NGT
Loss of   -Cell Function in People Who Develop Type 2 Diabetes: Longitudinal Data Insulin Action Insulin Secretion M-low (mg/kg EMBS/min) 0 1 2 3 4 NGT IGT Diabetes * AIR (  U/mL) * 0 50 100 150 200 250 300 NGT Diabetes † IGT * P <0.05;  † P <0.01 Adapted from Weyer C et al.  J Clin Invest . 1999;104:787-794. EMBS=estimated metabolic body size
Changing Glucose: Different Rates at Different Clinical Stages Ferrannini E et al.  Diabetes.  2004;53:160-165. Fasting plasma glucose  (mmol/L) Baseline 3.25 years 7 years 10 NGT  NGT    NGT NGT    D    D NGT    NGT    D IGT    D    D IGT    IGT    D 9 8 7 6 5 4 3
Functional Defects in   -Cells in the Development of Diabetes ,[object Object],[object Object],[object Object],[object Object]
UKPDS: Progressive Deterioration in Glycemic Control Over Time ,[object Object],Intensive Conventional Time from randomization (y) ,[object Object],[object Object],[object Object],[object Object],[object Object],Median A1C (%) ,[object Object],Years from diagnosis  -Cell function (%) 100 80 60 40 20 0 UKPDS Group.  Lancet . 1998;352:837-853. -12 -10 -8 -6 -4 -2 0 2 4 6 Holman RR.  Diabetes Res Clin Pract .  1998;40(suppl):S21-S25. 9 8 7 6 0
UKPDS: Progressive Deterioration in   -Cell Function Over Time Holman RR.  Diabetes Res Clin Pract . 1998;40(suppl):S21-S25.  -Cell function  (%) Years from diagnosis 100 80 60 40 20 0 -12 -10 -8 -6 -4 -2 0 2 4 6
Insulin and Glucose Patterns: Normal and Type 2 Diabetes  Polonsky KS et al.  N Engl J Med.  1988;318:1231-1239. 100 200 300 400 0600 1000 1800 1400 0200 2200 0600 Time of day 0600 1000 1800 1400 0200 2200 0600 Time of day 20 40 60 80 100 120 B L S B L S Normal Type 2 diabetes Glucose (mg/dL) Insulin (  U/mL) (meals) (meals)
Early Nutrient-Induced Insulin Secretion ,[object Object],[object Object],[object Object],[object Object]
Fasting Plasma Glucose and  the Acute Insulin Response Relative acute insulin response (% increase) Brunzell JD et al.  J Clin Endocrinol Metab . 1976;42:222-229. Time (min) 79–89 90–99 100–114 115–149 150–349 n 24 20 7 3 12 FPG (mg/dL) 800 600 400 200 0 -100 0 15 30 60 90 120
Acute Insulin Response to Glucose Time (min) Pfeifer MA et al.  Am J Med . 1981;70:579-588. Plasma IRI (  U/mL) Control (n=9) Type 2 Diabetes (n=9) =20g IV glucose 120 100 80 60 40 20 0 -30 0 30 -30 0 30 120 100 80 60 40 20 0 Plasma IRI (  U/mL) IRI=immunoreactive insulin
Acute Insulin Response to Arginine Ward WK et al.  J Clin Invest . 1984;74:1318-1328. Acute insulin response to arginine (  U/mL) Plasma glucose (mg/dL) 400 300 200 100 0 0 200 400 600 Controls (n=8) Type 2 diabetes (n=8)
Decreases in Insulin Response r=-0.58;  P =0.07 Røder ME et al.  J Clin Endocrinol Metab . 1998;83:604-608. AIR max (pmol/L) Fasting glucose (mmol/L) 0 4 8 12 16 20 0 200 400 600 800 1,000 Type 2 diabetes=9 Healthy subjects=10
Disproportionate Increase in Proinsulin in Patients With Type 2 Diabetes Ward WK et al.  Diabetologia . 1987;30:698-702. Basal   (%) PI IRI Controls (n=28) Type 2 diabetes (n=22) P <0.001 0 10 20 30 40 50 60 70
Mechanisms Responsible for Changes in   -Cell Function ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
 -Cell Mass in Normal Patients and Patients With Diabetes: Autopsy Study  -Cell  volume (%) Normal  Impaired Diabetes Normal  Diabetes Obese Lean 0 1 2 3 4 -   41% -   40% -63% * * † * P <0.05;  † P <0.01  Butler AE et al.  Diabetes.  2003;52:102-110.
Altered   -Cell Mass and Function in Islets From Subjects With Type 2 Diabetes 0 1,000 2,000 3,000 4,000 5,000 6,000 7,000 8,000 9,000 Control (n=14) Type 2  diabetes (n=14) Islet mass (IEq/g pancreas) GSIR=glucose-stimulated insulin release Deng S et al.  Diabetes.  2004;53:624-632. 0 0.5 1.0 1.5 2.0 2.5 3.0 3.5 4.0 Control (n=14) Type 2  diabetes (n=14) GSIR (ng/min/100 islets)  -Cell Mass  -Cell Function * P <0.001;  † P <0.05  * †
Potential Causes for Falling Insulin Secretion: Glucolipotoxicity ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Potential Causes for Falling Insulin Secretion: Glucolipotoxicity (cont.) ,[object Object],[object Object],[object Object],[object Object]
Role of Islet Amyloid in   -Cell Dysfunction ,[object Object],[object Object],[object Object],[object Object],[object Object],Kahn SE et al.  Diabetes . 1999;48:241-253.
Amyloid Deposits in Pancreatic Islets in Type 2 Diabetes Verchere CB et al.  Proc Natl Acad Sci USA . 1996;93:3492-3496. Amyloid deposits in pancreatic islets of human with type 2 diabetes 50  m

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Ndei Beta Cell Slide Kit Insulin Secretion

  • 1. Section 2 Pancreatic  -Cells and Insulin Secretion in Type 2 Diabetes
  • 2.  -Cell Adaptation and Failure: Opportunities for Prevention and Treatment of Type 2 Diabetes
  • 3.
  • 4. Hypothetical Relationships Determine Categories of Glucose Tolerance Adapted from Kahn SE et al. Diabetes . 1993;42:1663-1672. Type 2 Diabetes Insulin sensitivity index (x10 -5 min -1 /pmol/L) AIRglucose (pmol/L) IGT Normal 0 500 1,000 1,500 95th 75th 50th 25th 5th 0 2 4 6 8 10
  • 5. Hypothetical Outcomes of Interventions to Treat Type 2 Diabetes Adapted from Kahn SE et al. Diabetes . 1993;42:1663-1672. Type 2 Diabetes IGT Insulin sensitivity index (x10 -5 min -1 /pmol/L) Increased Insulin Secretion Normal Increased Insulin Sensitivity 0 500 1,000 1,500 95th 75th 50th 25th 5th 0 2 4 6 8 10 AIRglucose (pmol/L)
  • 6. Hypothetical Outcomes of Interventions to Prevent Type 2 Diabetes Adapted from Kahn SE et al. Diabetes . 1993;42:1663-1672. 0 0 2 4 6 8 10 Type 2 Diabetes 95th 75th 50th 25th 5th 500 1,000 1,500 IGT Insulin sensitivity index (x10 -5 min -1 /pmol/L) Increased Insulin Sensitivity Increased Insulin Secretion Normal AIRglucose (pmol/L)
  • 7.
  • 8.
  • 9. Decreased  -Cell Function in Groups With Diabetes and at High Risk Insulin sensitivity index ( S i ; x10 -5 min -1 /pmol/L) Vidal J, Kahn SE. In: Lowe WL Jr, ed. Genetics of Diabetes Mellitus . 2001:109-131. 0 1 2 3 4 5 6 7 0 100 200 300 400 500 600 700 50th 25th 75th 5th Relatives of Patients With Type 2 Diabetes PCOS Women Former GDMs IGT Type 2 Diabetes Older Subjects AIRglucose (pmol/L)
  • 10. Short-term  -Cell Adaptation: Response to Pregnancy Insulin sensitivity index (  mol/kg/min per pmol/L) Insulin secretion rate (pmol/min) Buchanan TA. J Clin Endocrinol Metab . 2001;86:989-993. 0.3 400 800 600 200 0 0 0.2 0.1 0.4 3rd trimester Nonpregnant postpartum Gestational Diabetes 1,000 Normal
  • 11.
  • 12. Declining  -Cell Function: Best Correlation of Progression Acute insulin response (  U/mL) Weyer C et al. J Clin Invest . 1999;104:787-794. EMBS=estimated metabolic body size 500 400 300 200 100 0 0 1 2 3 4 5 Measure of insulin resistance (mg/kg EMBS/min) Nonprogressors Progressors DIA IGT NGT NGT NGT NGT
  • 13. Loss of  -Cell Function in People Who Develop Type 2 Diabetes: Longitudinal Data Insulin Action Insulin Secretion M-low (mg/kg EMBS/min) 0 1 2 3 4 NGT IGT Diabetes * AIR (  U/mL) * 0 50 100 150 200 250 300 NGT Diabetes † IGT * P <0.05; † P <0.01 Adapted from Weyer C et al. J Clin Invest . 1999;104:787-794. EMBS=estimated metabolic body size
  • 14. Changing Glucose: Different Rates at Different Clinical Stages Ferrannini E et al. Diabetes. 2004;53:160-165. Fasting plasma glucose (mmol/L) Baseline 3.25 years 7 years 10 NGT  NGT  NGT NGT  D  D NGT  NGT  D IGT  D  D IGT  IGT  D 9 8 7 6 5 4 3
  • 15.
  • 16.
  • 17. UKPDS: Progressive Deterioration in  -Cell Function Over Time Holman RR. Diabetes Res Clin Pract . 1998;40(suppl):S21-S25.  -Cell function (%) Years from diagnosis 100 80 60 40 20 0 -12 -10 -8 -6 -4 -2 0 2 4 6
  • 18. Insulin and Glucose Patterns: Normal and Type 2 Diabetes Polonsky KS et al. N Engl J Med. 1988;318:1231-1239. 100 200 300 400 0600 1000 1800 1400 0200 2200 0600 Time of day 0600 1000 1800 1400 0200 2200 0600 Time of day 20 40 60 80 100 120 B L S B L S Normal Type 2 diabetes Glucose (mg/dL) Insulin (  U/mL) (meals) (meals)
  • 19.
  • 20. Fasting Plasma Glucose and the Acute Insulin Response Relative acute insulin response (% increase) Brunzell JD et al. J Clin Endocrinol Metab . 1976;42:222-229. Time (min) 79–89 90–99 100–114 115–149 150–349 n 24 20 7 3 12 FPG (mg/dL) 800 600 400 200 0 -100 0 15 30 60 90 120
  • 21. Acute Insulin Response to Glucose Time (min) Pfeifer MA et al. Am J Med . 1981;70:579-588. Plasma IRI (  U/mL) Control (n=9) Type 2 Diabetes (n=9) =20g IV glucose 120 100 80 60 40 20 0 -30 0 30 -30 0 30 120 100 80 60 40 20 0 Plasma IRI (  U/mL) IRI=immunoreactive insulin
  • 22. Acute Insulin Response to Arginine Ward WK et al. J Clin Invest . 1984;74:1318-1328. Acute insulin response to arginine (  U/mL) Plasma glucose (mg/dL) 400 300 200 100 0 0 200 400 600 Controls (n=8) Type 2 diabetes (n=8)
  • 23. Decreases in Insulin Response r=-0.58; P =0.07 Røder ME et al. J Clin Endocrinol Metab . 1998;83:604-608. AIR max (pmol/L) Fasting glucose (mmol/L) 0 4 8 12 16 20 0 200 400 600 800 1,000 Type 2 diabetes=9 Healthy subjects=10
  • 24. Disproportionate Increase in Proinsulin in Patients With Type 2 Diabetes Ward WK et al. Diabetologia . 1987;30:698-702. Basal (%) PI IRI Controls (n=28) Type 2 diabetes (n=22) P <0.001 0 10 20 30 40 50 60 70
  • 25.
  • 26.  -Cell Mass in Normal Patients and Patients With Diabetes: Autopsy Study  -Cell volume (%) Normal Impaired Diabetes Normal Diabetes Obese Lean 0 1 2 3 4 - 41% - 40% -63% * * † * P <0.05; † P <0.01 Butler AE et al. Diabetes. 2003;52:102-110.
  • 27. Altered  -Cell Mass and Function in Islets From Subjects With Type 2 Diabetes 0 1,000 2,000 3,000 4,000 5,000 6,000 7,000 8,000 9,000 Control (n=14) Type 2 diabetes (n=14) Islet mass (IEq/g pancreas) GSIR=glucose-stimulated insulin release Deng S et al. Diabetes. 2004;53:624-632. 0 0.5 1.0 1.5 2.0 2.5 3.0 3.5 4.0 Control (n=14) Type 2 diabetes (n=14) GSIR (ng/min/100 islets)  -Cell Mass  -Cell Function * P <0.001; † P <0.05 * †
  • 28.
  • 29.
  • 30.
  • 31. Amyloid Deposits in Pancreatic Islets in Type 2 Diabetes Verchere CB et al. Proc Natl Acad Sci USA . 1996;93:3492-3496. Amyloid deposits in pancreatic islets of human with type 2 diabetes 50  m

Hinweis der Redaktion

  1. Pancreatic  -Cells and Insulin Secretion in Type 2 Diabetes This section focuses on the pathophysiology of  -cells in type 2 diabetes.