Skip to main content
Erschienen in: Diabetologia 5/2004

01.05.2004 | Review

Control of glycaemia: from molecules to men. Minkowski Lecture 2003

verfasst von: M. Stumvoll

Erschienen in: Diabetologia | Ausgabe 5/2004

Einloggen, um Zugang zu erhalten

Abstract

Regulation of glycaemia represents a fundamental biological principle, and its failure underlies Type 2 diabetes. The complex aetiology of Type 2 diabetes, which probably involves a medley of molecular mechanisms, requires dissection out of diabetes-associated subphenotypes, such as the non-obese with increased liver fat or the obese with low plasma adiponectin. The concepts of the hyperbolic relationship of insulin secretion and insulin sensitivity with glucose allostasis help us to establish the pathophysiological framework within which such mechanisms must operate. The translation of burgeoning new basic science findings into a physiological and clinical context calls for novel and imaginative clinical experimental tools. For the purpose of this review, four molecules (adiponectin [APM1], stearoyl CoA desaturase-1 [SCD1], insulin receptor substrate-1 [IRS1], peroxisome proliferator-activated receptor-γ [PPARG]), each with a plausible role in the disease process, have been selected to illustrate the use of such techniques in humans. These include procedures as diverse as isotope dilution for turnover studies (e.g. glycerol turnover as a proxy for lipolysis), conventional and modified clamp procedures, association studies of functionally relevant single nucleotide polymorphisms in candidate genes (e.g. IRS-1 and PPARγ), multivariate correlational analyses (as with plasma adiponectin), magnetic resonance spectroscopy to quantify intra-tissue lipid deposition and regional fat distribution, and gas chromatography to determine fatty acid patterns in selected lipid fractions as proxy for intrahepatic enzyme activity. A concerted effort by scientists from many disciplines (genetics and cell biology, physiology and epidemiology) will be required to bridge the growing gap between basic scientific concepts of biological modifiers of glycaemia and concepts that are truly relevant for human Type 2 diabetes.
Literatur
1.
Zurück zum Zitat Fajans SS, Bell GI, Polonsky KS (2001) Molecular mechanisms and clinical pathophysiology of maturity-onset diabetes of the young. N Engl J Med 345:971–980PubMed Fajans SS, Bell GI, Polonsky KS (2001) Molecular mechanisms and clinical pathophysiology of maturity-onset diabetes of the young. N Engl J Med 345:971–980PubMed
2.
Zurück zum Zitat Maassen JA, Kadowaki T (1996) Maternally inherited diabetes and deafness: a new diabetes subtype. Diabetologia 39:375–382CrossRefPubMed Maassen JA, Kadowaki T (1996) Maternally inherited diabetes and deafness: a new diabetes subtype. Diabetologia 39:375–382CrossRefPubMed
3.
Zurück zum Zitat Pozzilli P, Di Mario U (2001) Autoimmune diabetes not requiring insulin at diagnosis (latent autoimmune diabetes of the adult): definition, characterization, and potential prevention. Diabetes Care 24:1460–1467PubMed Pozzilli P, Di Mario U (2001) Autoimmune diabetes not requiring insulin at diagnosis (latent autoimmune diabetes of the adult): definition, characterization, and potential prevention. Diabetes Care 24:1460–1467PubMed
4.
Zurück zum Zitat Bergman RN, Phillips LS, Cobelli C (1981) Physiologic evaluation of factors controlling glucose tolerance in man: measurement of insulin sensitivity and beta-cell glucose sensitivity from the response to intravenous glucose. J Clin Invest 68:1456–1467PubMed Bergman RN, Phillips LS, Cobelli C (1981) Physiologic evaluation of factors controlling glucose tolerance in man: measurement of insulin sensitivity and beta-cell glucose sensitivity from the response to intravenous glucose. J Clin Invest 68:1456–1467PubMed
5.
Zurück zum Zitat Bergman RN, Ader M, Huecking K et al. (2002) Accurate assessment of beta-cell function: the hyperbolic correction. Diabetes 51 [Suppl 1]:S212–S220 Bergman RN, Ader M, Huecking K et al. (2002) Accurate assessment of beta-cell function: the hyperbolic correction. Diabetes 51 [Suppl 1]:S212–S220
6.
Zurück zum Zitat Kahn SE, Prigeon RL, McCulloch DK et al. (1993) Quantification of the relationship between insulin sensitivity and beta-cell function in human subjects. Evidence for a hyperbolic function. Diabetes 42:1663–1672PubMed Kahn SE, Prigeon RL, McCulloch DK et al. (1993) Quantification of the relationship between insulin sensitivity and beta-cell function in human subjects. Evidence for a hyperbolic function. Diabetes 42:1663–1672PubMed
7.
Zurück zum Zitat Bergman RN (1989) Lilly lecture 1989. Toward physiological understanding of glucose tolerance. Minimal-model approach. Diabetes 38:1512–1527PubMed Bergman RN (1989) Lilly lecture 1989. Toward physiological understanding of glucose tolerance. Minimal-model approach. Diabetes 38:1512–1527PubMed
8.
Zurück zum Zitat Stumvoll M, Tataranni PA, Stefan N et al. (2003) Glucose allostasis. Diabetes 52:903–909PubMed Stumvoll M, Tataranni PA, Stefan N et al. (2003) Glucose allostasis. Diabetes 52:903–909PubMed
9.
Zurück zum Zitat Cannon WB (1929) Organization for physiological homeostasis. Physiol Rev 9:399–431 Cannon WB (1929) Organization for physiological homeostasis. Physiol Rev 9:399–431
10.
Zurück zum Zitat Sterling P, Eyer J (1988) Allostasis: a new paradigm to explain arousal pathology. In: Fisher S, Reason J (eds) Handbook of life stress, cognition and health. Wiley, New York, pp 629–649 Sterling P, Eyer J (1988) Allostasis: a new paradigm to explain arousal pathology. In: Fisher S, Reason J (eds) Handbook of life stress, cognition and health. Wiley, New York, pp 629–649
11.
Zurück zum Zitat McEwen BS (1998) Protective and damaging effects of stress mediators. N Engl J Med 338:171–179 McEwen BS (1998) Protective and damaging effects of stress mediators. N Engl J Med 338:171–179
12.
Zurück zum Zitat Seeman TE, McEwen BS, Rowe JW et al. (2001) Allostatic load as a marker of cumulative biological risk: MacArthur studies of successful aging. Proc Natl Acad Sci USA 98:4770–4775CrossRefPubMed Seeman TE, McEwen BS, Rowe JW et al. (2001) Allostatic load as a marker of cumulative biological risk: MacArthur studies of successful aging. Proc Natl Acad Sci USA 98:4770–4775CrossRefPubMed
13.
Zurück zum Zitat Goldstein DS, McEwen B (2002) Allostasis, homeostats, and the nature of stress. Stress 5:55–58CrossRefPubMed Goldstein DS, McEwen B (2002) Allostasis, homeostats, and the nature of stress. Stress 5:55–58CrossRefPubMed
14.
Zurück zum Zitat Goran MI, Gower BA (2001) Longitudinal study on pubertal insulin resistance. Diabetes 50:2444–2450PubMed Goran MI, Gower BA (2001) Longitudinal study on pubertal insulin resistance. Diabetes 50:2444–2450PubMed
15.
Zurück zum Zitat Montague CT, O’Rahilly S (2000) The perils of portliness: causes and consequences of visceral adiposity. Diabetes 49:883–888 Montague CT, O’Rahilly S (2000) The perils of portliness: causes and consequences of visceral adiposity. Diabetes 49:883–888
16.
Zurück zum Zitat Seppala-Lindroos A, Vehkavaara S, Hakkinen AM et al. (2002) Fat accumulation in the liver is associated with defects in insulin suppression of glucose production and serum free fatty acids independent of obesity in normal men. J Clin Endocrinol Metab 87:3023–3028 Seppala-Lindroos A, Vehkavaara S, Hakkinen AM et al. (2002) Fat accumulation in the liver is associated with defects in insulin suppression of glucose production and serum free fatty acids independent of obesity in normal men. J Clin Endocrinol Metab 87:3023–3028
17.
Zurück zum Zitat Thamer C, Machann J, Bachmann O et al. (2003) Intramyocellular lipids: anthropometric determinants and relationships with maximal aerobic capacity and insulin sensitivity. J Clin Endocrinol Metab 88:1785–1791CrossRefPubMed Thamer C, Machann J, Bachmann O et al. (2003) Intramyocellular lipids: anthropometric determinants and relationships with maximal aerobic capacity and insulin sensitivity. J Clin Endocrinol Metab 88:1785–1791CrossRefPubMed
18.
Zurück zum Zitat Medici F, Hawa M, Pyke DA et al. (1999) Concordance rate for type II diabetes mellitus in monozygotic twins: actuarial analysis. Diabetologia 42:146–150PubMed Medici F, Hawa M, Pyke DA et al. (1999) Concordance rate for type II diabetes mellitus in monozygotic twins: actuarial analysis. Diabetologia 42:146–150PubMed
19.
Zurück zum Zitat Poulsen P, Kyvik KO, Vaag A et al. (1999) Heritability of type II (non-insulin-dependent) diabetes mellitus and abnormal glucose tolerance—a population-based twin study. Diabetologia 42:139–145 Poulsen P, Kyvik KO, Vaag A et al. (1999) Heritability of type II (non-insulin-dependent) diabetes mellitus and abnormal glucose tolerance—a population-based twin study. Diabetologia 42:139–145
20.
Zurück zum Zitat Lehtovirta M, Kaprio J, Forsblom C et al. (2000) Insulin sensitivity and insulin secretion in monozygotic and dizygotic twins. Diabetologia 43:285–293 Lehtovirta M, Kaprio J, Forsblom C et al. (2000) Insulin sensitivity and insulin secretion in monozygotic and dizygotic twins. Diabetologia 43:285–293
21.
Zurück zum Zitat Lander ES, Schork NJ (1994) Genetic dissection of complex traits. Science 265:2037–2048PubMed Lander ES, Schork NJ (1994) Genetic dissection of complex traits. Science 265:2037–2048PubMed
22.
Zurück zum Zitat Hanis CL, Boerwinkle E, Chakraborty R et al. (1996) A genome-wide search for human non-insulin-dependent (Type 2) diabetes genes reveals a major susceptibility locus on chromosome 2. Nat Genet 13:161–166PubMed Hanis CL, Boerwinkle E, Chakraborty R et al. (1996) A genome-wide search for human non-insulin-dependent (Type 2) diabetes genes reveals a major susceptibility locus on chromosome 2. Nat Genet 13:161–166PubMed
23.
Zurück zum Zitat Permutt AM, Bernal-Mizrachi E, Inoue H (2000) Calpain 10: the first positional cloning of a gene for Type 2 diabetes. J Clin Invest 106:819–821PubMed Permutt AM, Bernal-Mizrachi E, Inoue H (2000) Calpain 10: the first positional cloning of a gene for Type 2 diabetes. J Clin Invest 106:819–821PubMed
24.
Zurück zum Zitat Ma H, Fukiage C, Kim YH et al. (2001) Characterization and expression of calpain 10. A novel ubiquitous calpain with nuclear localization. J Biol Chem 276:28525–28531CrossRefPubMed Ma H, Fukiage C, Kim YH et al. (2001) Characterization and expression of calpain 10. A novel ubiquitous calpain with nuclear localization. J Biol Chem 276:28525–28531CrossRefPubMed
25.
Zurück zum Zitat Baier LJ, Permana PA, Yang X et al. (2000) A calpain-10 gene polymorphism is associated with reduced muscle mRNA levels and insulin resistance. J Clin Invest 106:R69–R73PubMed Baier LJ, Permana PA, Yang X et al. (2000) A calpain-10 gene polymorphism is associated with reduced muscle mRNA levels and insulin resistance. J Clin Invest 106:R69–R73PubMed
26.
Zurück zum Zitat Oral EA, Simha V, Ruiz E et al. (2002) Leptin-replacement therapy for lipodystrophy. N Engl J Med 346:570–578PubMed Oral EA, Simha V, Ruiz E et al. (2002) Leptin-replacement therapy for lipodystrophy. N Engl J Med 346:570–578PubMed
27.
Zurück zum Zitat Weyer C, Funahashi T, Tanaka S et al. (2001) Hypoadiponectinemia in obesity and Type 2 diabetes: close association with insulin resistance and hyperinsulinemia. J Clin Endocrinol Metab 86:1930–1935PubMed Weyer C, Funahashi T, Tanaka S et al. (2001) Hypoadiponectinemia in obesity and Type 2 diabetes: close association with insulin resistance and hyperinsulinemia. J Clin Endocrinol Metab 86:1930–1935PubMed
28.
Zurück zum Zitat Takahashi M, Arita Y, Yamagata K et al. (2000) Genomic structure and mutations in adipose-specific gene, adiponectin. Int J Obes Relat Metab Disord 24:861–868PubMed Takahashi M, Arita Y, Yamagata K et al. (2000) Genomic structure and mutations in adipose-specific gene, adiponectin. Int J Obes Relat Metab Disord 24:861–868PubMed
29.
Zurück zum Zitat Yang WS, Lee WJ, Funahashi T et al. (2001) Weight reduction increases plasma levels of an adipose-derived anti-inflammatory protein, adiponectin. J Clin Endocrinol Metab 86:3815–3819PubMed Yang WS, Lee WJ, Funahashi T et al. (2001) Weight reduction increases plasma levels of an adipose-derived anti-inflammatory protein, adiponectin. J Clin Endocrinol Metab 86:3815–3819PubMed
30.
Zurück zum Zitat Lindsay RS, Funahashi T, Hanson RL et al. (2002) Adiponectin and development of Type 2 diabetes in the Pima Indian population. Lancet 360:57–58CrossRefPubMed Lindsay RS, Funahashi T, Hanson RL et al. (2002) Adiponectin and development of Type 2 diabetes in the Pima Indian population. Lancet 360:57–58CrossRefPubMed
31.
Zurück zum Zitat Spranger J, Kroke A, Mohlig M et al. (2003) Adiponectin and protection against Type 2 diabetes mellitus. Lancet 361:226–228CrossRef Spranger J, Kroke A, Mohlig M et al. (2003) Adiponectin and protection against Type 2 diabetes mellitus. Lancet 361:226–228CrossRef
32.
Zurück zum Zitat Yamauchi T, Kamon J, Waki H et al. (2001) The fat-derived hormone adiponectin reverses insulin resistance associated with both lipoatrophy and obesity. Nat Med 7:941–946PubMed Yamauchi T, Kamon J, Waki H et al. (2001) The fat-derived hormone adiponectin reverses insulin resistance associated with both lipoatrophy and obesity. Nat Med 7:941–946PubMed
33.
Zurück zum Zitat Combs TP, Pajvani UB, Berg AH et al. (2004) A transgenic mouse with a deletion in the collagenous domain of adiponectin displays elevated circulating adiponectin and improved insulin sensitivity. Endocrinology 145:367–383CrossRefPubMed Combs TP, Pajvani UB, Berg AH et al. (2004) A transgenic mouse with a deletion in the collagenous domain of adiponectin displays elevated circulating adiponectin and improved insulin sensitivity. Endocrinology 145:367–383CrossRefPubMed
34.
Zurück zum Zitat Tschritter O, Fritsche A, Thamer C et al. (2003) Plasma adiponectin concentrations predict insulin sensitivity of both glucose and lipid metabolism. Diabetes 52:239–243PubMed Tschritter O, Fritsche A, Thamer C et al. (2003) Plasma adiponectin concentrations predict insulin sensitivity of both glucose and lipid metabolism. Diabetes 52:239–243PubMed
35.
Zurück zum Zitat Combs TP, Berg AH, Obici S et al. (2001) Endogenous glucose production is inhibited by the adipose-derived protein Acrp30. J Clin Invest 108:1875–1881PubMed Combs TP, Berg AH, Obici S et al. (2001) Endogenous glucose production is inhibited by the adipose-derived protein Acrp30. J Clin Invest 108:1875–1881PubMed
36.
Zurück zum Zitat Stefan N, Stumvoll M, Vozarova B et al. (2003) Plasma adiponectin and endogenous glucose production in humans. Diabetes Care 26:3315–3319PubMed Stefan N, Stumvoll M, Vozarova B et al. (2003) Plasma adiponectin and endogenous glucose production in humans. Diabetes Care 26:3315–3319PubMed
37.
Zurück zum Zitat Stumvoll M, Tschritter O, Fritsche A et al. (2002) Association of the T-G polymorphism in adiponectin (exon 2) with obesity and insulin sensitivity. Interaction with family history of diabetes. Diabetes 51:37–42PubMed Stumvoll M, Tschritter O, Fritsche A et al. (2002) Association of the T-G polymorphism in adiponectin (exon 2) with obesity and insulin sensitivity. Interaction with family history of diabetes. Diabetes 51:37–42PubMed
38.
Zurück zum Zitat Yamauchi T, Kamon J, Ito Y et al. (2003) Cloning of adiponectin receptors that mediate antidiabetic metabolic effects. Nature 423:762–769CrossRefPubMed Yamauchi T, Kamon J, Ito Y et al. (2003) Cloning of adiponectin receptors that mediate antidiabetic metabolic effects. Nature 423:762–769CrossRefPubMed
39.
Zurück zum Zitat Cohen P, Miyazaki M, Socci ND et al. (2002) Role for stearoyl-CoA desaturase-1 in leptin-mediated weight loss. Science 297:240–243CrossRefPubMed Cohen P, Miyazaki M, Socci ND et al. (2002) Role for stearoyl-CoA desaturase-1 in leptin-mediated weight loss. Science 297:240–243CrossRefPubMed
40.
Zurück zum Zitat Zhang Y, Wat N, Stratton IM et al. (1996) UKPDS 19: heterogeneity in NIDDM: separate contributions of IRS-1 and beta 3-adrenergic-receptor mutations to insulin resistance and obesity respectively with no evidence for glycogen synthase gene mutations. UK Prospective Diabetes Study. Diabetologia 39:1505–1511PubMed Zhang Y, Wat N, Stratton IM et al. (1996) UKPDS 19: heterogeneity in NIDDM: separate contributions of IRS-1 and beta 3-adrenergic-receptor mutations to insulin resistance and obesity respectively with no evidence for glycogen synthase gene mutations. UK Prospective Diabetes Study. Diabetologia 39:1505–1511PubMed
41.
Zurück zum Zitat Koch M, Rett K, Volk A et al. (1999) Amino acid polymorphism Gly 972 Arg in IRS-1 is not associated to lower clamp-derived insulin sensitivity in young healthy first degree relatives of patients with Type 2 diabetes. Exp Clin Endocrinol Diabetes 107:318–322PubMed Koch M, Rett K, Volk A et al. (1999) Amino acid polymorphism Gly 972 Arg in IRS-1 is not associated to lower clamp-derived insulin sensitivity in young healthy first degree relatives of patients with Type 2 diabetes. Exp Clin Endocrinol Diabetes 107:318–322PubMed
42.
Zurück zum Zitat Hager J, Zouali H, Velho G et al. (1993) Insulin receptor substrate (IRS-1) gene polymorphisms in French NIDDM families. Lancet 342:1430–1430 Hager J, Zouali H, Velho G et al. (1993) Insulin receptor substrate (IRS-1) gene polymorphisms in French NIDDM families. Lancet 342:1430–1430
43.
Zurück zum Zitat Imai Y, Philippe N, Sesti G et al. (1997) Expression of variant forms of insulin receptor substrate-1 identified in patients with noninsulin-dependent diabetes mellitus. J Clin Endocrinol Metab 82:4201–4207 Imai Y, Philippe N, Sesti G et al. (1997) Expression of variant forms of insulin receptor substrate-1 identified in patients with noninsulin-dependent diabetes mellitus. J Clin Endocrinol Metab 82:4201–4207
44.
Zurück zum Zitat Ura S, Araki E, Kishikawa H et al. (1996) Molecular scanning of the insulin receptor substrate-1 (IRS-1) gene in Japanese patients with NIDDM: identification of five novel polymorphisms. Diabetologia 39:600–608 Ura S, Araki E, Kishikawa H et al. (1996) Molecular scanning of the insulin receptor substrate-1 (IRS-1) gene in Japanese patients with NIDDM: identification of five novel polymorphisms. Diabetologia 39:600–608
45.
Zurück zum Zitat Almind K, Bjorbaek C, Vestergaard H et al. (1993) Aminoacid polymorphisms of insulin receptor substrate-1 in non-insulin-dependent diabetes mellitus. Lancet 342:828–832PubMed Almind K, Bjorbaek C, Vestergaard H et al. (1993) Aminoacid polymorphisms of insulin receptor substrate-1 in non-insulin-dependent diabetes mellitus. Lancet 342:828–832PubMed
46.
Zurück zum Zitat Laakso M, Malkki M, Kekalainen P et al. (1994) Insulin receptor substrate-1 variants in non-insulin-dependent diabetes. J Clin Invest 94:1141–1146PubMed Laakso M, Malkki M, Kekalainen P et al. (1994) Insulin receptor substrate-1 variants in non-insulin-dependent diabetes. J Clin Invest 94:1141–1146PubMed
47.
Zurück zum Zitat Porzio O, Federici M, Hribal ML et al. (1999) The Gly972→Arg amino acid polymorphism in IRS-1 impairs insulin secretion in pancreatic beta cells. J Clin Invest 104:357–364PubMed Porzio O, Federici M, Hribal ML et al. (1999) The Gly972→Arg amino acid polymorphism in IRS-1 impairs insulin secretion in pancreatic beta cells. J Clin Invest 104:357–364PubMed
48.
Zurück zum Zitat Stumvoll M, Fritsche A, Volk A et al. (2001) The Gly972Arg polymorphism in the insulin receptor substrate-1 gene contributes to the variation in insulin secretion in normal glucose tolerant humans. Diabetes 50:882–885PubMed Stumvoll M, Fritsche A, Volk A et al. (2001) The Gly972Arg polymorphism in the insulin receptor substrate-1 gene contributes to the variation in insulin secretion in normal glucose tolerant humans. Diabetes 50:882–885PubMed
49.
Zurück zum Zitat Marchetti P, Lupi R, Federici M et al. (2002) Insulin secretory function is impaired in isolated human islets carrying the Gly(972)→Arg IRS-1 polymorphism. Diabetes 51:1419–1424 Marchetti P, Lupi R, Federici M et al. (2002) Insulin secretory function is impaired in isolated human islets carrying the Gly(972)→Arg IRS-1 polymorphism. Diabetes 51:1419–1424
50.
Zurück zum Zitat Fritsche A, Stefan N, Hardt E et al. (2000) A novel hyperglycemic clamp for characterization of islet function in humans: assessment of three different secretagogues, maximal insulin response and reproducibility. Eur J Clin Invest 30:411–418CrossRefPubMed Fritsche A, Stefan N, Hardt E et al. (2000) A novel hyperglycemic clamp for characterization of islet function in humans: assessment of three different secretagogues, maximal insulin response and reproducibility. Eur J Clin Invest 30:411–418CrossRefPubMed
51.
Zurück zum Zitat ’t Hart LM, Nijpels G, Dekker JM et al. (2002) Variations in insulin secretion in carriers of gene variants in IRS-1 and -2. Diabetes 51:884–887PubMed ’t Hart LM, Nijpels G, Dekker JM et al. (2002) Variations in insulin secretion in carriers of gene variants in IRS-1 and -2. Diabetes 51:884–887PubMed
52.
Zurück zum Zitat Desvergne B, Wahli W (1999) Peroxisome proliferator-activated receptors: nuclear control of metabolism. Endocr Rev 20:649–688PubMed Desvergne B, Wahli W (1999) Peroxisome proliferator-activated receptors: nuclear control of metabolism. Endocr Rev 20:649–688PubMed
53.
Zurück zum Zitat Stumvoll M, Haring HU (2002) Glitazones: clinical effects and molecular mechanisms. Ann Med 34:217–224PubMed Stumvoll M, Haring HU (2002) Glitazones: clinical effects and molecular mechanisms. Ann Med 34:217–224PubMed
54.
Zurück zum Zitat Olefsky JM (2000) Treatment of insulin resistance with peroxisome proliferator-activated receptor gamma agonists. J Clin Invest 106:467–472PubMed Olefsky JM (2000) Treatment of insulin resistance with peroxisome proliferator-activated receptor gamma agonists. J Clin Invest 106:467–472PubMed
55.
56.
Zurück zum Zitat Saltiel AR, Olefsky JM (1996) Thiazolidinediones in the treatment of insulin resistance and type II diabetes. Diabetes 45:1661–1669PubMed Saltiel AR, Olefsky JM (1996) Thiazolidinediones in the treatment of insulin resistance and type II diabetes. Diabetes 45:1661–1669PubMed
57.
Zurück zum Zitat Spiegelman BM (1998) PPAR-gamma: adipogenic regulator and thiazolidinedione receptor. Diabetes 47:507–514PubMed Spiegelman BM (1998) PPAR-gamma: adipogenic regulator and thiazolidinedione receptor. Diabetes 47:507–514PubMed
58.
59.
Zurück zum Zitat Beamer BA, Negri C, Yen CJ et al. (1997) Chromosomal localization and partial genomic structure of the human peroxisome proliferator activated receptor-gamma (hPPAR gamma) gene. Biochem Biophys Res Commun 233:756–759CrossRefPubMed Beamer BA, Negri C, Yen CJ et al. (1997) Chromosomal localization and partial genomic structure of the human peroxisome proliferator activated receptor-gamma (hPPAR gamma) gene. Biochem Biophys Res Commun 233:756–759CrossRefPubMed
60.
Zurück zum Zitat Yen CJ, Beamer BA, Negri C et al. (1997) Molecular scanning of the human peroxisome proliferator activated receptor gamma (hPPAR gamma) gene in diabetic Caucasians: identification of a Pro12Ala PPAR gamma 2 missense mutation. Biochem Biophys Res Commun 241:270–274CrossRefPubMed Yen CJ, Beamer BA, Negri C et al. (1997) Molecular scanning of the human peroxisome proliferator activated receptor gamma (hPPAR gamma) gene in diabetic Caucasians: identification of a Pro12Ala PPAR gamma 2 missense mutation. Biochem Biophys Res Commun 241:270–274CrossRefPubMed
61.
Zurück zum Zitat Altshuler D, Hirschhorn JN, Klannemark M et al. (2000) The common PPARγ Pro12Ala polymorphism is associated with decreased risk of Type 2 diabetes. Nat Genet 26:76–80PubMed Altshuler D, Hirschhorn JN, Klannemark M et al. (2000) The common PPARγ Pro12Ala polymorphism is associated with decreased risk of Type 2 diabetes. Nat Genet 26:76–80PubMed
62.
Zurück zum Zitat Memisoglu A, Hu FB, Hankinson SE et al. (2003) Interaction between a peroxisome proliferator-activated receptor {gamma} gene polymorphism and dietary fat intake in relation to body mass. Hum Mol Genet 12:2923–2929CrossRefPubMed Memisoglu A, Hu FB, Hankinson SE et al. (2003) Interaction between a peroxisome proliferator-activated receptor {gamma} gene polymorphism and dietary fat intake in relation to body mass. Hum Mol Genet 12:2923–2929CrossRefPubMed
63.
Zurück zum Zitat Ek J, Andersen G, Urhammer SA et al. (2001) Studies of the Pro12Ala polymorphism of the peroxisome proliferator-activated receptor-γ2 (PPAR-γ2) gene in relation to insulin sensitivity among glucose tolerant Caucasians. Diabetologia 44:1170–1176CrossRefPubMed Ek J, Andersen G, Urhammer SA et al. (2001) Studies of the Pro12Ala polymorphism of the peroxisome proliferator-activated receptor-γ2 (PPAR-γ2) gene in relation to insulin sensitivity among glucose tolerant Caucasians. Diabetologia 44:1170–1176CrossRefPubMed
64.
Zurück zum Zitat Deeb SS, Fajas L, Nemoto M et al. (1998) A Pro12Ala substitution in PPARγ2 associated with decreased receptor activity, lower body mass index and improved insulin sensitivity. Nat Genet 20:284–287CrossRefPubMed Deeb SS, Fajas L, Nemoto M et al. (1998) A Pro12Ala substitution in PPARγ2 associated with decreased receptor activity, lower body mass index and improved insulin sensitivity. Nat Genet 20:284–287CrossRefPubMed
65.
Zurück zum Zitat Jacob S, Stumvoll M, Becker R et al. (2000) The PPARgamma2 polymorphism Pro12Ala is associated with better insulin sensitivity in the offspring of Type 2 diabetic patients. Horm Metab Res 32:413–416PubMed Jacob S, Stumvoll M, Becker R et al. (2000) The PPARgamma2 polymorphism Pro12Ala is associated with better insulin sensitivity in the offspring of Type 2 diabetic patients. Horm Metab Res 32:413–416PubMed
66.
Zurück zum Zitat Hara K, Okada T, Tobe K et al. (2000) The Pro12Ala polymorphism in PPAR gamma2 may confer resistance to Type 2 diabetes. Biochem Biophys Res Commun 271:212–216PubMed Hara K, Okada T, Tobe K et al. (2000) The Pro12Ala polymorphism in PPAR gamma2 may confer resistance to Type 2 diabetes. Biochem Biophys Res Commun 271:212–216PubMed
67.
Zurück zum Zitat Koch M, Rett K, Maerker E et al. (1999) The PPARgamma2 amino acid polymorphism Pro 12 Ala is prevalent in offspring of Type II diabetic patients and is associated to increased insulin sensitivity in a subgroup of obese subjects. Diabetologia 42:758–762CrossRefPubMed Koch M, Rett K, Maerker E et al. (1999) The PPARgamma2 amino acid polymorphism Pro 12 Ala is prevalent in offspring of Type II diabetic patients and is associated to increased insulin sensitivity in a subgroup of obese subjects. Diabetologia 42:758–762CrossRefPubMed
68.
Zurück zum Zitat Muller YL, Bogardus C, Beamer BA et al. (2003) A functional variant in the peroxisome proliferator-activated receptor gamma2 promoter is associated with predictors of obesity and Type 2 diabetes in Pima Indians. Diabetes 52:1864–1871PubMed Muller YL, Bogardus C, Beamer BA et al. (2003) A functional variant in the peroxisome proliferator-activated receptor gamma2 promoter is associated with predictors of obesity and Type 2 diabetes in Pima Indians. Diabetes 52:1864–1871PubMed
69.
Zurück zum Zitat Stumvoll M, Wahl HG, Löblein K et al. (2001) The Pro12Ala polymorphism in the peroxisome proliferator activated receptor γ2 gene is associated with increased antilipolytic insulin sensitivity. Diabetes 50:876–881PubMed Stumvoll M, Wahl HG, Löblein K et al. (2001) The Pro12Ala polymorphism in the peroxisome proliferator activated receptor γ2 gene is associated with increased antilipolytic insulin sensitivity. Diabetes 50:876–881PubMed
70.
Zurück zum Zitat Boden G, Chen X, Capulong E et al. (2001) Effects of free fatty acids on gluconeogenesis and autoregulation of glucose production in Type 2 diabetes. Diabetes 50:810–816 Boden G, Chen X, Capulong E et al. (2001) Effects of free fatty acids on gluconeogenesis and autoregulation of glucose production in Type 2 diabetes. Diabetes 50:810–816
71.
Zurück zum Zitat Boden G (1997) Role of fatty acids in the pathogenesis of insulin resistance and NIDDM. Diabetes 46:3–10PubMed Boden G (1997) Role of fatty acids in the pathogenesis of insulin resistance and NIDDM. Diabetes 46:3–10PubMed
72.
Zurück zum Zitat Duckworth WC, Bennett RG, Hamel FG (1998) Insulin degradation: progress and potential. Endocr Rev 19:608–624CrossRefPubMed Duckworth WC, Bennett RG, Hamel FG (1998) Insulin degradation: progress and potential. Endocr Rev 19:608–624CrossRefPubMed
73.
Zurück zum Zitat Douglas JA, Erdos MR, Watanabe RM et al. (2001) The peroxisome proliferator-activated receptor-gamma2 Pro12A1a variant: association with Type 2 diabetes and trait differences. Diabetes 50:886–890 Douglas JA, Erdos MR, Watanabe RM et al. (2001) The peroxisome proliferator-activated receptor-gamma2 Pro12A1a variant: association with Type 2 diabetes and trait differences. Diabetes 50:886–890
74.
Zurück zum Zitat Ferrannini E, Wahren J, Faber OK et al. (1983) Splanchnic and renal metabolism of insulin in human subjects: a dose-response study. Am J Physiol 244:E517–E527PubMed Ferrannini E, Wahren J, Faber OK et al. (1983) Splanchnic and renal metabolism of insulin in human subjects: a dose-response study. Am J Physiol 244:E517–E527PubMed
75.
Zurück zum Zitat Campbell PJ, Carlson MG, Nurjhan N (1994) Fat metabolism in human obesity. Am J Physiol 266:E600–E605PubMed Campbell PJ, Carlson MG, Nurjhan N (1994) Fat metabolism in human obesity. Am J Physiol 266:E600–E605PubMed
76.
Zurück zum Zitat Iozzo P, Beck-Nielsen H, Laakso M et al. (1999) Independent influence of age on basal insulin secretion in nondiabetic humans. European Group for the Study of Insulin Resistance. J Clin Endocrinol Metab 84: 863–868CrossRefPubMed Iozzo P, Beck-Nielsen H, Laakso M et al. (1999) Independent influence of age on basal insulin secretion in nondiabetic humans. European Group for the Study of Insulin Resistance. J Clin Endocrinol Metab 84: 863–868CrossRefPubMed
77.
Zurück zum Zitat Jones CN, Pei D, Staris P et al. (1997) Alterations in the glucose-stimulated insulin secretory dose-response curve and in insulin clearance in nondiabetic insulin-resistant individuals. J Clin Endocrinol Metab 82:1834–1838CrossRefPubMed Jones CN, Pei D, Staris P et al. (1997) Alterations in the glucose-stimulated insulin secretory dose-response curve and in insulin clearance in nondiabetic insulin-resistant individuals. J Clin Endocrinol Metab 82:1834–1838CrossRefPubMed
78.
Zurück zum Zitat Luan J, Browne PO, Harding AH et al. (2001) Evidence for gene-nutrient interaction at the PPARgamma locus. Diabetes 50:686–689PubMed Luan J, Browne PO, Harding AH et al. (2001) Evidence for gene-nutrient interaction at the PPARgamma locus. Diabetes 50:686–689PubMed
79.
Zurück zum Zitat Mori H, Ikegami H, Kawaguchi Y et al. (2001) The Pro12 -->Ala substitution in PPAR-gamma is associated with resistance to development of diabetes in the general population: possible involvement in impairment of insulin secretion in individuals with Type 2 diabetes. Diabetes 50:891–894PubMed Mori H, Ikegami H, Kawaguchi Y et al. (2001) The Pro12 -->Ala substitution in PPAR-gamma is associated with resistance to development of diabetes in the general population: possible involvement in impairment of insulin secretion in individuals with Type 2 diabetes. Diabetes 50:891–894PubMed
80.
Zurück zum Zitat Bergman RN (2000) Non-esterified fatty acids and the liver: why is insulin secreted into the portal vein? Diabetologia 43:946–952PubMed Bergman RN (2000) Non-esterified fatty acids and the liver: why is insulin secreted into the portal vein? Diabetologia 43:946–952PubMed
81.
Zurück zum Zitat Michael MD, Kulkarni RN, Postic C et al. (2000) Loss of insulin signaling in hepatocytes leads to severe insulin resistance and progressive hepatic dysfunction. Mol Cell 6:87–97PubMed Michael MD, Kulkarni RN, Postic C et al. (2000) Loss of insulin signaling in hepatocytes leads to severe insulin resistance and progressive hepatic dysfunction. Mol Cell 6:87–97PubMed
82.
Zurück zum Zitat Chen X, Iqbal N, Boden G (1999) The effects of free fatty acids on gluconeogenesis and glycogenolysis in normal subjects. J Clin Invest 103:365–372PubMed Chen X, Iqbal N, Boden G (1999) The effects of free fatty acids on gluconeogenesis and glycogenolysis in normal subjects. J Clin Invest 103:365–372PubMed
83.
Zurück zum Zitat Tschritter O, Fritsche A, Stefan N et al. (2003) Increased insulin clearance in peroxisome proliferator-activated receptor gamma2 Pro12Ala. Metabolism 52:778–783CrossRefPubMed Tschritter O, Fritsche A, Stefan N et al. (2003) Increased insulin clearance in peroxisome proliferator-activated receptor gamma2 Pro12Ala. Metabolism 52:778–783CrossRefPubMed
84.
Zurück zum Zitat Poy MN, Yang Y, Rezaei K et al. (2002) CEACAM1 regulates insulin clearance in liver. Nat Genet 30:270–276CrossRefPubMed Poy MN, Yang Y, Rezaei K et al. (2002) CEACAM1 regulates insulin clearance in liver. Nat Genet 30:270–276CrossRefPubMed
85.
Zurück zum Zitat Stumvoll M, Mitrakou A, Pimenta W et al. (2000) Use of the oral glucose tolerance test to assess insulin release and insulin sensitivity. Diabetes Care 23:295–301 Stumvoll M, Mitrakou A, Pimenta W et al. (2000) Use of the oral glucose tolerance test to assess insulin release and insulin sensitivity. Diabetes Care 23:295–301
86.
Zurück zum Zitat Matsuda A, DeFronzo R (1999) Insulin sensitivity indices obtained from oral glucose tolerance testing. Diabetes Care 22:1462–1470PubMed Matsuda A, DeFronzo R (1999) Insulin sensitivity indices obtained from oral glucose tolerance testing. Diabetes Care 22:1462–1470PubMed
87.
Zurück zum Zitat Stumvoll M, Häring H (2002) The Pro12Ala polymorphism in the peroxisome proliferator-activated receptor γ. Diabetes 51:2341–2347 Stumvoll M, Häring H (2002) The Pro12Ala polymorphism in the peroxisome proliferator-activated receptor γ. Diabetes 51:2341–2347
Metadaten
Titel
Control of glycaemia: from molecules to men. Minkowski Lecture 2003
verfasst von
M. Stumvoll
Publikationsdatum
01.05.2004
Verlag
Springer-Verlag
Erschienen in
Diabetologia / Ausgabe 5/2004
Print ISSN: 0012-186X
Elektronische ISSN: 1432-0428
DOI
https://doi.org/10.1007/s00125-004-1400-0

Weitere Artikel der Ausgabe 5/2004

Diabetologia 5/2004 Zur Ausgabe

Leitlinien kompakt für die Innere Medizin

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Notfall-TEP der Hüfte ist auch bei 90-Jährigen machbar

26.04.2024 Hüft-TEP Nachrichten

Ob bei einer Notfalloperation nach Schenkelhalsfraktur eine Hemiarthroplastik oder eine totale Endoprothese (TEP) eingebaut wird, sollte nicht allein vom Alter der Patientinnen und Patienten abhängen. Auch über 90-Jährige können von der TEP profitieren.

Niedriger diastolischer Blutdruck erhöht Risiko für schwere kardiovaskuläre Komplikationen

25.04.2024 Hypotonie Nachrichten

Wenn unter einer medikamentösen Hochdrucktherapie der diastolische Blutdruck in den Keller geht, steigt das Risiko für schwere kardiovaskuläre Ereignisse: Darauf deutet eine Sekundäranalyse der SPRINT-Studie hin.

Bei schweren Reaktionen auf Insektenstiche empfiehlt sich eine spezifische Immuntherapie

Insektenstiche sind bei Erwachsenen die häufigsten Auslöser einer Anaphylaxie. Einen wirksamen Schutz vor schweren anaphylaktischen Reaktionen bietet die allergenspezifische Immuntherapie. Jedoch kommt sie noch viel zu selten zum Einsatz.

Therapiestart mit Blutdrucksenkern erhöht Frakturrisiko

25.04.2024 Hypertonie Nachrichten

Beginnen ältere Männer im Pflegeheim eine Antihypertensiva-Therapie, dann ist die Frakturrate in den folgenden 30 Tagen mehr als verdoppelt. Besonders häufig stürzen Demenzkranke und Männer, die erstmals Blutdrucksenker nehmen. Dafür spricht eine Analyse unter US-Veteranen.

Update Innere Medizin

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.