Skip to main content
Log in

The Role of Insulin Resistance in the Pathogenesis of Alzheimer’s Disease

Implications for Treatment

  • Review Article
  • Published:
CNS Drugs Aims and scope Submit manuscript

Abstract

An emerging body of evidence suggests that an increased prevalence of insulin abnormalities and insulin resistance in Alzheimer’s disease may contribute to the disease pathophysiology and clinical symptoms. It has long been known that insulin is essential for energy metabolism in the periphery. In the past 2 decades, convergent findings have begun to demonstrate that insulin also plays a role in energy metabolism and other aspects of CNS function. Investigators reported 20 years ago that insulin and insulin receptors were densely but selectively expressed in the brain, including the medial temporal regions that support the formation of memory. It has recently been demonstrated that insulin-sensitive glucose transporters are localised to the same regions supporting memory and that insulin plays a role in memory functions. Collectively, these findings suggest that insulin may contribute to normal cognitive functioning and that insulin abnormalities may exacerbate cognitive impairments, such as those associated with Alzheimer’s disease.

Insulin may also play a role in regulating the amyloid precursor protein and its derivative β-amyloid (Aβ), which is associated with senile plaques, a neuro-pathological hallmark of Alzheimer’s disease. It has been proposed that insulin can accelerate the intracellular trafficking of Aβ and interfere with its degradation. These findings are consistent with the notion that insulin abnormalities may potentially influence levels of Aβ in the brains of patients with Alzheimer’s disease.

The increased occurrence of insulin resistance in Alzheimer’s disease and the numerous mechanisms through which insulin may affect clinical and pathological aspects of the disease suggest that improving insulin effectiveness may have therapeutic benefit for patients with Alzheimer’s disease. The thiazolidinedione rosiglitazone has been shown to have a potent insulin-sensitising action that appears to be mediated through the peroxisome proliferator-activated receptor-γ (PPAR-γ). PPAR-γ agonists, such as rosiglitazone, also have anti-inflammatory effects that may be of therapeutic benefit in patients with Alzheimer’s disease.

This review presents evidence suggesting that insulin resistance plays a role in the pathophysiology and clinical symptoms of Alzheimer’s disease. Based on this evidence, we propose that treatment of insulin resistance may reduce the risk or retard the development of Alzheimer’s disease.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Table I

Similar content being viewed by others

References

  1. Banks WA, Jaspan JB, Kastin AJ. Selective, physiological transport of insulin across the blood-brain barrier: novel demonstration by species-specific radioimmunoassays. Peptides 1997; 18(8): 1257–62

    Article  PubMed  CAS  Google Scholar 

  2. Banks WA, Jaspan JB, Huang W, et al. Transport of insulin across the blood-brain barrier: saturability at euglycemic doses of insulin. Peptides 1997; 18(9): 1423–9

    Article  PubMed  CAS  Google Scholar 

  3. Baskin D, Figlewicz D, Woods S, et al. Insulin in the brain. Annu Rev Physiol 1987; 49: 335–47

    Article  PubMed  CAS  Google Scholar 

  4. Baura GD, Foster DM, Porte Jr D, et al. Saturable transport of insulin from plasma into the central nervous system of dogs in vivo: a mechanism for regulated insulin delivery to the brain. J Clin Invest 1993; 92(4): 1824–30

    Article  PubMed  CAS  Google Scholar 

  5. Wallum BJ, Taborsky GJ, Porte D, et al. Cerebrospinal fluid insulin levels increase during intravenous insulin infusions in man. J Clin Endocrinol Metab 1987; 64(1): 190–4

    Article  PubMed  CAS  Google Scholar 

  6. Havrankova J, Roth J. Insulin receptors are widely distributed in the central nervous system of the rat. Nature 1978; 272: 827–9

    Article  PubMed  CAS  Google Scholar 

  7. Havrankova J, Schmechel D, Roth J, et al. Identification of insulin in rat brain. Proc Natl Acad Sci U S A 1978; 75(11): 5737–41

    Article  PubMed  CAS  Google Scholar 

  8. Unger J, Livingston J, Moss A. Insulin receptors in the central nervous system: localization, signalling mechanisms and functional aspects. Prog Neurobiol 1991; 36: 343–62

    Article  PubMed  CAS  Google Scholar 

  9. Reagan L, Gorovits N, Hoskin E, et al. Localization and regulation of GLUTx1 glucose transporter in the hippocampus of streptozotocin diabetic rats. Proc Natl Acad Sci U S A 2001; 98(5): 2820–5

    Article  PubMed  CAS  Google Scholar 

  10. Apelt J, Mehlhorn G, Schliebs R. Insulin-sensitive GLUT4 glucose transporters are colocalized with GLUT3-expressing cells and demonstrate a chemically distinct neuron-specific localization in the brain. J Neurosci Res 1999; 57: 693–705

    Article  PubMed  CAS  Google Scholar 

  11. Brant A, Jess T, Milligan G, et al. Immunological analysis of glucose transporters expressed in different regions of the rat brain and central nervous system. Biochem Biophys Res Commun 1993; 192(3): 1297–302

    Article  PubMed  CAS  Google Scholar 

  12. El-Messari S, Leloup C, Quignon M, et al. Immunocytochemical localization of the insulin-responsive glucose transporter 4 (Glut4) in the rat central nervous system. J Comp Neurol 1998; 399(4): 492–512

    Article  PubMed  CAS  Google Scholar 

  13. Livingstone C, Lyall H, Gould G. Hypothalamic GLUT 4 expression: a glucose- and insulin-sensing mechanism? Mol Cell Endocrinol 1995; 107(1): 67–70

    Article  PubMed  CAS  Google Scholar 

  14. Braak H, Braak E. Frequency of stages of Alzheimer-related lesions in different age categories. Neurobiol Aging 1997 Jul–Aug; 18(4): 351–7

    Article  PubMed  CAS  Google Scholar 

  15. Gasparini L, Gouras GK, Wang R, et al. Stimulation of β-amyloid precursor protein trafficking by insulin reduces intraneuronal β-amyloid and required mitogen-activated protein kinase signaling. J Neurosci 2001; 21(8): 2561–70

    PubMed  CAS  Google Scholar 

  16. Davis SN, Granner DK. Insulin, oral hypoglycemic agents, and the pharmacology of the endocrine pancreas. In: Hardman JG, Gilman AG, Limbird LE, editors. Gilman and Goodman’s the pharmacological basis of therapeutics. 9th ed. New York: McGraw-Hill, 1996: 1487–1517

    Google Scholar 

  17. Shii K, Roth RA. Inhibition of insulin degradation by hepatoma cells after microinjection of monoclonal antibodies to a specific cytosolic protease. Proc Natl Acad Sci U S A 1986; 83(12): 4147–51

    Article  PubMed  CAS  Google Scholar 

  18. Joost HG, Thorens B. The extended GLUT-family of sugar/polyol transport facilitators: nomenclature, sequence characteristics, and potential function of its novel members. Mol Membr Biol 2001; 18(4): 247–56

    Article  PubMed  CAS  Google Scholar 

  19. Schulingkamp R, Pagano T, Hung D, et al. Insulin receptors and insulin action in the brain: review and clinical implications. Neurosci Biobehav Rev 2000; 24: 855–72

    Article  PubMed  CAS  Google Scholar 

  20. Ibberson M, Uldry M, Thorens B. GLUTX1, a novel mammalian glucose transporter expressed in the central nervous system and insulin-sensitive tissues. J Biol Chem 2000; 275(7): 4607–12

    Article  PubMed  CAS  Google Scholar 

  21. Kahn BB. Lilly lecture 1995. Glucose transport: pivotal step in insulin action. Diabetes 1996; 45(11): 1644–54

    Article  PubMed  CAS  Google Scholar 

  22. Rea S, James DE. Moving GLUT4: the biogenesis and trafficking of GLUT4 storage vesicles. Diabetes 1997; 46(11): 1667–77

    Article  PubMed  CAS  Google Scholar 

  23. Expert Committee on the Diagnosis and Classification of Diabetes Mellitus. Report of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus. Diabetes Care 2002; 25Suppl. 1: S5–20

    Google Scholar 

  24. Reaven G. Insulin resistance in noninsulin-dependent diabetes mellitus: does it exist and can it be measured? Am J Med 1983; 74(1A): 3–17

    Article  PubMed  CAS  Google Scholar 

  25. Ramlo-Halsted B, Edelman S. The natural history of type 2 diabetes: implications for clinical practice. Prim Care 1999; 26(4): 771–89

    Article  PubMed  CAS  Google Scholar 

  26. Leyva F, Godsland I, Worthington M, et al. Factors of the metabolic syndrome: baseline interrelationships in the first follow-up cohort of the HDDRISC Study (HDDRISC-1). Arterioscler Thromb Vasc Biol 1998; 18: 208–14

    Article  PubMed  CAS  Google Scholar 

  27. Meigs J, Mittleman M, Nathan D, et al. Hyperinsulinemia, hyperglycemia, and impaired hemostasis: the Framingham Offspring study. JAMA 2000; 283(2): 221–8

    Article  PubMed  CAS  Google Scholar 

  28. Boyko E, de Courten M, Zimmet P, et al. Features of the metabolic syndrome predict higher risk of diabetes and impaired glucose tolerance. Diabetes Care 2000; 23: 1242–8

    Article  PubMed  CAS  Google Scholar 

  29. Craft S, Asthana S, Newcomer JW, et al. Enhancement of memory in Alzheimer’s disease with insulin and somatostatin, but not glucose. Arch Gen Psychiatry 1999; 56: 1135–40

    Article  PubMed  CAS  Google Scholar 

  30. Fruehwald-Shultes B, Kern W, Bong W, et al. Supraphysiological hyperinsulinemia acutely increases hypothalamic-pituitary-adrenal secretory activity in humans. J Clin Endocrinol Metab 1999; 84: 3041–6

    Article  Google Scholar 

  31. Tappy L, Randin D, Vollenweider P, et al. Mechanisms of dexamethasone-induced insulin resistance in healthy humans. J Clin Endocrinol Metab 1994; 79: 1063–9

    Article  PubMed  CAS  Google Scholar 

  32. Weinstein SP, Paquin T, Pritsker A, et al. Glucocorticoid-induced insulin resistance: dexamethasone inhibits the activation of glucose transport in rat skeletal muscle by both insulin- and non-insulin-related stimuli. Diabetes 1995; 44: 441–5

    Article  PubMed  CAS  Google Scholar 

  33. Tojo C, Takao T, Nishioka T, et al. Hypothalamic-pituitary-adrenal axis in WBN/Kob rats with non-insulin dependent diabetes mellitus. Endocr J 1995; 43(2): 233–9

    Article  Google Scholar 

  34. Lee Z, Chan J, Yeung V, et al. Plasma insulin, growth hormone, cortisol, and central obesity among young Chinese type 2 diabetic patients. Diabetes Care 1999; 22(9): 1450–7

    Article  PubMed  CAS  Google Scholar 

  35. Meneilly G, Hill A. Alterations in glucose metabolism in patients with Alzheimer’s disease. J Am Geriatr Soc 1993; 41: 710–4

    PubMed  CAS  Google Scholar 

  36. Spyer G, Hattersley A, MacDonald I, et al. Hypoglycaemic counter-regulation at normal blood glucose concentrations in patients with well controlled type-2 diabetes. Lancet 2000; 356(9246): 1970–4

    Article  PubMed  CAS  Google Scholar 

  37. Devaskar SU, Giddings SJ, Rajakumar PA, et al. Insulin gene expression and insulin synthesis in mammalian neuronal cells. J Biol Chem 1994; 269(11): 8445–54

    PubMed  CAS  Google Scholar 

  38. Rulifson EJ, Kim SK, Nusse R. Ablation of insulin-producing neurons in flies: growth and diabetic phenotypes. Science 2002; 296: 1118–20

    Article  PubMed  CAS  Google Scholar 

  39. Schechter R, Holtzclaw L, Sadiq F, et al. Insulin synthesis by isolated rabbit neurons. Endocrinology 1988; 23(1): 505–13

    Article  Google Scholar 

  40. Singh BS, Rajakumar PA, Eves EM, et al. Insulin gene expression in immortalized rat hippocampal and pheochromocytoma-12 cell lines. Regul Pept 1997; 69(1): 7–14

    Article  PubMed  CAS  Google Scholar 

  41. Hasselbalch SG, Knudsen GM, Videbaek C, et al. No effect of insulin on glucose blood-brain barrier transport and cerebral metabolism in humans. Diabetes 1999 Oct; 48(10): 1915–21

    Article  PubMed  CAS  Google Scholar 

  42. Squire L, Zola-Morgan S. The medial temporal lobe memory system. Science 1991; 253: 1380–6

    Article  PubMed  CAS  Google Scholar 

  43. Squire L, Ojemann J, Miezin F, et al. Activation of the hippocampus in normal humans: a functional anatomical study of memory. Proc Natl Acad Sci U S A 1992; 89: 1837–41

    Article  PubMed  CAS  Google Scholar 

  44. Squire L. Memory and the hippocampus: a synthesis from findings with rats, monkeys, and humans. Psychol Rev 1992; 99(2): 195–231

    Article  PubMed  CAS  Google Scholar 

  45. Park CR, Seeley RJ, Craft S, et al. Intracerebroventricular insulin enhances memory in a passive-avoidance task. Physiol Behav 2000; 68: 509–14

    Article  PubMed  CAS  Google Scholar 

  46. Zhao W, Chen H, Xu H, et al. Brain insulin receptors and spatial memory: correlated changes in gene expression, tyrosine phosphorylation, and signaling molecules in the hippocampus of the water maze trained rats. J Biol Chem 1999; 274(49): 34893–902

    Article  PubMed  CAS  Google Scholar 

  47. Marfaing-Jallat P, Portha B, Penicaud L. Altered conditioned taste aversion and glucose utilization in related brain nuclei of diabetic GK rats. Brain Res Bull 1995; 37(6): 639–43

    Article  PubMed  CAS  Google Scholar 

  48. Greenwood C, Winocur G. Glucose treatment reduces memory deficits in young rats fed high-fat diets. Neurobiol Learn Mem 2001; 75(2): 179–89

    Article  PubMed  CAS  Google Scholar 

  49. Elias PK, Elias MF, D’Agostino RB, et al. NIDDM and blood pressure as risk factors for poor cognitive performance: the Framingham Study. Diabetes Care 1997; 20(9): 1388–95

    Article  PubMed  CAS  Google Scholar 

  50. Helkala E-L, Niskanen L, Viinamaki H, et al. Short-term and long-term memory in elderly patients with NIDDM. Diabetes Care 1995; 18(5): 681–5

    Article  PubMed  CAS  Google Scholar 

  51. Perlmuter LC, Hakami MK, Hodgson-Harrington C, et al. Decreased cognitive function in aging non-insulin-dependent diabetic patients. Am J Med 1984; 77: 1043–8

    Article  PubMed  CAS  Google Scholar 

  52. Strachan M, Deary I, Ewing F, et al. Is type II diabetes associated with an increased risk of cognitive dysfunction? A critical review of published studies. Diabetes Care 1997 Mar; 20(3): 438–45

    Article  PubMed  CAS  Google Scholar 

  53. Vanhanen M, Kuusisto J, Koivisto K, et al. Type-2 diabetes and cognitive function in a non-demented population. Acta Neurol Scand 1999; 100: 97–101

    Article  PubMed  CAS  Google Scholar 

  54. Vanhanen M, Koivisto K, Kuusisto J, et al. Cognitive function in an elderly population with persistent impaired glucose tolerance. Diabetes Care 1998; 21(3): 398–402

    Article  PubMed  CAS  Google Scholar 

  55. Ryan C, Geckle M. Why is learning and memory dysfunction in type 2 diabetes limited to older adults? Diabetes Metab Res Rev 2000; 16: 308–15

    Article  PubMed  CAS  Google Scholar 

  56. Gregg E, Yaffe K, Cauley J, et al. Is diabetes associated with cognitive impairment and cognitive decline among older women? Arch Intern Med 2000; 160: 174–80

    Article  PubMed  CAS  Google Scholar 

  57. Kalmijn S, Feskens E, Launer L, et al. Glucose intolerance, hyperinsulinemia and cognitive function in a general population of elderly men. Diabetologia 1995; 38: 1096–102

    Article  PubMed  CAS  Google Scholar 

  58. Meneilly GS, Cheung E, Tessier D, et al. The effect of improved glycemic control on cognitive functions in the elderly patient with diabetes. J Gerontol 1993; 48(4): M117–M21

    Article  PubMed  CAS  Google Scholar 

  59. Reaven G, Thompson L, Nahum D, et al. Relationship between hyperglycemia and cognitive function in older NIDDM patients. Diabetes Care 1990; 13(1): 16–21

    Article  PubMed  CAS  Google Scholar 

  60. Skeberdis V, Lan J, Zheng X, et al. Insulin promotes rapid delivery of N-methyl-D-aspartate receptors to the cell surface by exocytosis. Proc Natl Acad Sci U S A 2001; 98(6): 3561–6

    Article  PubMed  CAS  Google Scholar 

  61. Gould E, Tanapat P. Stress and hippocampal neurogenesis. Biol Psychiatry 1999; 46(11): 1472–9

    Article  PubMed  CAS  Google Scholar 

  62. Joels M, de Kloet E. Effects of glucocorticoids and norepinephrine on the excitability in the hippocampus. Science 1989; 245(4925): 1502–5

    Article  PubMed  CAS  Google Scholar 

  63. Pavlides C, McEwen BS. Effects of mineralocorticoid and glucocorticoid receptors on long-term potentiation in the CA3 hippocampal field. Brain Res 1999; 851: 204–14

    Article  PubMed  CAS  Google Scholar 

  64. Xu L, Holscher C, Anwyl R, et al. Glucocorticoid receptor and protein/RNA synthesis-dependent mechanisms underlie the control of synaptic by stress. Proc Natl Acad Sci U S A 1998; 95: 3204–8

    Article  PubMed  CAS  Google Scholar 

  65. de Quervain DJ, Roozendaal B, Nitsch RM, et al. Acute cortisone administration impairs retrieval of long-term declarative memory in humans. Nat Neurosci 2000; 3(4): 313–4

    Article  PubMed  Google Scholar 

  66. Forget H, Lacroix A, Somma M, et al. Cognitive decline in patients with Cushing’s syndrome. J Int Neuropsychol Soc 2000; 6: 20–9

    PubMed  CAS  Google Scholar 

  67. Greendale G, Kritz-Silverstein D, Seeman T, et al. Higher basal cortisol predicts verbal memory loss in postmenopausal women: Rancho Bernardo study. J Am Geriatr Soc 2000; 48(12): 1655–8

    PubMed  CAS  Google Scholar 

  68. Lupien S, Lecours AR, Lussier I, et al. Basal cortisol levels and cognitive deficits in human aging. J Neurosci 1994; 14 (5 Pt 1): 2893–903

    PubMed  CAS  Google Scholar 

  69. Miller T, Taylor J, Rogerson S, et al. Cognitive and noncognitive symptoms in dementia patients: relationship to cortisol and dehydroepiandrosterone. Int Psychogeriatr 1998; 10(1): 85–96

    Article  PubMed  CAS  Google Scholar 

  70. Newcomer J, Craft S, Hershey T, et al. Glucocorticoid-induced impairment in declarative memory performance in adult humans. J Neurosci 1994; 14: 2047–53

    PubMed  CAS  Google Scholar 

  71. Newcomer JW, Selke G, Melson AK, et al. Decreased memory performance in healthy humans induced by stress-level cortisol treatment. Arch Gen Psychiatry 1999; 56: 527–33

    Article  PubMed  CAS  Google Scholar 

  72. Young A, Sahakian B, Robbins T, et al. The effects of chronic administration of hydrocortisone on cognitive function in normal male volunteers. Psychopharmacology (Berl) 1999; 145(3): 260–6

    Article  CAS  Google Scholar 

  73. Brown ES, Rush J, McEwen BS. Hippocampal remodeling and damage by corticosteroids: implications for mood disorders. Neuropsychopharmacology 1999; 21(4): 74–84

    Article  Google Scholar 

  74. Brunetti A, Fulham JJ, Aloj L, et al. Decreased brain glucose utilization in patients with Cushing’s disease. J Nucl Med 1998; 39(5): 786–90

    PubMed  CAS  Google Scholar 

  75. Sapolsky R, Uno H, Rebert C, et al. Hippocampal damage associated with prolonged glucocorticoid exposure in primates. J Neurosci 1990; 10(9): 2897–902

    PubMed  CAS  Google Scholar 

  76. Sapolsky R. Glucocorticoids and hippocampal atrophy in neuropsychiatric disorders. Arch Gen Psychiatry 2000; 57(10): 925–35

    Article  PubMed  CAS  Google Scholar 

  77. Starkman M, Giordani B, Gebarski S, et al. Decrease in cortisol reverses human hippocampal atrophy following treatment of Cushing’s disease. Biol Psychiatry 1999; 46(12): 1595–602

    Article  PubMed  CAS  Google Scholar 

  78. LeMay DR, Gehua L, Zelenock GB, et al. Insulin administration protects neurologic function in cerebral ischemia in rats. Stroke 1988 Nov; 19(11): 1411–9

    Article  PubMed  CAS  Google Scholar 

  79. Li PA, Shuaib A, Miyashita H, et al. Hyperglycemia enhances extracellular glutamate accumulation in rats subjected to forebrain ischemia. Stroke 2000; 31(1): 183–92

    Article  PubMed  CAS  Google Scholar 

  80. Atlante A, Calissano P, Bobba A, et al. Glutamate neurotoxicity, oxidative stress and mitochondria. FEBS Lett 2001; 497(1): 1–5

    Article  PubMed  CAS  Google Scholar 

  81. Coyle JT, Puttfarcken P. Oxidative stress, glutamate, and neuro-degenerative disorders. Science 1993; 262(5134): 689–95

    Article  PubMed  CAS  Google Scholar 

  82. Brookmeyer R, Gray S, Kawas C. Projections of Alzheimer’s disease in the United States and the public health impact of delaying disease onset. Am J Public Health 1998; 88(9): 1337–42

    Article  PubMed  CAS  Google Scholar 

  83. Kawas C, Gray S, Brookmeyer R, et al. Age-specific incidence rates of Alzheimer’s disease: the Baltimore Longitudinal Study of Aging. Neurology 2000; 13(411): 2072–7

    Article  Google Scholar 

  84. Polvikoski T, Sulkava R, Myllykangas L, et al. Prevalence of Alzheimer’s disease in very elderly people: a prospective neuropathological study. Neurology 2001; 56: 1690–6

    Article  PubMed  CAS  Google Scholar 

  85. American Psychiatric Association. Diagnostic and statistical manual of mental disorders. 4th ed. Washington, DC: American Psychiatric Association, 1994

    Google Scholar 

  86. Petersen RC, Smith GE, Waring SC, et al. Mild cognitive impairment: clinical characterization and outcome. Arch Neurol 1999; 56: 303–8

    Article  PubMed  CAS  Google Scholar 

  87. Petersen RC, Doody R, Kurz A, et al. Current concepts in mild cognitive impairment. Arch Neurol 2001; 58(12): 1985–92

    Article  PubMed  CAS  Google Scholar 

  88. Razay G, Wilcock GK. Hyperinsulinemia and Alzheimer’s disease. Age Ageing 1994; 23: 396–9

    Article  PubMed  CAS  Google Scholar 

  89. Craft S, Asthana S, Schellenberg GD, et al. Insulin metabolism in Alzheimer’s disease differs according to apolipoprotein E genotype and gender. Neuroendocrinology 1999; 70: 146–52

    Article  PubMed  CAS  Google Scholar 

  90. Craft S, Peskind E, Schwartz MW, et al. Cerebrospinal fluid and plasma insulin levels in Alzheimer’s disease: relationship to severity of dementia and apolipoprotein E genotype. Neurology 1998; 50: 164–8

    Article  PubMed  CAS  Google Scholar 

  91. Leibson C, Rocca W, Hanson V, et al. The risk of dementia among persons with diabetes mellitus: a population-based cohort study. Ann N Y Acad Sci 1997; 826: 422–7

    Article  PubMed  CAS  Google Scholar 

  92. Ott A, Stolk RP, van Harskamp F, et al. Diabetes mellitus and the risk of dementia: the Rotterdam study. Neurology 1999; 10: 1937–42

    Article  Google Scholar 

  93. Corder E, Saunders A, Strittmatter W, et al. Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer’s disease in late onset families. Science 1993; 261(5123): 921–3

    Article  PubMed  CAS  Google Scholar 

  94. Kuusisto J, Koivisto K, Mykkanen L, et al. Association between features of the insulin resistance syndrome and Alzheimer’s disease independently of apolipoprotein E4 phenotype: cross sectional population based study. BMJ 1997; 315: 1045–9

    Article  PubMed  CAS  Google Scholar 

  95. Foster NL, Chase TN, Fedio P, et al. Alzheimer’s disease: focal cortical changes shown by positron emission tomography. Neurology 1983; 33(8): 961–5

    Article  PubMed  CAS  Google Scholar 

  96. Rodriguez G, Vitali P, Calvini P, et al. Hippocampal perfusion in mild Alzheimer’s disease. Psychiatry Res 2000; 100(2): 65–74

    Article  PubMed  CAS  Google Scholar 

  97. De Santi S, de Leon MJ, Rusinek H, et al. Hippocampal formation glucose metabolism and volume losses in MCI and Alzheimer’s disease. Neurobiol Aging 2001; 22(4): 529–39

    Article  PubMed  Google Scholar 

  98. Craft S, Asthana S, Newcomer J, et al. Insulin-induced enhancement of memory in Alzheimer’s disease is independent of glucose. Soc Neurosci Abstr 1996; 22(2): 1177

    Google Scholar 

  99. Craft S, Zallen G, Baker LD. Glucose and memory in mild senile dementia of the Alzheimer’s type. J Clin Exp Neuropsychol 1992; 14: 253–67

    Article  PubMed  CAS  Google Scholar 

  100. Craft S, Murphy C, Wemstrom J. Glucose effects on complex memory and non-memory tasks: the influence of age, sex, and glucoregulatory response. Psychobiology 1994; 22: 95–105

    CAS  Google Scholar 

  101. Newcomer JW, Craft S, Fucetola R, et al. Glucose-induced increase in memory performance in patients with schizophrenia. Schizophr Bull 1999; 25(2): 321–35

    Article  PubMed  CAS  Google Scholar 

  102. Craft S, Newcomer J, Kanne S, et al. Memory improvement following induced hyperinsulinemia in Alzheimer’s disease. Neurobiol Aging 1996; 17(1): 123–30

    Article  PubMed  CAS  Google Scholar 

  103. Craft S, Asthana S, Schellenberg G, et al. Insulin effects on glucose metabolism, memory, and plasma amyloid precursor protein in Alzheimer’s disease differ according to apolipoprotein-E genotype. Ann N Y Acad Sci 2000; 903: 222–8

    Article  PubMed  CAS  Google Scholar 

  104. Craft S, Asthana S, Cook DG, et al. Insulin dose response effects on memory and amyloid precursor protein in Alzheimer’s disease: interactions with apolipoprotein E genotype. Psychoneuroendocrinology. In press

  105. Sinha S, Lieberburg I. Cellular mechanisms of beta-amyloid production and secretion. Proc Natl Acad Sci U S A 1999; 96(20): 11049–53

    Article  PubMed  CAS  Google Scholar 

  106. Kienlen-Campard P, Miolet S, Tasiaux B, et al. Intracellular amyloid-beta 1-42, but not extracellular soluble amyloid-beta peptides, induces neuronal apoptosis. J Biol Chem 2002; 277(18): 15666–70

    Article  PubMed  CAS  Google Scholar 

  107. Naslund J, Haroutunian V, Mohs R, et al. Correlation between elevated levels of amyloid beta-peptide in the brain and cognitive decline. JAMA 2000; 283(12): 1571–7

    Article  PubMed  CAS  Google Scholar 

  108. Parvathy S, Davies P, Haroutunian V, et al. Correlation between Abetax-40-, Abetax-42-, and Abetax-43-containing amyloid plaques and cognitive decline. Arch Neurol 2001; 58(12): 2025–32

    Article  PubMed  CAS  Google Scholar 

  109. Arriagada PV, Growdon JH, Hedley-Whyte ET, et al. Neurofibrillary tangles but not senile plaques parallel duration and severity of Alzheimer’s disease. Neurology 1992; 42: 631–9

    Article  PubMed  CAS  Google Scholar 

  110. Jellinger KA. The neuropathological diagnosis of Alzheimer disease. J Neural Transm Suppl 1998; 53: 97–118

    Article  PubMed  CAS  Google Scholar 

  111. Tilley L, Morgan K, Kalsheker N. Genetic risk factors in Alzheimer’s disease. Mol Pathol 1998; 51: 293–304

    Article  PubMed  CAS  Google Scholar 

  112. Gyure KA, Durham R, Stewart WF, et al. Intraneuronal abeta-amyloid precedes development of amyloid plaques in Down syndrome. Arch Pathol Lab Med 2001; 125(4): 489–92

    PubMed  CAS  Google Scholar 

  113. Xia W, Ostaszewski BL, Kimberly WT, et al. Alzheimer’s disease mutations in presenilin-1 or amyloid precursor protein decrease the efficacy of a gamma-secretase inhibitor: evidence for direct involvement of PS 1 in the gamma-secretase cleavage complex. Neurobiol Dis 2000; 7 (6 Pt B): 673–81

    Article  PubMed  CAS  Google Scholar 

  114. Authier F, Posner BI, Bergeron JJM. Insulin-degrading enzyme. Clin Invest Med 1996; 19(3): 149–60

    PubMed  CAS  Google Scholar 

  115. Kurochkin IV, Goto S. Alzheimer’s B-amyloid peptide specifically interacts with and is degraded by insulin degrading enzyme. FEBS Lett 1994; 345: 33–7

    Article  PubMed  CAS  Google Scholar 

  116. McDermott JR, Gibson AM. Degradation of Alzheimer’s beta-amyloid protein by human and rat brain peptidases: involvement of insulin-degrading enzyme. Neurochem Res 1997; 22(1): 49–56

    Article  PubMed  CAS  Google Scholar 

  117. Qiu W, Walsh D, Ye Z, et al. Insulin-degrading enzyme regulates extracellular levels of amyloid beta-protein by degradation. J Biol Chem 1998; 273(49): 32730–8

    Article  PubMed  CAS  Google Scholar 

  118. Vekrellis K, Ye Z, Qiu WQ, et al. Neurons regulate extracellular levels of amyloid beta-protein via proteolysis by insulin-degrading enzyme. J Neurosci 2000; 20(5): 1657–65

    PubMed  CAS  Google Scholar 

  119. Sudoh S, Frosch MP, Wolf BA. Differential effects of proteases involved in intracellular degradation of amyloid β-protein between detergent-soluble and -insoluble pools in CHO-695 cells. Biochemistry 2002; 41(4): 1091–9

    Article  PubMed  CAS  Google Scholar 

  120. Edbauer D, Willem M, Lammich S, et al. Insulin-degrading enzyme rapidly removes the β-amyloid precursor protein intracellular domain (AICD). J Biol Chem 2002; 277(16): 13389–93

    Article  PubMed  CAS  Google Scholar 

  121. Akiyama H, Barger S, Barnum S, et al. Inflammation and Alzheimer’s disease. Neurobiol Aging 2000; 21(3): 383–421

    Article  PubMed  CAS  Google Scholar 

  122. Rogers J, Shen Y. A perspective on inflammation in Alzheimer’s disease. Ann N Y Acad Sci 2000; 924: 132–5

    Article  PubMed  CAS  Google Scholar 

  123. Lue LF, Walker DG, Rogers J. Modeling microglial activation in Alzheimer’s disease with human postmortem microglial cultures. Neurobiol Aging 2001; 22(6): 945–56

    Article  PubMed  CAS  Google Scholar 

  124. Lim GP, Yang F, Chu T, et al. Ibuprofen suppresses plaque pathology and inflammation in a mouse model for Alzheimer’s disease. J Neurosci 2000; 20(15): 5709–14

    PubMed  CAS  Google Scholar 

  125. Anthony JC, Breitner JC, Zandi PP, et al. Reduced prevalence of Alzheimer’s disease in users of NSAIDs and H2 receptor antagonists: the Cache County study. Neurology 2000; 54(11): 2066–71

    Article  PubMed  CAS  Google Scholar 

  126. Broe GA, Grayson DA, Creasey HM, et al. Anti-inflammatory drugs protect against Alzheimer disease at low doses. Arch Neurol 2000; 57(11): 1586–91

    Article  PubMed  CAS  Google Scholar 

  127. Rosier N, Wichart I, Jellinger KA. Intra vitam lumbar and post mortem ventricular cerebrospinal fluid immunoreactive interleukin-6 in Alzheimer’s disease patients. Acta Neurol Scand 2001; 103(2): 126–30

    Article  Google Scholar 

  128. Hull M, Strauss S, Berger M, et al. The participation of interleukin-6, a stress-inducible cytokine, in the pathogenesis of Alzheimer’s disease. Behav Brain Res 1996; 78(1): 37–41

    Article  PubMed  CAS  Google Scholar 

  129. Hak AE, Pols HA, Stehouwer CD, et al. Markers of inflammation and cellular adhesion molecules in relation to insulin resistance in nondiabetic elderly: the Rotterdam study. J Clin Endocrinol Metab 2001; 86(9): 4398–405

    Article  PubMed  CAS  Google Scholar 

  130. Pickup JC, Mattock MB, Chusney GD, et al. NIDDM as a disease of the innate immune system: association of acute-phase reactants and interleukin-6 with metabolic syndrome X. Diabetologia 1997; 40(11): 1286–92

    Article  PubMed  CAS  Google Scholar 

  131. Fernandez-Real JM, Broch M, Vendrell J, et al. Interleukin-6 gene polymorphism and insulin sensitivity. Diabetes 2000; 49: 517–20

    Article  PubMed  CAS  Google Scholar 

  132. Combs CK, Johnson DE, Karlo JC, et al. Inflammatory mechanisms in Alzheimer’s disease: inhibition of β-amyloid-stimulated proinflammatory responses and neurotoxicity by PPAR-γ agonists. J Neurosci 2000; 20(2): 558–67

    PubMed  CAS  Google Scholar 

  133. Hoyer S. Brain glucose and energy metabolism abnormalities in sporadic Alzheimer disease. Causes and consequences: an update. Exp Gerontol 2000; 35: 1363–72

    Article  PubMed  CAS  Google Scholar 

  134. Frölich L, Blum-Degen D, Bernstein HG, et al. Brain insulin and insulin receptors in aging and sporadic Alzheimer’s disease. J Neural Transm 1998; 105: 423–38

    Article  PubMed  Google Scholar 

  135. Hoyer S, Lee SK, Loffler T, et al. Inhibition of the neuronal insulin receptor: an in vivo model for sporadic Alzheimer disease? Ann N Y Acad Sci 2000; 920: 256–8

    Article  PubMed  CAS  Google Scholar 

  136. Kagansky N, Levy S, Knobler H. The role of hyperglycemia in acute stroke. Arch Neurol 2001 Aug; 58(8): 1209–12

    Article  PubMed  CAS  Google Scholar 

  137. Harris MI. Diabetes in America: epidemiology and scope of the problem. Diabetes Care 1998 Dec; 21 Suppl. 3: C11–4

    Google Scholar 

  138. Malinowski J, Bolesta S. Rosiglitazone in the treatment of type 2 diabetes mellitus: a critical review. Clin Ther 2000; 22(10): 1151–68

    Article  PubMed  CAS  Google Scholar 

  139. da Silva B, Molitch M. Pharmacologic management of type 2 diabetes in the elderly: overview of treatment options. Formulary 2000; 35: 580–94

    Google Scholar 

  140. Dunn C, Faulds D. Nateglinide. Drugs 2000; 60(3): 607–15

    Article  PubMed  CAS  Google Scholar 

  141. Evans AJ, Krentz AJ. Recent developments and emerging therapies for type 2 diabetes mellitus. Drugs R D 1999; 2: 75–94

    Article  PubMed  CAS  Google Scholar 

  142. Hevener AL, Reichart D, Olefsky J. Exercise and thiazolid-inedione therapy normalize insulin action in the obese Zucker fatty rat. Diabetes 2000; 49(12): 2154–9

    Article  PubMed  CAS  Google Scholar 

  143. Kennedy JW, Hirshman MF, Gervino EV, et al. Acute exercise induces GLUT4 translocation in skeletal muscle of normal human subjects and subjects with type 2 diabetes. Diabetes 1999; 48(5): 1192–7

    Article  PubMed  CAS  Google Scholar 

  144. Young PW, Cawthorne MA, Coyle PJ, et al. Repeat treatment of obese mice with BRL 49653, a new potent insulin sensitizer, enhances insulin action in white adipocytes: association with increased insulin binding and cell-surface GLUT4 as measured by photoaffinity labeling. Diabetes 1995; 44(9): 1087–92

    Article  PubMed  CAS  Google Scholar 

  145. Gibbs EM, Stock JL, McCoid SC, et al. Glycemic improvement in diabetic db/db mice by overexpression of the human insulin-regulatable glucose transporter (GLUT4). J Clin Invest 1995; 95(4): 1512–8

    Article  PubMed  CAS  Google Scholar 

  146. Kuusisto J, Koivisto K, Mykkanen L, et al. Essential hypertension and cognitive function: the role of hyperinsulinemia. Hypertension 1993; 22: 771–9

    Article  PubMed  CAS  Google Scholar 

  147. Stolk R, Breteler M, Alewijn O, et al. Insulin and cognitive function in an elderly population. Diabetes Care 1997; 20(5): 792–5

    Article  PubMed  CAS  Google Scholar 

  148. Richardson JTE. Cognitive function in diabetes mellitus. Neurosci Behav Rev 1989; 14: 385–8

    Article  Google Scholar 

  149. Reaven G, Thompson L. Reduced cognitive function in older patients with non-insulin dependent diabetes: relationship and severity of hyperglycemia. Diabetes Care 1990; 13(1): 16–21

    Article  PubMed  CAS  Google Scholar 

  150. Gradman T, Laws A, Thompson L, et al. Verbal learning and/or memory improves with glycemic control in older subjects with non-insulin-dependent diabetes mellitus. J Am Geriatr Soc 1993; 41: 1305–12

    PubMed  CAS  Google Scholar 

  151. De Angelis Lobo d’Avila K, Gadonski G, Fang J, et al. Exercise reverses peripheral insulin resistance in trained L-NAME-hypertensive rats. Hypertension 1999; 34: 768–22

    Article  PubMed  Google Scholar 

  152. Mayer-Davis E, D’Agostino R, Karter A, et al. Intensity and amount of physical activity in relation to insulin sensitivity: the insulin resistance atherosclerosis study. JAMA 1998; 279(9): 669–74

    Article  PubMed  CAS  Google Scholar 

  153. Carro E, Trejo JL, Busiguina S, et al. Circulating insulin-like growth factor I mediates the protective effects of physical exercise against brain insults of different etiology and anatomy. J Neurosci 2001; 21(15): 5678–84

    PubMed  CAS  Google Scholar 

  154. Laurin D, Verreault R, Lindsay J, et al. Physical activity and risk of cognitive impairment and dementia in elderly persons. Arch Neurol 2001; 58(3): 498–504

    Article  PubMed  CAS  Google Scholar 

  155. Pignatti F, Rozzini R, Trabucchi M. Physical activity and cognitive decline in elderly persons. Arch Intern Med 2002; 11(62): 361–2

    Article  Google Scholar 

  156. Yaffe K, Barnes D, Nevitt M, et al. A prospective study of physical activity and cognitive decline in elderly women: women who walk. Arch Intern Med 2001; 161(14): 1703–8

    Article  PubMed  CAS  Google Scholar 

  157. Kramer AF, Hahn S, Cohen NJ, et al. Ageing, fitness and neuro-cognitive function. Nature 1999; 400(6743): 418–9

    Article  PubMed  CAS  Google Scholar 

  158. Watson GS, Fujimoto W, Petrova A, et al. Exercise and diet are associated with improved memory in Japanese-Americans with impaired glucose tolerance (IGT) [abstract #72]. Society of Neuroscience’s 31st Annual Meeting; 2001 Nov 10–15; San Diego. Soc Neurosci Abstr 2001; 27 (Program no. 72.13)

  159. Peskind ER, Wilkinson CW, Petrie EC, et al. Increased CSF cortisol in Alzheimer’s disease is a function of APOE genotype. Neurology 2001; 56(8): 1094–8

    Article  PubMed  CAS  Google Scholar 

  160. Jack CR, Dickson DW, Parisi JE, et al. Antemortem MRI findings correlate with hippocampal neuropathology in typical aging and dementia. Neurology 2002; 58(5): 750–7

    Article  PubMed  Google Scholar 

  161. Delerive P, Fruchart J-C, Staels B. Paroxisome proliferator-activated receptors in inflammation control. J Endocrinol 2001; 169: 453–9

    Article  PubMed  CAS  Google Scholar 

  162. Paik JH, Ju JH, Lee JY, et al. Two opposing effects of non-steroidal anti-inflammatory drugs on the expression of inducible cyclooxygenase: mediation through different signaling pathways. J Biol Chem 2000; 275(36): 28173–9

    PubMed  CAS  Google Scholar 

  163. Longstreth Jr WT, Dulberg C, Manolio TA, et al. Incidence, manifestations, and predictors of brain infarcts defined by serial cranial magnetic resonance imaging in the elderly: the Cardiovascular Health Study. Stroke 2002 Oct; 33(10): 2376–82

    Article  PubMed  Google Scholar 

Download references

Acknowledgements

This work was supported in part by the Department of Veterans Affairs, USA, and grants (AG00258, AG05136 and AG10880) from the National Institutes of Health, USA, and from GlaxoSmithKline. The authors have no conflicts of interest that are directly relevant to the content of this manuscript.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Suzanne Craft.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Watson, G.S., Craft, S. The Role of Insulin Resistance in the Pathogenesis of Alzheimer’s Disease. Mol Diag Ther 17, 27–45 (2003). https://doi.org/10.2165/00023210-200317010-00003

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.2165/00023210-200317010-00003

Keywords

Navigation