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Erschienen in: Pituitary 4/2007

01.12.2007 | Case Report

Management of type 2 diabetes mellitus associated with pituitary gigantism

verfasst von: Omar Ali, Swati Banerjee, Daniel F. Kelly, Phillip D. K. Lee

Erschienen in: Pituitary | Ausgabe 4/2007

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Abstract

Pituitary gigantism, a condition of endogenous growth hormone (GH) hypersecretion prior to epiphyseal closure, is a rare condition. In the adult condition of GH excess, acromegaly, the occurrence of type 2 diabetes mellitus (T2DM) and diabetic ketoacidosis (DKA) have been reported, with resolution following normalization of GH levels. We report the case of a 16-year-old male with pituitary gigantism due to a large invasive suprasellar adenoma who presented with T2DM and DKA. Despite surgical de-bulking, radiotherapy and medical treatment with cabergoline and pegvisomant, GH and insulin-like growth factor-I (IGF-I) levels remained elevated. However, the T2DM and recurrent DKA were successfully managed with metformin and low-dose glargine insulin, respectively. We review the pathophysiology of T2DM and DKA in growth hormone excess and available treatment options.
Literatur
1.
Zurück zum Zitat Bergson BA, Eden S, Ernest I, Oden A et al (1988) Epidemiology and long-term survival in acromegaly. A study of 166 cases diagnosed between 1955 and 1984. Acta Med Scand 223:327–335 Bergson BA, Eden S, Ernest I, Oden A et al (1988) Epidemiology and long-term survival in acromegaly. A study of 166 cases diagnosed between 1955 and 1984. Acta Med Scand 223:327–335
2.
Zurück zum Zitat Alexander L, Appleton D, Hall R et al (1980) Epidemiology of acromegaly in the Newcastle region. Clin Endocrinol 12:71–79 Alexander L, Appleton D, Hall R et al (1980) Epidemiology of acromegaly in the Newcastle region. Clin Endocrinol 12:71–79
3.
Zurück zum Zitat Etxabe J, Gaztambide S, Latorre P, Vazquez JA (1993) Acromegaly: an epidemiological study. J Endocrinol Invest 16:181–187PubMed Etxabe J, Gaztambide S, Latorre P, Vazquez JA (1993) Acromegaly: an epidemiological study. J Endocrinol Invest 16:181–187PubMed
5.
Zurück zum Zitat Sönksen PH, Greenwood FC, Ellis JP et al (1967) Changes of carbohydrate tolerance in acromegaly with progress of the disease and in response to treatment. J Clin Endocrinol Metab 27:1418–1430PubMedCrossRef Sönksen PH, Greenwood FC, Ellis JP et al (1967) Changes of carbohydrate tolerance in acromegaly with progress of the disease and in response to treatment. J Clin Endocrinol Metab 27:1418–1430PubMedCrossRef
6.
Zurück zum Zitat Møller N, Jørgensen JO, Abildgaard N, Ørskov L, Schmitz O, Christiansen JS (1991) Effects of growth hormone on glucose metabolism. Horm Res 36(suppl 1):32–35PubMed Møller N, Jørgensen JO, Abildgaard N, Ørskov L, Schmitz O, Christiansen JS (1991) Effects of growth hormone on glucose metabolism. Horm Res 36(suppl 1):32–35PubMed
7.
Zurück zum Zitat Arya KR, Pathare AV, Chadda M, Menon PS (1997) Diabetes in acromegaly—a study of 34 cases. J Indian Med Assoc 95:546–547PubMed Arya KR, Pathare AV, Chadda M, Menon PS (1997) Diabetes in acromegaly—a study of 34 cases. J Indian Med Assoc 95:546–547PubMed
8.
Zurück zum Zitat Ezzat S, Forster MJ, Berchtold P et al (1994) Acromegaly. Clinical and biochemical features in 500 patients. Medicine 73:233–240PubMedCrossRef Ezzat S, Forster MJ, Berchtold P et al (1994) Acromegaly. Clinical and biochemical features in 500 patients. Medicine 73:233–240PubMedCrossRef
9.
Zurück zum Zitat Szeto CC, Li KY, Ko GT et al (1997) Acromegaly in a woman presenting with diabetic ketoacidosis and insulin resistance. Int J Clin Pract 51:476–477PubMed Szeto CC, Li KY, Ko GT et al (1997) Acromegaly in a woman presenting with diabetic ketoacidosis and insulin resistance. Int J Clin Pract 51:476–477PubMed
10.
Zurück zum Zitat Katz JR, Edwards R, Khan M, Conway GS (1996) Acromegaly presenting with diabetic ketoacidosis. Postgrad Med J 72:682–683PubMed Katz JR, Edwards R, Khan M, Conway GS (1996) Acromegaly presenting with diabetic ketoacidosis. Postgrad Med J 72:682–683PubMed
11.
Zurück zum Zitat Westphal SA (2000) Concurrent diagnosis of acromegaly and diabetic ketoacidosis. Endocr Pract 6:450–452PubMed Westphal SA (2000) Concurrent diagnosis of acromegaly and diabetic ketoacidosis. Endocr Pract 6:450–452PubMed
12.
Zurück zum Zitat Kuzuya T, Matsuda A, Sakamoto Y et al (1983) A case of pituitary gigantism who had two episodes of diabetic ketoacidosis followed by complete recovery of diabetes. Endocrinol Jpn 30:329–334PubMed Kuzuya T, Matsuda A, Sakamoto Y et al (1983) A case of pituitary gigantism who had two episodes of diabetic ketoacidosis followed by complete recovery of diabetes. Endocrinol Jpn 30:329–334PubMed
13.
Zurück zum Zitat Alvi NS, Kirk JM (1999) Pituitary gigantism causing diabetic ketoacidosis. J Pediatr Endocrinol Metab 12:907–909PubMed Alvi NS, Kirk JM (1999) Pituitary gigantism causing diabetic ketoacidosis. J Pediatr Endocrinol Metab 12:907–909PubMed
14.
Zurück zum Zitat Holt RI, Simpson HL, Sonksen PH (2003) The role of the growth hormone-insulin-like growth factor axis in glucose homeostasis. Diabet Med 20:3–15PubMedCrossRef Holt RI, Simpson HL, Sonksen PH (2003) The role of the growth hormone-insulin-like growth factor axis in glucose homeostasis. Diabet Med 20:3–15PubMedCrossRef
15.
Zurück zum Zitat Møller N, Gjedsted J, Gormsen L et al (2003) Effects of growth hormone on lipid metabolism in humans. Growth Horm IGF Res 13(Suppl A):S18–S21PubMedCrossRef Møller N, Gjedsted J, Gormsen L et al (2003) Effects of growth hormone on lipid metabolism in humans. Growth Horm IGF Res 13(Suppl A):S18–S21PubMedCrossRef
16.
Zurück zum Zitat Kaiser N, Leibowitz G, Nesher R (2003) Glucotoxicity and beta-cell failure in type 2 diabetes mellitus. Pediatr Endocrinol Metab 16:5–22 Kaiser N, Leibowitz G, Nesher R (2003) Glucotoxicity and beta-cell failure in type 2 diabetes mellitus. Pediatr Endocrinol Metab 16:5–22
17.
Zurück zum Zitat McGarry JD, Dobbins RL (1999) Fatty acids, lipotoxicity and insulin secretion. Diabetologia 42:128–138PubMedCrossRef McGarry JD, Dobbins RL (1999) Fatty acids, lipotoxicity and insulin secretion. Diabetologia 42:128–138PubMedCrossRef
18.
Zurück zum Zitat Newton CA, Raskin P (2004) Diabetic ketoacidosis in type 1 and type 2 diabetes mellitus: clinical and biochemical differences. Arch Intern Med 164:1925–1931PubMedCrossRef Newton CA, Raskin P (2004) Diabetic ketoacidosis in type 1 and type 2 diabetes mellitus: clinical and biochemical differences. Arch Intern Med 164:1925–1931PubMedCrossRef
19.
Zurück zum Zitat Arafah BM, Nasrallah MP (2001) Pituitary tumors: pathophysiology, clinical manifestations and management. Endocr Relat Cancer 8:287–305PubMedCrossRef Arafah BM, Nasrallah MP (2001) Pituitary tumors: pathophysiology, clinical manifestations and management. Endocr Relat Cancer 8:287–305PubMedCrossRef
20.
Zurück zum Zitat Zada G, Kelly DF, Cohan P et al (2003) Endonasal transsphenoidal approach for pituitary adenomas and other sellar lesions: an assessment of efficacy, safety, and patient impressions. J Neurosurg 98:350–358PubMed Zada G, Kelly DF, Cohan P et al (2003) Endonasal transsphenoidal approach for pituitary adenomas and other sellar lesions: an assessment of efficacy, safety, and patient impressions. J Neurosurg 98:350–358PubMed
21.
Zurück zum Zitat Ahmed S, Elsheikh M, Stratton IM et al (1999) Outcome of transphenoidal surgery for acromegaly and its relationship to surgical experience. Clin Endocrinol 50:561–567CrossRef Ahmed S, Elsheikh M, Stratton IM et al (1999) Outcome of transphenoidal surgery for acromegaly and its relationship to surgical experience. Clin Endocrinol 50:561–567CrossRef
22.
Zurück zum Zitat Thorner MO (2003) Controversy: radiotherapy for acromegaly. Clin Endocrinol 58:136–137CrossRef Thorner MO (2003) Controversy: radiotherapy for acromegaly. Clin Endocrinol 58:136–137CrossRef
23.
Zurück zum Zitat Wass JA (2003) Radiotherapy in acromegaly: a protagonists viewpoint. Clin Endocrinol 58:128–131CrossRef Wass JA (2003) Radiotherapy in acromegaly: a protagonists viewpoint. Clin Endocrinol 58:128–131CrossRef
24.
Zurück zum Zitat Barkan AL (2003) Radiotherapy in acromegaly: the argument against. Clin Endocrinol 58:132–135CrossRef Barkan AL (2003) Radiotherapy in acromegaly: the argument against. Clin Endocrinol 58:132–135CrossRef
25.
Zurück zum Zitat Racine M, Barkan A (2003) Somatostatin analogs in medical treatment of acromegaly. Endocrine 20:271–278PubMedCrossRef Racine M, Barkan A (2003) Somatostatin analogs in medical treatment of acromegaly. Endocrine 20:271–278PubMedCrossRef
26.
Zurück zum Zitat Koop BL, Harris AG, Ezzat S (1994) Effect of octreotide on glucose tolerance in acromegaly. Eur J Endocrinol 130:581–586PubMedCrossRef Koop BL, Harris AG, Ezzat S (1994) Effect of octreotide on glucose tolerance in acromegaly. Eur J Endocrinol 130:581–586PubMedCrossRef
27.
Zurück zum Zitat Webb SM, Ortega E, Rodriguez-Espinosa J et al (2001) Decreased insulin requirements after LAR-octreotide but not after lanreotide in an acromegalic patient. Pituitary 4:275–278PubMedCrossRef Webb SM, Ortega E, Rodriguez-Espinosa J et al (2001) Decreased insulin requirements after LAR-octreotide but not after lanreotide in an acromegalic patient. Pituitary 4:275–278PubMedCrossRef
28.
Zurück zum Zitat Trainer PJ, Drake WM, Katznelson L et al (2000) Treatment of acromegaly with the growth hormone-receptor antagonist pegvisomant. N Engl J Med 342:1171–1177PubMedCrossRef Trainer PJ, Drake WM, Katznelson L et al (2000) Treatment of acromegaly with the growth hormone-receptor antagonist pegvisomant. N Engl J Med 342:1171–1177PubMedCrossRef
29.
Zurück zum Zitat Drake WM, Parkinson C, Besser GM, Trainer PJ (2001) Clinical use of a growth hormone receptor antagonist in the treatment of acromegaly. Trends Endocrinol Metab 12:408–413PubMedCrossRef Drake WM, Parkinson C, Besser GM, Trainer PJ (2001) Clinical use of a growth hormone receptor antagonist in the treatment of acromegaly. Trends Endocrinol Metab 12:408–413PubMedCrossRef
30.
Zurück zum Zitat Friend KE (2002) Acromegaly: a new therapy. Cancer Control 9:232–235PubMed Friend KE (2002) Acromegaly: a new therapy. Cancer Control 9:232–235PubMed
31.
Zurück zum Zitat Schreiber I, Buchfelder M, Droste M et al (2007) Treatment of acromegaly with the GH receptor antagonist pegvisomant in clinical practice: Safety and efficacy evaluation from the German Pegvisomant Observational Study. Eur J Endocrinol 156:75–82PubMedCrossRef Schreiber I, Buchfelder M, Droste M et al (2007) Treatment of acromegaly with the GH receptor antagonist pegvisomant in clinical practice: Safety and efficacy evaluation from the German Pegvisomant Observational Study. Eur J Endocrinol 156:75–82PubMedCrossRef
32.
Zurück zum Zitat Zhou G, Myers R, Li Y et al (2001) Role of AMP-activated protein kinase in mechanism of metformin action. J Clin Invest 108:1167–1174PubMedCrossRef Zhou G, Myers R, Li Y et al (2001) Role of AMP-activated protein kinase in mechanism of metformin action. J Clin Invest 108:1167–1174PubMedCrossRef
33.
Zurück zum Zitat Hawley SA, Gadalla AE, Olsen GS, Hardie DG (2002) The antidiabetic drug metformin activates the AMP-activated protein kinase cascade via an adenine nucleotide-independent mechanism. Diabetes 51:2420–2425PubMedCrossRef Hawley SA, Gadalla AE, Olsen GS, Hardie DG (2002) The antidiabetic drug metformin activates the AMP-activated protein kinase cascade via an adenine nucleotide-independent mechanism. Diabetes 51:2420–2425PubMedCrossRef
34.
Zurück zum Zitat Hardie DG, Carling D (1997) The AMP-activated protein kinase: fuel gauge of the mammalian cell? Eur J Biochem 246:259–273PubMedCrossRef Hardie DG, Carling D (1997) The AMP-activated protein kinase: fuel gauge of the mammalian cell? Eur J Biochem 246:259–273PubMedCrossRef
35.
Zurück zum Zitat Lochhead PA, Salt IP, Walker KS et al (2000). 5-aminoimidazole-4-carboxamide riboside mimics the effects of insulin on the expression of the 2 key gluconeogenic genes PEPCK and glucose-6-phosphatase. Diabetes 49:896–903PubMedCrossRef Lochhead PA, Salt IP, Walker KS et al (2000). 5-aminoimidazole-4-carboxamide riboside mimics the effects of insulin on the expression of the 2 key gluconeogenic genes PEPCK and glucose-6-phosphatase. Diabetes 49:896–903PubMedCrossRef
36.
Zurück zum Zitat Hundal RS, Krssak M, Dufour S et al (2000) Mechanism by which metformin reduces glucose production in type 2 diabetes. Diabetes. 49:2063–2069PubMedCrossRef Hundal RS, Krssak M, Dufour S et al (2000) Mechanism by which metformin reduces glucose production in type 2 diabetes. Diabetes. 49:2063–2069PubMedCrossRef
37.
Zurück zum Zitat Towler MC, Hardie DG (2007) AMP-activated protein kinase in metabolic control and insulin signaling. Circ Res 100:328–341PubMedCrossRef Towler MC, Hardie DG (2007) AMP-activated protein kinase in metabolic control and insulin signaling. Circ Res 100:328–341PubMedCrossRef
38.
Zurück zum Zitat Perriello G, Misericordia P, Volpi E et al (1994) Acute antihyperglycemic mechanisms of metformin in NIDDM. Evidence for suppression of lipid oxidation and hepatic glucose production. Diabetes 43:920–928PubMedCrossRef Perriello G, Misericordia P, Volpi E et al (1994) Acute antihyperglycemic mechanisms of metformin in NIDDM. Evidence for suppression of lipid oxidation and hepatic glucose production. Diabetes 43:920–928PubMedCrossRef
39.
Zurück zum Zitat Lupi R, Del Guerra S, Fierabracci V et al (2002) Lipotoxicity in human pancreatic islets and the protective effect of metformin. Diabetes. 51(Suppl 1):S134–S137PubMedCrossRef Lupi R, Del Guerra S, Fierabracci V et al (2002) Lipotoxicity in human pancreatic islets and the protective effect of metformin. Diabetes. 51(Suppl 1):S134–S137PubMedCrossRef
40.
Zurück zum Zitat Wiernsperger NF, Bailey CJ (1999) The antihyperglycaemic effect of metformin: therapeutic and cellular mechanisms. Drugs 58 Suppl 1:31–39; discussion 75–82 Wiernsperger NF, Bailey CJ (1999) The antihyperglycaemic effect of metformin: therapeutic and cellular mechanisms. Drugs 58 Suppl 1:31–39; discussion 75–82
41.
Zurück zum Zitat Ikeda T, Iwata K, Murakami H (2000) Inhibitory effect of metformin on intestinal glucose absorption in the perfused rat intestine. Biochem Pharmacol 59:887–890PubMedCrossRef Ikeda T, Iwata K, Murakami H (2000) Inhibitory effect of metformin on intestinal glucose absorption in the perfused rat intestine. Biochem Pharmacol 59:887–890PubMedCrossRef
42.
Zurück zum Zitat Drake WM, Rowles SV, Roberts ME et al (2003) Insulin sensitivity and glucose tolerance improve in patients with acromegaly converted from depot octreotide to pegvisomant. Eur J Endocrinol 149:521–527PubMedCrossRef Drake WM, Rowles SV, Roberts ME et al (2003) Insulin sensitivity and glucose tolerance improve in patients with acromegaly converted from depot octreotide to pegvisomant. Eur J Endocrinol 149:521–527PubMedCrossRef
43.
Zurück zum Zitat Kay JP, Alemzadeh R, Langley G et al (2001) Beneficial effects of metformin in normoglycemic morbidly obese adolescents. Metabolism 50:1457–1461PubMedCrossRef Kay JP, Alemzadeh R, Langley G et al (2001) Beneficial effects of metformin in normoglycemic morbidly obese adolescents. Metabolism 50:1457–1461PubMedCrossRef
44.
Zurück zum Zitat Lee A, Morley JE (1998) Metformin decreases food consumption and induces weight loss in subjects with obesity with type II non-insulin-dependent diabetes. Obes Res 6:47–53PubMed Lee A, Morley JE (1998) Metformin decreases food consumption and induces weight loss in subjects with obesity with type II non-insulin-dependent diabetes. Obes Res 6:47–53PubMed
Metadaten
Titel
Management of type 2 diabetes mellitus associated with pituitary gigantism
verfasst von
Omar Ali
Swati Banerjee
Daniel F. Kelly
Phillip D. K. Lee
Publikationsdatum
01.12.2007
Verlag
Springer US
Erschienen in
Pituitary / Ausgabe 4/2007
Print ISSN: 1386-341X
Elektronische ISSN: 1573-7403
DOI
https://doi.org/10.1007/s11102-007-0060-8

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