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Psychopharmaka und Diabetes

Psychotropic drugs and diabetes

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Summary

Psychotropic drugs, such as antipsychotics and antidepressants, are widely used substances which can display marked metabolic side effects. Psychiatric patients display increased morbidity and mortality which, besides disease specific factors, may be attributed to metabolic side effects of psychotropic drugs. Commonly observed side effects of antipsychotics are weight gain as well as disturbances in glucose and lipid metabolism. Additionally, antipsychotics have been shown to increase diabetes risk. Also, the use of some of the antidepressant substances is associated with an increased diabetes risk. However, large inter-substance variations have been observed. Conversely, diabetics have an increased risk of depression. Metabolic side effects of psychotropic drugs pose a serious impairment for psychiatric patients and their management can play a pivotal role in therapeutic compliance and success. This review aims to give an overview of metabolic side effects of commonly used psychotic drugs and to give an insight into possible underlying mechanisms.

Zusammenfassung

Psychopharmaka, wie zum Beispiel Antipsychotika oder Antidepressiva, sind weit verbreitete Substanzen, welche in vielen Fällen ein ungünstiges metabolisches Nebenwirkungsprofil aufweisen. Die zu erwartenden metabolischen Nebenwirkungen unter Antipsychotikatherapie umfassen eine teilweise stark ausgeprägte Gewichtszunahme, eine Erhöhung des Diabetesrisikos und die Ausbildung eines atherogenen Lipidprofils. Die Einnahme von Antidepressiva geht ebenfalls mit einem erhöhten Risiko an Diabetes zu erkranken einher, wobei große Unterschiede zwischen den einzelnen Substanzen bestehen. Zusätzlich scheint es sich um eine wechselseitige Beziehung zwischen Depressionen und Diabetes zu handeln, da Diabetiker ein signifikant höheres Risiko haben an Depressionen zu erkranken als die Normalbevölkerung. Metabolische Nebenwirkungen von Psychopharmaka stellen eine ernst zu nehmende Beeinträchtigung für psychisch kranke Patienten dar und ihre Behandlungsregime können einen entscheidenden Faktor für die Compliance und damit einhergehend dem Therapieerfolg der betroffenen Patienten darstellen. Dieser Beitrag soll einen Überblick über die metabolischen Nebenwirkungen häufig verwendeter Psychopharmaka und einen Einblick in mögliche zugrundeliegende Mechanismen bieten.

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Literatur

  • Newcomer JW, Hennekens CH. Severe mental illness and risk of cardiovascular disease. JAMA, 298: 1794–1796, 2007

    PubMed  CAS  Google Scholar 

  • Roick C, Fritz-Wieacker A, Matschinger H, et al. Health habits of patients with schizophrenia. Soc Psychiatry Psychiatr Epidemiol, 42: 268–276, 2007

    PubMed  Google Scholar 

  • Lindamer LA, McKibbin C, Norman GJ, et al. Assessment of physical activity in middle-aged and older adults with schizophrenia. Schizophr Res, 104: 294–301, 2008

    PubMed  Google Scholar 

  • Gracious BL, Cook SR, Meyer AE, et al. Prevalence of overweight and obesity in adolescents with severe mental illness: a cross-sectional chart review. J Clin Psychiatry, 71: 949–954, 2010

    PubMed  Google Scholar 

  • Sundell KA, Gissler M, Petzold M, et al. Antidepressant utilization patterns and mortality in Swedish men and women aged 20–34 years. Eur J Clin Pharmacol, 67: 169–178, 2011

    PubMed  Google Scholar 

  • Jin H, Folsom D, Sasaki A, et al. Increased Framingham 10-year risk of coronary heart disease in middle-aged and older patients with psychotic symptoms. Schizophr Res, 125: 295–299, 2011

    PubMed  Google Scholar 

  • Haslam DW, James WP. Obesity. Lancet, 366: 1197–1209, 2005

    PubMed  Google Scholar 

  • Tschoner A, Engl J, Laimer M, et al. Metabolic side effects of antipsychotic medication. Int J Clin Pract, 61: 1356–1370, 2007

    PubMed  CAS  Google Scholar 

  • Smith M, Hopkins D, Peveler RC, et al. First- v. second-generation antipsychotics and risk for diabetes in schizophrenia: systematic review and meta-analysis. Br J Psychiatry, 192: 406–411, 2008

    PubMed  CAS  Google Scholar 

  • Rouillon F, Sorbara F. Schizophrenia and diabetes: epidemiological data. Eur Psychiatry, 20(Suppl 4): S345–S348, 2005

    PubMed  Google Scholar 

  • Allison DB, Casey DE. Antipsychotic-induced weight gain: a review of the literature. J Clin Psychiatry, 62(Suppl 7): 22–31, 2001

    PubMed  CAS  Google Scholar 

  • Allison DB, Mentore JL, Heo M, et al. Antipsychotic-induced weight gain: a comprehensive research synthesis. Am J Psychiatry, 156: 1686–1696, 1999

    PubMed  CAS  Google Scholar 

  • Coodin S. Body mass index in persons with schizophrenia. Can J Psychiatry, 46: 549–555, 2001

    PubMed  CAS  Google Scholar 

  • Kessing LV, Thomsen AF, Mogensen UB, et al. Treatment with antipsychotics and the risk of diabetes in clinical practice. Br J Psychiatry, 197: 266–271, 2010

    PubMed  Google Scholar 

  • Chen DC, Zhou MA, Zhou DH, et al. Gender differences in the prevalence of diabetes mellitus in chronic hospitalized patients with schizophrenia on long-term antipsychotics. Psychiatry Res, 186: 451–453, 2011

    CAS  Google Scholar 

  • Consensus development conference on antipsychotic drugs and obesity and diabetes. Diabetes Care, 27: 596–601, 2004

    Google Scholar 

  • Komossa K, Rummel-Kluge C, Hunger H, et al. Olanzapine versus other atypical antipsychotics for schizophrenia. Cochrane Database Syst Rev, 2010: CD006654, 2010

    Google Scholar 

  • Lieberman JA, Stroup TS, McEvoy JP, et al. Effectiveness of antipsychotic drugs in patients with chronic schizophrenia. N Engl J Med, 353: 1209–1223, 2005

    PubMed  CAS  Google Scholar 

  • Eder U, Mangweth B, Ebenbichler C, et al. Association of olanzapine-induced weight gain with an increase in body fat. Am J Psychiatry, 158: 1719–1722, 2001

    PubMed  CAS  Google Scholar 

  • Wetterling T. Bodyweight gain with atypical antipsychotics. A comparative review. Drug Saf, 24: 59–73, 2001

    PubMed  CAS  Google Scholar 

  • Tschoner A, Engl J, Rettenbacher M, et al. Effects of six second generation antipsychotics on body weight and metabolism – risk assessment and results from a prospective study. Pharmacopsychiatry, 42: 29–34, 2009

    PubMed  CAS  Google Scholar 

  • Ebenbichler CF, Laimer M, Eder U, et al. Olanzapine induces insulin resistance: results from a prospective study. J Clin Psychiatry, 64: 1436–1439, 2003

    PubMed  CAS  Google Scholar 

  • Avram AM, Patel V, Taylor HC, et al. Euglycemic clamp study in clozapine-induced diabetic ketoacidosis. Ann Pharmacother, 35: 1381–1387, 2001

    PubMed  CAS  Google Scholar 

  • Koro CE, Fedder DO, L'Italien GJ, et al. Assessment of independent effect of olanzapine and risperidone on risk of diabetes among patients with schizophrenia: population based nested case-control study. BMJ, 325: 243, 2002

    PubMed  CAS  Google Scholar 

  • Koro CE, Fedder DO, L'Italien GJ, et al. An assessment of the independent effects of olanzapine and risperidone exposure on the risk of hyperlipidemia in schizophrenic patients. Arch Gen Psychiatry, 59: 1021–1026, 2002

    PubMed  CAS  Google Scholar 

  • Daumit GL, Goff DC, Meyer JM, et al. Antipsychotic effects on estimated 10-year coronary heart disease risk in the CATIE schizophrenia study. Schizophr Res, 105: 175–187, 2008

    PubMed  Google Scholar 

  • American Diabetes Association; American Psychiatric Association; American Association of Clinical Endocrinologists; North American Association for the Study of Obesity. Consensus development conference on antipsychotic drugs and obesity and diabetes. J Clin Psychiatry, 65: 267–272, 2004

    Google Scholar 

  • Parsons B, Allison DB, Loebel A, et al. Weight effects associated with antipsychotics: a comprehensive database analysis. Schizophr Res, 110: 103–110, 2009

    PubMed  Google Scholar 

  • De Hert M, Mittoux A, He Y, et al. Metabolic parameters in the short- and long-term treatment of schizophrenia with sertindole or risperidone. Eur Arch Psychiatry Clin Neurosci, 261: 231–239, 2011

    PubMed  Google Scholar 

  • Kibbey KJ, Roberts AM, Nicholson GC. Diabetic ketoacidosis and elevated serum lipase in the setting of aripiprazole therapy. Diabetes Care, 33: e96, 2010

    PubMed  Google Scholar 

  • Church CO, Stevens DL, Fugate SE. Diabetic ketoacidosis associated with aripiprazole. Diabet Med, 22: 1440–1443, 2005

    PubMed  CAS  Google Scholar 

  • Reddymasu S, Bahta E, Levine S, et al. Elevated lipase and diabetic ketoacidosis associated with aripiprazole. JOP, 7: 303–305, 2006

    PubMed  Google Scholar 

  • Peuskens J, De Hert M, Mortimer A. Metabolic control in patients with schizophrenia treated with amisulpride or olanzapine. Int Clin Psychopharmacol, 22: 145–152, 2007

    PubMed  Google Scholar 

  • Blonde L, Kan HJ, Gutterman EM, et al. Predicted risk of diabetes and coronary heart disease in patients with schizophrenia: aripiprazole versus standard of care. J Clin Psychiatry, 69: 741–748, 2008

    PubMed  Google Scholar 

  • Meyer JM, Davis VG, McEvoy JP, et al. Impact of antipsychotic treatment on nonfasting triglycerides in the CATIE Schizophrenia Trial phase 1. Schizophr Res, 103: 104–109, 2008

    PubMed  Google Scholar 

  • Yood MU, DeLorenze G, Quesenberry CP Jr, et al. The incidence of diabetes in atypical antipsychotic users differs according to agent – results from a multisite epidemiologic study. Pharmacoepidemiol Drug Saf, 18: 791–799, 2009

    PubMed  Google Scholar 

  • McIntyre RS, Cragin L, Sorensen S, et al. Comparison of the metabolic and economic consequences of long-term treatment of schizophrenia using ziprasidone, olanzapine, quetiapine and risperidone in Canada: a cost-effectiveness analysis. J Eval Clin Pract, 16: 744–755, 2010

    PubMed  Google Scholar 

  • Bushe CJ, Leonard BE. Blood glucose and schizophrenia: a systematic review of prospective randomized clinical trials. J Clin Psychiatry, 68: 1682–1690, 2007

    PubMed  CAS  Google Scholar 

  • Nasrallah HA, Meyer JM, Goff DC, et al. Low rates of treatment for hypertension, dyslipidemia and diabetes in schizophrenia: data from the CATIE schizophrenia trial sample at baseline. Schizophr Res, 86: 15–22, 2006

    PubMed  Google Scholar 

  • De Hert M, Schreurs V, Sweers K, et al. Typical and atypical antipsychotics differentially affect long-term incidence rates of the metabolic syndrome in first-episode patients with schizophrenia: a retrospective chart review. Schizophr Res, 101: 295–303, 2008

    PubMed  Google Scholar 

  • De Hert M, Dekker JM, Wood D, et al. Cardiovascular disease and diabetes in people with severe mental illness position statement from the European Psychiatric Association (EPA), supported by the European Association for the Study of Diabetes (EASD) and the European Society of Cardiology (ESC). Eur Psychiatry, 24: 412–424, 2009

    PubMed  CAS  Google Scholar 

  • Nasrallah HA. Atypical antipsychotic-induced metabolic side effects: insights from receptor-binding profiles. Mol Psychiatry, 13: 27–35, 2008

    PubMed  CAS  Google Scholar 

  • Leibowitz SF, Alexander JT. Hypothalamic serotonin in control of eating behavior, meal size, and body weight. Biol Psychiatry, 44: 851–864, 1998

    PubMed  CAS  Google Scholar 

  • Sicard MN, Zai CC, Tiwari AK, et al. Polymorphisms of the HTR2C gene and antipsychotic-induced weight gain: an update and meta-analysis. Pharmacogenomics, 11: 1561–1571, 2010

    PubMed  CAS  Google Scholar 

  • De Luca V, Mueller DJ, de Bartolomeis A, et al. Association of the HTR2C gene and antipsychotic induced weight gain: a meta-analysis. Int J Neuropsychopharmacol, 10: 697–704, 2007

    PubMed  CAS  Google Scholar 

  • Nonogaki K, Strack AM, Dallman MF, et al. Leptin-independent hyperphagia and type 2 diabetes in mice with a mutated serotonin 5-HT2C receptor gene. Nat Med, 4: 1152–1156, 1998

    PubMed  CAS  Google Scholar 

  • Reynolds GP, Kirk SL. Metabolic side effects of antipsychotic drug treatment – pharmacological mechanisms. Pharmacol Ther, 125: 169–179, 2010

    PubMed  CAS  Google Scholar 

  • Reynolds GP, Zhang ZJ, Zhang XB. Association of antipsychotic drug-induced weight gain with a 5-HT2C receptor gene polymorphism. Lancet, 359: 2086–2087, 2002

    PubMed  CAS  Google Scholar 

  • Templeman LA, Reynolds GP, Arranz B, et al. Polymorphisms of the 5-HT2C receptor and leptin genes are associated with antipsychotic drug-induced weight gain in Caucasian subjects with a first-episode psychosis. Pharmacogenet Genomics, 15: 195–200, 2005

    PubMed  CAS  Google Scholar 

  • Garcia-Tornadu I, Perez-Millan MI, Recouvreux V, et al. New insights into the endocrine and metabolic roles of dopamine D2 receptors gained from the Drd2 mouse. Neuroendocrinology, 92: 207–214, 2010

    PubMed  CAS  Google Scholar 

  • Muller DJ, Zai CC, Sicard M, et al. Systematic analysis of dopamine receptor genes (DRD1-DRD5) in antipsychotic-induced weight gain. Pharmacogenomics J, 2010 Aug 17. [Epub ahead of print]

  • Lencz T, Robinson DG, Napolitano B, et al. DRD2 promoter region variation predicts antipsychotic-induced weight gain in first episode schizophrenia. Pharmacogenet Genomics, 20: 569–572, 2010

    PubMed  CAS  Google Scholar 

  • Ratliff JC, Barber JA, Palmese LB, et al. Association of prescription H1 antihistamine use with obesity: results from the National Health and Nutrition Examination Survey. Obesity (Silver Spring), 18: 2398–2400, 2010

    CAS  Google Scholar 

  • Han M, Deng C, Burne TH, et al. Short- and long-term effects of antipsychotic drug treatment on weight gain and H1 receptor expression. Psychoneuroendocrinology, 33: 569–580, 2008

    PubMed  CAS  Google Scholar 

  • Kroeze WK, Hufeisen SJ, Popadak BA, et al. H1-histamine receptor affinity predicts short-term weight gain for typical and atypical antipsychotic drugs. Neuropsychopharmacology, 28: 519–526, 2003

    PubMed  CAS  Google Scholar 

  • Deng C, Weston-Green K, Huang XF. The role of histaminergic H1 and H3 receptors in food intake: a mechanism for atypical antipsychotic-induced weight gain? Prog Neuropsychopharmacol Biol Psychiatry, 34: 1–4, 2010

    PubMed  Google Scholar 

  • Arrang JM. Histamine and schizophrenia. Int Rev Neurobiol, 78: 247–287, 2007

    PubMed  CAS  Google Scholar 

  • Friedman JM, Halaas JL. Leptin and the regulation of body weight in mammals. Nature, 395: 763–770, 1998

    PubMed  CAS  Google Scholar 

  • Laimer M, Kramer-Reinstadler K, Rauchenzauner M, et al. Effect of mirtazapine treatment on body composition and metabolism. J Clin Psychiatry, 67: 421–424, 2006

    PubMed  CAS  Google Scholar 

  • Melkersson KI, Hulting AL. Insulin and leptin levels in patients with schizophrenia or related psychoses – a comparison between different antipsychotic agents. Psychopharmacology (Berl), 154: 205–212, 2001

    CAS  Google Scholar 

  • Venkatasubramanian G, Chittiprol S, Neelakantachar N, et al. A longitudinal study on the impact of antipsychotic treatment on serum leptin in schizophrenia. Clin Neuropharmacol, 33: 288–292, 2010

    PubMed  CAS  Google Scholar 

  • Calarge CA, Ellingrod VL, Zimmerman B, et al. Leptin gene -2548G/A variants predict risperidone-associated weight gain in children and adolescents. Psychiatr Genet, 19: 320–327, 2009

    PubMed  Google Scholar 

  • Perez-Iglesias R, Mata I, Amado JA, et al. Effect of FTO, SH2B1, LEP, and LEPR polymorphisms on weight gain associated with antipsychotic treatment. J Clin Psychopharmacol, 30: 661–666, 2010

    PubMed  CAS  Google Scholar 

  • Opgen-Rhein C, Brandl EJ, Muller DJ, et al. Association of HTR2C, but not LEP or INSIG2, genes with antipsychotic-induced weight gain in a German sample. Pharmacogenomics, 11: 773–780, 2010

    PubMed  CAS  Google Scholar 

  • Engl J, Laimer M, Niederwanger A, et al. Olanzapine impairs glycogen synthesis and insulin signaling in L6 skeletal muscle cells. Mol Psychiatry, 10: 1089–1096, 2005

    PubMed  CAS  Google Scholar 

  • Pollmacher T, Hinze-Selch D, Mullington J. Effects of clozapine on plasma cytokine and soluble cytokine receptor levels. J Clin Psychopharmacol, 16: 403–409, 1996

    PubMed  CAS  Google Scholar 

  • Haack M, Hinze-Selch D, Fenzel T, et al. Plasma levels of cytokines and soluble cytokine receptors in psychiatric patients upon hospital admission: effects of confounding factors and diagnosis. J Psychiatr Res, 33: 407–418, 1999

    PubMed  CAS  Google Scholar 

  • Johnson DE, Yamazaki H, Ward KM, et al. Inhibitory effects of antipsychotics on carbachol-enhanced insulin secretion from perifused rat islets: role of muscarinic antagonism in antipsychotic-induced diabetes and hyperglycemia. Diabetes, 54: 1552–1558, 2005

    PubMed  CAS  Google Scholar 

  • Sasaki N, Iwase M, Uchizono Y, et al. The atypical antipsychotic clozapine impairs insulin secretion by inhibiting glucose metabolism and distal steps in rat pancreatic islets. Diabetologia, 49: 2930–2938, 2006

    PubMed  CAS  Google Scholar 

  • Tschoner A, Fleischhacker WW, Ebenbichler CF. Experimental antipsychotics and metabolic adverse effects – findings from clinical trials. Curr Opin Investig Drugs, 10: 1041–1048, 2009

    PubMed  CAS  Google Scholar 

  • Olfson M, Marcus SC. National patterns in antidepressant medication treatment. Arch Gen Psychiatry, 66: 848–856, 2009

    PubMed  Google Scholar 

  • Anderson RJ, Freedland KE, Clouse RE, et al. The prevalence of comorbid depression in adults with diabetes: a meta-analysis. Diabetes Care, 24: 1069–1078, 2001

    PubMed  CAS  Google Scholar 

  • Toplak H, Abrahamian H. Impact of depression on diabetes mellitus. Obes Facts, 2: 211–215, 2009

    PubMed  Google Scholar 

  • Hennings JM, Ising M, Grautoff S, et al. Glucose tolerance in depressed inpatients, under treatment with mirtazapine and in healthy controls. Exp Clin Endocrinol Diabetes, 118: 98–100, 2010

    PubMed  CAS  Google Scholar 

  • Simon GE, Von Korff M, Saunders K, et al. Association between obesity and psychiatric disorders in the US adult population. Arch Gen Psychiatry, 63: 824–830, 2006

    PubMed  Google Scholar 

  • Rubin RR, Ma Y, Marrero DG, et al. Elevated depression symptoms, antidepressant medicine use, and risk of developing diabetes during the diabetes prevention program. Diabetes Care, 31: 420–426, 2008

    PubMed  Google Scholar 

  • Knol MJ, Geerlings MI, Egberts AC, et al. No increased incidence of diabetes in antidepressant users. Int Clin Psychopharmacol, 22: 382–386, 2007

    PubMed  Google Scholar 

  • Andersohn F, Schade R, Suissa S, et al. Long-term use of antidepressants for depressive disorders and the risk of diabetes mellitus. Am J Psychiatry, 166: 591–598, 2009

    PubMed  Google Scholar 

  • Himmerich H, Fulda S, Schaaf L, et al. Changes in weight and glucose tolerance during treatment with mirtazapine. Diabetes Care, 29: 170, 2006

    PubMed  Google Scholar 

  • Kraus T, Haack M, Schuld A, et al. Body weight, the tumor necrosis factor system, and leptin production during treatment with mirtazapine or venlafaxine. Pharmacopsychiatry, 35: 220–225, 2002

    PubMed  CAS  Google Scholar 

  • Chiu HW, Li TC. Rapid weight gain during mirtazapine treatment. J Neuropsychiatry Clin Neurosci, 23: E7, 2011

    PubMed  Google Scholar 

  • Fisfalen ME, Hsiung RC. Glucose dysregulation and mirtazapine-induced weight gain. Am J Psychiatry, 160: 797, 2003

    PubMed  Google Scholar 

  • Serretti A, Mandelli L. Antidepressants and body weight: a comprehensive review and meta-analysis. J Clin Psychiatry, 71: 1259–1272, 2010

    PubMed  Google Scholar 

  • Lustman PJ, Williams MM, Sayuk GS, et al. Factors influencing glycemic control in type 2 diabetes during acute- and maintenance-phase treatment of major depressive disorder with bupropion. Diabetes Care, 30: 459–466, 2007

    PubMed  CAS  Google Scholar 

  • Greenway FL, Fujioka K, Plodkowski RA, et al. Effect of naltrexone plus bupropion on weight loss in overweight and obese adults (COR-I): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial. Lancet, 376: 595–605, 2010

    PubMed  CAS  Google Scholar 

  • Katsiki N, Hatzitolios AI, Mikhailidis DP. Naltrexone sustained-release (SR) + bupropion SR combination therapy for the treatment of obesity: 'A new kid on the block'? Ann Med, 43: 249–258, 2011

    PubMed  CAS  Google Scholar 

  • Raeder MB, Bjelland I, Emil Vollset S, et al. Obesity, dyslipidemia, and diabetes with selective serotonin reuptake inhibitors: the Hordaland Health Study. J Clin Psychiatry, 67: 1974–1982, 2006

    PubMed  CAS  Google Scholar 

  • Xiong GL, Jiang W, Clare R, et al. Prognosis of patients taking selective serotonin reuptake inhibitors before coronary artery bypass grafting. Am J Cardiol, 98: 42–47, 2006

    PubMed  CAS  Google Scholar 

  • McIntyre RS, Soczynska JK, Konarski JZ, et al. The effect of antidepressants on glucose homeostasis and insulin sensitivity: synthesis and mechanisms. Expert Opin Drug Saf, 5: 157–168, 2006

    PubMed  CAS  Google Scholar 

  • Gray DS, Fujioka K, Devine W, et al. A randomized double-blind clinical trial of fluoxetine in obese diabetics. Int J Obes Relat Metab Disord, 16(Suppl 4): S67–S72, 1992

    PubMed  Google Scholar 

  • Maheux P, Ducros F, Bourque J, et al. Fluoxetine improves insulin sensitivity in obese patients with non-insulin-dependent diabetes mellitus independently of weight loss. Int J Obes Relat Metab Disord, 21: 97–102, 1997

    PubMed  CAS  Google Scholar 

  • Potter van Loon BJ, Radder JK, Frolich M, et al. Fluoxetine increases insulin action in obese nondiabetic and in obese non-insulin-dependent diabetic individuals. Int J Obes Relat Metab Disord, 16: 79–85, 1992

    PubMed  CAS  Google Scholar 

  • Dastjerdi MS, Kazemi F, Najafian A, et al. An open-label pilot study of the combination therapy of metformin and fluoxetine for weight reduction. Int J Obes (Lond), 31: 713–717, 2007

    Google Scholar 

  • Rudolph RL, Fabre LF, Feighner JP, et al. A randomized, placebo-controlled, dose-response trial of venlafaxine hydrochloride in the treatment of major depression. J Clin Psychiatry, 59: 116–122, 1998

    PubMed  CAS  Google Scholar 

  • Harrison CL, Ferrier N, Young AH. Tolerability of high-dose venlafaxine in depressed patients. J Psychopharmacol, 18: 200–204, 2004

    PubMed  CAS  Google Scholar 

  • Abrahamian H, Hofmann P, Prager R, et al. Diabetes mellitus and co-morbid depression: treatment with milnacipran results in significant improvement of both diseases (results from the Austrian MDDM study group). Neuropsychiatr Dis Treat, 5: 261–266, 2009

    PubMed  CAS  Google Scholar 

  • Aronne LJ, Segal KR. Weight gain in the treatment of mood disorders. J Clin Psychiatry, 64(Suppl 8): 22–29, 2003

    PubMed  CAS  Google Scholar 

  • Papakostas GI, Nelson JC, Kasper S, et al. A meta-analysis of clinical trials comparing reboxetine, a norepinephrine reuptake inhibitor, with selective serotonin reuptake inhibitors for the treatment of major depressive disorder. Eur Neuropsychopharmacol, 18: 122–127, 2008

    PubMed  CAS  Google Scholar 

  • Kopf D, Westphal S, Luley CW, et al. Lipid metabolism and insulin resistance in depressed patients: significance of weight, hypercortisolism, and antidepressant treatment. J Clin Psychopharmacol, 24: 527–531, 2004

    PubMed  CAS  Google Scholar 

  • Gutierrez A, Saracibar G, Casis L, et al. Effects of fluoxetine administration on neuropeptide y and orexins in obese zucker rat hypothalamus. Obes Res, 10: 532–540, 2002

    PubMed  CAS  Google Scholar 

  • Myung CS, Kim BT, Choi SH, et al. Role of neuropeptide Y and proopiomelanocortin in fluoxetine-induced anorexia. Arch Pharm Res, 28: 716–721, 2005

    PubMed  CAS  Google Scholar 

  • Dryden S, Frankish HM, Wang Q, et al. Increased feeding and neuropeptide Y (NPY) but not NPY mRNA levels in the hypothalamus of the rat following central administration of the serotonin synthesis inhibitor p-chlorophenylalanine. Brain Res, 724: 232–237, 1996

    PubMed  CAS  Google Scholar 

  • Kalra SP, Kalra PS. Neuropeptide Y: a physiological orexigen modulated by the feedback action of ghrelin and leptin. Endocrine, 22: 49–56, 2003

    PubMed  CAS  Google Scholar 

  • Nguyen AD, Herzog H, Sainsbury A. Neuropeptide Y and peptide YY: important regulators of energy metabolism. Curr Opin Endocrinol Diabetes Obes, 18: 56–60, 2011

    PubMed  CAS  Google Scholar 

  • Levkovitz Y, Ben-Shushan G, Hershkovitz A, et al. Antidepressants induce cellular insulin resistance by activation of IRS-1 kinases. Mol Cell Neurosci, 36: 305–312, 2007

    PubMed  CAS  Google Scholar 

  • Raeder MB, Ferno J, Vik-Mo AO, et al. SREBP activation by antipsychotic- and antidepressant-drugs in cultured human liver cells: relevance for metabolic side-effects? Mol Cell Biochem, 289: 167–173, 2006

    PubMed  CAS  Google Scholar 

  • Shimano H. SREBPs: physiology and pathophysiology of the SREBP family. FEBS J, 276: 616–621, 2009

    PubMed  CAS  Google Scholar 

  • Hinze-Selch D, Schuld A, Kraus T, et al. Effects of antidepressants on weight and on the plasma levels of leptin, TNF-alpha and soluble TNF receptors: A longitudinal study in patients treated with amitriptyline or paroxetine. Neuropsychopharmacology, 23: 13–19, 2000

    PubMed  CAS  Google Scholar 

  • Hotamisligil GS. The role of TNFalpha and TNF receptors in obesity and insulin resistance. J Intern Med, 245: 621–625, 1999

    PubMed  CAS  Google Scholar 

  • Burgi S, Baltensperger K, Honegger UE. Antidepressant-induced switch of beta 1-adrenoceptor trafficking as a mechanism for drug action. J Biol Chem, 278: 1044–1052, 2003

    PubMed  Google Scholar 

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Ress, C., Tschoner, A., Kaser, S. et al. Psychopharmaka und Diabetes. Wien Med Wochenschr 161, 531–542 (2011). https://doi.org/10.1007/s10354-011-0004-9

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