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Síndrome metabólico en pacientes ambulatorios con tratamiento antipsicótico en la práctica clínica habitual: evaluación transversal de una base de datos de atención primaria

Published online by Cambridge University Press:  12 May 2020

Antoni Sicras-Mainar
Affiliation:
Junta Directiva de Planificación, Servicios Asistenciales Badalona SA, Gaietá Soler, Entresuelo 8, 08911Badalona (Barcelona), España
Milagrosa Blanca-Tamayo
Affiliation:
Departamento de Psiquiatría, Servicios Asistenciales de Badalona, Badalona (Barcelona), España
Javier Rejas-Gutiérrez
Affiliation:
Departmento de Investigación de Variables Médicas, Unidad Médica, Pfizer España, Alcobendas (Madrid), España
Ruth Navarro-Artieda
Affiliation:
Servicio de Documentación Médica, Hospital Germans Trías i Pujol, Badalona (Barcelona), España
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Resumen

Objetivo.

Determinar la prevalencia del síndrome metabólico (SM) en pacientes ambulatorios tratados con antipsicóticos incluidos en una base de datos de atención primaria.

Métodos.

Se realizó un estudio transversal mediante evaluación de una base de datos administrativa de reclamaciones de pacientes ambulatorios de 5 centros de atención primaria. Se incluyeron los pacientes tratados con antipsicóticos durante más de 3 meses. El grupo de control se compuso de pacientes ambulatorios incluidos en la base de datos sin exposición a ningún antipsicótico. El SM se definió según los criterios modificados del NCEP-ATP III y para su confirmación se exigieron, al menos, 3 de los 5 componentes siguientes: índice de masa corporal > 28,8 kg/m2, triglicéridos > 150 mg/ml, colesterol-HDL < 40 mg/ml (hombres) y < 50 mg/ml (mujeres), presión arterial > 130/85 mm Hg y glucosa sérica en ayunas > 110 mg/dl.

Resultados.

Identificamos a 742 pacientes [mujeres 51,5%, edad 55,1 (20,7) años] tratados con antipsicóticos de primera o segunda generación durante 27,6 (20,3) meses. Los controles fueron 85.286 pacientes ambulatorios [mujeres 50,5%, edad 45,5 (17,7) años]. La prevalencia de SM fue significativamente mayor en los sujetos tratados con antipsicóticos: 27% (IC 95%, 23,8-30,1) frente a 14,4% (14,1- 14,6%); CP ajustado a edad y sexo=l,38 (1,16-1,65, P < 0,001). Todos los componentes del SM, excepto la hipertensión, fueron significativamente más frecuentes en el grupo tratado con antipsicóticos, en particular, el índice de masa corporal > 28,8 kg/m2: 33% (29,6- 36,4%) frente al 17,8% (17,6-18,1%), CP ajustado=l,63 (1,39-1,92, P < 0,001), y niveles bajos de colesterol-HDL: 48,4% (44,8-52%) frente a 29,3% (29-29,6%); CP ajustado=l,65 (1,42-1,93, P < 0,001). Comparados con la población de referencia, los sujetos con esquizofrenia o trastorno bipolar (TB), pero no los que tenían demencia, mostraron una prevalencia mayor de SM.

Conclusión.

Comparados con la población general de pacientes ambulatorios, la prevalencia de SM fue significativamente mayor en pacientes con esquizofrenia o TB tratados con antipsicóticos.

Type
Artículo original
Copyright
Copyright © European Psychiatric Association 2008

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References

Bibliografía

[1]Alegría, ECordero, ALaclaustra, MGrima, ALeón, MCasasnovas, JA, et al. en representación de los investigadores del registro MESYAS. Prevalencia del síndrome metabólico en población laboral española: registro MESYAS. Rev Esp Cardiol 2005; 58: 797806.Google Scholar
[2] 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. Diabetes Care 2004; 27(2):596-601.Google Scholar
[3]Basu, RBrar, JSChengappa, KNRJohn, VParepally, HGershon, S, et al. The prevalence of the metabolic syndrome in patients with schizoaffective disorder- bipolar subtype. Bipolar Disord 2004; 6: 314–8.Google ScholarPubMed
[4]Bautista, MCEngler, MM. The Mediterranean diet: is it cardioprotective? Prog Cardiovasc Nurs 2005; 20: 70–6.Google ScholarPubMed
[5]Bobes, JArango, CAranda, PCarmena, RGarcía-García, MRejas, J, on behalf of CLAMORS collaborative study group. Cardiovascular and metabolic risk in outpatients with schizophrenia treated with antipsychotics: Results of the CLAMORS Study. Schizophr Res 2007; 90: 162–73.CrossRefGoogle ScholarPubMed
[6]Calbo, JMTerrancle, de Juari IFernández, PRodríguez, MJMartínez, VSantisteban, Y, et al. Prevalencia del síndrome metabólico en la provincia de Albacete. Rev Clin Esp 2007;207(2):64-8.CrossRefGoogle Scholar
[7]Casey, D. Metabolic issues and cardiovascular disease in patients with psychiatric disorders. Am J Med 2005; 118: 164–120.Google ScholarPubMed
[8]Chrousos, GP. The role of stress and the hypothalamic-pituitaryadrenal axis in the pathogenesis of the metabolic syndrome: neuroendocrine and target tissue-related causes. Int J Obes Relat Metab Disord 2000; 24(Suppl 2): S50-5.CrossRefGoogle Scholar
[9]Citrome, L. Metabolic syndrome and cardiovascular disease. Psychopharmacology 2005;19(Suppl. 6):8493.CrossRefGoogle ScholarPubMed
[10]Coca, MMHernanz, PVega, MSuárez, C. Prevalencia de síndrome metabólico en la población de un centro de atención primaria urbano. Aten Primaria 2005; 35: 436–7.CrossRefGoogle Scholar
[11]Cohn, TPrud'homme, DStreiner, DKameh, HRemington, G. Characterizing coronary hearth disease risk in chronic schizophrenia: High prevalence of the metabolic syndrome. Can J Psychiatry 2004; 49: 753–60.CrossRefGoogle Scholar
[12]Correll, CUFrederickson, AMKane, JMManu, P. Metabolic syndrome and the risk of coronary heart disease in 367 patients treated with second-generation antipsychotics drugs. J Clin Psychiatry 2006; 67: 575–83.CrossRefGoogle Scholar
[13]De, Hert MAVan, Winkel RVan, Eyck DHanssens, LWampers, MScheen, A, et al. Prevalence of metabolic syndrome in patients with schizophrenia treated with antipsychotic medication. Schizophr Res 2006; 83: 8793.Google Scholar
[14]Elman, IAdler, CMMalhotra, AKBir, CPickar, DBreier, A. Effect of acute metabolic stress on pituitary-adrenal axis activation in patients with schizophrenia. Am J Psychiatry 1988; 155: 979–81.CrossRefGoogle Scholar
[15]Enger, CWeatherby, LReynolds, RFGlasser, DBWalker, AM. Serious cardiovascular events and mortality among patients with schizophrenia. J Nerv Ment Dis 2004; 192: 1927.Google ScholarPubMed
[16]Fagiolini, AFrank, EScott, JATurkin, SKupfer, DJ. Metabolic syndrome in bipolar disorder: findings from the Bipolar Disorder Center for Pennsylvanians. Bipolar Disord 2005; 7: 424–30.CrossRefGoogle ScholarPubMed
[17]Hagg, SLindblom, YMjorndal, T, Adolfsson R. High prevelence of the metabolic syndrome among a Swedish cohort of patients with schizophrenia. Int Clin Psychopharmacol 2006; 21: 93–8.Google Scholar
[18]Kaneda, YFujii, AOhmori, T. The hypothalamic-pituitary-adrenal axis in chronic schizophrenic patients long-term treated with neuroleptics. Prog Neuropsychopharmacol Biol Psychiatry 2002; 26: 935–8.Google ScholarPubMed
[19]Kilbourne, AMCornelius, JRHan, XPincus, HAShad, MSalloum, I. Burden of general medical conditions among individuals with bipolar disorder. Bipolar Disord 2004; 6: 368–73.Google ScholarPubMed
[20]Kokkinos, PPanagiotakos, DBPolychronopoulos, E. Dietary Influences on blood pressure: the effect of the Mediterranean diet on the prevalence of hypertension. J Clin Hypertens (Greenwich) 2005; 7: 165–70.Google ScholarPubMed
[21]Lakka, HMLaaksonen, DELakka, TANiskanen, LKKumpusalo, ETuomilheto, J, et al. The metabolic syndrome and total and cardiovascular disease mortality in middle-aged men. JAMA 2002; 288: 2709-16.CrossRefGoogle ScholarPubMed
[22]Lamberti, JSCrilly, JFMaharaj, KOlson, DWiener, KDvorin, S, et al. Prevalence of diabetes mellitus among outpatients with severe mental disorders receiving atypical antipsychotic drugs. J Clin Psychiatry 2004; 65: 702–6.CrossRefGoogle ScholarPubMed
[23]Lamberts, HWood, M. Clasificación Internacional de la Atención Primaria CIAP-2, Clasificación de razones de consulta. Barcelona: Masson/SG; 1990.Google Scholar
[24]Lindenmayer, JPCzobor, PVolavka, JCitrome, LSheitman, BMcEvoy, JP, et al. Changes in glucose and cholesterol levels in patients with schizophrenia treated with typical or atypical antipsychotic. Am J Psychiatry 2003; 160: 290–6.CrossRefGoogle ScholarPubMed
[25]Lorenzo, CSerrano-Ríos, MMartínez-Larrad, MTGabriel, RWilliams, KGómez-Genque, JA, et al. Central adiposity determines prevalence differences of the metabolic syndrome. Obes Res 2003; 11: 1480-7.Google ScholarPubMed
[26]Martínez-Larrad, MTFernández-Pérez, CGonzález-Sánchez, JLLópez, AFernández-Álvarez, JRiviriego, J. et al. Prevalence of the metabolic syndrome (ATP-1I1 criterio). Population-based study of rural and urban areas in the Spanish province of Segovia. Med Clin (Barc) 2005; 125: 481–6.Google Scholar
[27]McEvoy, JPMeyer, JMGoff, DCNasrallah, HADavis, SMSullivan, L, et al. Prevalence of the metabolic syndrome in patients with schizophrenia: Baseline results from the Clinical Antipsychotic Triais of Intervention Effectiveness (CAT1E) schizophrenia trial and comparison with national estimates from NHANES III. Schizophr Res 2005; 80: 1932.CrossRefGoogle Scholar
[28]Mclntyre, RSMcCann, SMKennedy, SH. Antipsychotic metabolic – effects: weight gain, diabetes mellitus, and lipid abnormalities. Can J Psychiatry 2001; 46: 273–81.CrossRefGoogle Scholar
[29]Meltzer, HYDavidson, MGlassman, AHVieweg, WV. Assessing cardiovascular risks versus clinical benefits of atypical antipsychotic drug treatment. J Clin Psychiatry 2002; 63: 25–9.Google ScholarPubMed
[30]Meyer, JLoh, CLeckband, SGBoyd, JAWirshing, WCPierre, JM. et al. Prevalence of the metabolic syndrome in veterans with schizophrenia. J Psychiatr Pract 2006; 12: 510.Google Scholar
[31] National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment on High Blood Cholesterol in Adults (Adult Treatment Panel III). Third report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults. Adult Treatment Panel III final report. Circulation 2002; 106: 3143-421.Google Scholar
[32]Newcomer, JW. Second-generation (atypical) antipsychotics and metabolic effects: a comprehensive literature review. CNS Drugs 2005;19(Suppl l):l93.Google ScholarPubMed
[33]Reaven, GM. Role of insulin resistance in human disease. Diabetes 1988; 37: 1595–607.Google ScholarPubMed
[34]Ridker, PMBuring, JECook, NRRifai, N. C-reactive protein, the metabolic syndrome, and risk of incident cardiovascular events: an 8-year follow-up of 14,719 initially healthy American women. Circulation 2003; 107: 391–7.CrossRefGoogle ScholarPubMed
[35]Rodríguez-Artalejo, FBaca, EEsmatjes, EMerino-Torres, JFMonereo, SMoreno, B, et al. Assessment and control of metabolic and cardiovascular risk in patients with schizophrenia. Med Clin (Barc) 2006; 127(14): 542-8.CrossRefGoogle ScholarPubMed
[36]Ryan, MCThakore, JH. Physical consequences of schizophrenia and its treatment: the metabolic syndrome. Life Sci 2002; 71: 239–57.CrossRefGoogle ScholarPubMed
[37]Saltar, NGaw, AScherbakova, OFord, IO'Reilly, DSHaffner, SM, et al. Metabolic syndrome with and without C-reactive protein as a predictor of coronary heart disease and diabetes in the West of Scotland Coronary Prevention Study. Circulation 2003; 108: 414–9.Google Scholar
[38]Sicras, ARejas, JNavarro, RSerrat, JBlanca, M. Metabolic syndrome in bipolar disorder: a cross-sectional assessment of a Health Management Organization database. Bipolar Disord, in press.Google Scholar
[39]Thakore, JHMann, JNVlahos, IMartin, AReznek, R. Increased visceral fat distribution in drug-naive and drug-free patients with schizophrenia. Int J Obes Relat Metab Disord 2002; 26: 137–41.CrossRefGoogle ScholarPubMed
[40]Tunstall-Pedoe, HKuulasmaa, KMahonen, MTolonen, HRuokokoski, EAmouyel, P. Contribution of trends in survival and coronary- event rates to changes in coronary heart disease mortality: 10- year results from 37 WHO MONICA Project populations. Lancet 1999; 353: 1547–57.CrossRefGoogle ScholarPubMed
[41]Yumru, MSavas, HAKurt, EKaya, MCSelek, SSavas, E, et at. Atypical antipsychotics related metabolic syndrome in bipolar patients. J Affect Disord 2007; 98: 247–52.CrossRefGoogle ScholarPubMed