¿Qué es?
La DHEA es producida por las glándulas suprarrenales y por el hígado. Los niveles de DHEA parecen disminuir a medida que las personas envejecen. Los niveles de DHEA parecen ser más bajos en personas con depresión y después de la menopausia.
Las personas comúnmente usan DHEA recetado para el adelgazamiento del tejido vaginal. Los suplementos de DHEA se usan para el envejecimiento de la piel, la depresión, la infertilidad, la fuerza muscular, las enfermedades cardíacas, la disfunción eréctil (DE) y muchas otras afecciones, pero no existe una buena evidencia científica que respalde muchos de estos otros usos.
¿Qué tan efectivo es?
Natural Medicines Comprehensive Database (La Base Exhaustiva de Datos de Medicamentos Naturales) clasifica la eficacia, basada en evidencia científica, de acuerdo a la siguiente escala: Eficaz, Probablemente Eficaz, Posiblemente Eficaz, Posiblemente Ineficaz, Probablemente Ineficaz, Ineficaz, e Insuficiente Evidencia para Hacer una Determinación.
La clasificación de la eficacia para este producto es la siguiente:
Probablemente eficaz para...
- Adelgazamiento del tejido vaginal (atrofia vaginal). El uso de insertos vaginales que contienen DHEA puede reducir el dolor durante las relaciones sexuales hasta en un 15% después de la menopausia. Un producto de DHEA recetado está disponible para esta condición.
Posiblemente eficaz para...
- Envejecimiento de la piel. La ingesta de DHEA o su aplicación sobre la piel puede mejorar la apariencia de la piel después de la menopausia y en personas mayores de 60 años.
- Depresión. La ingesta diaria de 30-500 mg de DHEA parece mejorar los síntomas de la depresión. Las dosis más bajas no parecen ayudar.
- Incapacidad para quedar embarazada dentro de un año de intentar concebir (infertilidad). La ingesta de DHEA antes de la fertilización in vitro (FIV) podría mejorar las posibilidades de embarazo y de tener un bebé. Pero no está claro si tomar DHEA ayuda a prevenir el aborto espontáneo después de la FIV.
Posiblemente ineficaz para...
- Envejecimiento. La ingesta diaria de DHEA durante un máximo de 2 años no parece mejorar la forma del cuerpo, la fuerza ósea, la fuerza muscular o la calidad de vida en personas mayores de 60 años que tienen niveles bajos de DHEA.
- Fuerza muscular. La ingesta de DHEA no mejora la fuerza muscular en los adultos.
- Rendimiento físico en adultos mayores. La ingesta de DHEA no mejora el rendimiento físico en los adultos mayores.
Probablemente ineficaz para...
- Habilidades de memoria y pensamiento (función cognitiva). La ingesta de DHEA no parece mejorar la función mental ni disminuir el deterioro mental en personas mayores sanas, personas con VIH o adultos jóvenes sanos.
- Un trastorno autoinmune en el que se dañan las glándulas que producen lágrimas y saliva (síndrome de Sjogren). La ingesta de DHEA no mejora los síntomas de esta condición.
¿Es seguro?
La DHEA posiblemente no sea segura cuando se usa en dosis altas o a largo plazo. No use DHEA en dosis superiores a 50-100 mg al día o durante un período prolongado. Usar dosis más altas o usarlo a largo plazo puede aumentar el riesgo de efectos secundarios graves, incluido el cáncer.
Cuando se aplica sobre la piel: La DHEA es posiblemente segura cuando se usa de manera apropiada. La crema de DHEA se ha utilizado de forma segura hasta por 1 año.
Cuando se aplica en la vagina: La DHEA es posiblemente segura cuando se usa apropiadamente. Los insertos vaginales de DHEA se han utilizado con seguridad hasta por 3 meses.
Advertencias y precauciones especiales:
Embarazo y lactancia: Es posible que la DHEA no sea segura cuando se toma durante el embarazo o la lactancia. Puede causar niveles más altos de lo normal de una hormona masculina llamada andrógeno. Esto podría ser perjudicial para el bebé. No use DHEA si está embarazada o amamantando.Diabetes: La DHEA puede afectar el funcionamiento de la insulina en el cuerpo. Si tiene diabetes, controle cuidadosamente su nivel de azúcar en sangre si está tomando DHEA.
Condiciones sensibles a hormonas como cáncer de mama, cáncer de útero, cáncer de ovario, endometriosis o fibromas uterinos: La DHEA es una hormona que puede afectar el funcionamiento del estrógeno en el cuerpo. Si tiene alguna afección que podría empeorar con el estrógeno, no use DHEA.
Colesterol alto: La DHEA puede reducir el colesterol de las lipoproteínas de alta densidad (HDL o "bueno"), especialmente en las mujeres. Si tiene colesterol alto o una enfermedad cardíaca, hable con su proveedor de atención médica antes de tomar DHEA.
Problemas hepáticos: La DHEA puede empeorar los problemas hepáticos. No use DHEA si tiene problemas hepáticos.
Depresión y trastornos del estado de ánimo: La DHEA puede provocar excitabilidad, impulsividad e irritabilidad en personas con trastornos del estado de ánimo. Si tiene un trastorno del estado de ánimo, hable con su proveedor de atención médica antes de tomar DHEA.
Síndrome de ovario poliquístico (SOP): La ingesta de DHEA podría empeorar esta condición. No use DHEA si tiene SOP.
¿Existen interacciones con medicamentos?
- Fulvestrant (Faslodex)
- Los cánceres sensibles al estrógeno son cánceres que se ven afectados por los niveles de estrógeno en el cuerpo. Fulvestrant se usa para estos tipos de cáncer. La DHEA podría aumentar el estrógeno en el cuerpo y disminuir los efectos del fulvestrant para tratar el cáncer. No tome DHEA si está tomando fulvestrant.
- Medicamentos modificados por el hígado (sustratos del citocromo P450 3A4 (CYP3A4))
- Algunos medicamentos son modificados y degradados por el hígado. La DHEA podría cambiar la rapidez con que el hígado descompone estos medicamentos. Esto podría cambiar los efectos y los efectos secundarios de estos medicamentos.
- Medicamentos para cánceres sensibles al estrógeno (inhibidores de aromatasa)
- El cuerpo convierte la DHEA en estrógeno en el cuerpo. Los inhibidores de la aromatasa se utilizan para ayudar a reducir los niveles de estrógeno en el cuerpo. La ingesta de DHEA podría disminuir los efectos de los inhibidores de la aromatasa.
- Medicamentos para la depresión (medicamentos antidepresivos)
- Existe cierta preocupación de que la ingesta de DHEA junto con medicamentos antidepresivos pueda aumentar el riesgo de efectos secundarios graves. Hable con un proveedor de atención médica antes de tomar DHEA si está tomando un antidepresivo.
- Medicamentos que retardan la coagulación de la sangre (medicamentos anticoagulantes / antiplaquetarios)
- La DHEA podría retardar la coagulación sanguínea. La ingesta de DHEA junto con medicamentos que también retardan la coagulación de la sangre puede aumentar el riesgo de hematomas y hemorragias.
- Tamoxifeno (Nolvadex)
- Los cánceres sensibles al estrógeno son cánceres que se ven afectados por los niveles de estrógeno en el cuerpo. El tamoxifeno se usa para ayudar a tratar y prevenir estos tipos de cáncer. La DHEA aumenta los niveles de estrógeno en el cuerpo y podría disminuir los efectos del tamoxifeno. No tome DHEA si está tomando tamoxifeno.
- Triazolam (Halción)
- La DHEA podría disminuir la rapidez con que el cuerpo descompone el triazolam. La ingesta de DHEA con triazolam podría aumentar los efectos y los efectos secundarios del triazolam.
- Vacuna contra la tuberculosis
- Tomar DHEA podría reducir los efectos de la vacuna contra la tuberculosis. No tome DHEA si está recibiendo una vacuna contra la tuberculosis.
- Estrógenos
- La DHEA puede aumentar los niveles de estrógeno en el cuerpo. La ingesta de DHEA junto con estrógeno puede causar demasiado estrógeno en el cuerpo.
- Testosterona
- Tomar DHEA con testosterona puede hacer que haya demasiada testosterona en el cuerpo. Esto podría aumentar los efectos y los efectos secundarios de la testosterona.
¿Existen interacciones con hierbas y suplementos?
- Hierbas y suplementos que pueden retardar la coagulación sanguínea
- La DHEA podría retardar la coagulación sanguínea y aumentar el riesgo de hemorragia. Tomarlo con otros suplementos con efectos similares podría aumentar el riesgo de hemorragia en algunas personas. Ejemplos de suplementos con este efecto incluyen ajo, jengibre, ginkgo, natokinasa y Panax ginseng.
- Regaliz
- El consumo de regaliz aumenta los niveles de DHEA en el cuerpo. La ingesta de regaliz con DHEA podría aumentar los efectos secundarios de la DHEA.
- Soja
- Anteriormente se pensaba que la soya podría disminuir los efectos de la DHEA, pero esto no parece ser una preocupación importante.
¿Existen interacciones con alimentos?
- Anteriormente se pensaba que comer soya o una dieta alta en fibra podría disminuir los efectos de la DHEA, pero esto no parece ser una preocupación importante.
¿Como se usa normalmente?
Otros nombres
Metodología
Para saber más sobre cómo este artículo fue escrito, refiérase a la metodología de la Base exhaustiva de datos de medicamentos naturales.
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- Romanutti, C., Bruttomesso, A. C., Castilla, V., Bisceglia, J. A., Galagovsky, L. R., and Wachsman, M. B. In vitro antiviral activity of dehydroepiandrosterone and its synthetic derivatives against vesicular stomatitis virus. Vet.J 2009;182:327-335. View abstract.
- Sawalha, A. H. and Kovats, S. Dehydroepiandrosterone in systemic lupus erythematosus. Curr Rheumatol.Rep. 2008;10:286-291. View abstract.
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- Charlton, M., Angulo, P., Chalasani, N., Merriman, R., Viker, K., Charatcharoenwitthaya, P., Sanderson, S., Gawrieh, S., Krishnan, A., and Lindor, K. Low circulating levels of dehydroepiandrosterone in histologically advanced nonalcoholic fatty liver disease. Hepatology 2008;47:484-492. View abstract.
- Bednarek-Tupikowska, G., Tworowska-Bardzinska, U., Tupikowski, K., Bohdanowicz-Pawlak, A., Szymczak, J., Kubicka, E., Skoczynska, A., and Milewicz, A. The correlations between endogenous dehydroepiandrosterone sulfate and some atherosclerosis risk factors in premenopausal women. Med Sci Monit. 2008;14:CR37-CR41. View abstract.
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- Maggio, M., Lauretani, F., Ceda, G. P., Bandinelli, S., Ling, S. M., Metter, E. J., Artoni, A., Carassale, L., Cazzato, A., Ceresini, G., Guralnik, J. M., Basaria, S., Valenti, G., and Ferrucci, L. Relationship between low levels of anabolic hormones and 6-year mortality in older men: the aging in the Chianti Area (InCHIANTI) study. Arch.Intern.Med 11-12-2007;167:2249-2254. View abstract.
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- Ahboucha, S., Pomier-Layrargues, G., Vincent, C., Hassoun, Z., Tamaz, R., Baker, G., and Butterworth, R. F. Reduced plasma dehydroepiandrosterone sulfate levels are significantly correlated with fatigue severity in patients with primary biliary cirrhosis. Neurochem.Int. 2008;52(4-5):569-574. View abstract.
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- Zenk, J. L., Frestedt, J. L., and Kuskowski, M. A. HUM5007, a novel combination of thermogenic compounds, and 3-acetyl-7-oxo-dehydroepiandrosterone: each increases the resting metabolic rate of overweight adults. J Nutr Biochem 2007;18:629-634. View abstract.
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- Ritsner, M. S., Gibel, A., Ratner, Y., Tsinovoy, G., and Strous, R. D. Improvement of sustained attention and visual and movement skills, but not clinical symptoms, after dehydroepiandrosterone augmentation in schizophrenia: a randomized, double-blind, placebo-controlled, crossover trial. J Clin Psychopharmacol. 2006;26:495-499. View abstract.
- Yehuda, R., Brand, S. R., Golier, J. A., and Yang, R. K. Clinical correlates of DHEA associated with post-traumatic stress disorder. Acta Psychiatr.Scand. 2006;114:187-193. View abstract.
- Brooke, A. M., Kalingag, L. A., Miraki-Moud, F., Camacho-Hubner, C., Maher, K. T., Walker, D. M., Hinson, J. P., and Monson, J. P. Dehydroepiandrosterone improves psychological well-being in male and female hypopituitary patients on maintenance growth hormone replacement. J Clin Endocrinol.Metab 2006;91:3773-3779. View abstract.
- Solano, M. E., Elia, E., Luchetti, C. G., Sander, V., Di, Girolamo G., Gonzalez, C., and Motta, A. B. Metformin prevents embryonic resorption induced by hyperandrogenisation with dehydroepiandrosterone in mice. Reprod.Fertil.Dev. 2006;18:533-544. View abstract.
- Villareal, D. T. and Holloszy, J. O. DHEA enhances effects of weight training on muscle mass and strength in elderly women and men. Am J Physiol Endocrinol.Metab 2006;291:E1003-E1008. View abstract.
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- Christiansen, J. J., Gravholt, C. H., Fisker, S., Moller, N., Andersen, M., Svenstrup, B., Bennett, P., Ivarsen, P., Christiansen, J. S., and Jorgensen, J. O. Very short term dehydroepiandrosterone treatment in female adrenal failure: impact on carbohydrate, lipid and protein metabolism. Eur J Endocrinol. 2005;152:77-85. View abstract.
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- Williams, M. R., Dawood, T., Ling, S., Dai, A., Lew, R., Myles, K., Funder, J. W., Sudhir, K., and Komesaroff, P. A. Dehydroepiandrosterone increases endothelial cell proliferation in vitro and improves endothelial function in vivo by mechanisms independent of androgen and estrogen receptors. J.Clin.Endocrinol.Metab 2004;89:4708-4715. View abstract.
- Rasmussen, K. R., Arrowood, M. J., and Healey, M. C. Effectiveness of dehydroepiandrosterone in reduction of cryptosporidial activity in immunosuppressed rats. Antimicrob.Agents Chemother 1992;36:220-222. View abstract.
- Buster, J. E., Casson, P. R., Straughn, A. B., Dale, D., Umstot, E. S., Chiamori, N., and Abraham, G. E. Postmenopausal steroid replacement with micronized dehydroepiandrosterone: preliminary oral bioavailability and dose proportionality studies. Am J Obstet Gynecol 1992;166:1163-1170. View abstract.
- Morgan, C. A., III, Southwick, S., Hazlett, G., Rasmusson, A., Hoyt, G., Zimolo, Z., and Charney, D. Relationships among plasma dehydroepiandrosterone sulfate and cortisol levels, symptoms of dissociation, and objective performance in humans exposed to acute stress. Arch.Gen.Psychiatry 2004;61:819-825. View abstract.
- Straub, R. H., Weidler, C., Demmel, B., Herrmann, M., Kees, F., Schmidt, M., Scholmerich, J., and Schedel, J. Renal clearance and daily excretion of cortisol and adrenal androgens in patients with rheumatoid arthritis and systemic lupus erythematosus. Ann Rheum.Dis 2004;63:961-968. View abstract.
- Miller, K. K., Cai, J., Ripp, S. L., Pierce, W. M., Jr., Rushmore, T. H., and Prough, R. A. Stereo- and regioselectivity account for the diversity of dehydroepiandrosterone (DHEA) metabolites produced by liver microsomal cytochromes P450. Drug Metab Dispos. 2004;32:305-313. View abstract.
- Dolecek, R., Tymonova, J., Adamkova, M., Kadlcik, M., Pohlidal, A., and Zavodna, R. Endocrine changes after burns: the bone involvement. Acta Chir Plast. 2003;45:95-103. View abstract.
- Defay, R., Pinchinat, S., Lumbroso, S., Sultan, C., Papoz, L., and Delcourt, C. Relationships between hormonal status and cataract in french postmenopausal women: the POLA study. Ann.Epidemiol. 2003;13:638-644. View abstract.
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- Armanini, D., Vecchio, F., Basso, A., Milone, F. F., Simoncini, M., Fiore, C., Mattarello, M. J., Sartorato, P., and Karbowiak, I. Alzheimer's disease: pathophysiological implications of measurement of plasma cortisol, plasma dehydroepiandrosterone sulfate, and lymphocytic corticosteroid receptors. Endocrine. 2003;22:113-118. View abstract.
- Leal, A. M., Magalhaes, P. K., Souza, C. S., and Foss, N. T. Adrenocortical hormones and interleukin patterns in leprosy. Parasite Immunol. 2003;25(8-9):457-461. View abstract.
- Gobbi, D., Rhoden, E. L., Menti, E., Lulhier, F., and Rhoden, C. Effects of the chronic use of dehydroepiandrosterone (DHEA) on testicular weight and spermatogenesis: experimental study in rats. Int.Urol.Nephrol. 2003;35:119-122. View abstract.
- Maayan, R., Yoran-Hegesh, R., Strous, R., Nechmad, A., Averbuch, E., Weizman, A., and Spivak, B. Three-month treatment course of methylphenidate increases plasma levels of dehydroepiandrosterone (DHEA) and dehydroepiandrosterone-sulfate (DHEA-S) in attention deficit hyperactivity disorder. Neuropsychobiology 2003;48:111-115. View abstract.
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- Tagliaferro, A. R., Roebuck, B. D., Ronan, A. M., and Meeker, L. D. Enhancement of pancreatic carcinogenesis by dehydroepiandrosterone. Adv.Exp.Med Biol. 1992;322:119-129. View abstract.
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- Howard, J. S., III. Severe psychosis and the adrenal androgens. Integr Physiol Behav.Sci 1992;27:209-215. View abstract.
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- Valtysdottir, S. T., Wide, L., and Hallgren, R. Mental wellbeing and quality of sexual life in women with primary Sjogren's syndrome are related to circulating dehydroepiandrosterone sulphate. Ann Rheum.Dis 2003;62:875-879. View abstract.
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- Mayer, D., Forstner, K., and Kopplow, K. Induction and modulation of hepatic preneoplasia and neoplasia in the rat by dehydroepiandrosterone. Toxicol.Pathol. 2003;31:103-112. View abstract.
- Chang, D. M., Lan, J. L., Lin, H. Y., and Luo, S. F. Dehydroepiandrosterone treatment of women with mild-to-moderate systemic lupus erythematosus: a multicenter randomized, double-blind, placebo-controlled trial. Arthritis Rheum. 2002;46:2924-2927. View abstract.
- Josipovic, B. and Josipovic, A. Basal levels of DHEAS as a marker for disease activity in premenopausal women with recent onset rheumatoid arthritis. J Rheumatol. 2002;29:1803-1805. View abstract.
- Takayanagi, R., Goto, K., Suzuki, S., Tanaka, S., Shimoda, S., and Nawata, H. Dehydroepiandrosterone (DHEA) as a possible source for estrogen formation in bone cells: correlation between bone mineral density and serum DHEA-sulfate concentration in postmenopausal women, and the presence of aromatase to be enhanced by 1,25-dihydroxyvitamin D3 in human osteoblasts. Mech.Ageing Dev. 4-30-2002;123:1107-1114. View abstract.
- Liu, D. and Dillon, J. S. Dehydroepiandrosterone activates endothelial cell nitric-oxide synthase by a specific plasma membrane receptor coupled to Galpha(i2,3). J Biol.Chem 6-14-2002;277:21379-21388. View abstract.
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- Feldman, H. A., Longcope, C., Derby, C. A., Johannes, C. B., Araujo, A. B., Coviello, A. D., Bremner, W. J., and McKinlay, J. B. Age trends in the level of serum testosterone and other hormones in middle-aged men: longitudinal results from the Massachusetts male aging study. J Clin Endocrinol.Metab 2002;87:589-598. View abstract.
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- Bhattoa, H. P., Kiss, E., Bettembuk, P., and Balogh, A. Bone mineral density, biochemical markers of bone turnover, and hormonal status in men with systemic lupus erythematosus. Rheumatol.Int 2001;21:97-102. View abstract.
- Morrison, M. F., Ten Have, T., Freeman, E. W., Sammel, M. D., and Grisso, J. A. DHEA-S levels and depressive symptoms in a cohort of African American and Caucasian women in the late reproductive years. Biol Psychiatry 11-1-2001;50:705-711. View abstract.
- Umezaki, H., Hess, D. L., Valenzuela, G. J., and Ducsay, C. A. Fetectomy alters maternal pituitary-adrenal function in pregnant rhesus macaques. Biol Reprod. 2001;65:1616-1621. View abstract.
- Barbetta, L., Dall'Asta, C., Re, T., Colombo, P., Travaglini, P., and Ambrosi, B. Androgen secretion in ectopic ACTH syndrome and in Cushing's disease: modifications before and after surgery. Horm.Metab Res 2001;33:596-601. View abstract.
- Luboshitzky, R., Qupti, G., Ishay, A., Shen-Orr, Z., and Herer, P. Increased urinary 6-sulfatoxymelatonin excretion in women with non- classical steroid 21-hydroxylase deficiency. Neuroendocrinol.Lett 2001;22:332-336. View abstract.
- Ciotta, L., Calogero, A. E., Farina, M., De, Leo, V, La Marca, A., and Cianci, A. Clinical, endocrine and metabolic effects of acarbose, an alpha- glucosidase inhibitor, in PCOS patients with increased insulin response and normal glucose tolerance. Hum Reprod. 2001;16:2066-2072. View abstract.
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- Van Niekerk, J. K., Huppert, F. A., and Herbert, J. Salivary cortisol and DHEA: association with measures of cognition and well-being in normal older men, and effects of three months of DHEA supplementation. Psychoneuroendocrinology 2001;26:591-612. View abstract.
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- Murialdo, G., Barreca, A., Nobili, F., Rollero, A., Timossi, G., Gianelli, M. V., Copello, F., Rodriguez, G., and Polleri, A. Relationships between cortisol, dehydroepiandrosterone sulphate and insulin-like growth factor-I system in dementia. J Endocrinol Invest 2001;24:139-146. View abstract.
- Sulcova, J., Hill, M., Hampl, R., Masek, Z., Novacek, A., Ceska, R., and Starka, L. Effects of transdermal application of DHEA on the levels of steroids, gonadotropins and lipids in men. Physiol Res 2000;49:685-693. View abstract.
- Oberbeck, R., Dahlweid, M., Koch, R., van Griensven, M., Emmendorfer, A., Tscherne, H., and Pape, H. C. Dehydroepiandrosterone decreases mortality rate and improves cellular immune function during polymicrobial sepsis. Crit Care Med 2001;29:380-384. View abstract.
- Straub, R. H., Scholmerich, J., and Zietz, B. Replacement therapy with DHEA plus corticosteroids in patients with chronic inflammatory diseases--substitutes of adrenal and sex hormones. Z Rheumatol. 2000;59 Suppl 2:II/108-II/118. View abstract.
- Casson, P. R., Lindsay, M. S., Pisarska, M. D., Carson, S. A., and Buster, J. E. Dehydroepiandrosterone supplementation augments ovarian stimulation in poor responders: a case series. Hum.Reprod. 2000;15:2129-2132. View abstract.
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