Abriendo caminos: una revisión para develar la sexualidad en el autismo

Manzo Jorge, Ma. Elena Hernández-Aguilar, Ma. Rebeca Toledo-Cárdenas, Deissy Herrera-Covarrubias, Genaro A. Coria-Ávila

Resumen


La conducta sexual se asocia a una base neural que involucra múltiples áreas de la corteza cerebral y estructuras subcorticales, muchas de las cuales están alteradas en personas con autismo. Las alteraciones neurobiológicas en el autismo dificultan la comprensión de normas sociales, lo que puede llevar a comportamientos sexuales inapropiados como la masturbación pública o el contacto no consensuado. En cuanto a la capacidad reproductiva, las mujeres con autismo de alto funcionamiento son fisiológicamente capaces de concebir, aunque el embarazo presenta retos significativos, incluyendo un aumento en el estrés y un mayor riesgo de complicaciones obstétricas, tales como partos prematuros y la necesidad de intervenciones quirúrgicas, como la cesárea. Estos factores sugieren la necesidad de un enfoque de atención prenatal adaptado a las necesidades de esta población. Otro aspecto crucial es la orientación sexual de las personas con autismo, donde se observa una diversidad significativamente mayor en comparación con la población neurotípica, así como una inversión en la proporción de orientaciones sexuales: alrededor del 30% de individuos con autismo se identifica como heterosexual, mientras que el 70% reporta orientaciones dentro del espectro LGTB+. A pesar de que las personas con autismo tienden a establecer relaciones afectivas con menor frecuencia en comparación con las neurotípicas, aquellas que lo hacen reportan un alto grado de satisfacción, destacando la complejidad de la experiencia de pareja en personas con autismo. Este panorama subraya la urgencia de desarrollar programas de educación sexual inclusivos y específicamente diseñados para abordar las particularidades de la población con autismo.

 Abstract

Sexual behavior is associated with a neural base that involves multiple areas of the cerebral cortex and subcortical structures, many of which are altered in individuals with autism. These neurobiological alterations contribute to the multiple challenges these individuals face in their sexuality. Inappropriate sexual behaviors such as public masturbation and non-consensual physical contact prevail, reflecting problems in understanding social norms. Regarding reproductive capacity, women with high-functioning autism could conceive, but pregnancy presents significant challenges, including increased stress and obstetric complications such as premature births and cesarean sections, suggesting the need for a specific prenatal care approach for this population. A crucial aspect of sexuality in autism is sexual orientation. There is greater diversity among individuals with autism compared to the neurotypical population, with a notable inversion in the proportion of sexual orientations: about 30% of individuals with autism identify as heterosexual, while 70% report orientations within the LGBT spectrum. Although these individuals have a lower frequency of affective relationships compared to neurotypicals, those who are in relationships report high satisfaction, highlighting the complexity of the relationship experience in people with autism. This landscape underscores the importance of developing sexual education programs that are inclusive and specifically designed to address the particularities of the autism population.

 Keywords: Autism spectrum disorder; ASD; pregnancy; sexual orientation; sexuality.


Palabras clave


Trastorno del espectro autista; TEA; embarazo; orientación sexual; sexualidad.

Texto completo:

PDF

Referencias


American Psychiatric Association. Diagnostic and statistical manual of mental disorders (DSM-5®). Am Psych Assoc, Arlington, VA. 2013

Manzo J. Un segundo espectro del autismo: de la conducta a la neurona. eNeurobiol 2019 10: 1501.

Manzo J. Autismo y sexualidad. La ciencia y el hombre 2018 3: 2-3.

Calabrò RS, Cacciola A, Bruschetta D, Milardi D, Quattrini F, Sciarrone F, La Rosa G, Bramanti P, Anastasi G. Neuroanatomy and function of human sexual behavior: A neglected or unknown issue? Brain Behav 2019 9: e01389.

Manzo J, Carrillo P, Coria-Avila GA, Garcia LI. The sexual cerebellum. En: Komisaruk BR, González-Mariscal G. Behavioral neuroendocrinology. CRC Press, Boca Raton, FL 2017.

Courchesne E, Mouton PR, Calhoun ME, Semendeferi K, Ahrens-Barbeau C, Hallet MJ, Barnes CC, Pierce K. Neuron number and size in prefrontal cortex of children with autism. JAMA 2011 306: 2001–2010.

Morgan JT, Chana G, Abramson I, Semendeferi K, Courchense E, Everall IP. Abnormal microglial–neuronal spatial organization in the dorsolateral prefrontal cortex in autism. Brain Res 2012 1456: 72–81.

Vargas DL, Nascimbene C, Krishnan C, Zimmerman AW, Pardo CA. Neuroglial activation and neuroinflammation in the brain of patients with autism. Ann Neurol 2005 57: 67–81.

Watanabe H, Nakamura M, Ohno T, Itahashi T, Tanaka E, Ohta H, Yamada T, Kanai C, Iwanami A, Kato N, Hashimoto R. Altered orbitofrontal sulcogyral patterns in adult males with high-functioning autism spectrum disorders. Soc Cogn Affect Neur 2014 9: 520–528.

Girgis RR, Minshew NJ, Melhem NM, Nutche JJ, Keshavan MS, Hardan AY. Volumetric alterations of the orbitofrontal cortex in autism. Prog Neuro-Psychopharmacol Biol Psychiatry 2007 31: 41–45.

Hardan AY, Girgis RR, Lacerda ALT, Yorbik O, Kilpatrick M, Keshavan MS, Minshew NJ. Magnetic resonance imaging study of the orbitofrontal cortex in autism. J Child Neurol 2006 21: 866–871.

Zikopoulos B, Barbas H. Changes in prefrontal axons may disrupt the network in autism. J Neurosci 2010 30: 14595–14609.

Libero LE, Reid MA, White DM, Salibi N, Lahti AC, Kana RK. Biochemistry of the cingulate cortex in autism: An MR spectroscopy study. Autism Res 2016 9: 643–657.

Polk M, Ikuta T. Disrupted functional connectivity between the nucleus accumbens and posterior cingulate cortex in autism spectrum disorder. NeuroReport 2022 33: 43–47.

Laidi C, Boisgontier J, de Pierrefeu A, Duchesnay E, Hotier S, d’Albis MA, Delorme R, Bolognani F, Czech C, Bouquet C, Amestoy A, Petit J, Holiga S, Dukart J, Gaman A, Toledano E, Moal ML, Scheid I, Leboyer M, Houenou J. Decreased cortical thickness in the anterior cingulate cortex in adults with autism. J Autism Dev Disord 2019 49: 1402–1409.

Simms ML, Kemper TL, Timbie CM, Bauman ML, Blatt GJ. The anterior cingulate cortex in autism: heterogeneity of qualitative and quantitative cytoarchitectonic features suggests possible subgroups. Acta Neuropathol 2009 118: 673–684.

Sato M, Nakai N, Fujima S, Choe KY, Takumi T. Social circuits and their dysfunction in autism spectrum disorder. Mol Psychiatry 2023 28: 3194–3206.

Nomi JS, Molnar-Szakacs I, Uddin LQ. Insular function in autism: Update and future directions in neuroimaging and interventions. Prog Neuro-Psychopharmacol Biol Psychiatry 2019 89: 412–426.

Doyle-Thomas KAR, Kushki A, Duerden EG, Taylor MJ, Lerch JP, Soorya LV, Wang AT, Fan J, Anagnostou E. The effect of diagnosis, age, and symptom severity on cortical surface area in the cingulate cortex and insula in autism spectrum disorders. J Child Neurol 2012 28: 732–739.

Uddin LQ, Menon V. The anterior insula in autism: Under-connected and under-examined. Neurosci Biobehav Rev 2009 33: 1198–1203.

Caria A, Falco S. Anterior insular cortex regulation in autism spectrum disorders. Front Behav Neurosci 2015 9: 38.

Bayless DW, Davis CO, Yang R, Ding JB, Luo L, Shah NM. A neural circuit for male sexual behavior and reward. Cell 2023 186: 3862-3881.

Ågmo A. Neuroendocrinology of sexual behavior. Int J Impot Res 2024 36: 305–311.

Asimakopoulos B. Hypothalamus-pituitary-gonadal axis: It is time for revision. Hum Genet Embryol 2012 2: 1.

Caria A, Ciringione L, Falco S. Morphofunctional alterations of the hypothalamus and social behavior in autism spectrum disorders. Brain Sci 2020 10: 435.

Ménard S, Gelez H, Coria-Avila GA, Pfaus JG. Sexual experience increases oxytocin, but not vasopressin, receptor densities in the medial preoptic area, ventromedial hypothalamus, and central amygdala of male rats. Psychoneuroendocrinology 2022 146: 105900.

Aiello TP, Whitaker‐Azmitia PM. Sexual differentiation and the neuroendocrine hypothesis of autism. Anat Rec 211 294: 1663–1670.

Carter CS. Sex differences in oxytocin and vasopressin: Implications for autism spectrum disorders? Behav Brain Res 2007 176: 170–186.

Harris VS, Sachs BD. Copulatory behavior in male rats following amygdaloid lesions. Brain Res. 1975 86: 514–518.

Kondo Y. Lesions of the medial amygdala produce severe impairment of copulatory behavior in sexually inexperienced male rats. Physiol Behav 1992 51: 939–943.

Hamann S, Herman RA, Nolan CL, Wallen K. Men and women differ in amygdala response to visual sexual stimuli. Nat Neurosci 2004 7: 411–416.

Hamann S. Sex differences in the responses of the human amygdala. Neurosci 2005 11: 288–293.

Holder MK, Mong JA. The role of ovarian hormones and the medial amygdala in sexual motivation. Curr Sex Heal Rep 2017 9: 262–270.

Lee JK, Andrews DS, Ozturk A, Solomon M, Rogers S, Amaral DG, Nordahl CW. Altered development of amygdala-connected brain regions in males and females with autism. J Neurosci 2022 42: 6145–6155.

Zou Y, Lu Q, Zheng D, Chu Z, Liu Z, Chen H, Ruan Q, Ge X, Zhang Z, Wang X, Lou W, Huang Y, Wang Y, Huang X, Liu Z, Xie W, Zhou Y, Yao P. Prenatal levonorgestrel exposure induces autism-like behavior in offspring through ERβ suppression in the amygdala. Mol Autism 2017 8: 46.

Kondo Y, Shinoda A, Yamanouchi K, Arai Y. Role of septum and preoptic area in regulating masculine and feminine sexual behavior in male rats. Horm Behav 1990 24: 421–434.

Gogate MG, Brid SV, Wingkar KC, Kantak NM. Septal regulation of male sexual behavior in rats. Physiol Behav 1995 57: 1205–1207.

Tsukahara S, Kanaya M, Yamanouchi K. Neuroanatomy and sex differences of the lordosis-inhibiting system in the lateral septum. Front Neurosci 2014 8: 299.

Bauman M, Kemper TL. Histoanatomic observations of the brain in early infantile autism. Neurology 1985 35: 866–866.

Cera N, Vargas-Cáceres S, Oliveira C, Monteiro J, Bronco D, Pignatelli D, Rebelo S. How relevant is the systemic oxytocin concentration for human sexual behavior? A systematic review. Sex Med 2021 9: 100370.

Melis MR, Argiolas A. Oxytocin, erectile function and sexual behavior: Last discoveries and possible advances. Int J Mol Sci 2021 22: 10376.

Pedersen CA, Boccia ML. Oxytocin maintains as well as initiates female sexual behavior: Effects of a highly selective oxytocin antagonist. Horm Behav 2002 41: 170–177.

Horiai M, Otsuka A, Hidema S, Hiraoka Y, Hayashi R, Miyazaki S, Furuse T, Mizukami H, Teruyama R, Tamura M, Bito H, Maejima Y, Shimomura K, Nishimori K. Targeting oxytocin receptor (Oxtr)-expressing neurons in the lateral septum to restore social novelty in autism spectrum disorder mouse models. Sci Rep 2020 10: 22173.

Bartheld CS, von Bahney J, Herculano‐Houzel S. The search for true numbers of neurons and glial cells in the human brain: A review of 150 years of cell counting. J Comp Neurol 2016 524: 3865–3895.

Voogd J, Glickstein M. The anatomy of the cerebellum. Trends Neurosci 1998 21: 370–375.

Habas C. Functional imaging of the deep cerebellar nuclei: A review. Cerebellum 2010 9: 22–28.

Doty RL. Odor-guided behavior in mammals. Experientia 1986 42: 257–271.

Manzo J, Miquel M, Toledo R, Mayor-Mar JA, Garcia LI, Aranda-Abreu G, Caba M, Hernandez ME. Fos expression at the cerebellum following non-contact arousal and mating behavior in male rats. Physiol Behav 2008 93: 357–363.

Sachs BD. Erection evoked in male rats by airborne scent from estrous females. Physiol Behav 1997 62: 921–924.

Dubuc C, Allen WL, Maestripieri D, Higham JP. Is male rhesus macaque red color ornamentation attractive to females? Behav Ecol Sociobiol 2014 68: 1215–1224.

Hu SH, Wei N, Wang QD, Yan LQ, Wei EQ, Zhang MM, Hu JB, Huang MI, Zhou WH, Xu Y. Patterns of brain activation during visually evoked sexual arousal differ between homosexual and heterosexual men. Am J Neuroradiol 2008 29: 1890–1896.

Hawk ST, Tolman R, Mueller CW. The effects of target attractiveness on men’s sexual arousal in response to erotic auditory stimuli. J Sex Res 2007 44: 96–103.

Tsujimura A, Miyagawa Y, Fujita K, Matsuoka Y, Takahashi T, Takao T, Matsumiya K, Osaki Y, Takasawa M, Oku N, Hatazawa J, Kaneko S, Okuyama A. Brain processing of audiovisual sexual stimuli inducing penile erection: A positron emission tomography study. J Urol 2006 176: 679–683.

Ortiz-Pulido R, Miquel M, Garcia LI, Perez CA, Aranda-Abreu GE, Toledo R, Hernandez ME, Manzo J. Sexual behavior and locomotion induced by sexual cues in male rats following lesion of Lobules VIa and VII of the cerebellar vermis. Physiol Behav 2011 103: 330–335.

Perez-Pouchoulen M, Toledo R, Garcia LI, Perez-Estudillo CA, Coria-Avila GA, Hernandez ME, Carrillo P, Manzo J. Androgen receptors in Purkinje neurons are modulated by systemic testosterone and sexual training in a region-specific manner in the male rat. Physio Behav 2016 156: 191–198.

Courchesne, E. Brainstem, cerebellar and limbic neuroanatomical abnormalities in autism. Curr Opin Neurobiol 1997 7: 269–278.

Crippa A, Del Vecchio G, Ceccarelli SB, Nobile M, Arrigoni F, Brambilla P. Cortico-cerebellar connectivity in autism spectrum disorder: What do we know so far? Front Psychiatry 2016 7: 20.

Cruz-Magos OE, Herrera-Meza G, García LI, Coria-Avila GA, Herrera-Covarrubias D, Toledo-Cárdenas MR, Hernández-Aguilar ME, Manzo J. Multiunit recording of cerebellar cortex in autistic male rats during social interaction in enriched environments. NeuroSci 2023 4: 178–185.

Fatemi SH, Aldinger KA, Ashwood P, Bauman ML, Blaha CD, Blatt GJ, Chauhan A, Chauhan V, Dager SR, Dickson PE, Estes AM, Goldowitz D, Heck DH, Kemper TL, King BH, Martin LA, Millen KJ, Mittleman G, Mosconi MW, Persico AM, Sweeney JA, Webb SJ, Welsh JP. Consensus paper: Pathological role of the cerebellum in autism. Cerebellum 2012 11: 777–807.

Perez-Pouchoulen M, Miquel M, Saft P, Brug B, Toledo R, Hernandez ME, Manzo J. Prenatal exposure to sodium valproate alters androgen receptor expression in the developing cerebellum in a region and age specific manner in male and female rats. Int J Dev Neurosci 2016 53: 46–52.

Manzo J, Coria-Avila GA, García LI, Hernández ME, Herrera-Covarrubias D, Toledo R, Monje-Reyna D, Santamaria F. Male sexual behavior and prostate histology in a rat model of autism. eNeurobiol. 2019 25: 280919.

Velázquez-Landa X, Carrillo P, Coria-Avila GA, Herrera-Covarrubias D, García LI, Toledo-Cárdenas MR, Hernández-Aguilar ME, Manzo J. Zebrafish sexual behavior in plain and enriched environments: Parameters in the valproate model of autism. Fishes 2023 8: 156.

Grumbach MM. The neuroendocrinology of human puberty revisited. Horm Res Paediatr 2002 57: 2–14.

Crone EA, Dahl RE. Understanding adolescence as a period of social–affective engagement and goal flexibility. Nat Rev Neurosci 2012 13: 636–650.

Seltzer MM, Shattuck P, Abbeduto L, Greenberg JS. Trajectory of development in adolescents and adults with autism. Ment Retard Dev Disabil Res Rev 2004 10: 234–247.

Corbett BA, Vandekar S, Muscatello RA, Tanguturi Y. Pubertal timing during early adolescence: Advanced pubertal onset in females with autism spectrum disorder. Autism Res 2020 13: 2202–2215.

Kellaher DC. Sexual behavior and autism spectrum disorders: An update and discussion. Curr Psychiat Rep 2015 17: 562.

Bourgondien MEV, Reichle NC, Palmer A. Sexual behavior in adults with autism. J Autism Dev Disord 1997 27: 113–125.

Stokes MA, Kaur A. High-functioning autism and sexuality: A parental perspective. Autism 2005 9: 266–289.

Brown-Lavoie SM, Viecili MA, Weiss JA. Sexual knowledge and victimization in adults with autism spectrum disorders. J Autism Dev Disord 2014 44: 2185–2196.

Beddows N, Brooks R. Inappropriate sexual behaviour in adolescents with autism spectrum disorder: What education is recommended and why. Early Interv Psychiatry 2016 10: 282–289.

Ballan MS, Freyer MB. Autism spectrum disorder, adolescence, and sexuality education: Suggested interventions for mental health professionals. Sex Disabil 2017 35: 261–273.

Ballan MS. Parental perspectives of communication about sexuality in families of children with autism spectrum disorders. J Autism Dev Disord 2012 42: 676–684.

Coskun M, Karakoc S, Kircelli F, Mukaddes NM. Effectiveness of mirtazapine in the treatment of inappropriate sexual behaviors in individuals with autistic disorder. J Child Adolesc 2009 Psychopharmacol 19: 203–206.

Rogers C, Lepherd L, Ganguly R, Jacob-Rogers S. Perinatal issues for women with high functioning autism spectrum disorder. Women Birth 2017 30: e89–e95.

Ferrara R, Ricci P, Damato FM, Iovino L, Ricci L, Cicinelli G, Simeoli R, Keller R. Pregnancy in autistic women and social medical considerations: Scoping review and meta- synthesis. Front Psychiatry 2023 14: 1222127.

Sundelin HE, Stephansson O, Hultman CM, Ludvigsson JF. Pregnancy outcomes in women with autism: A nationwide population-based cohort study. Clin Epidemiology 2018 10: 1817–1826.

George R, Stokes MA. Sexual orientation in autism spectrum disorder. Autism Res 2018 11: 133-141.

Weir E, Allison C, Baron‐Cohen S. The sexual health, orientation, and activity of autistic adolescents and adults. Autism Res. 2021 14: 2342–2354.

Dewinter J, Graaf HD, Begeer S. Sexual orientation, gender identity, and romantic relationships in adolescents and adults with autism spectrum disorder. J Autism Dev Disord 2017 47: 2927–2934.




DOI: https://doi.org/10.25009/eb.v15i39.2635

Enlaces refback

  • No hay ningún enlace refback.


 

eNeurobiología es una publicación cuatrimestral editada por el Instituto de Investigaciones Cerebrales de la Universidad Veracruzana. Estamos ubicados en Av. Dr. Luis Castelazo Ayala, s/n, colonia Industrial Ánimas, C.P. 91190, Xalapa-Enríquez, Veracruz, México. Teléfono: 8418900 ext. 13062, www.iice.uv.mx; eneurobiologia@uv.mx. Reserva de Derechos al Uso Exclusivo 04-2023-061314100600-102, otorgada por el Instituto Nacional de Derechos de Autor. ISSN: 2007-3054. Esta obra está bajo una Licencia Creative Commons Attribution 4.0 International.