PAIS and MAIS Ligand-Selective and the Organic Ethiology of Gender Dysphorias
By Wal Torres# & Pedro Jurberg *
# Wal was a MS in sexology candidate, at UGF-Rio, Brazil
* Pedro Jurberg,PhD, is a neurobiologist from Instituto Oswaldo Cruz, Rio, Brazil.
Gender may not be defined anymore only by genitals and sex of rearing as determining factors: after David Reimer's revelation of the truth about what he suffered oppressed by sex of rearing "therapy", we need to renew our gender criterias. We propose the neuro-psychical identity as a new gender main criteria, and that gender is independent of the genital conformation because the sex hormone that determines genital external conformation is DHT, thru its action over the androgen receptor AR, but testosterone-T is the main responsible for the neural gender organization in humans. The gender discord between those two biological systems may occur, generating the dysphoria, naturally or thru a genital surgery (as in David Reimer's case). It is important to study the hormone-selective binding characteristics and expression (T-AR and DHT-AR) to know if that action in mild androgen insensitivity syndromes-MAIS and partial syndromes-PAIS explain some dysphoric situations in transsexuals (MAIS) and intersexuals (PAIS). A diagnosis test for children and youths may be developed, and gender understanding must be renewed.
The androgen receptor (AR) is a ligand-activated transcription factor
that mediates male sexual development. AR binds the two biologically
active androgens, testosterone(T) and dihydrotestosterone(DHT), with
high affinity (Zhou et al 1995b). AR is not tissue or ligand specific,
but its action is ligand dependent. There is a database
(Gottlieb et al,1998) of AR mutations. Despite AR being not ligand
specific, its action may be ligand-selective. Sometimes both ligands
T and DHT are uneffective; sometimes DHT is less effective;
sometimes T (Gottlieb et al, 1999) .|
In PAIS and CAIS (complete AIS), the action of DHT-AR is abnormal (it generates genital malformations- levels 2 to 7 in Quigley's scale--- see Quigley et al 1995); in MAIS maybe there is no problem with DHT-AR (they don't show any genital malformation- level 1 in Quigley's scale), but possibly T-AR may have important abnormalities (they show undervirilization: gynecomastia, or small penis, and/or a dysphoria, etc.). The abnormalities in T-AR are less visible and less studied than DHT-AR, because they mediate--- during fetal stage--- "more invisible processes" (Zhou et al,1995b), in more invisible tissues.
Some genital malformation or intersex don't generate gender dysphorias. Gender dysphoria means "to have an uneasiness with its genitals". CAIS don't generate dysphorias, because all tissues remain female and there is no inner discord. Some PAIS and MAIS cases also don't generate dysphorias. Gender dysphorias happens when there is a gender discord between genital and neural tissues. That situation may happens:
(1) When baby boys have their genitals mutilated, or micropenis, and are surgically transgenitalized to females and reared as girls. For example, the John/Joan case (David Reimer's), described by Nussbaum,2000;Diamond & Sigmundson,1997; Fausto-Sterling,2000; Colapinto,2000;
(2) when happens the discord between the neural gender (male) with ambiguous (female like) genitals, as in Imperato McGinley's syndromes: recognized as girls, reared as girls in all cultures and continents, later they show they are boys;
(3) some PAIS situations, when the genitals are more female, but the neural male (in most PAIS cases there is harmony between genital and neural gender, both female or male);
(4) True hermafroditism when the genital option (by surgery decision made by adults: parents, psychiatrists or surgeons) is not in accord with the child neuro-psychical gender identity (showed later by the child expression and living);
(5) "transsexuals", when the neural and genital gender are naturally in radical discord, without any visible genital external conformation problem.
How we may evaluate those situations?
What could be a good criteria?
John Money's criteria (genital conformation and sex of rearing --- see Money & Ehrhardt 1972; Money & Tucker 1975) really isn't a good criteria: the true story of David Reimer show us John Money's model of gender identity formation was a fake and not the reality (see Diamond 1996; Diamond & Sigmundson 1997; Colapinto 2000; Fausto-Sterling 2000) --- Money and his co-workers wrote and published their opinions and not what the patient (David Reimer) really lived as gender identity, as truth-they ignored the patient's reality, publishing their opinions as truth and unfortunately being believed: they trapped doctors, sexologists and psychologists.
(a) Our neural organization has its congenital and irreversible gender determined in a neuroendocrinal way (Imperato McGinley et al, 1979; Bonsall & Michael 1989; Resko et al 1988; McEwen, 1994, Zhou et al, 1995a; Kruijver et al, 2000);
(b) That gender neural organization generates in the foetus and baby a psychical gender identity as an emotional priming (see Damasio 1994; Torres & Jurberg 2000; and Torres & Jurberg in other article in this volume); and that
(c) rearing, culture, hormones at puberty: modulate, inhibit or reinforce, but don't determine the gender of our identity (Imperato McGinley1979; Wilson,JD, 1999);
we propose as a 1st gender classification criteria:
what determines the neural gender is prenatal T as what determines the external genitals gender is prenatal DHT: in humans as in other primates (Bonsall & Michael 1989, Resko et al, 1988). The gender identity is determined by the dynamic complex evolution and psychical expression of that neural differentiation (see the other article of Torres & Jurberg in this volume).
To evaluate properly gender in transsexual and intersexual dysphorics it is important the selective action of T-AR and DHT-AR in PAIS and MAIS, researching functional activity and gene expression not only of DHT-AR and artificial steroids-AR, but also T-AR (see Gottlieb et al 1999).
What we may today do in mosaic situations? In the genital tract (DHT-AR action) we may know , but in the neural (T-AR)?
We propose as a 2nd gender classification criteria:
in complex situations: wait the child own manifestation thru its neural system of who it is, boy or girl: they have the best neural sensor possible: their selves .
Whe propose a 3rd gender classification criteria:
When happens a dysphoria in a genetically male child, it would be important to study the child in the molecular level, with or without genital malformations , when it is feasible --- or wait and believe in the identity showed by the child.
Those 3 criterias may prevent dysphorias
when there are genital malformations, and a test procedure to evaluate dysphorias in children may be developed. When malformations don't happen we may not prevent, but we may diagnosis soon (the child show a dysphoria between 5 to 8 years old if with liberty and no social repression --- as a "sissi boy" or "effeminate gay boy", for example), and correct the children as soon as possible--- beginning with 10 to 12 years old at least, before the child will be too traumatized by society (see Cohen et al, 1997) and the body structure defformed by hormones.
The ligand-selective test may prevent consequences. If not, we will need to wait that the victim show its identity freely, before any surgery and final legal gender classification is irreversibly d etermined. It is better to sacrifice family and society, delaying the social and civil legal decision --- as Freitas, 1998 proposed --- knowing that doing this way we will prevent some children sufferings.
The ethical position we support today is:
don't define anymore gender in a rash, heteronomous and authoritary way, because that rash action may mutilate children, and originate dysphorias --- see David Reimer's and Cheryl Chase's stories and arguments (Fausto-Sterling 2000; Colapinto 2000). Therapists and surgeons know gender dysphorics by the outside only --- thinking they have problems to understand reality (see Mormont, Michel, Wauthy, 1995), when they are the only to really know and live themselves by the inside, knowing their true reality (see Freitas 1998).
Today, no result or fact is in contradiction with our 3 criterias; but first of al we need a positive confirmation of them from lab gene expression results in PAIS and MAIS intersex and transsex --- and to do that we need a molecular endocrinology lab to continue our project .
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Paris, June 2001
Universidade Gama Filho- Rio, Brazil
WF Torres supported by Capes.
Presented at the 15th World Congress of Sexology, Paris 2001