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Neurointersexuality - Sex Difference in the human brain

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A sex difference in the human brain and its relationship to transsexuality

From J.-N. Zhou, M.A. Hofman, L.J. Gooren and D.F. Swaab

Transsexuals have the strong feeling, often from childhood onwards, of having been born the wrong sex. The possible psychogenic or biological etiology of transsexuality has been the subject of debate for many years[1,2]. Here we show that the volume of the central subdivision of the bed nucleus of the stria terminalis (BSTc), a brain area that is essential for sexual behaviour [3,4], is larger in men than in women. A female-sized BSTc was found in male-to-female transsexuals. The sizeof the BSTc was not influenced by sex hormones in adulthood and was independent of sexual orientation. Our study is the first to show afemale brain structure in genetically male transsexuals and supports the hypothesis that gender identity develops as a result of an interaction between the developing brain and sex hormones [5,6].

Investigation of genetics, gonads, genitalia or hormone level of transsexuals has not, so far, produced any results that explain their status [1,2]. In experimental animals, however, the same gonadal hormones that prenatally determine the morphology of the genitalia alsoinfluence the morphology and function of the brain in experimental animals in a sexually dimorphic fashion [6,7]. This led to the hypothesis that sexual differentiation of the brain in transsexuals might not have followed the line of sexual differentiation of the body as a whole. In thepast few years, several anatomical differences in relation to sex and sexual orientation have been observed in the human hypothalamus (see[6] for a review), but so far no neuroanatomical investigations have been made in relation to the expression of cross-gender identity (transsexuality).

We have studied the hypothalamus of six male-to-female transsexuals(T1-T6); this material that was collected over the last eleven years. We searched for a brain structure that was sexually dimorphic, but not influenced by sexual orientation, as male-to-female transsexuals may be"oriented" to either sex with respect to sexual behaviour. Our earlier observations showed that the paraventricular nucleus (PVN), sexually dimorphic nucleus (SDN) and suprachiasmatic nucleus (SCN) did not meet these criteria ([6] and unpublished data). Although there is no accepted animal model for gender identity alterations, the bed nucleus of the stria terminalis (BST) turned out to be an appropriate candidate to study for the following reasons. First, it is known that the BST plays anessential part in rodent sexual behaviour [3,4]. Not only have oestrogen and androgen receptors been found in the BST [8,9], it is also a majoraromatization centre in the developing rat brain [10]. The BST in the ratreceives projections mainly from the amygdala and provides a strong input in the preoptic-hypothalamic region [11,12]. Reciprocal connections between hypothalamus, BST and amygdala are also well documented in experimental animals [13-15]. In addition, sex differences in the size and cell number of the BST have been described in rodents which are influenced by gonadal steroids in development[16-18]. Also in humans a particular caudal part of the BST(BNST-dspm) has been reported to be 2.5 times larger in men than in women [19].

Figure 1: Schematic frontal section through two subdivisions of the bed nucleus of the stria terminalis (BST) that are hatched. III: third ventricle; AC: anterior commissure; BSTc and BSTv: central and ventral subdivisions of the BST; FX: fornix; IC: internal capsule; LV: lateral ventricle; NBM: nucleus basalis of Meynert; OT: optic tract; PVN: paraventricular nucleus; SDN: sexually dimorphic nucleus; SON: supraoptic nucleus.

The localization of the BST is shown in figure 1. The central part of the BST (BSTc) is characterized by its somatostatin cells and vasoactiveintestinal polypeptide (VIP) innervation [20]. We measured the volumeof the BSTc on the basis of its VIP innervation (Fig. 2).

Heterosexual Cis-Man

Heterosexual Cis-Woman

Homosexual Cis-Man

Lesbian NGS-Woman

Figure 2: Representative sections of the BSTc innervated by vasoactive intestinal polypeptide (VIP). A: heterosexual man; B: heterosexual woman; C: homosexual man; D: male-to-female transsexual. Bar=0.5 mm. LV: lateral ventricle. Note there are two parts of the BST in A and B: small sized medial subdivision (BSTm), and large oval-sized central subdivision (BSTc).

The BSTc volume in heterosexual men (2.49±0.16 mm3) was 44%
larger than in heterosexual women (1.73±0.13 mm3) (P<0.005) (Fig. 3). The volume of the BSTc of heterosexual and homosexual men was
found not to differ in any statistically significant way (2.81±0.20 mm3) (P=0.26). The BSTc was 62% larger in homosexual men than inheterosexual women (P<0.005). AIDS did not seem to influence the size of the BSTc: the BSTc size of two heterosexual AIDS-infected women and three heterosexual AIDS-infected men remained well within the range of the corresponding reference group (Fig. 3). The AIDS-infected heterosexuals were therefore included in the corresponding reference group for statistical purposes. A small volume of the BSTc (1.30±0.23 mm3) was found in the male-to-female transsexuals (Fig. 3). Its size was only 52% of that found in the reference males (P<0.005) and 46% of the BSTc of homosexual males(P<0.005). Although the mean BSTc volume in the transsexuals was even smaller than that in the female group, the difference did not reach statistical significance (P=0.13). The volume of the BSTc was not related to age in any of the reference groups studied (P>0.15), indicating that the observed small size of the BSTc in transsexuals was not due tothe fact that they were, on average, 10 to 13 years older than the hetero-and homosexual men.

The BST plays an essential role in masculine sexual behaviour and in the regulation of gonadotrophin release, as shown by studies in the rat[3,4,21]. There has been no direct evidence that the BST has such a rolein human sexual behaviour but our demonstration of a sexually dimorphic pattern in the size of the human BSTc, which is in agreement with the previously described sex difference in a more caudal part of the BST (BNST-dspm) [19], indicates that this nucleus may also be involved in human sexual or reproductive functions. It has been proposed that neurochemical sex differences in the rat BST may be dueto effects of sex hormones on the brain during development and in adulthood [22,23]. Our data from humans however, indicate that BSTcvolume is not affected by varying sex hormone levels in adulthood. The BSTc volume of a 46-year-old woman who had suffered for at least 1 year from a tumour of the adrenal cortex that produced very high blood levels of androstenedione and testosterone, was within the range of that of other women (Fig. 3: S1). Furthermore, two postmenopausal women (aged over 70 years) showed a completely normal female-sized BSTc (Fig. 3: M1, M2). As all the transsexuals had been treated with oestrogens, the reduced size of the BSTc could possibly have been due to the presence of high levels of oestrogen in the blood. Evidence against this comes from the fact that transsexual T2 and T3 both showeda small, female-like BSTc (Fig. 3), although T2 stopped taking oestrogen about 15 months before death, since her prolactin levels were too high and T3 stopped hormone treatment since a sarcoma was foundabout three months before death; also a 31-year-old man who sufferedfrom a feminizing adrenal tumour which induced high blood levels of oestrogen, nevertheless had a very large BSTc (Fig. 3: S2).


Figure 3: Volume of the BSTc innervated by VIP fibres in presumed heterosexual males (M), homosexual males (HM), presumed heterosexual females (F) and male-to-female transsexuals (TM). The six transsexuals are numbered T1-T6. The patients with abnormal sex hormone levels are numbered S1-S4. M1 and M2: postmenopausal women. Bars indicate mean±SEM. Open symbols: individuals who died of AIDS. METHODS. Brains of 42 subjects matched for age, postmortem time and duration of formalin fixation were investigated. The autopsy was performed following the required permission. For immunocytochemical staining of VIP, the paraffin sections were hydrated and rinsed in TBS (Tris-buffered-saline: 0.05 M tris, 0.9% NaCl, pH 7.6). The sections were incubated with 200 µl anti-VIP (Viper, 18/9/86) 1:1000 in 0.5% triton in TBS overnight at 4° C. The immunocytochemical and morphometric procedures were performed as described extensively elsewhere [25-27]. In brief, serial 6 m m sections of the BSTc were studied by means of a digitizer (Calcomp 2000) connected to a HP-UX 9.0, using a Zeiss microscope equipped with a 2.5x objective and with 10x (PLAN) oculars. Staining was performed on every 50th section with anti-VIP. The rostral and caudal borders of the BSTc were assessed by staining every 10th section in the area. The volume of the BSTc was determined by integrating all the area measurements of the BSTc sections that were innervated by VIP fibres. In a pilot study, the size of the BSTc was measured on both sides in eight subjects (five females and three males) and no left-right asymmetries were observed: the left BSTc (1.71±0.16 mm3) was comparable in size to that of the right BSTc (1.83±0.30 mm3) (P=0.79). No asymmetry was observed in the BNST-dspm either [19]. The rest of our study was therefore performed on one side of the brain only. Brain weight of the male transsexuals (1385±75 g) was not different from that of the reference males (1453±25 g) (P=0.61) or that of the females (1256±35 g) (P=0.23). The cause of death of the six transsexuals was suicide (T1), cardiovascular disease (T2,T6), sarcoma (T3), AIDS, pneumonia, pericarditis (T4) and hepatitic failure (T5). Sexual orientation of the subjects of the reference group (12 men and 11 women) was generally not known, but presumably most of them were heterosexual. Sexual orientation of nine homosexuals was registered in the clinical records [28]. Differences among the groups were tested two-tailed using the Mann-Whitney U test. A 5% level of significance was used in all statistical tests.

Our results might also be explained if the female-sized BSTc in the transsexual group was due to the lack of androgens, because they had all been orchidectomized except for T4. We therefore studied two other men who had been orchidectomized because of cancer of the prostate (one and three months before death: S4 and S3, respectively), and found that their BSTc sizes were at the high end of the normal male range. The BSTc size of the single transsexual who had not been orchidectomized (T4) ranged in the middle of the transsexual scores (Fig. 3). Not only were five of the transsexuals orchidectomized, they all used the antiandrogen cyproterone acetate (CPA). A CPA effect on the BSTc does not seem likely, because T6 had not taken CPA for the past 10 years, and T3 took no CPA during the two years before death and still had a female-sized BSTc.

In summary, our observations suggest that the small size of the BSTc in male-to-female transsexuals cannot be explained by differences in adult sex hormone levels, but is established during development by anorganizing action of sex hormones, an idea supported by the fact that neonatal gonadectomy of male rats and androgenization of the female rats indeed induced significant changes in the number of neurons of the BST and suppressed its sexual dimorphism [17,18].

Considered together with information from animals, then our study supports the hypothesis that gender identity alterations may develop as aresult of an altered interaction between the development of the brain andsex hormones [5,6]. The direct action of genetic factors should also beconsidered on the basis of animal experiments [24].

We found no relationship between BSTc size and the sexual orientation of transsexuals, that is, whether they were male-oriented (T1,T6), female-oriented (T3,T2,T5), or both (T4). Furthermore, the size of the BSTc of heterosexual men and homosexual men did not differ, which reinforced the idea that the reduced BSTc size is independent of sexual orientation. In addition, there was no difference in BSTc size between early-onset (T2,T5,T6) and late-onset transsexuals (T1, T3), indicating that the decreased size is related to the gender identity alteration per serather than to the age at which it becomes apparent. Interestingly, thevery small BSTc in transsexuals appears to be a very local brain difference. We failed to observe similar changes in three other hypothalamic nuclei, namely, PVN, SDN or SCN in the same individuals (unpublished data). This might be due to the fact that thesenuclei do not all develop at the same time, or to a difference between these nuclei and the BST with respect to the presence of sex hormone receptors or aromatase. We are now studying the distribution of sexhormone receptors and the aromatase activity in various hypothalamicnuclei in relation to sexual orientation and gender.


We thank Mr. B. Fisser, Mr. H. Stoffels, Mr. G. van der Meulen, and Ms. T. Eikelboom and Ms. W.T.P. Verweij for their help, and Drs.R.M. Buijs, M.A. Corner, E. Fliers, A. Walter and F.W. van Leeuwenfor their comments. Brain material was provided by the Netherlands Brain Bank (coordinator Dr. R. Ravid). This study was supported by NWO.


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Correspondence and requests for materials to:
J.-N. Zhou, M.A. Hofman and D.F. Swaab
Graduate School Neurosciences Amsterdam
Netherlands Institute for Brain Research
Meibergdreef 33 
1105 AZ Amsterdam ZO
The Netherlands 

L.J.G. Gooren
Department of Endocrinology
Free University Hospital
1007 MB Amsterdam
The Netherlands




Letzte Bearbeitung: 12.02.2024, 18:39



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Neurointersexualität / Neurointersexuelle Körperdiskrepanz (NIBD)
Eine Zusatz-Bezeichnung, die gerne von manchen originär transsexuellen Menschen benutzt wird, um sich von der inflationären Benutzung des Begriffes "Transsexualität", welche durch die genderorientierte Trans*-Community, aber auch durch die Medien getätigt wird, abzugrenzen. NIBD-Betroffene wollen einfach nicht mit anderen Phänomenlagen, die entweder nur ein Lifestyle, Rollenproblem oder sexueller Fetisch sind, verwechselt und/oder in einen Topf geworfen werden. Die Bezeichnung NIBD bezieht sich auf die wissenschaftliche Arbeit von Dr. Haupt.


Neurointersexuality / Neurointersexual Body Discrepancy (NIBD)
An additional term which is often used by originally transsexual people to differentiate themselves from the inflationary use of the term "transsexuality" by the gender-oriented trans* community, but also by the media. NIBD patients simply do not want to be confused and/or lumped together with other phenomena that are either just a lifestyle, role problem or sexual fetish. The term NIBD refers to the scientific work of Dr. Haupt.





Transgender - Transidentität
Transgender hadern hauptsächlich mit der sozialen Geschlechterrolle (gender), die ihnen seitens der Gesellschaft und kulturellen Konventionen aufgedrückt wird. Einen körperlichen Leidensdruck, wie ihn originär transsexuelle Menschen (NIBD) verspüren, ist bei ihnen nicht gegeben. Gerne und immer wieder wird, auch von Fachleuten, Transgenderismus mit originärer Transsexualität verwechselt.
Transidente hadern mit ihrer Identität als Mann oder Frau. Dieses Problem ist rein psychisch bedingt, einen körperlichen Leidensdruck, wie ihn originär transsexuelle Menschen (NIBD) verspüren, ist bei ihnen ebenfalls nicht gegeben. Auch hier wird das Phänomen gerne mit originärer Transsexualität verwechselt.


Transgender - Transidentity
Transgender people mainly struggle with the social gender role (gender) that is imposed on them by society and cultural conventions. They do not experience the kind of physical distress felt by originally transsexual people (NIBD). Transgenderism is often and repeatedly confused with original transsexuality, even by experts.
Transident people struggle with their identity as a man or a woman. This problem is purely psychological; they do not experience the kind of physical suffering that original transsexual people (NIBD) do. Here too, the phenomenon is often confused with original transsexuality.

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