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Zhou Brain Research (1995): what the study does and does not show
"Studies show that trans women have female brains" — that claim often rests on one study: Zhou (1995) on the brain nucleus BSTc. It was a small post-mortem study of brains of people who had used hormones, from a single research group. According to the Cass Review, brain research has so far not reliably identified brain changes directly linked to gender incongruence.
What Zhou did
Zhou, Hofman, Gooren and Swaab (Nature, 1995) examined post-mortem brains of six male transsexuals (source) and measured the volume of the bed nucleus of the stria terminalis, central subdivision (BSTc). The volume was larger in men than in women, and in the transsexual participants the BSTc was female-sized (source). The six participants had used cross-sex hormones (source).
Limitation 1 — brains after hormone use
The authors themselves concluded that the size of the BSTc was not influenced by sex hormones in adulthood (source). The Cass Review, however, writes (para. 8.18) that most brain studies examined brains after treatment with feminising hormones, rather than before and after treatment, so changes could be caused by the treatment rather than by an inherent difference (source).
Limitation 2 — the difference only emerges in adulthood
Chung, De Vries and Swaab (2002) found that the difference in BSTc volume between men and women only becomes significant in adulthood, and call that late differentiation unexpected (source). That fits poorly with the idea that this brain feature is fixed early in development and would explain a sense of gender identity in childhood.
Limitation 3 — small sample, post-mortem, limited replication
Six participants is few for an anatomical claim. The Cass Review writes (para. 8.18) that most brain studies are based on small numbers and have not been reliably replicated (source). A follow-up study by Kruijver et al. (2000), with 42 participants, also found a female-range number of neurons in the BSTc in trans women (source), but it came from the same research group, and according to a critical analysis 26 of the 34 participants in its main analysis were the same as in Zhou (source). See also publication bias and scientific problems.
Limitation 4 — no reliable brain marker
The Cass Review writes (para. 8.20) that research in this area has so far not reliably identified brain changes directly linked to gender incongruence, and that even if it could, this would say nothing about cause and effect; brains change through plasticity (para. 8.17) (source). See also no brain marker and no measurable marker.
What this means
The claim that "trans brains" exist rests on small post-mortem studies from thirty years ago from a single research group. Cass also writes that it cannot be ruled out that a biological predisposition plays a part in some individuals, in ways not yet understood (para. 8.21 and 8.23) (source).
A mega-analysis of imaging studies reported that trans people appear to have their own "unique brain phenotype", but Cass writes that this type of analysis commonly generates false-positive findings and that the group is highly heterogeneous (para. 8.19). See no brain marker.
Cass writes that there is no clear evidence for a straightforward biological cause of gender incongruence, that a biological predisposition is possible in some individuals, and that brain research has so far not reliably shown brain changes directly linked to gender incongruence (para. 8.20-8.21).
They found a female-sized BSTc in trans women and concluded that this supports the hypothesis that gender identity develops from an interaction between the developing brain and sex hormones.
Sources
- Zhou, J.N. et al. (1995). A sex difference in the human brain and its relation to transsexuality. Nature. Europe PMC
- Chung, W.C.J., De Vries, G.J. & Swaab, D.F. (2002). Sexual differentiation of the bed nucleus of the stria terminalis in humans may extend into adulthood. J. Neuroscience. Europe PMC
- Kruijver, F.P.M. et al. (2000). Male-to-female transsexuals have female neuron numbers in a limbic nucleus. J. Clin. Endocrinol. Metab. Europe PMC
- Cass, H. (2024). Independent Review — Final Report, chapter 8.