# Differential genome-wide association analysis of schizophrenia and post-traumatic stress disorder identifies opposing effects at the MAPT/CRHR1 locus

**Authors:** Zhong‐shan Cheng

PMC · DOI: 10.3389/fgene.2026.1728494 · Frontiers in Genetics · 2026-02-13

## TL;DR

This study finds opposing genetic effects at the MAPT/CRHR1 locus in schizophrenia and PTSD, suggesting distinct biological pathways for these disorders.

## Contribution

The study identifies a specific genetic locus with opposing effects in schizophrenia and PTSD, revealing distinct neurodevelopmental and stress-related pathways.

## Key findings

- Four independent loci show genome-wide significant differential associations between schizophrenia and PTSD.
- The MAPT/CRHR1 locus at 17q21.31 exhibits opposing regulatory effects on gene expression in brain tissues.
- Opposite directions of effect at rs62062288 suggest divergent genetic contributions to schizophrenia and PTSD.

## Abstract

Schizophrenia (SCZ) and post-traumatic stress disorder (PTSD) are severe psychiatric conditions with overlapping yet distinct symptomatology and pathophysiology.

We conducted a differential genome-wide association study (GWAS) to directly compare the genetic architectures of SCZ and PTSD using publicly available GWAS summary statistics from the Psychiatric Genomics Consortium (PGC).

We identified four independent loci reaching genome-wide significance (P < 5 × 10−8) for differential associations between SCZ and PTSD in individuals of European ancestry. These loci (rs62062288, rs58120505, rs12536395, and rs11057189) showed genome-wide significant associations with SCZ and nominal associations with PTSD (all Ps < 0.05) but with opposite directions of effect. Among these, only rs62062288 retained genome-wide significance for PTSD in trans-ancestry meta-analysis, whereas the other three loci showed markedly attenuated PTSD associations (all Ps > 0.001). rs62062288 maps to the 17q21.31 MAPT/CRHR1 locus, exhibiting a risk effect for PTSD and a protective effect for SCZ. GTEx analyses revealed that MAPT and CRHR1 are highly expressed across multiple brain tissues and that rs62062288 shows opposite regulatory effects on MAPT and CRHR1 expression in the brain tissue caudate basal ganglia, with the PTSD risk allele associated with increased MAPT expression and decreased CRHR1 expression. Additional brain-region–specific expression quantitative trait locus (eQTL) effects on CRHR1 were observed in frontal cortex BA9, hippocampus, and spinal cord, indicating tissue-dependent regulation.

These findings provide evidence for distinct and opposing genetic contributions to SCZ and PTSD. The identification of the MAPT/CRHR1 locus with brain-region–specific and gene-specific regulatory effects highlights divergent neurodevelopmental and stress-related pathways underlying these disorders.

## Linked entities

- **Genes:** MAPT (microtubule associated protein tau) [NCBI Gene 4137], CRHR1 (corticotropin releasing hormone receptor 1) [NCBI Gene 1394]
- **Diseases:** schizophrenia (MONDO:0005090), post-traumatic stress disorder (MONDO:0005146)

## Full-text entities

- **Genes:** LRRC37A2 (leucine rich repeat containing 37 member A2) [NCBI Gene 474170] {aka LRRC37}, CRHR1 (corticotropin releasing hormone receptor 1) [NCBI Gene 1394] {aka CRF-R, CRF-R-1, CRF-R1, CRF1, CRFR-1, CRFR1}, BBS9 (Bardet-Biedl syndrome 9) [NCBI Gene 27241] {aka B1, C18, D1, PTHB1}, MAD1L1 (mitotic arrest deficient 1 like 1) [NCBI Gene 8379] {aka MAD1, MVA7, PIG9, TP53I9, TXBP181}, SPPL2C (signal peptide peptidase like 2C) [NCBI Gene 162540] {aka IMP5}, IMMP2L (inner mitochondrial membrane peptidase subunit 2) [NCBI Gene 83943] {aka IMMP2L-IT1, IMP2, IMP2-LIKE}, MPHOSPH9 (M-phase phosphoprotein 9) [NCBI Gene 10198] {aka MPP-9, MPP9}, ARL17B (ARF like GTPase 17B) [NCBI Gene 100506084] {aka ARL17}, KANSL1 (KAT8 regulatory NSL complex subunit 1) [NCBI Gene 284058] {aka C17DELq21.31, CENP-36, DEL17Q21.31, KDVS, KIAA1267, MSL1v1}, LRRC37A (leucine rich repeat containing 37A) [NCBI Gene 9884] {aka LRRC37, LRRC37A1}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, ARL17A (ARF like GTPase 17A) [NCBI Gene 51326] {aka ARF1P2, ARL17P1}, IGKV5-2 (immunoglobulin kappa variable 5-2) [NCBI Gene 28907] {aka B2, IGKV52}, FUT2 (fucosyltransferase 2 (H blood group)) [NCBI Gene 2524] {aka B12QTL1, SE, SEC2, Se2, sej}
- **Diseases:** COVID-19 (MESH:D000086382), stress-related (MESH:D000079225), cognitive impairment (MESH:D003072), bipolar disorder (MESH:D001714), SCZ (MESH:D012559), neuroinflammation (MESH:D000090862), neurodevelopmental abnormalities (MESH:D063647), Psychiatric (MESH:D001523), substance abuse (MESH:D019966), neurodevelopmental disruptions (MESH:D015451), mitochondrial dysfunction (MESH:D028361), neurodevelopmental disease (MESH:D004194), neurodegeneration (MESH:D019636), trauma (MESH:D014947), inflammatory (MESH:D007249), PTSD (MESH:D013313), emotional dysregulation (MESH:D021081), major depressive disorder (MESH:D003865), HPA-axis (MESH:D007029)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** rs58120505, rs11057189, rs2532252, rs62062288, S356T, rs12536395

## Full text

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## Figures

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## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12945334/full.md

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Source: https://tomesphere.com/paper/PMC12945334