Abstract
Background: Numerous studies have documented that patients with schizophrenia show neurocognitive impairments, which are also heritable in schizophrenia families. In view of these findings, the current investigation tested the hypothesis that neurocognitive performance of schizophrenia probands can predict the neurocognitive performance of their unaffected family members. Methods: Participants (n=1967; schizophrenia=369; first-degree relatives=1072; community comparison subjects=526) in the Consortium on the Genetics of Schizophrenia were administered the Penn Computerized Neurocognitive Battery. Results: Consistent with prior work, probands showed significant neurocognitive impairment, and neurocognitive ability was significantly heritable across domains. On average, unaffected relatives did not differ from community comparison subjects in their neurocognitive performance. However, in six of seven domains, proband scores predicted the performance of their unaffected siblings. Male, but not female, proband performance was predictive of their unaffected relatives' (siblings and mothers) performance, most consistently in face memory and spatial processing. Conclusions: Using a novel approach in which individual probands are paired with their respective unaffected relatives within each family, we found that male proband performance predicted both sister and brother performance, an effect that was most powerfully observed for face memory and spatial processing. Results suggest that the familial transmission of sexually dimorphic neurocognitive domains, in which a particular sex tends to show a performance advantage over the other, may not itself be sex specific in schizophrenia families.
| Original language | English |
|---|---|
| Pages (from-to) | 976-984 |
| Number of pages | 9 |
| Journal | Biological Psychiatry |
| Volume | 73 |
| Issue number | 10 |
| DOIs | |
| State | Published - 15 May 2013 |
| Externally published | Yes |
Bibliographical note
Funding Information:This study was supported by National Institute of Mental Health Grants R01 MH086135, R01 MH65571, R01 MH42228, R01 MH65588, R01 MH65562, R01 MH65707, R01 MH65554, R01 MH65578, R01 MH65558, and K08 MH79364; a Neuropsychiatry Postdoctoral traineeship (MH19112); and a Scottish Rite Schizophrenia Research Fellowship.
Funding
This study was supported by National Institute of Mental Health Grants R01 MH086135, R01 MH65571, R01 MH42228, R01 MH65588, R01 MH65562, R01 MH65707, R01 MH65554, R01 MH65578, R01 MH65558, and K08 MH79364; a Neuropsychiatry Postdoctoral traineeship (MH19112); and a Scottish Rite Schizophrenia Research Fellowship.
| Funders | Funder number |
|---|---|
| Scottish Rite Schizophrenia Research Fellowship | |
| National Institute of Mental Health | R01 MH65558, R01 MH42228, K08 MH79364, MH19112, R01MH065707, R01 MH65562, R01 MH086135, R01 MH65571, R01 MH65578, R01 MH65588, R01 MH65554 |
Keywords
- Endophenotype
- genetics
- heritability
- neurocognition
- schizophrenia
- sex differences
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