A Genome-Wide Linkage Scan for Distinct Subsets of Schizophrenia Characterized by Age at Onset and Neurocognitive Deficits
2011

Linkage Scan for Subsets of Schizophrenia Based on Age at Onset and Cognitive Deficits

Sample size: 1242 publication 10 minutes Evidence: moderate

Author Information

Author(s): Lien Yin-Ju, Hsiao Po-Chang, Liu Chih-Min, Faraone Stephen V., Tsuang Ming T., Hwu Hai-Gwo, Chen Wei J.

Primary Institution: National Taiwan University

Hypothesis

Using a homogeneous subtype of schizophrenia based on age at onset or neurocognitive deficits can help obtain increased linkage signals.

Conclusion

The study found possible evidence of linkage on chromosome 2q22.1 in families of schizophrenia patients with more cognitive deficits and younger age at onset.

Supporting Evidence

  • A maximum LOD score of 4.17 was found at 2q22.1 in families ranked by age at onset.
  • Further subsetting by cognitive test performance increased the LOD score to 7.71.
  • Significant familial resemblance was observed for age at onset and neurocognitive performance.

Takeaway

Researchers looked at families with schizophrenia to find genetic clues based on when symptoms started and how well they think. They found a possible link to a specific part of a chromosome.

Methodology

Patients with schizophrenia and their first-degree relatives were genotyped and assessed using various cognitive tests.

Potential Biases

The study may have risks of false positives due to multiple testing.

Limitations

The study's sample consisted only of adults with Han Chinese ancestry, which may limit the generalizability of the findings.

Participant Demographics

The study included patients with schizophrenia and their first-degree relatives, primarily of Han Chinese ancestry.

Statistical Information

P-Value

p<0.001

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1371/journal.pone.0024103

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