4.4 Article

Paternal age related schizophrenia (PARS): Latent subgroups detected by k-means clustering analysis

期刊

SCHIZOPHRENIA RESEARCH
卷 128, 期 1-3, 页码 143-149

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ELSEVIER
DOI: 10.1016/j.schres.2011.02.006

关键词

Cluster analysis; k-Means clustering; Paternal age related schizophrenia; PARS; Schizophrenia

资金

  1. [RC1MH088843-02]
  2. [2K24MH00169]

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Background: Paternal age related schizophrenia (PARS) has been proposed as a subgroup of schizophrenia with distinct etiology, pathophysiology and symptoms. This study uses a k-means clustering analysis approach to generate hypotheses about differences between PARS and other cases of schizophrenia. Methods: We studied PARS (operationally defined as not having any family history of schizophrenia among first and second-degree relatives and fathers' age at birth >= 35 years) in a series of schizophrenia cases recruited from a research unit. Data were available on demographic variables, symptoms (Positive and Negative Syndrome Scale; PANSS), cognitive tests (Wechsler Adult Intelligence Scale-Revised; WAIS-R) and olfaction (University of Pennsylvania Smell Identification Test; UPSIT). We conducted a series of k-means clustering analyses to identify clusters of cases containing high concentrations of PARS. Results: Two analyses generated clusters with high concentrations of PARS cases. The first analysis (N = 136; PARS = 34) revealed a cluster containing 83% PARS cases, in which the patients showed a significant discrepancy between verbal and performance intelligence. The mean paternal and maternal ages were 41 and 33, respectively. The second analysis (N = 123; PARS = 30) revealed a cluster containing 71% PARS cases, of which 93% were females; the mean age of onset of psychosis, at 17.2, was significantly early. Conclusions: These results strengthen the evidence that PARS cases differ from other patients with schizophrenia. Hypothesis-generating findings suggest that features of PARS may include a discrepancy between verbal and performance intelligence, and in females, an early age of onset. These findings provide a rationale for separating these phenotypes from others in future clinical, genetic and pathophysiologic studies of schizophrenia and in considering responses to treatment. (C) 2011 Elsevier BM. All rights reserved.

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