Tsuang Debby, Esterberg Michelle, Braff David, Calkins Monica, Cadenhead Kristin, Dobie Dorcas, Freedman Robert, Green Michael F, Greenwood Tiffany, Gur Raquel, Gur Ruben, Horan William, Lazzeroni Laura C, Light Gregory A, Millard Steven P, Olincy Ann, Nuechterlein Keith, Seidman Larry, Siever Larry, Silverman Jeremy, Stone William, Sprock Joyce, Sugar Catherine, Swerdlow Neal, Tsuang Ming, Turetsky Bruce, Radant Allen
VISN-20 Geriatric Research, Education, and Clinical Center, VA Puget Sound Health Care System, Seattle, Washington, United States of America ; Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, Washington, United States of America.
Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, Washington, United States of America.
PLoS One. 2014 Feb 11;9(2):e88379. doi: 10.1371/journal.pone.0088379. eCollection 2014.
The children of older fathers have increased risks of developing schizophrenia spectrum disorders, and among those who develop these disorders, those with older fathers present with more severe clinical symptoms. However, the influence of advanced paternal age on other important domains related to schizophrenia, such as quantitative endophenotype deficit levels, remains unknown. This study investigated the associations between paternal age and level of endophenotypic impairment in a well-characterized family-based sample from the Consortium on the Genetics of Schizophrenia (COGS). All families included at least one affected subject and one unaffected sibling. Subjects met criteria for schizophrenia (probands; n = 293) or were unaffected first-degree siblings of those probands (n = 382). Paternal age at the time of subjects' birth was documented. Subjects completed a comprehensive clinical assessment and a battery of tests that measured 16 endophenotypes. After controlling for covariates, potential paternal age-endophenotype associations were analyzed using one model that included probands alone and a second model that included both probands and unaffected siblings. Endophenotype deficits in the Identical Pairs version of the 4-digit Continuous Performance Test and in the Penn Computerized Neurocognitive Battery verbal memory test showed significant associations with paternal age. However, after correcting for multiple comparisons, no endophenotype was significantly associated with paternal age. These findings suggest that factors other than advanced paternal age at birth may account for endophenotypic deficit levels in schizophrenia.
父亲年龄较大的孩子患精神分裂症谱系障碍的风险增加,在那些患这些疾病的孩子中,父亲年龄较大的孩子临床症状更严重。然而,父亲年龄较大对与精神分裂症相关的其他重要领域的影响,如定量内表型缺陷水平,仍不清楚。本研究在来自精神分裂症遗传学联盟(COGS)的一个特征明确的基于家庭的样本中,调查了父亲年龄与内表型损害水平之间的关联。所有家庭至少包括一名受影响的受试者和一名未受影响的兄弟姐妹。记录了受试者出生时父亲的年龄。受试者完成了全面的临床评估和一系列测量16种内表型的测试。在控制协变量后,使用一个仅包括先证者的模型和一个包括先证者和未受影响的兄弟姐妹的第二个模型,分析了潜在的父亲年龄与内表型的关联。四位数连续性能测试同卵对版本和宾夕法尼亚计算机化神经认知电池言语记忆测试中的内表型缺陷与父亲年龄存在显著关联。然而,在进行多重比较校正后,没有内表型与父亲年龄显著相关。这些发现表明,出生时父亲年龄较大以外的因素可能是精神分裂症内表型缺陷水平的原因。