Advanced paternal age and risk of psychotic-like symptoms in adult offspring

Abstract Between 2% and 12% of adults in the general population report experiencing psychotic-like symptoms, and there is suggestive evidence that these symptoms are associated with risk of schizophrenia and other forms of psychopathology. Older parental age is an established risk factor for schizop...

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Published inSchizophrenia research Vol. 165; no. 2; pp. 123 - 127
Main Authors Foutz, Julia, Mezuk, Briana
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.07.2015
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Abstract Abstract Between 2% and 12% of adults in the general population report experiencing psychotic-like symptoms, and there is suggestive evidence that these symptoms are associated with risk of schizophrenia and other forms of psychopathology. Older parental age is an established risk factor for schizophrenia, however few studies have attempted to extend this relationship to psychotic-like symptoms. Data come from the National Comorbidity Survey—Replication and analysis is restricted to a subset of respondents who completed questions on psychosis ( N = 924). Lifetime occurrence of six psychotic-like symptoms (i.e., see a vision others couldn't see, hear voices others couldn't hear) was assessed by self-report. These symptoms were combined into a single binary (any vs. none) variable and analyzed using logistic regression, accounting for the complex survey design. Models were adjusted for age, sex, race/ethnicity, socioeconomic status, marital status, birth order, and history of mood, anxiety, and substance use disorders. Approximately 9% ( n = 103) of respondents reported at least one psychotic-like symptom. In fully-adjusted models, paternal age was significantly associated with experiencing psychotic-like symptoms ( χ2 = 13.34, p = .010). Relative to respondents whose fathers were aged 25 to 29 at the time of their birth, those with fathers aged > 35 had 2.12 times higher odds (95% confidence interval: 1.08–4.16) of psychotic-like symptoms. There was no relationship between maternal age (younger or older) and psychotic-like symptoms ( χ2 = 0.54, p = .909). Older paternal, but not maternal, age at birth is associated with psychotic-like symptoms in adult offspring.
AbstractList Abstract Between 2% and 12% of adults in the general population report experiencing psychotic-like symptoms, and there is suggestive evidence that these symptoms are associated with risk of schizophrenia and other forms of psychopathology. Older parental age is an established risk factor for schizophrenia, however few studies have attempted to extend this relationship to psychotic-like symptoms. Data come from the National Comorbidity Survey—Replication and analysis is restricted to a subset of respondents who completed questions on psychosis ( N = 924). Lifetime occurrence of six psychotic-like symptoms (i.e., see a vision others couldn't see, hear voices others couldn't hear) was assessed by self-report. These symptoms were combined into a single binary (any vs. none) variable and analyzed using logistic regression, accounting for the complex survey design. Models were adjusted for age, sex, race/ethnicity, socioeconomic status, marital status, birth order, and history of mood, anxiety, and substance use disorders. Approximately 9% ( n = 103) of respondents reported at least one psychotic-like symptom. In fully-adjusted models, paternal age was significantly associated with experiencing psychotic-like symptoms ( χ2 = 13.34, p = .010). Relative to respondents whose fathers were aged 25 to 29 at the time of their birth, those with fathers aged > 35 had 2.12 times higher odds (95% confidence interval: 1.08–4.16) of psychotic-like symptoms. There was no relationship between maternal age (younger or older) and psychotic-like symptoms ( χ2 = 0.54, p = .909). Older paternal, but not maternal, age at birth is associated with psychotic-like symptoms in adult offspring.
Between 2% and 12% of adults in the general population report experiencing psychotic-like symptoms, and there is suggestive evidence that these symptoms are associated with risk of schizophrenia and other forms of psychopathology. Older parental age is an established risk factor for schizophrenia, however few studies have attempted to extend this relationship to psychotic-like symptoms. Data come from the National Comorbidity Survey—Replication and analysis is restricted to a subset of respondents who completed questions on psychosis (N=924). Lifetime occurrence of six psychotic-like symptoms (i.e., see a vision others couldn't see, hear voices others couldn't hear) was assessed by self-report. These symptoms were combined into a single binary (any vs. none) variable and analyzed using logistic regression, accounting for the complex survey design. Models were adjusted for age, sex, race/ethnicity, socioeconomic status, marital status, birth order, and history of mood, anxiety, and substance use disorders. Approximately 9% (n=103) of respondents reported at least one psychotic-like symptom. In fully-adjusted models, paternal age was significantly associated with experiencing psychotic-like symptoms (χ2=13.34, p=.010). Relative to respondents whose fathers were aged 25 to 29 at the time of their birth, those with fathers aged >35 had 2.12 times higher odds (95% confidence interval: 1.08–4.16) of psychotic-like symptoms. There was no relationship between maternal age (younger or older) and psychotic-like symptoms (χ2=0.54, p=.909). Older paternal, but not maternal, age at birth is associated with psychotic-like symptoms in adult offspring.
Between 2% and 12% of adults in the general population report experiencing psychotic-like symptoms, and there is suggestive evidence that these symptoms are associated with risk of schizophrenia and other forms of psychopathology. Older parental age is an established risk factor for schizophrenia, however few studies have attempted to extend this relationship to psychotic-like symptoms. Data come from the National Comorbidity Survey-Replication and analysis is restricted to a subset of respondents who completed questions on psychosis (N=924). Lifetime occurrence of six psychotic-like symptoms (i.e., see a vision others couldn’t see, hear voices others couldn’t hear) was assessed by self-report. These symptoms were combined into a single binary (any vs. none) variable and analyzed using logistic regression, accounting for the complex survey design. Models were adjusted for age, sex, race/ethnicity, socioeconomic status, marital status, birth order, and history of mood, anxiety, and substance use disorders. Approximately 9% (n=103) of respondents reported at least one psychotic-like symptom. In fully-adjusted models, paternal age was significantly associated with experiencing psychotic-like symptoms (X 2 = 13.34, p = 0.010). Relative to respondents whose fathers were aged 25 to 29 at the time of their birth, those with fathers aged >35 had 2.12 times higher odds (95% Confidence Interval: 1.08 – 4.16) of psychotic-like symptoms. There was no relationship between maternal age (younger or older) and psychotic-like symptoms (X 2 = 0.54, p = .909). Older paternal, but not maternal, age at birth is associated with psychotic-like symptoms in adult offspring.
Between 2% and 12% of adults in the general population report experiencing psychotic-like symptoms, and there is suggestive evidence that these symptoms are associated with risk of schizophrenia and other forms of psychopathology. Older parental age is an established risk factor for schizophrenia, however few studies have attempted to extend this relationship to psychotic-like symptoms. Data come from the National Comorbidity Survey-Replication and analysis is restricted to a subset of respondents who completed questions on psychosis (N=924). Lifetime occurrence of six psychotic-like symptoms (i.e., see a vision others couldn't see, hear voices others couldn't hear) was assessed by self-report. These symptoms were combined into a single binary (any vs. none) variable and analyzed using logistic regression, accounting for the complex survey design. Models were adjusted for age, sex, race/ethnicity, socioeconomic status, marital status, birth order, and history of mood, anxiety, and substance use disorders. Approximately 9% (n=103) of respondents reported at least one psychotic-like symptom. In fully-adjusted models, paternal age was significantly associated with experiencing psychotic-like symptoms (χ(2)=13.34, p=.010). Relative to respondents whose fathers were aged 25 to 29 at the time of their birth, those with fathers aged >35 had 2.12 times higher odds (95% confidence interval: 1.08-4.16) of psychotic-like symptoms. There was no relationship between maternal age (younger or older) and psychotic-like symptoms (χ(2)=0.54, p=.909). Older paternal, but not maternal, age at birth is associated with psychotic-like symptoms in adult offspring.
Author Mezuk, Briana
Foutz, Julia
AuthorAffiliation c Institute for Social Research, University of Michigan, Ann Arbor, MI
a Division of Epidemiology, Department of Family Medicine and Population Health, Virginia Commonwealth University, Richmond, VA
b Virginia Institute of Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, VA
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Keywords Psychosis
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Epidemiology
Risk factors
Parental age
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SSID ssj0001507
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Snippet Abstract Between 2% and 12% of adults in the general population report experiencing psychotic-like symptoms, and there is suggestive evidence that these...
Between 2% and 12% of adults in the general population report experiencing psychotic-like symptoms, and there is suggestive evidence that these symptoms are...
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elsevier
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Aggregation Database
Index Database
Publisher
StartPage 123
SubjectTerms Adolescent
Adult
Age Distribution
Age Factors
Epidemiology
Female
Humans
Male
Maternal Age
Middle Aged
Odds Ratio
Parental age
Paternal Age
Population
Psychiatry
Psychosis
Psychotic Disorders - epidemiology
Retrospective Studies
Risk Factors
Statistics, Nonparametric
Young Adult
Title Advanced paternal age and risk of psychotic-like symptoms in adult offspring
URI https://www.clinicalkey.es/playcontent/1-s2.0-S0920996415001875
https://dx.doi.org/10.1016/j.schres.2015.04.014
https://www.ncbi.nlm.nih.gov/pubmed/25972109
https://www.proquest.com/docview/1686415367
https://pubmed.ncbi.nlm.nih.gov/PMC4472338
Volume 165
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