Literature DB >> 28285739

Neuropsychiatric comorbidities in adults with phenylketonuria: A retrospective cohort study.

Deborah A Bilder1, Joyce A Kobori2, Jessica L Cohen-Pfeffer3, Erin M Johnson3, Elaina R Jurecki3, Mitzie L Grant4.   

Abstract

Adults with phenylketonuria (PKU) may experience neurologic and psychiatric disorders, including intellectual disability, anxiety, depression, and neurocognitive dysfunction. Identifying the prevalence and prevalence ratios of these conditions will inform clinical treatment. This nested, case-controlled study used International Classification of Diseases, Ninth Revision (ICD-9) codes from the MarketScan® insurance claims databases from 2006 to 2012 and healthcare claims data for US-based employer and government-sponsored health plans. Prevalence and prevalence ratio calculations of neuropsychiatric comorbidities for adults (≥20years old) with PKU were compared with two groups [diabetes mellitus (DM) and general population (GP)] matched by age, gender, geographic location, and insurance type. Age cohorts (i.e., 20-29, 30-39, 40-49, 50-59, 60-69, and 70+years, and a combined subset of 20-39) were used to stratify data. The PKU cohort experienced significantly higher rates of several comorbid neurologic, psychiatric and developmental conditions. Compared to GP, PKU was associated with significantly higher prevalence for numerous neuropsychiatric conditions, most notably for intellectual disability (PR=7.9, 95% CI: 6.4-9.9), autism spectrum disorder (PR=6.1, 95% CI: 3.6-10.4), Tourette/tic disorders (PR=5.4, 95% CI: 2.1-14.1), and eating disorders (4.0, 95% CI: 3.2-5.0). Rates of fatigue/malaise, epilepsy/convulsions, sleep disturbance, personality disorders, phobias, psychosis, and migraines among those with PKU exceeded rates for the GP but were comparable to those with DM, with significantly lower rates of concomitant disorders occurring in younger, compared to older, adults with PKU. Lifelong monitoring and treatment of co-occurring neuropsychiatric conditions are important for effective PKU management.
Copyright © 2017 The Authors. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Comorbidity; Neurodevelopmental; Neurologic; Neuropsychiatric; Phenylalanine hydroxylase deficiency; Phenylketonuria

Mesh:

Year:  2017        PMID: 28285739     DOI: 10.1016/j.ymgme.2017.03.002

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  31 in total

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5.  Improved attention linked to sustained phenylalanine reduction in adults with early-treated phenylketonuria.

Authors:  Deborah A Bilder; Georgianne L Arnold; David Dimmock; Mitzie L Grant; Darren Janzen; Nicola Longo; Mina Nguyen-Driver; Elaina Jurecki; Markus Merilainen; Gianni Amato; Susan Waisbren
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8.  The Impact of the COVID-19 Pandemic on the Perception of Health and Treatment-Related Issues among Patients with Phenylketonuria in Poland-The Results of a National Online Survey.

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9.  Vitamin K Status in Adherent and Non-Adherent Patients with Phenylketonuria: A Cross-Sectional Study.

Authors:  Renata Mozrzymas; Dariusz Walkowiak; Sławomira Drzymała-Czyż; Patrycja Krzyżanowska-Jankowska; Monika Duś-Żuchowska; Łukasz Kałużny; Jarosław Walkowiak
Journal:  Nutrients       Date:  2020-06-14       Impact factor: 5.717

10.  Salivary serotonin does not correlate with central serotonin turnover in adult phenylketonuria (PKU) patients.

Authors:  Joseph Leung; Caroline Selvage; Taryn Bosdet; Jennifer Branov; Annie Rosen-Heath; Carole Bishop; Sandra Sirrs; Gabriella Horvath
Journal:  Mol Genet Metab Rep       Date:  2018-04-05
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