Literature DB >> 23266195

A diversified approach for PKU treatment: routine screening yields high incidence of psychiatric distress in phenylketonuria clinics.

Barbara K Burton1, Lauren Leviton, Hazel Vespa, Hilary Coon, Nicola Longo, Bridget D Lundy, Maria Johnson, Andrew Angelino, Ada Hamosh, Deborah Bilder.   

Abstract

OBJECTIVES: Individuals with phenylketonuria (PKU) treated early and continuously are reported to have psychiatric and executive function impairments. The feasibility of screening for psychiatric distress and executive function impairment in individuals with PKU was tested in 3 separate clinics in North America.
METHODS: Individuals were offered screening for psychiatric distress using the Pediatric Symptom Checklist, the PSC-Youth Report or the Brief Symptom Inventory and executive function impairment using the Behavior Rating Inventory of Executive Function. Gender, age and blood phenylalanine (Phe) concentrations obtained most recently and during the 2 years prior to screening were assessed.
RESULTS: More than 90% of patients with PKU accepted the screening for psychiatric distress during their routine clinic visit. The screening took 15-20 min. 32% of patients screened positive for psychiatric distress and 19% for executive function impairment. More individuals >18 years screened positive for psychiatric distress while a similar number screened positive for executive function impairment across age groups. Lower blood Phe levels correlated with negative screening for psychiatric distress. Patients positive for psychiatric distress had higher (p=0.009) median and most recent blood Phe values (p=0.05). DISCUSSION/
CONCLUSIONS: Routine screening for psychiatric distress of patients with phenylketonuria could be easily implemented in current clinic structures. High incidences of positive screens reinforce the need for regular psychiatric assessments of individuals with PKU. Identification and referral to local mental health providers might help to improve the standard of care for individuals with PKU.
Copyright © 2012. Published by Elsevier Inc.

Entities:  

Mesh:

Year:  2012        PMID: 23266195     DOI: 10.1016/j.ymgme.2012.11.003

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


  9 in total

1.  Expanding research to provide an evidence base for nutritional interventions for the management of inborn errors of metabolism.

Authors:  Kathryn M Camp; Michele A Lloyd-Puryear; Lynne Yao; Stephen C Groft; Melissa A Parisi; Andrew Mulberg; Rashmi Gopal-Srivastava; Stephen Cederbaum; Gregory M Enns; Abby G Ershow; Dianne M Frazier; John Gohagan; Cary Harding; R Rodney Howell; Karen Regan; Peter W Stacpoole; Charles Venditti; Jerry Vockley; Michael Watson; Paul M Coates
Journal:  Mol Genet Metab       Date:  2013-05-23       Impact factor: 4.797

2.  Extended Experience of Lower Dose Sapropterin in Irish Adults with Mild Phenylketonuria.

Authors:  S Doyle; M O'Regan; C Stenson; J Bracken; U Hendroff; A Agasarova; D Deverell; E P Treacy
Journal:  JIMD Rep       Date:  2017-10-14

Review 3.  Inherited Metabolic Disorders: Aspects of Chronic Nutrition Management.

Authors:  Suzanne W Boyer; Lisa J Barclay; Lindsay C Burrage
Journal:  Nutr Clin Pract       Date:  2015-06-16       Impact factor: 3.080

4.  Long-Term Neurological Outcomes of Adult Patients with Phenylketonuria before and after Newborn Screening in Japan.

Authors:  Kenji Yamada; Seiji Yamaguchi; Kazunori Yokoyama; Kikumaro Aoki; Takeshi Taketani
Journal:  Int J Neonatal Screen       Date:  2021-04-14

5.  Tetrahydrobiopterin responsiveness in a series of 53 cases of phenylketonuria and hyperphenylalaninemia in Iran.

Authors:  Aria Setoodeh; Bahram Yarali; Ali Rabbani; Shohreh Khatami; Sedigheh Shams
Journal:  Mol Genet Metab Rep       Date:  2015-01-28

6.  Psychological well-being of early and continuously treated phenylketonuria patients.

Authors:  Alena Gerlinde Thiele; Nicole Spieß; Rudolf Ascherl; Maria Arelin; Carmen Rohde; Wieland Kiess; Skadi Beblo
Journal:  JIMD Rep       Date:  2021-02-21

7.  Mental health diagnoses in adults with phenylketonuria: a retrospective systematic audit in a large UK single centre.

Authors:  George Altman; Kamran Hussain; Diane Green; Boyd J G Strauss; Gisela Wilcox
Journal:  Orphanet J Rare Dis       Date:  2021-12-20       Impact factor: 4.123

8.  Longitudinal quality of life analysis in a phenylketonuria cohort provided sapropterin dihydrochloride.

Authors:  Teresa D Douglas; Usha Ramakrishnan; Julie A Kable; Rani H Singh
Journal:  Health Qual Life Outcomes       Date:  2013-12-30       Impact factor: 3.186

9.  Targeting mGlu5 Metabotropic Glutamate Receptors in the Treatment of Cognitive Dysfunction in a Mouse Model of Phenylketonuria.

Authors:  Francesca Nardecchia; Rosamaria Orlando; Luisa Iacovelli; Marco Colamartino; Elena Fiori; Vincenzo Leuzzi; Sonia Piccinin; Robert Nistico; Stefano Puglisi-Allegra; Luisa Di Menna; Giuseppe Battaglia; Ferdinando Nicoletti; Tiziana Pascucci
Journal:  Front Neurosci       Date:  2018-03-16       Impact factor: 4.677

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.