4.0 Article

Living with phenylketonuria in adulthood: The PKU ATTITUDE study

Journal

MOLECULAR GENETICS AND METABOLISM REPORTS
Volume 16, Issue -, Pages 39-45

Publisher

ELSEVIER
DOI: 10.1016/j.ymgmr.2018.06.007

Keywords

Phenylketonuria (PKU); Diet; Adulthood; Compliance; Amino acid

Funding

  1. Nutricia Italia

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Dietary treatment is the cornerstone of therapy for phenylketonuria (PKU), but adherence to low-phenylalanine diet progressively decreases after adolescence. We designed a survey to characterize the dietary habits of Italian adult PKU patients and to identify psychological factors influencing disease perception and adherence to diet. Participants to the survey (n = 111; response rate 94%) were asked to complete a structured questionnaire. Patients appeared to have an altered perception and awareness of the disease. About 40% of them did not consider PKU a disease and, despite declaring regular monitoring of phenylalanine levels (85%), nearly half of them reported a high plasma value over the last 6 months (> 600 mu mol/L, 48%) or were unable to specify it (31%). Adherence to PKU diet was unsatisfactory, with increased consumption of natural protein sources and reduced daily use of amino-acid supplements (< 4-5 times/day in 82% patients). In addition to the intrinsic characteristics of AA formula (palatability, ease of use), the most important factor influencing their consumption was the increased social pressure associated with their use (55%). Plasma phenylalanine periodical measurements (61%) and examinations at metabolic centers (49%) were considered relevant for compliance to diet. In Italian adult PKU patients dietary management was found to be inadequate, likely due to inappropriate perception and knowledge of the disease, and lack of awareness of the negative impact of poor metabolic control in adult life. Clinicians should consider implementing more intense and tailored educational measures, as well as structured transitional care processes.

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