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Systematic literature review of the somatic comorbidities experienced by adults with phenylketonuria.
Whitehall, Kaleigh B; Rose, Sarah; Clague, Gillian E; Ahring, Kirsten K; Bilder, Deborah A; Harding, Cary O; Hermida, Álvaro; Inwood, Anita; Longo, Nicola; Maillot, François; Muntau, Ania C; Pessoa, André L S; Rocha, Júlio C; Rohr, Fran; Sivri, Serap; Said, Jack; Oshinbolu, Sheun; Sibbring, Gillian C.
Affiliation
  • Whitehall KB; BioMarin Pharmaceutical Inc., 105 Digital Drive, Novato, CA, 94949, USA. Kaleigh.Whitehall@bmrn.com.
  • Rose S; BioMarin Pharmaceutical Inc., 105 Digital Drive, Novato, CA, 94949, USA.
  • Clague GE; BioMarin Pharmaceutical Inc., 105 Digital Drive, Novato, CA, 94949, USA.
  • Ahring KK; Clinic for PKU, Copenhagen University Hospital, Copenhagen, Denmark.
  • Bilder DA; Huntsman Mental Health Institute, University of Utah, Salt Lake City, UT, USA.
  • Harding CO; Oregon Health & Science University, Portland, OR, USA.
  • Hermida Á; University of Santiago de Compostela, Santiago de Compostela, Spain.
  • Inwood A; Queensland Lifespan Metabolic Medicine Service, Queensland Children's Hospital, South Brisbane, QLD, Australia.
  • Longo N; University of Utah School of Medicine, Salt Lake City, UT, USA.
  • Maillot F; Internal Medicine Department and Reference Center for Inherited Metabolic Disease, and the University of Tours, Tours, France.
  • Muntau AC; University Children's Hospital, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Pessoa ALS; Federal University of Ceará - UFC, Fortaleza, Ceará, Brazil.
  • Rocha JC; Hospital Infantil Albert Sabin, Fortaleza, Ceará, Brazil.
  • Rohr F; NOVA Medical School/Faculdade de Ciências Médicas (NMS/FCM), Universidade NOVA de Lisboa, Lisbon, Portugal.
  • Sivri S; Reference Centre of Inherited Metabolic Diseases (RC-IMD), Centro Hospitalar Universitário de Lisboa Central, Lisbon, Portugal.
  • Said J; Nutrition & Metabolism, CINTESIS, NOVA Medical School, Faculdade de Ciências Médicas, Universidade NOVA de Lisboa, Lisbon, Portugal.
  • Oshinbolu S; Met Ed Consultants, Boulder, CO, USA.
  • Sibbring GC; Hacettepe University, Ankara, Turkey.
Orphanet J Rare Dis ; 19(1): 293, 2024 Aug 12.
Article in En | MEDLINE | ID: mdl-39135125
ABSTRACT

BACKGROUND:

Phenylketonuria (PKU) is an inborn error of phenylalanine (Phe) metabolism that, if untreated, causes Phe accumulation in the brain leading to neurophysiologic alterations and poor outcomes. Lifelong management centers on dietary Phe restriction, yet long-term complete metabolic control is unachievable for many adults. High blood Phe levels or chronic Phe and intact protein restriction in the diet may lead to somatic comorbidities. A systematic literature review was conducted to evaluate somatic comorbidities experienced by adults with PKU.

METHODS:

Clinical and observational studies reporting somatic comorbidities experienced by individuals with PKU aged ≥ 16 years (or classified as adults) evaluating a Phe-restricted diet with or without pharmacologic therapy versus no therapeutic intervention (including healthy controls), or pharmacologic therapy versus a Phe-restricted diet alone, were identified. PubMed® was searched (February 1, 2022 and updated November 1, 2023), using a pre-defined search strategy, followed by two-stage screening and data extraction. Included studies were grouped by PKU population comparison.

RESULTS:

1185 records were screened; 51 studies across 12,602 individuals were extracted. Bone-related abnormalities were the most reported outcome (n = 21); several outcome measures were used. Original study groupings included Phe-restricted diet versus healthy controls or reference values (n = 40); treatment-adherent versus those non-adherent (n = 12). Additional groups added as part of a protocol amendment included different Phe-restricted diets (n = 4); severe versus less severe disease (n = 5). Vote counting indicated a higher burden of ≥ 1 comorbidity (or outcome measure) for the Phe-restricted diet group by 37 of 38 studies included in the analysis of Phe-restricted diet versus healthy controls; higher burden in healthy controls was reported in 12 studies. Vote counting was similar between those treatment adherent (n = 7) versus non-adherent (n = 10).

CONCLUSIONS:

Adults with PKU have a higher comorbidity burden than a non-PKU population. More robust studies are needed to better understand the relationship between effective metabolic control and comorbidity burden, using consistent outcome measures. This SLR was supported by BioMarin Pharmaceutical Inc., Novato, CA, and is registered with the Research Registry (reviewregistry1476).
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenylketonurias / Comorbidity Limits: Adult / Humans Language: En Journal: Orphanet J Rare Dis Journal subject: MEDICINA Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenylketonurias / Comorbidity Limits: Adult / Humans Language: En Journal: Orphanet J Rare Dis Journal subject: MEDICINA Year: 2024 Document type: Article Affiliation country: Country of publication: