Amino Acid Plasma Profiles from a Prolonged-Release Protein Substitute for Phenylketonuria: A Randomized, Single-Dose, Four-Way Crossover Trial in Healthy Volunteers

dc.contributor.authorMika Scheinin
dc.contributor.authorAnna Barassi
dc.contributor.authorJouni Junnila
dc.contributor.authorZsófia Lovró
dc.contributor.authorGiorgio Reiner
dc.contributor.authorEssi Sarkkinen
dc.contributor.authorAnita MacDonald
dc.contributor.organizationfi=biolääketieteen laitos|en=Institute of Biomedicine|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.77952289591
dc.converis.publication-id48961756
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/48961756
dc.date.accessioned2022-10-27T12:24:04Z
dc.date.available2022-10-27T12:24:04Z
dc.description.abstractSeveral disorders of amino acid (AA) metabolism are treated with a protein-restricted diet supplemented with specific AA mixtures. Delivery kinetics impacts AA absorption and plasma concentration profiles. We assessed plasma profiles after ingestion of an AA mixture engineered to prolong AA absorption with Physiomimic Technology(TM)(Test) in a randomized, single-dose, four-way crossover trial in healthy volunteers (Trial Registration: ISRCTN11016729). In a two-step hypothesis, the primary endpoints were (i) significant reduction in peak plasma concentrations (C-max) of essential amino acids (EAAs) while (ii) maintaining EAA bioavailability (AUC(0-300 min)) compared to a free AA mixture (Reference). Secondary endpoints included effects on plasma profiles of other AA groups and effects on several metabolic markers. Thirty subjects completed the study. Both co-primary endpoints were met: C(max)for EAAs was 27% lower with the Test product compared to the Reference product (ratio, 0.726,p< 0.0001); overall plasma EAA levels from the two AA mixtures was within the pre-specified bioequivalence range (AUC(0-300min)ratio, 0.890 (95% CI: 0.865, 0.915)). These findings were supported by the results of secondary endpoints. Prolongation of AA absorption was associated with modulation of several metabolic markers. It will be important to understand whether this can improve the long-term management of disorders of AA metabolism.
dc.identifier.eissn2072-6643
dc.identifier.olddbid175254
dc.identifier.oldhandle10024/158348
dc.identifier.urihttps://www.utupub.fi/handle/11111/35871
dc.identifier.urnURN:NBN:fi-fe2021042823563
dc.language.isoen
dc.okm.affiliatedauthorScheinin, Mika
dc.okm.affiliatedauthorLovro, Zsofia
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3121 Internal medicineen_GB
dc.okm.discipline3121 Sisätauditfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherMDPI
dc.publisher.countrySwitzerlanden_GB
dc.publisher.countrySveitsifi_FI
dc.publisher.country-codeCH
dc.relation.articlenumberARTN 1653
dc.relation.doi10.3390/nu12061653
dc.relation.ispartofjournalNutrients
dc.relation.issue6
dc.relation.volume12
dc.source.identifierhttps://www.utupub.fi/handle/10024/158348
dc.titleAmino Acid Plasma Profiles from a Prolonged-Release Protein Substitute for Phenylketonuria: A Randomized, Single-Dose, Four-Way Crossover Trial in Healthy Volunteers
dc.year.issued2020

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