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dc.date.accessioned2024-02-17T17:50:23Z
dc.date.available2024-02-17T17:50:23Z
dc.date.created2023-10-13T13:55:42Z
dc.date.issued2023
dc.identifier.citationFung, Erik Ng, Kwan Hung Kwok, Timothy Lui, Leong-Ting Palaniswamy, Saranya Chan, Queenie Lim, Lee-Ling Wiklund, Petri Xie, Suyi Turner, Cheryl Elshorbagy, Amany K. Refsum, Helga Leung, Jason C. S. Kong, Alice P. S. Chan, Juliana C. N. Järvelin, Marjo-Riitta Woo, Jean . Divergent Survival Outcomes Associated with Elevated Branched-Chain Amino Acid Levels among Older Adults with or without Hypertension and Diabetes: A Validated, Prospective, Longitudinal Follow-Up Study. Biomolecules. 2023, 13(8)
dc.identifier.urihttp://hdl.handle.net/10852/108196
dc.description.abstractBranched-chain amino acids are critical metabolic intermediates that can indicate increased risk of cardiometabolic disease when levels are elevated or, alternatively, suggest sufficient mitochondrial energy metabolism and reserve in old age. The interpretation of BCAA levels can be context-dependent, and it remains unclear whether abnormal levels can inform prognosis. This prospective longitudinal study aimed to determine the interrelationship between mortality hazard and fasting serum BCAA levels among older men and women aged ≥65 years with or without hypertension and diabetes mellitus. At baseline (0Y), fasting serum BCAA concentration in 2997 community-living older men and women were measured. Approximately 14 years later (14Y), 860 study participants returned for repeat measurements. Deaths were analysed and classified into cardiovascular and non-cardiovascular causes using International Classification of Diseases codes. Survival analysis and multivariable Cox regression were performed. During a median follow-up of 17Y, 971 (78.6%) non-cardiovascular and 263 (21.4%) cardiovascular deaths occurred among 1235 (41.2%) deceased (median age, 85.8 years [IQR 81.7–89.7]). From 0Y to 14Y, BCAA levels declined in both sexes, whereas serum creatinine concentration increased (both p < 0.0001). In older adults without hypertension or diabetes mellitus, the relationship between mortality hazard and BCAA level was linear and above-median BCAA levels were associated with improved survival, whereas in the presence of cardiometabolic disease the relationship was U-shaped. Overall, adjusted Cox regression determined that each 10% increment in BCAA concentration was associated with a 7% (p = 0.0002) and 16% (p = 0.0057) reduction in mortality hazard estimated at 0Y and 14Y, respectively. Our findings suggested that abnormally high or low (dyshomeostatic) BCAA levels among older adults with hypertension and/or diabetes mellitus were associated with increased mortality, whereas in those with neither disease, increased BCAA levels was associated with improved survival, particularly in the oldest-old.
dc.languageEN
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleDivergent Survival Outcomes Associated with Elevated Branched-Chain Amino Acid Levels among Older Adults with or without Hypertension and Diabetes: A Validated, Prospective, Longitudinal Follow-Up Study
dc.title.alternativeENEngelskEnglishDivergent Survival Outcomes Associated with Elevated Branched-Chain Amino Acid Levels among Older Adults with or without Hypertension and Diabetes: A Validated, Prospective, Longitudinal Follow-Up Study
dc.typeJournal article
dc.creator.authorFung, Erik
dc.creator.authorNg, Kwan Hung
dc.creator.authorKwok, Timothy
dc.creator.authorLui, Leong-Ting
dc.creator.authorPalaniswamy, Saranya
dc.creator.authorChan, Queenie
dc.creator.authorLim, Lee-Ling
dc.creator.authorWiklund, Petri
dc.creator.authorXie, Suyi
dc.creator.authorTurner, Cheryl
dc.creator.authorElshorbagy, Amany K.
dc.creator.authorRefsum, Helga
dc.creator.authorLeung, Jason C. S.
dc.creator.authorKong, Alice P. S.
dc.creator.authorChan, Juliana C. N.
dc.creator.authorJärvelin, Marjo-Riitta
dc.creator.authorWoo, Jean
cristin.unitcode185,51,13,20
cristin.unitnameSeksjon for klinisk ernæring
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin2184509
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Biomolecules&rft.volume=13&rft.spage=&rft.date=2023
dc.identifier.jtitleBiomolecules
dc.identifier.volume13
dc.identifier.issue8
dc.identifier.pagecount0
dc.identifier.doihttps://doi.org/10.3390/biom13081252
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn2218-273X
dc.type.versionPublishedVersion
cristin.articleid1252


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