Sex-based estimation of biological variation in plasma-free amino acid concentrations among healthy adults

[Display omitted] •Updated analytical goals set for plasma amino acids based on biological variation.•Within-subject biological variations of four amino acids differ by sex.•No sex-based differences were observed in between-subject biological variations.•Sex-stratified indices of individuality help...

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Published inJournal of mass spectrometry and advances in the clinical lab Vol. 37; pp. 1 - 8
Main Authors Ercan, Müjgan, Akbulut, Emiş Deniz, Caniklioğlu, Ayşen, Fırat Oğuz, Esra, Dülgeroğlu, Yakup, Avcı, Esin, Ercan, Şerif
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.08.2025
Elsevier
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ISSN2667-145X
2667-1468
2667-145X
DOI10.1016/j.jmsacl.2025.04.010

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Abstract [Display omitted] •Updated analytical goals set for plasma amino acids based on biological variation.•Within-subject biological variations of four amino acids differ by sex.•No sex-based differences were observed in between-subject biological variations.•Sex-stratified indices of individuality help to assess utility of reference intervals. Free amino acid (FAA) analysis plays a crucial role in diagnosing and monitoring inborn errors of metabolism, assessing nutritional status, and identifying metabolic imbalances associated with various diseases. This study aimed to provide updated biological variation (BV) data to support the reliable clinical application of FAA concentrations in plasma samples, utilizing LC-MS/MS. Venous blood was collected from 22 healthy Turkish adults (9 men and 13 women) over approximately nine weeks. Plasma FAAs were measured in duplicate. BV estimates with 95 % confidence intervals were determined using nested ANOVA for the entire study group and sex-stratified subgroups, following analysis of outliers, normality, steady-state conditions, and variance homogeneity. Within-subject variation (CVI) and between-subject variation (CVG) estimates ranged from 9.5 % to 32.5 % and 8.6 % to 50.0 %, respectively. The estimated CVI values for essential amino acids were significantly lower than those for non-essential amino acids (P = 0.03). For most plasma FAAs, no significant differences in CVI (except for alanine, arginine, glutamic acid, and threonine) or CVG were observed between sexes. However, differences in the indices of individuality were noted between men and women for some plasma FAAs. This Biological Variation Data Critical Appraisal Checklist-compliant study provides the first updated BV data for plasma FAAs. The significant variation observed in CVI estimates is hypothesized to result from differences in the metabolic regulation of essential versus non-essential amino acids. The sex-stratified indices obtained in this study will aid in the appropriate application of population-based reference intervals for plasma FAA assessment.
AbstractList Introduction: Free amino acid (FAA) analysis plays a crucial role in diagnosing and monitoring inborn errors of metabolism, assessing nutritional status, and identifying metabolic imbalances associated with various diseases. This study aimed to provide updated biological variation (BV) data to support the reliable clinical application of FAA concentrations in plasma samples, utilizing LC-MS/MS. Materials and methods: Venous blood was collected from 22 healthy Turkish adults (9 men and 13 women) over approximately nine weeks. Plasma FAAs were measured in duplicate. BV estimates with 95 % confidence intervals were determined using nested ANOVA for the entire study group and sex-stratified subgroups, following analysis of outliers, normality, steady-state conditions, and variance homogeneity. Results: Within-subject variation (CVI) and between-subject variation (CVG) estimates ranged from 9.5 % to 32.5 % and 8.6 % to 50.0 %, respectively. The estimated CVI values for essential amino acids were significantly lower than those for non-essential amino acids (P = 0.03). For most plasma FAAs, no significant differences in CVI (except for alanine, arginine, glutamic acid, and threonine) or CVG were observed between sexes. However, differences in the indices of individuality were noted between men and women for some plasma FAAs. Conclusions: This Biological Variation Data Critical Appraisal Checklist-compliant study provides the first updated BV data for plasma FAAs. The significant variation observed in CVI estimates is hypothesized to result from differences in the metabolic regulation of essential versus non-essential amino acids. The sex-stratified indices obtained in this study will aid in the appropriate application of population-based reference intervals for plasma FAA assessment.
• Updated analytical goals set for plasma amino acids based on biological variation. • Within-subject biological variations of four amino acids differ by sex. • No sex-based differences were observed in between-subject biological variations. • Sex-stratified indices of individuality help to assess utility of reference intervals.
[Display omitted] •Updated analytical goals set for plasma amino acids based on biological variation.•Within-subject biological variations of four amino acids differ by sex.•No sex-based differences were observed in between-subject biological variations.•Sex-stratified indices of individuality help to assess utility of reference intervals. Free amino acid (FAA) analysis plays a crucial role in diagnosing and monitoring inborn errors of metabolism, assessing nutritional status, and identifying metabolic imbalances associated with various diseases. This study aimed to provide updated biological variation (BV) data to support the reliable clinical application of FAA concentrations in plasma samples, utilizing LC-MS/MS. Venous blood was collected from 22 healthy Turkish adults (9 men and 13 women) over approximately nine weeks. Plasma FAAs were measured in duplicate. BV estimates with 95 % confidence intervals were determined using nested ANOVA for the entire study group and sex-stratified subgroups, following analysis of outliers, normality, steady-state conditions, and variance homogeneity. Within-subject variation (CVI) and between-subject variation (CVG) estimates ranged from 9.5 % to 32.5 % and 8.6 % to 50.0 %, respectively. The estimated CVI values for essential amino acids were significantly lower than those for non-essential amino acids (P = 0.03). For most plasma FAAs, no significant differences in CVI (except for alanine, arginine, glutamic acid, and threonine) or CVG were observed between sexes. However, differences in the indices of individuality were noted between men and women for some plasma FAAs. This Biological Variation Data Critical Appraisal Checklist-compliant study provides the first updated BV data for plasma FAAs. The significant variation observed in CVI estimates is hypothesized to result from differences in the metabolic regulation of essential versus non-essential amino acids. The sex-stratified indices obtained in this study will aid in the appropriate application of population-based reference intervals for plasma FAA assessment.
Free amino acid (FAA) analysis plays a crucial role in diagnosing and monitoring inborn errors of metabolism, assessing nutritional status, and identifying metabolic imbalances associated with various diseases. This study aimed to provide updated biological variation (BV) data to support the reliable clinical application of FAA concentrations in plasma samples, utilizing LC-MS/MS. Venous blood was collected from 22 healthy Turkish adults (9 men and 13 women) over approximately nine weeks. Plasma FAAs were measured in duplicate. BV estimates with 95 % confidence intervals were determined using nested ANOVA for the entire study group and sex-stratified subgroups, following analysis of outliers, normality, steady-state conditions, and variance homogeneity. Within-subject variation (CV ) and between-subject variation (CV ) estimates ranged from 9.5 % to 32.5 % and 8.6 % to 50.0 %, respectively. The estimated CV values for essential amino acids were significantly lower than those for non-essential amino acids (  =  ). For most plasma FAAs, no significant differences in CV (except for alanine, arginine, glutamic acid, and threonine) or CV were observed between sexes. However, differences in the indices of individuality were noted between men and women for some plasma FAAs. This Biological Variation Data Critical Appraisal Checklist-compliant study provides the first updated BV data for plasma FAAs. The significant variation observed in CV estimates is hypothesized to result from differences in the metabolic regulation of essential versus non-essential amino acids. The sex-stratified indices obtained in this study will aid in the appropriate application of population-based reference intervals for plasma FAA assessment.
Free amino acid (FAA) analysis plays a crucial role in diagnosing and monitoring inborn errors of metabolism, assessing nutritional status, and identifying metabolic imbalances associated with various diseases. This study aimed to provide updated biological variation (BV) data to support the reliable clinical application of FAA concentrations in plasma samples, utilizing LC-MS/MS.IntroductionFree amino acid (FAA) analysis plays a crucial role in diagnosing and monitoring inborn errors of metabolism, assessing nutritional status, and identifying metabolic imbalances associated with various diseases. This study aimed to provide updated biological variation (BV) data to support the reliable clinical application of FAA concentrations in plasma samples, utilizing LC-MS/MS.Venous blood was collected from 22 healthy Turkish adults (9 men and 13 women) over approximately nine weeks. Plasma FAAs were measured in duplicate. BV estimates with 95 % confidence intervals were determined using nested ANOVA for the entire study group and sex-stratified subgroups, following analysis of outliers, normality, steady-state conditions, and variance homogeneity.Materials and methodsVenous blood was collected from 22 healthy Turkish adults (9 men and 13 women) over approximately nine weeks. Plasma FAAs were measured in duplicate. BV estimates with 95 % confidence intervals were determined using nested ANOVA for the entire study group and sex-stratified subgroups, following analysis of outliers, normality, steady-state conditions, and variance homogeneity.Within-subject variation (CVI) and between-subject variation (CVG) estimates ranged from 9.5 % to 32.5 % and 8.6 % to 50.0 %, respectively. The estimated CVI values for essential amino acids were significantly lower than those for non-essential amino acids (P = 0.03). For most plasma FAAs, no significant differences in CVI (except for alanine, arginine, glutamic acid, and threonine) or CVG were observed between sexes. However, differences in the indices of individuality were noted between men and women for some plasma FAAs.ResultsWithin-subject variation (CVI) and between-subject variation (CVG) estimates ranged from 9.5 % to 32.5 % and 8.6 % to 50.0 %, respectively. The estimated CVI values for essential amino acids were significantly lower than those for non-essential amino acids (P = 0.03). For most plasma FAAs, no significant differences in CVI (except for alanine, arginine, glutamic acid, and threonine) or CVG were observed between sexes. However, differences in the indices of individuality were noted between men and women for some plasma FAAs.This Biological Variation Data Critical Appraisal Checklist-compliant study provides the first updated BV data for plasma FAAs. The significant variation observed in CVI estimates is hypothesized to result from differences in the metabolic regulation of essential versus non-essential amino acids. The sex-stratified indices obtained in this study will aid in the appropriate application of population-based reference intervals for plasma FAA assessment.ConclusionsThis Biological Variation Data Critical Appraisal Checklist-compliant study provides the first updated BV data for plasma FAAs. The significant variation observed in CVI estimates is hypothesized to result from differences in the metabolic regulation of essential versus non-essential amino acids. The sex-stratified indices obtained in this study will aid in the appropriate application of population-based reference intervals for plasma FAA assessment.
Author Avcı, Esin
Ercan, Şerif
Fırat Oğuz, Esra
Caniklioğlu, Ayşen
Akbulut, Emiş Deniz
Dülgeroğlu, Yakup
Ercan, Müjgan
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Keywords CRP
EFLM
RCV
Index of individuality
prRI
LC-MS/MS
EFLM WG-BV
Biological variation
BV
BIVAC
popRI
Between-subject variation
BAPS
BMI
II
ERNDIM
Plasma-free amino acids
TEaAPS
CI
FAA
Within-subject variation
CK
EuBIVAS
CVAPS
CVA
RP-HPLC
APSs
NHSP
CVG
GGT
CVI
Language English
License This is an open access article under the CC BY-NC-ND license.
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Snippet [Display omitted] •Updated analytical goals set for plasma amino acids based on biological variation.•Within-subject biological variations of four amino acids...
Free amino acid (FAA) analysis plays a crucial role in diagnosing and monitoring inborn errors of metabolism, assessing nutritional status, and identifying...
• Updated analytical goals set for plasma amino acids based on biological variation. • Within-subject biological variations of four amino acids differ by sex....
Introduction: Free amino acid (FAA) analysis plays a crucial role in diagnosing and monitoring inborn errors of metabolism, assessing nutritional status, and...
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SubjectTerms Between-subject variation
Biological variation
Index of individuality
Plasma-free amino acids
Within-subject variation
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Title Sex-based estimation of biological variation in plasma-free amino acid concentrations among healthy adults
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