Immunity, inflammation and disease · 2021
Estimating the within-subject (CVI ) and between-subject (CVG ) biological variation of serum tryptase.
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Skarbø Birthe R, Vinnes Erik W, Wentzel-Larsen Tore, Sylte Marit S, Apelseth Torunn O
Аннотация
BACKGROUND: Tryptase is used as a biomarker to support the diagnosis of anaphylaxis and hematologic diseases. In the event of a mast cell activation during anaphylaxis, a temporary increase in the concentration of tryptase may be seen. On the basis of clinical studies, an increase of 2 µg/L + 20% from basis level has been proposed as significant. To evaluate the increase in tryptase levels, the within-subject (CVI ) and between-subject (CVG ) biological variations should be known. This study was conducted to estimate the biological variation of tryptase and to identify the reference change value (RCV).
METHODS: Blood samples were collected from healthy volunteers once a week consecutively over a 10-week period. Tryptase was measured by the use of a fluoroenzyme immunoassay (ImmunoCAPTM ; Thermo Fisher Scientific), and linear mixed-effects models were used to calculate the biological variation and RCV for both nontransformed and log-transformed tryptase.
RESULTS: Fourteen presumably healthy young adults (six males and eight females, age 23-35 years) were included. The CVI was 5.6% and the CVG was 31.5% (nontransformed data). Log-transformed data showed similar results. The analytical variation (CVA ) was 6.3% and the RCV was 23.5%.
CONCLUSIONS: Young healthy adults without ongoing allergic reactions show low within-subject biological variation. Higher biological variation was observed between subjects.
METHODS: Blood samples were collected from healthy volunteers once a week consecutively over a 10-week period. Tryptase was measured by the use of a fluoroenzyme immunoassay (ImmunoCAPTM ; Thermo Fisher Scientific), and linear mixed-effects models were used to calculate the biological variation and RCV for both nontransformed and log-transformed tryptase.
RESULTS: Fourteen presumably healthy young adults (six males and eight females, age 23-35 years) were included. The CVI was 5.6% and the CVG was 31.5% (nontransformed data). Log-transformed data showed similar results. The analytical variation (CVA ) was 6.3% and the RCV was 23.5%.
CONCLUSIONS: Young healthy adults without ongoing allergic reactions show low within-subject biological variation. Higher biological variation was observed between subjects.