Key result
The Hb Tacoma variant caused a clinically significant 38% mean relative bias (17 mmol/mol absolute bias) when measured with the Standard F immunoassay, whereas other methods showed < ±6% bias.
Why the study?
Hemoglobin Tacoma is known to potentially interfere with HbA1c assays, but its effect across multiple HbA1c measurement methods needed investigation.
Does the Hb Tacoma variant cause interference in HbA1c measurement across different point-of-care methods?
Observational (n=40)
Does the Hb Tacoma variant cause interference in HbA1c measurement across different point-of-care methods?
The Hb Tacoma variant causes clinically significant interference with the Standard F HbA1c assay, highlighting the need to understand hemoglobin variants in HbA1c testing.
Answers are grounded in this paper and cite their sources.
Hb Tacoma may require avoiding Standard F for HbA1c; extends evidence on variant-specific assay interferences.
Hemoglobin Tacoma is known to potentially interfere HbA1c assays. The variant is common in Finland with prevalence of up to 2% regionally and cases are also reported in areas that have attracted Finnish immigrants, especially in Sweden and North America. Here, we investigated the effect of Hb Tacoma on seven HbA1c methods. 20 non-variant and 20 Hb Tacoma samples were measured with Tina-quant Gen. 3 (immunoassay, considered as reference) and the following point of care instruments: Afinion 2, HbA1c 501 (both utilizing boronate affinity), QuikRead go, cobas b 101, DCA Atellica, and Standard F (all immunoassays). Repeatability was also assessed by measuring both non-variant and Hb Tacoma samples five times each at two different levels. For non-variant samples, the mean relative bias with all methods was < ±4%, whereas for Hb Tacoma samples Standard F had 38% mean relative bias. In absolute bias, the difference was 17 mmol/mol on average and constant through the measured range. For other methods the mean relative bias for Hb Tacoma samples was < ±6%. The repeatability with all methods was similar for non-variant and Hb Tacoma samples and at highest 4.1% (mean CV% of two levels). The observed interference by Standard F is likely due to two-antibody assay design as Hb Tacoma has been shown to result in conformational change. This interference is clinically significant and highlight the need for better controlling and better understanding hemoglobin variants in HbA1c testing.
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Mäenpää et al. (2024) conducted an observational in Hb Tacoma variant (n=40). Hb Tacoma variant vs. Non-variant samples was evaluated on Mean relative bias. The Hb Tacoma variant caused a clinically significant 38% mean relative bias (17 mmol/mol absolute bias) when measured with the Standard F immunoassay, whereas other methods showed < ±6% bias.
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