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Variability In Hb A2 levels among Individuals with Beta-Thalassemia Trait: Is Iron Deficiency Associated with Abnormally Low Hb A2?

2010· article· en· W2588104813 on OpenAlexaff
Madeleine Verhovsek, Tim O’Shea, Geoff Gibney, Jason C. C. So, Edmond S.K., Li Chong Chan, Martin H. Steinberg, David H.K. Chui

Bibliographic record

VenueBlood · 2010
Typearticle
Languageen
FieldMedicine
TopicHemoglobinopathies and Related Disorders
Canadian institutionsMcMaster University
Fundersnot available
KeywordsHemoglobin A2Beta thalassemiaIron deficiencyFerritinHemoglobinMedicineThalassemiaInternal medicineSerum ironAlpha-thalassemiaAnemiaBiologyGeneticsGenotypeGene

Abstract

fetched live from OpenAlex

Abstract Abstract 4281 Introduction: Quantification of HbA2 is a well established screening test for beta-thalassemia trait (BTT). However, there is a small subset of individuals heterozygous for beta-thalassemia mutations who have HbA2 levels less than or equal to 3.5%. Some reports have suggested that iron deficiency in BTT patients causes HbA2 to be lower than expected, while others have found no significant relationship between iron deficiency and the level of HbA2. These conflicting reports have led to confusion amongst clinicians as to the reliability of HbA2 measurement when screening for BTT in iron deficient individuals. Methods: From a database of 444 individuals with heterozygous beta-thalassemia, confirmed by molecular testing, we assessed the variability in HbA2. Individuals were classified as “iron deficient” or “non-iron deficient” based on their serum ferritin, using two definitions of iron deficiency (serum ferritin <15 ug/L or <30 ug/L), and data was analyzed independently. The association of HbA2 levels with gender, iron deficiency or beta-thalassemia mutation type was evaluated using a two-sample T-test. The relationship of HbA2 with gender, hemoglobin level, Hb F percentage, reticulocyte percentage and/or the natural logarithm of serum ferritin was evaluated using single and multiple linear regression analysis. Results: HbA2 ranged from 2.0 to 8.1%, with a mean of 5.5%. Mean HbA2 in females (5.4%, SD 0.6%) was lower than that in males (5.6%, SD 0.6%) (p=0.003). Seven individuals had a HbA2 level below 3.5% (range 2.0–3.1%), all of whom had serum ferritin ≥15 ug/L. Of these people, five had the Chinese (Aγδβ)0-thalassemia deletion, and would thus be expected to have a normal HbA2 level; one woman had a HbA2 of 3.1% and was found to be heterozygous for a novel point mutation at codon 29 of the delta-globin gene (GGC>GAC or Gly29Asp); and another woman with HbA2 of 2.0% had unexplained elevation of Hb F (8.0%). The 30 patients with serum ferritin <15 ug/L had evidence of iron-deficient hematopoiesis (significantly lower hemoglobin concentration and MCV than patients with ferritin ≥ 15), and none had HbA2 <3.5%. However, HbA2 was lower (5.3%) versus HbA2 in non-iron deficient individuals (5.5%; p=0.04). Individuals with the Chinese (Aγδβ)0-thalassemia deletion had a mean Hb A2 of 2.8%. Of the remaining beta-thalassemia genotypes, IVSII-645 and Nt -29 beta+ mutations were associated with HbA2 values significantly below the group mean, and -28 beta+ and the Codon 17, Codons 41/42 and Codon 43 beta0 mutations were associated with significantly higher HbA2 values. Multiple linear-regression analysis demonstrated a significant association of low HbA2 with low ferritin (p=0.04) and beta+-thalassemia mutation type (p<0.001). There was no significant association with gender (p=0.1), hemoglobin (p=0.2), reticulocyte count (p=0.08) or hemoglobin F level (p=1.0). Conclusions: From our population of patients with BTT, we have shown that individuals with overt iron deficiency all had HbA2 within the range expected for an individual with BTT (Hb A2 >3.5%). Nonetheless, serum ferritin < 15 ug/L was associated with a small but significant decrease in HbA2 (mean HbA2 of 5.3%, versus 5.5% in non-iron deficient individuals; p=0.04). Although a multivariate analysis confirmed that ferritin under 15 ug/L was associated with lower HbA2 levels, beta+-thalassemia mutation type explained more of the variability than did iron status in individuals with lower HbA2 values. Six out of seven patients who had HbA2 <3.5% were found to have heterozygous deletion or mutation of the delta-globin gene. Based on the results of our study, HbA2 remains a reliable test for BTT screening, even in the presence of iron deficiency. In patients known or suspected to have BTT, but in whom HbA2 is found to be <3.5%, testing for delta-globin abnormalities should be pursued. Disclosures: No relevant conflicts of interest to declare.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.002
metaresearch head score (Gemma)0.005
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.002
Threshold uncertainty score0.010

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0020.005
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0020.002
Science and technology studies0.0000.000
Scholarly communication0.0010.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0010.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.007
GPT teacher head0.216
Teacher spread0.209 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations1
Published2010
Admission routes1
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