To the Editor,
Recently, Violi et al. described a link between hypoalbuminemia and hypercoagulability, revealed by increased plasma D-dimer levels, in a group of 73 COVID-19 patients [1]. The authors found that patients with serum albumin <35 g/L showed significantly higher concentrations of D-dimer compared to patients with albumin ≥35 g/L and, more importantly, had a higher probability of intensive care treatment. Furthermore, the percentage of patients with D-dimer results 4-fold above the upper reference limit (URL) was significantly higher in patients with low albumin concentrations.
We recently performed a study on 427 COVID-19 patients deriving cut-off values for six biochemistry tests showing high sensitivity and negative predictive value for excluding the need of admission in intensive care unit (ICU) during hospital stay [2]. Particularly, the best cut-offs for serum albumin and plasma D-dimer, the latter expressed as fibrinogen-equivalent units (FEU), associated with the ability in detecting patients not at risk of ICU admission, were ≥29 g/L and <1704 μg/L FEU, respectively. It is interesting to note that for D-dimer this cut-off is only slightly lower than the 4-fold change above the URL (in our laboratory: 500 μg/L FEU for patients ≤50 years old and ‘age years × 10’ µg/L FEU for patients >50 years old) reported as a sign of increased thrombin generation by Violi et al. and other authors [1], [3].
In the population of our original study, 349 patients out of 427 had at least one determination of both D-dimer and serum albumin, and were therefore included in the following evaluation. Characteristics of these patients are reported in Table 1. Quite similarly to Violi et al. [1], we found that serum albumin concentrations inversely correlated with D-dimer (r=−0.351, p<0.001), and that D-dimer values 4-fold above URL were significantly associated both with serum albumin <29 g/L and an increased probability of ICU admission. In terms of absolute biomarker levels in the respective populations, it is however somewhat difficult to compare our results with those of Violi et al. as the authors do not make any remark about the methodology used to determine albumin nor about the units used to express D-dimer results. It is known that immunoturbidimetric assays for the determination of serum albumin, such as the one in use in our institution, are specific for the protein measurement contrary to nonspecific colorimetric methods which are in use in the majority of clinical institutions worldwide [4]. This issue probably explains why albumin concentrations in our population appear to be lower than those reported by Violi et al. and also why the great majority of our COVID-19 patients (89%) had albumin levels <35 g/L, regardless of ICU admission (Table 1). In our clinical setting, the application of the <35 g/L cut-off, which in our laboratory simply represents the lower limit derived from a reference population, is unable to discriminate efficaciously between complicated COVID-19 patients requiring ICU admission and other patients. On the other hand, the expression of D-dimer results as µg/L FEU, which relate the mass of D-dimer to the mass of fibrinogen, or as D-dimer µg/L units (DDU), which relate to the mass of D-dimer alone, leads in average to a 1.75-fold difference in the numerical result obtained by measuring the same sample, with results expressed as FEU being higher than those expressed as DDU. The use of FEU has been recommended to avoid erroneous classification of normal and abnormal D-dimer results and reporting values using alternative units may be misleading [5]. Although Violi et al. did not explicitly mention in which unit their D-dimer results are expressed, one can speculate the use of DDU and this may represent a confounding factor for result interpretation and application in other settings.
Characteristics of studied COVID-19 patients according to intensive care unit (ICU) admission and serum albumin concentrations.
| All patients | Non-ICU | ICU | p | Albumin <29 g/L |
Albumin ≥29 g/L |
p | |
|---|---|---|---|---|---|---|---|
| n | 349 | 302 (87%) | 47 (13%) | 232 (66%) | 117 (34%) | ||
| Age, years | 62 (50–72) | 61 (50–73) | 64 (57–70) | 0.791 | 68 (58–74) | 50 (44–60) | <0.001 |
| Male | 241 (69%) | 200 (66%) | 41 (87%) | 0.007 | 170 (73%) | 71 (61%) | 0.030 |
| D-Dimer, µg/L FEU | 1554 (796–5650) | 1299 (727–4355) | 11,870 (3614–28,919) | <0.001 | 3109 (1172–9271) | 762 (474–1526) | <0.001 |
| D-Dimer >4 × upper reference limit |
135 (37%) | 95 (31%) | 40 (85%) | <0.001 | 116 (50%) | 19 (16%) | <0.001 |
| Albumin, g/L | 26 (22–30) | 27 (24–31) | 18 (16–20) | <0.001 | - | - | - |
| Albumin <35 g/L |
310 (89%) | 263 (87%) | 47 (100%) | 0.018 | - | - | - |
| Albumin <29 g/L |
232 (66%) | 188 (62%) | 44 (94%) | <0.001 | - | - | - |
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Data are reported as absolute number with percentage for categorical variables and median with interquartile range for quantitative variables. Differences between variables were assessed by applying the chi-squared test (categorical) and the Mann-Whitney rank-sum test (quantitative). Normality was preemptively excluded for all continuous variables by performing the Shapiro-Wilk test.
In conclusion, our data support the hypothesis that hypoalbuminemia may be related to hypercoagulability, a condition that has been widely associated with severe clinical conditions in COVID-19, and that the cause-effect relationship between these two biomarkers should be investigated more thoroughly [1]. We want, however, to remark here how the issues of analytical and post-analytical harmonization are fundamental for providing optimal health care. Only the use of assays and units of measurement providing harmonized results will allow the application of common decision limits and the comparability of results obtained in clinical studies performed in different institutions, without any ambiguity in their interpretation. Quite recently, Favaloro and Thachil have similarly stressed the need to harmonize D-dimer assays to a single unit of measurement in order to decrease confusion and avoid misinformation [5].
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Research funding: None declared.
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Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.
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Competing interests: Authors state no conflict of interest.
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Ethical approval: Research involving human subjects complied with all relevant national regulations, institutional policies and is in accordance with the tenets of the Helsinki Declaration (as revised in 2013), and has been approved by the authors’ Institutional Review.
References
1. Violi, F, Ceccarelli, G, Cangemi, R, Alessandri, F, d’Ettorre, G, Oliva, A, et al. Hypoalbuminemia, coagulopathy and vascular disease in Covid-19. Circ Res 2020. https://doi.org/10.1161/CIRCRESAHA.120.317173 [Epub ahead of print].Suche in Google Scholar PubMed
2. Aloisio, E, Chibireva, M, Serafini, L, Pasqualetti, S, Falvella, FS, Dolci, A, et al. A comprehensive appraisal of laboratory biochemistry tests as major predictors of COVID-19 severity. Arch Pathol Lab Med 2020, in press.10.5858/arpa.2020-0389-SASuche in Google Scholar PubMed
3. Thachil, J, Tang, N, Gando, S, Falanga, A, Cattaneo, M, Levi, M, et al. ISTH interim guidance on recognition and management of coagulopathy in COVID-19. J Thromb Haemostasis 2020. https://doi.org/10.1111/jth.14810 [Epub ahead of print].Suche in Google Scholar PubMed PubMed Central
4. Infusino, I, Panteghini, M. Serum albumin: accuracy and clinical use. Clin Chim Acta 2013; 419: 15–8. https://doi.org/10.1016/j.cca.2013.01.005.Suche in Google Scholar PubMed
5. Favaloro, EJ, Thachil, J. Reporting of D-dimer data in COVID-19: some confusion and potential for misinformation. Clin Chem Lab Med 2020; 58: 1191–9. https://doi.org/10.1515/cclm-2020-0573.Suche in Google Scholar PubMed
© 2020 Walter de Gruyter GmbH, Berlin/Boston
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Artikel in diesem Heft
- Frontmatter
- Editorial
- Biotin interference in cardiac troponin immunoassay – where the wild things are?
- Review
- Laboratory-related issues in the measurement of cardiac troponins with highly sensitive assays
- Mini Review
- Chromatographic methods development for clinical practice: requirements and limitations
- Opinion Paper
- Harmonising EQA schemes the next frontier: challenging the status quo
- Genetics and Molecular Diagnostics
- Direct comparison study between droplet digital PCR and a combination of allele-specific PCR, asymmetric rapid PCR and melting curve analysis for the detection of BRAF V600E mutation in plasma from melanoma patients
- A novel mitochondrial m.14430A>G (MT-ND6, p.W82R) variant causes complex I deficiency and mitochondrial Leigh syndrome
- Obesity status modifies the association between rs7556897T>C in the intergenic region SLC19A3-CCL20 and blood pressure in French children
- General Clinical Chemistry and Laboratory Medicine
- Influence of reagent lots and multiple measuring systems on estimating the coefficient of variation from quality control data; implications for uncertainty estimation and interpretation of QC results
- Electrophoretic α1-globulin for screening of α1-antitrypsin deficient variants
- A continued method performance monitoring approach for the determination of pediatric renin samples – application within a European clinical trial
- Pilot study for cystic fibrosis neonatal screening: the Cuban experience
- Validation of the analytical performance of the NOVEOS™ System, a system which improves upon the third-generation in vitro allergy testing technology
- IgE cross-reactivity measurement of cashew nut, hazelnut and peanut using a novel IMMULITE inhibition method
- Sexual dimorphism in the cerebrospinal fluid total protein content
- Current state of the morphological assessment of urinary erythrocytes in The Netherlands: a nation-wide questionnaire
- Reference Values and Biological Variations
- Within-subject and between-subject biological variation of first morning void urine amino acids in 12 healthy subjects
- Proenkephalin as a new biomarker for pediatric acute kidney injury – reference values and performance in children under one year of age
- Hematology and Coagulation
- Quality performance for indirect Xa inhibitor monitoring in patients using international external quality data
- Cardiovascular Diseases
- Clinical risk assessment of biotin interference with a high-sensitivity cardiac troponin T assay
- Short- and long-term biological variation of cardiac troponin I in healthy individuals, and patients with end-stage renal failure requiring haemodialysis or cardiomyopathy
- Infectious Diseases
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- Letters to the Editors
- Evaluation of an ELISA for SARS-CoV-2 antibody testing: clinical performances and correlation with plaque reduction neutralization titer
- Preliminary evaluation of Roche Cobas Elecsys Anti-SARS-CoV-2 chemiluminescence immunoassay
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- Total pathway to method validation
- Derivation of performance specifications for uncertainty of serum C-reactive protein measurement according to the Milan model 3 (state of the art)
- FGF23 measurement in burosumab-treated patients: an emerging treatment may induce a new analytical interference
- Use of a modified IDS-ISYS intact PTH assay for intraoperative PTH measurements
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- Influence of delayed separation of plasma from whole blood and centrifugation protocol on Zn plasma concentration
- A survey of order of draw on inpatient wards and adherence to EFLM-COLABIOCLI recommendations
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