# Association Between ADA (Age–D-dimer–Albumin) Score and Chest CT Severity Score in COVID-19 Pneumonia

**Authors:** Enrico Maggio, Giacomo Bonito, Alessandra Oliva, Claudio Maria Mastroianni, Riccardo Vezza, Francesco Pugliese, Francesco Violi, Paolo Ricci, Lorenzo Loffredo, Pasquale Pignatelli

PMC · DOI: 10.3390/jpm16020102 · 2026-02-09

## TL;DR

This study shows that the ADA score is linked to the severity of lung damage in hospitalized COVID-19 patients, as seen on chest CT scans.

## Contribution

The study demonstrates a novel association between the ADA score and CT severity in hospitalized COVID-19 patients.

## Key findings

- The ADA score is statistically associated with the CT severity score in hospitalized COVID-19 patients.
- An ADA score cut-off of 44.5 predicts severe CT findings with high sensitivity.
- The ADA score, along with GFR and CRP, helps identify patients with extensive lung involvement.

## Abstract

Background/Objectives: This study aims to assess the relation between the ADA score with the severity of pneumonia, as evaluated by chest tomography using a severity score. Methods: In this observational study we enrolled 350 consecutive adult patients (≥18 years) with COVID-19-related severe acute pneumonia requiring hospitalization, consecutively admitted to non-intensive care unit (ICU) medical wards from April 2020 to March 2022. A standard high-resolution chest computed tomography (HRCT) was performed in all cases with a multidetector CT scanner without intravenous contrast injection, except in case of suspicion of pulmonary embolism. The ADA score and semi-quantitative 25-point CT Severity Score (CTSS) were calculated for all patients. Results: A total of 350 COVID-19 patients (154 males (44%) and 196 females (56%)) were recruited. A logistic regression analysis showed that CTSS is statistically associated with the ADA score (Exp(B): 1.116; 95% CI: 1.027–1.212; p = 0.009) and the need for ICU (Exp(B): 8.719; 95% CI: 2.994–25.390; p < 0.001), while the linear regression analysis showed a relation between the CTSS and ADA score, GFR and CRP (p = 0.003) (predictors: ADA score [β coeff 0.276; 95% CI: 0.041–−0.402; p = 0.017], GFR [β coeff −0.219; 95% CI: −0.095–−0.001; p = 0.045], CRP [β coeff −0.226; IC 95% −0.077–−0.001; p = 0.044]). Furthermore, a ROC curve analysis determined the optimal ADA score cut-off values for predicting severe CT findings at 44.5 (sensibility: 0.971; 1-specificity: 0.670; AUC: 0.750; SE 0.039; p < 0.001; 95% CI: 0.674–0.826; Youden’s J index= 0.301). Conclusions: This study highlights the potential clinical utility of integrating laboratory- and imaging-based scores for a comprehensive assessment of patients hospitalized with SARS-CoV-2 infection. The combined use of these scores may enable a more accurate identification of patients with extensive pulmonary involvement and an increased prothrombotic burden at hospital admission, facilitating the early recognition of high-risk patients.

## Linked entities

- **Diseases:** COVID-19 (MONDO:0100096), pneumonia (MONDO:0005249), pulmonary embolism (MONDO:0005279)

## Full-text entities

- **Genes:** FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}, CTSS (cathepsin S) [NCBI Gene 1520], CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** lymphadenopathy (MESH:D008206), impaired diffusion lung carbon monoxide (MESH:D002249), pleural effusion (MESH:D010996), obesity (MESH:D009765), stroke (MESH:D020521), hypercoagulation (MESH:D019851), COVID-related pneumonia (MESH:D011014), ARDS (MESH:D012128), pulmonary embolism (MESH:D011655), injury to (MESH:D014947), pulmonary involvement (MESH:C566343), hyperglycemia (MESH:D006943), dyslipidemia (MESH:D050171), acute coronary syndromes (MESH:D054058), coronary heart disease (MESH:D003327), pleural (MESH:D010995), lung abnormalities (MESH:D008171), diabetes mellitus (MESH:D003920), cancer (MESH:D009369), CKD (MESH:D051436), embolism (MESH:D004617), CT (MESH:C000719218), heart failure (MESH:D006333), thromboembolic disorders (MESH:D013923), septic shock (MESH:D012772), honeycombing (MESH:C537412), Severe acute respiratory COVID infection (MESH:D045169), long COVID (MESH:D000094024), Thrombotic (MESH:D013927), hypertension (MESH:D006973), venous thromboembolism (MESH:D054556), death (MESH:D003643), bronchiectasis (MESH:D001987), cardiovascular disease (MESH:D002318), infected (MESH:D007239), COVID (MESH:D000086382), arterial and venous thrombosis (MESH:D020246)
- **Chemicals:** ethanol (MESH:D000431), blood glucose (MESH:D001786), oxygen (MESH:D010100), ADA (-), D (MESH:D003903), sodium hypochlorite (MESH:D012973)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12941901/full.md

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Source: https://tomesphere.com/paper/PMC12941901