A true Agatston score is produced by dedicated calcium-scoring software: on each slice, every calcified focus (peak ≥130 HU, area ≥1 mmΒ²) has its area (mmΒ²) multiplied by a density factor based on peak HU β 1 for 130–199, 2 for 200–299, 3 for 300–399, 4 for ≥400 HU β then summed across all foci and slices.
That needs a dedicated, usually ECG-gated, thin-section acquisition β a routine abdominal CT is not validated to produce one. Because this is an opportunistic screen, we report a qualitative none / mild / moderate / severe estimate instead; any calcification is still a cardiovascular-risk marker.
Enter any measurement above.
>200 HU: osteoporosis effectively excluded (NPV ~99%). 110–160 HU: indeterminate (the 90%-sensitive-to-90%-specific zone) — consider DXA. <110 HU: suspicious for osteoporosis (>90% specific); <100 HU PPV ≥68%. Most vertebral fractures occurred at ≤145 HU. IV contrast did not significantly affect performance. Pickhardt et al., Ann Intern Med 2013 (doi:10.7326/0003-4819-158-8-201304160-00003).
Low muscle attenuation independently predicts mortality. 90%-specificity thresholds: 23 HU (men), 13 HU (women); the men's death-optimized cut was ~31 HU. Lee et al., Radiology 2023 (doi:10.1148/radiol.220574).
Cutpoints men <52.4, women <38.5 cmΒ²/mΒ² (Martin et al., J Clin Oncol 2013). Population-specific cutoffs vary; interpret with clinical context.
Reported here as a qualitative visual estimate (none/mild/moderate/severe) β a routine abdominal CT is not validated for a true Agatston score. With dedicated scoring, the sex-specific 90%-specificity Agatston thresholds for 10-year death were ≥1475 (men) and ≥735 (women) β Lee et al. note these values “would all be considered a severe or advanced category” of aortic calcium, so the mortality signal is best established at moderate-to-severe burden. Lee et al., Radiology 2023 (doi:10.1148/radiol.220574). A pooled meta-analysis found any-or-advanced calcification associated with higher cardiovascular and all-cause mortality, though this is a heterogeneous, less granular estimate: Leow et al., J Am Heart Assoc 2021 (doi:10.1161/JAHA.120.017205).
The VAT/SAT ratio reflects fat distribution but is strongly sex-dependent β men normally have much higher ratios than women (apple vs pear habitus) β and has no validated universal cutoff. A ratio of ~1 is therefore not a risk threshold; interpret a visceral-predominant (apple) pattern in the context of sex. Reported here descriptively. Pickhardt, Radiology 2022 (doi:10.1148/radiol.211561).
On non-contrast CT, liver attenuation <40 HU (which corresponds to ~15% MRI-PDFF) indicates at least moderate steatosis; a liver−spleen difference <−10 HU is a supporting sign. A screen only β for MASLD, fibrosis is the outcome that matters, so stratify risk non-invasively first (e.g., FIB-4) and reserve MRI-PDFF for selected cases needing fat quantification or monitoring rather than imaging every fatty liver. Pickhardt, Radiology 2022 (liver <40 HU β 15% PDFF; doi:10.1148/radiol.211561); Starekova/Reeder/Pickhardt, Radiology 2021 (doi:10.1148/radiol.2021204288); AASLD 2023.
Portal-venous phase. Contrast-enhanced CT can still flag moderate steatosis with its own cutoffs: automated liver attenuation <80 HU gives 78% sensitivity and 93% specificity, and <90 HU gives 91% sensitivity and 78% specificity. On this phase absolute liver HU outperforms the liver−spleen difference, so the spleen is not used. Pickhardt et al., AJR 2023;221:748–758; Pickhardt et al., Eur Radiol 2024;34:7041–7052; summarized in Dogra et al., RadioGraphics 2026 (doi:10.1148/rg.260009). Arterial phase remains unvalidated.
Overview: Pickhardt et al., RadioGraphics 2021 (doi:10.1148/rg.2021200056); Pickhardt, Radiology 2022 (doi:10.1148/radiol.211561). Educational tool β thresholds are population-derived and must be integrated with the clinical context.