ArticleFrontiers in immunology2026
Lactate dehydrogenase-to-albumin ratio as a potential prognostic indicator in glucocorticoid-treated severe pneumonia: a multicenter retrospective study with external validation.
Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Background: Glucocorticoids are widely used in severe pneumonia but can mask clinical symptoms and traditional severity scores. The lactate dehydrogenase-to-albumin ratio (LAR) reflects the balance between tissue injury and metabolic reserve, yet its prognostic value in steroid-treated pneumonia remains undefined. Methods: This multicenter study utilized a primary cohort (n=500) and an independent external validation cohort (n=354) of pneumonia patients receiving glucocorticoid therapy. The primary endpoints were 30-day and 90-day all-cause mortality. We employed Cox regression, restricted cubic splines (RCS), and ROC analysis to evaluate LAR performance. Results: High admission LAR (≥10.48) was identified as a potential prognostic indicator of mortality, associated with a more than twofold risk increase at 30 days (Adjusted HR 2.54; 95% CI: 1.56-4.12) and 90 days (Adjusted HR 2.44; 95% CI: 1.56-3.82). RCS analysis confirmed a non-linear risk escalation with a biological threshold of 10.22 (P non-linearity < 0.001). LAR demonstrated improved predictive discrimination (AUC 0.742) compared to PSI (AUC 0.700) and CURB-65 (AUC 0.654). Although the high LAR group received lower median cumulative glucocorticoid doses (3.0g vs. 5.8g; P < 0.001), this finding was associated with more rapid clinical progression and truncated treatment windows in high-risk patients, reflecting a survival-time-dependent exposure rather than a lack of therapeutic intensity. Conclusions: Admission LAR is a potential, easily accessible biochemical marker that provides prognostic value independent of typical inflammatory signs masked by steroids. In patients exceeding the 10.22 threshold, our findings suggest a potential efficacy bottleneck for conventional steroid dosing, highlighting a high-risk subpopulation that may require optimized early intervention.
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