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The ACTH test fails to diagnose adrenal insufficiency and augments cytokine production in sepsis
Dan Hao, … , Philip W. Shaul, Xiang-An Li
Dan Hao, … , Philip W. Shaul, Xiang-An Li
Published March 6, 2025
Citation Information: JCI Insight. 2025;10(8):e187487. https://doi.org/10.1172/jci.insight.187487.
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Research Article Infectious disease Inflammation

The ACTH test fails to diagnose adrenal insufficiency and augments cytokine production in sepsis

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Abstract

The adrenocorticotropic hormone (ACTH) test diagnoses relative adrenal insufficiency (RAI) or critical illness–related corticosteroid insufficiency (CIRCI). Initially, guidelines recommended corticosteroid/glucocorticoid (GC) therapy for septic patients with RAI, but later trials did not show a survival benefit, leading to updated guidelines that abandon targeting RAI or CIRCI. Recent studies with an RAI mouse model showed a clear survival benefit from GC therapy in mice with RAI, suggesting that inconclusive GC clinical trials might be due to issues with the ACTH test rather than targeting RAI. To investigate, we performed the ACTH test in septic mice. Interestingly, the ACTH test identified most mice as having adrenal insufficiency in early and middle stages of sepsis, even those with a normal adrenal stress response. Surprisingly, the ACTH test increased inflammatory cytokines to lethal levels, moderately increasing mortality in septic mice. This study revealed significant flaws in the ACTH test for diagnosing RAI/CIRCI. It not only fails to correctly identify these conditions, leading to misguided use of GCs, but also induces a lethal inflammatory response in sepsis. These findings suggest that inconclusive GC therapy trials may be due to the problematic nature of the ACTH test rather than ineffectiveness of targeting RAI/CIRCI.

Authors

Dan Hao, Qian Wang, Misa Ito, Jianyao Xue, Ling Guo, Bin Huang, Chieko Mineo, Philip W. Shaul, Xiang-An Li

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Figure 3

ACTH test augments inflammatory response in the adrenal gland through transcriptional regulation of AP-1 in sepsis.

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ACTH test augments inflammatory response in the adrenal gland through tr...
C57BL/6J mice were challenged with CLP (25G, full ligation) for 3 hours, and then treated with PBS or 4 IU ACTH. After 45 minutes, RNA from different tissues was isolated. (A) IL-6 mRNA expression was quantified by qRT-PCR. IL-6 relative mRNA expression was normalized to U36B4 expression and analyzed using a 2-tailed Student’s t test. (B–J) Adrenal RNA-seq analysis. (B) Volcano plot. (C) Differentially expressed cytokine genes. (D) The top 6 activated signaling pathways by KEGG enrichment analysis. (E) The top 21 differentially expressed genes in the adrenal gland. (F) The upstream transcriptional regulators analyzed by IPA. (G–J) Graphs showing upregulation of AP-1 signaling but not other signaling pathways (n = 3). *P < 0.05, **P < 0.01. RNA-seq analysis was performed using pairwise comparisons between conditions, applying a negative binomial generalized log-linear model with the glmLRT function in edgeR (https://bioconductor.org/packages/release/bioc/html/edgeR.html). (K) Schematic model of ACTH triggering inflammatory cytokine production in the adrenal gland.

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