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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 4

ACTH test augments inflammatory cytokine production in septic mice with RAI.

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ACTH test augments inflammatory cytokine production in septic mice with ...
(A and B) SRBIfl/fl and SF1CreSRBIfl/fl mice were challenged with CLP (25G, half ligation), serum corticosterone was measured at 3, 24, and 48 hours after CLP, and IL-6 levels were measured at 3 and 24 hours after CLP (n = 5–10). (C and D) SRBIfl/fl and SF1CreSRBIfl/fl mice were challenged with CLP (25G, half ligation); 3, 24, and 48 hours later, the mice were treated with 0.1 IU ACTH. Corticosterone was measured before and 1 hour after ACTH treatment (n = 5–10). (E) SF1CreSRBIfl/fl mice (n = 3–19) were challenged with CLP for 3 hours and then treated with different doses of ACTH (0.1, 0.2, 0.3, 4 IU). Serum IL-6 levels were quantified 1 hour later. (F) SRBIfl/fl (n = 5) and SF1CreSRBIfl/fl mice (n = 10) were challenged with CLP (25G, half ligation); 3 and 24 hours later, the mice were treated with 4 IU ACTH and serum cytokines were measured 1 hour later with the 31-plex cytokine method. *P < 0.05; **P < 0.01; ***P < 0.001 by 1-way ANOVA with Tukey’s multiple-comparison correction (A–F). In F, *P < 0.05, **P < 0.01 for SF1CreSRBIfl/fl mice; #P < 0.05 for SRBIfl/fl mice.

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