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Infrared Thermography of Acupoints Shows Correlation with Depression Severity in Adolescents

Infrared Thermography of Acupoints Shows Correlation with Depression Severity in Adolescents
Photo by Cht Gsml / Unsplash
Key Takeaway
Consider infrared thermography of acupoints as a potential non-invasive tool for assessing depression severity in adolescents, but validation is needed.

This prospective, multi-center observational study evaluated infrared thermography (IRT) of acupoints as a diagnostic tool for major depressive disorder (MDD) in adolescents. The study included 108 participants: 65 adolescents with MDD and 43 healthy controls. Infrared relative temperatures were measured at several acupoints.

Negative correlations were found between depression severity and temperatures at Taiyang (EX-HN5, r = -0.319, P = 0.001), Quchi (LI11, r = -0.229, P = 0.022), and Waiqiu (GB36, r = -0.325, P = 0.001). A weak positive correlation was observed at Yanggu (SI5, r = 0.202, P = 0.043). A diagnostic model using these temperatures yielded an AUC of 0.785 (95% CI: 0.693 - 0.876), with an internal validation C-index of 0.752 (95% CI: 0.617 - 0.877).

Safety and tolerability were not reported. The study did not report adverse events or discontinuations. Limitations include the need to validate findings across diverse populations and integrate multi-modal biomarkers to enhance diagnostic precision.

These results suggest that IRT of acupoints may offer a non-invasive adjunct for assessing depression severity in adolescents. However, given the observational design and modest sample size, clinicians should interpret these findings cautiously and await further validation before considering clinical application.

Study Details

Study typeCohort
EvidenceLevel 3
PublishedApr 2026
View Original Abstract ↓
BackgroundThe prevalence of adolescent major depressive disorder (MDD) is rising; however, diagnosis relies on subjective measures due to a lack of objective biomarkers. This study explored infrared thermography (IRT) as a non-invasive tool to quantify thermal radiation characteristics of acupoints in adolescents with MDD. The objective was to establish diagnostic models based on acupoint temperature-derived biomarkers.MethodsA prospective, multi-center observational study enrolled 108 participants (65 adolescents with MDD and 43 healthy controls [HCs]). We first examined correlations between acupoint temperatures and depression severity using Pearson analysis. Multiple linear and binary logistic regression models were developed to diagnose MDD and assess severity. The diagnostic model for MDD was visualized as a nomogram and validated using Receiver Operating Characteristic (ROC) curves, Hosmer-Lemeshow tests, calibration plots, and decision curve analysis (DCA). Internal validation was performed using the bootstrap method.ResultsAmong 27 acupoints analyzed, adolescents with MDD exhibited altered acupoint temperatures at Taiyang (EX-HN5), Quchi (LI11), Yanggu (SI5), and Waiqiu (GB36). Subsequent Pearson correlation analysis revealed negative correlations between the infrared relative temperatures of Taiyang (EX-HN5), Quchi (LI11), and Waiqiu (GB36) and depression severity (P = 0.001, r = -0.319; P = 0.022, r = -0.229; P = 0.001, r = -0.325) and a weak positive correlation between the infrared relative temperature of Yanggu (SI5) and depression severity (P = 0.043, r = 0.202). Building on these findings, two diagnostic models were developed: a linear regression model for depression severity of adolescents (Y = 52.25-9.52*TEX-HN5-13.07*TGB36) and a logistic regression model for adolescents with MDD diagnosis (P = ex/(1+ex), x = 0.22-1.14*TEX-HN5+0.45*TSI5-2.19*TGB36). The nomogram-based model demonstrated good calibration (Hosmer-Lemeshow P = 0.855), discrimination (AUC = 0.785, 95%CI: 0.693 - 0.876), and clinical utility. Internal validation using the bootstrap method produced a C-index of 0.752 (95% CI: 0.617 - 0.877), further confirming the model’s robustness.ConclusionsIn conclusion, acupoint temperature-based models show promising efficacy for the objective and non-invasive diagnosis and severity quantification of adolescents with MDD, offering valuable tools for early clinical intervention. Future studies should validate these findings across diverse populations and integrate multi-modal biomarkers to enhance diagnostic precision.Clinical Trial RegistrationClinicalTrials.gov, identifier NCT06750640.
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