Precision psychiatry with immunological and cognitive biomarkers: a multi-domain prediction for the diagnosis of bipolar disorder or schizophrenia using machine learning

Brisa S. Fernandes, Chandan Karmakar, Ryad Tamouza, Truyen Tran, John Yearwood, Nora Hamdani, H. Laouamri, Jean‐Romain Richard, Robert H. Yolken, Michael Berk,

Translational Psychiatry · 2020 · 72 citations · 19 references

DOIFull text

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Concepts

TL;DR

Precision psychiatry is gaining priority, yet cognitive, inflammatory, and immunological alterations in bipolar disorder and schizophrenia vary widely and have not reliably distinguished these diagnoses, underscoring the need for independent validation. The study aimed to create a probabilistic multi‑domain model that integrates peripheral immune and inflammatory biomarkers with cognitive measures via machine learning to objectively predict bipolar disorder and schizophrenia diagnoses. The model was trained on 416 participants (323 for blood biomarkers, 372 for cognitive tests, and 279 for combined analysis) using machine‑learning algorithms to integrate immune/inflammatory and cognitive data. The multi‑domain model achieved 80 % sensitivity and 71 % specificity for BD vs.

Abstract

Abstract Precision psychiatry is attracting increasing attention lately as a recognized priority. One of the goals of precision psychiatry is to develop tools capable of aiding a clinically informed psychiatric diagnosis objectively. Cognitive, inflammatory and immunological factors are altered in both bipolar disorder (BD) and schizophrenia (SZ), however, most of these alterations do not respect diagnostic boundaries from a phenomenological perspective and possess great variability in different individuals with the same phenotypic diagnosis and, consequently, none so far has proven to have the ability of reliably aiding in the differential diagnosis of BD and SZ. We developed a probabilistic multi-domain data integration model consisting of immune and inflammatory biomarkers in peripheral blood and cognitive biomarkers using machine learning to predict diagnosis of BD and SZ. A total of 416 participants, being 323, 372, and 279 subjects for blood, cognition and combined biomarkers analysis, respectively. Our multi-domain model performances for the BD vs. control (sensitivity 80% and specificity 71%) and for the SZ vs. control (sensitivity 84% and specificity 81%) pairs were high in general, however, our multi-domain model had only moderate performance for the differential diagnosis of BD and SZ (sensitivity 71% and specificity 73%). In conclusion, our results show that the diagnosis of BD and of SZ, and that the differential diagnosis of BD and SZ can be predicted with possible clinical utility by a computational machine learning algorithm employing blood and cognitive biomarkers, and that their integration in a multi-domain outperforms algorithms based in only one domain. Independent studies are needed to validate these findings.

References

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