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Published on: November 21, 2013
The immunophenotypes indicating suicide risk in adolescent with bipolar disorder type I
Aysegul Tonyali1, Binay Kayan Ocakoglu, Esra Bulanik Koc
1Department of Child and Adolescent Psychiatry, Prof Mazhar Osman Mental Health and Disease Training and Research Hospital, University of Health Sciences, Istanbul, Turkiye.
None:
This study aims to investigate the relation between inflammatory markers such as neutrophil-to-lymphocyte ratio (NLR), lymphocyte-to-monocyte ratio (LMR), platelet-to-monocyte ratio, and suicide attempts in adolescents with bipolar disorder and to define a patient phenotype based on inflammatory markers. All patients under 18 years old diagnosed with bipolar disorder type I according to the diagnostic and statistical manual of mental disorders-5 criteria were included the study. NLR, platelet-to-lymphocyte ratio, LMR, and neutrophil-to-monocyte ratio were calculated. The median-split classification yielded 12 distinct inflammatory phenotypes (low-high-high-high [LHHH], low-low-low-low, high-high-high-high, low-low-high-high, low-high-high-low, high-low-low-high, high-high-low-low, low-high-low-low, high-high-low-high, low-low-high-low, high-low-high-high, and high-low-low-low). A total of 145 patients with bipolar disorder type I were included in the analysis. Thirty-five patients (24.1%) had a lifetime history of suicide attempts. None of the 4 inflammatory ratios differed significantly between patients with and without suicide attempt history (NLR: 1.93 ± 0.93 vs 2.11 ± 1.49, P = .864; platelet-to-lymphocyte ratio: 122.37 ± 41.74 vs 123.64 ± 50.23, P = .837; LMR: 3.97 ± 1.66 vs 3.76 ± 1.33, P = .600; neutrophil-to-monocyte ratio: 6.91 ± 2.49 vs 7.14 ± 4.59, P = .762). We identified 12 distinct inflammatory phenotypes represented markedly different suicide risks ranging from 0% to 57.1% (LHHH: 57.1%, low-low-low-low: 40%, high-high-high-high: 35.7%, low-low-high-high: 30.8). The LHHH phenotype, characterized by low NLR but high other ratios, emerged as a particularly high-risk profile requiring intensive clinical attention. The inflammatory phenotypes identified here may be a first step toward biologically informed suicide prevention in bipolar disorder.
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