RNA Biomarkers in Bipolar Disorder and Response to Mood Stabilizers

被引:5
作者
Pisanu, Claudia [1 ]
Squassina, Alessio [1 ,2 ]
机构
[1] Univ Cagliari, Dept Biomed Sci, Sect Neurosci & Clin Pharmacol, I-09042 Monserrato, Italy
[2] Dalhousie Univ, Fac Med, Dept Psychiat, Halifax, NS B3H 2E2, Canada
关键词
bipolar disorder; biomarker; transcript; microRNA; miRNA; circular RNA; circRNA; lithium; pharmacogenetics; precision medicine; personalized medicine; LYMPHOBLASTOID CELL-LINES; LONG NONCODING RNAS; GENE-EXPRESSION; LITHIUM RESPONSE; STEM-CELLS; BRAIN; DYSREGULATION; ASSOCIATION; DEPRESSION; MICRORNAS;
D O I
10.3390/ijms241210067
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bipolar disorder (BD) is a severe chronic disorder that represents one of the main causes of disability among young people. To date, no reliable biomarkers are available to inform the diagnosis of BD or clinical response to pharmacological treatment. Studies focused on coding and noncoding transcripts may provide information complementary to genome-wide association studies, allowing to correlate the dynamic evolution of different types of RNAs based on specific cell types and developmental stage with disease development or clinical course. In this narrative review, we summarize findings from human studies that evaluated the potential utility of messenger RNAs and noncoding transcripts, such as microRNAs, circular RNAs and long noncoding RNAs, as peripheral markers of BD and/or response to lithium and other mood stabilizers. The majority of available studies investigated specific targets or pathways, with large heterogeneity in the included type of cells or biofluids. However, a growing number of studies are using hypothesis-free designs, with some studies also integrating data on coding and noncoding RNAs measured in the same participants. Finally, studies conducted in neurons derived from induced-pluripotent stem cells or in brain organoids provide promising preliminary findings supporting the power and utility of these cellular models to investigate the molecular determinants of BD and clinical response.
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