Urinary exosomal microRNAs as predictive biomarkers for persistent psychotic-like experiences

被引:6
作者
Tomita, Yasufumi [1 ,2 ]
Suzuki, Kazuhiro [1 ,3 ,4 ]
Yamasaki, Syudo [5 ]
Toriumi, Kazuya [1 ]
Miyashita, Mitsuhiro [1 ,5 ]
Ando, Shuntaro [6 ]
Endo, Kaori [5 ]
Yoshikawa, Akane [7 ]
Tabata, Koichi [1 ,8 ]
Usami, Satoshi [9 ]
Hiraiwa-Hasegawa, Mariko [10 ]
Itokawa, Masanari [1 ,2 ]
Kawaji, Hideya [11 ]
Kasai, Kiyoto [6 ,12 ]
Nishida, Atsushi [5 ]
Arai, Makoto [1 ]
机构
[1] Tokyo Metropolitan Inst Med Sci, Dept Psychiat & Behav Sci, Schizophrenia Res Project, Tokyo, Japan
[2] Univ Tokyo, Grad Sch Frontier Sci, Dept Comp Biol & Med Sci, Tokyo, Japan
[3] Shinshu Univ, Sch Med, Dept Psychiat, Matsumoto, Japan
[4] Shinshu Univ, Sch Med, Dept Community Mental Hlth, Matsumoto, Japan
[5] Tokyo Metropolitan Inst Med Sci, Res Ctr Social Sci & Med, Unit Mental Hlth Promot, Tokyo, Japan
[6] Univ Tokyo, Grad Sch Med, Dept Neuropsychiat, Tokyo, Japan
[7] Juntendo Uni, Grad Sch Med, Dept Psychiat & Behav Sci, Tokyo, Japan
[8] Tokyo Med & Dent Univ, Grad Sch Med & Dent Sci, Dept Psychiat & Behav Sci, Tokyo, Japan
[9] Univ Tokyo, Ctr Res & Dev Transit Secondary Higher Educ, Tokyo, Japan
[10] Grad Univ Adv Studies, Dept Evolutionary Studies Biosyst, SOKENDAI, Hayama, Japan
[11] Tokyo Metropolitan Inst Med Sci, Res Ctr Genome & Med Sci, Tokyo, Japan
[12] Univ Tokyo, Univ Tokyo Inst Adv Study, Int Res Ctr Neurointelligence, Tokyo, Japan
基金
日本学术振兴会;
关键词
MOVEMENT ABNORMALITIES; SCHIZOPHRENIA; EXPRESSION; CHILDHOOD; SYMPTOMS; RISK; METAANALYSIS; ADOLESCENCE; BIOGENESIS; PATHWAY;
D O I
10.1038/s41537-023-00340-5
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Psychotic-like experiences (PLEs) occur occasionally in adolescence and mostly disappear with increasing age. Their presence, if persistent, is considered a robust risk factor for subsequent psychiatric disorders. To date, only a few biological markers have been investigated for persistent PLE prediction. This study identified urinary exosomal microRNAs that can serve as predictive biomarkers for persistent PLEs. This study was part of a population-based biomarker subsample study of the Tokyo Teen Cohort Study. A total of 345 participants aged 13 (baseline) and 14 (follow-up) years underwent PLE assessments by experienced psychiatrists using semi-structured interviews. We defined remitted and persistent PLEs based on longitudinal profiles. We obtained urine at baseline and the expression levels of urinary exosomal miRNAs were compared between 15 individuals with persistent PLEs and 15 age- and sex-matched individuals with remitted PLEs. We constructed a logistic regression model to examine whether miRNA expression levels could predict persistent PLEs. We identified six significant differentially expressed microRNAs, namely hsa-miR-486-5p, hsa-miR-199a-3p, hsa-miR-144-5p, hsa-miR-451a, hsa-miR-143-3p, and hsa-miR-142-3p. The predictive model showed an area under the curve of 0.860 (95% confidence interval: 0.713-0.993) for five-fold cross-validation. We found a subset of urinary exosomal microRNAs that were differentially expressed in persistent PLEs and presented the likelihood that a microRNA-based statistical model could predict them with high accuracy. Therefore, urine exosomal miRNAs may serve as novel biomarkers for the risk of psychiatric disorders.
引用
收藏
页数:7
相关论文
共 68 条
  • [1] Kinesin Kif3b mutation reduces NMDAR subunit NR2A trafficking and causes schizophrenia-like phenotypes in mice
    Alsabban, Ashwaq Hassan
    Morikawa, Momo
    Tanaka, Yosuke
    Takei, Yosuke
    Hirokawa, Nobutaka
    [J]. EMBO JOURNAL, 2020, 39 (01)
  • [2] Cohort Profile: The Tokyo Teen Cohort study (TTC)
    Ando, Shuntaro
    Nishida, Atsushi
    Yamasaki, Syudo
    Koike, Shinsuke
    Morimoto, Yuko
    Hoshino, Aya
    Kanata, Sho
    Fujikawa, Shinya
    Endo, Kaori
    Usami, Satoshi
    Furukawa, Toshiaki A.
    Hiraiwa-Hasegawa, Mariko
    Kasai, Kiyoto
    [J]. INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2019, 48 (05) : 1414 - +
  • [3] [Anonymous], 2010, GENOME BIOL, DOI DOI 10.1186/gb-2010-11-10-r106
  • [4] MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004)
    Bartel, David P.
    [J]. CELL, 2007, 131 (04) : 11 - 29
  • [5] Extracellular matrix abnormalities in schizophrenia
    Berretta, Sabina
    [J]. NEUROPHARMACOLOGY, 2012, 62 (03) : 1584 - 1597
  • [6] The neuregulin signaling pathway and schizophrenia: From genes to synapses and neural circuits
    Buonanno, Andres
    [J]. BRAIN RESEARCH BULLETIN, 2010, 83 (3-4) : 122 - 131
  • [7] Persistence of psychosis spectrum symptoms in the Philadelphia Neurodevelopmental Cohort: a prospective two-year follow-up
    Calkins, Monica E.
    Moore, Tyler M.
    Satterthwaite, Theodore D.
    Wolf, Daniel H.
    Turetsky, Bruce I.
    Roalf, David R.
    Merikangas, Kathleen R.
    Ruparel, Kosha
    Kohler, Christian G.
    Gur, Ruben C.
    Gur, Raquel E.
    [J]. WORLD PSYCHIATRY, 2017, 16 (01) : 62 - 76
  • [8] Integrin Structure, Activation, and Interactions
    Campbell, Iain D.
    Humphries, Martin J.
    [J]. COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, 2011, 3 (03): : 1 - 14
  • [9] Does normal developmental expression of psychosis combine with environmental risk to cause persistence of psychosis? A psychosis proneness-persistence model
    Cougnard, Audrey
    Marcelis, Machteld
    Myin-Germeys, Inez
    De Graaf, Ron
    Vollebergh, Wilma
    Krabbendam, Lydia
    Lieb, Roselind
    Wittchen, Hans-Ulrich
    Henquet, Cecile
    Spauwen, Janneke
    Van Os, Jim
    [J]. PSYCHOLOGICAL MEDICINE, 2007, 37 (04) : 513 - 527
  • [10] Neuronal KIF5b deletion induces striatum-dependent locomotor impairments and defects in membrane presentation of dopamine D2 receptors
    Cromberg, Lucas E.
    Saez, Trinidad M. M.
    Otero, Maria G.
    Tomasella, Eugenia
    Alloatti, Matias
    Damianich, Ana
    Devoto, Victorio Pozo
    Ferrario, Juan
    Gelman, Diego
    Rubinstein, Marcelo
    Falzone, Tomas L.
    [J]. JOURNAL OF NEUROCHEMISTRY, 2019, 149 (03) : 362 - 380