Long Noncoding RNA VLDLR-AS1 Levels in Serum Correlate with Combat-Related Chronic Mild Traumatic Brain Injury and Depression Symptoms in US Veterans

被引:6
作者
Patel, Rekha S. [1 ]
Krause-Hauch, Meredith [2 ]
Kenney, Kimbra [3 ]
Miles, Shannon [1 ,4 ]
Nakase-Richardson, Risa [5 ,6 ]
Patel, Niketa A. [1 ,2 ]
机构
[1] James A Haley Vet Hosp, Res Serv, 13000 Bruce B Downs Blvd, Tampa, FL 33612 USA
[2] Univ S Florida, Dept Mol Med, Tampa, FL 33612 USA
[3] Uniformed Serv Univ Hlth Sci, Dept Neurol, Bethesda, MD 20814 USA
[4] Univ S Florida, Morsani Coll Med, Dept Psychiat & Behav Neurosci, Tampa, FL 33620 USA
[5] James A Haley Vet Hosp, Staff Off, Tampa, FL 33612 USA
[6] Univ S Florida, Dept Internal Med Pulm Crit Care & Sleep Med, Tampa, FL 33620 USA
关键词
mild traumatic brain injury; lncRNA; lincRNA; exosomes; VLDLR-AS1; MALAT1; depression; LIMBIC CENC; neurological diseases; neuropsychological symptoms; genetic serum biomarker; veterans; PTSD; LNCRNA; GAS5; MECHANISMS; EXPRESSION; INVENTORY; SEVERITY; PROFILES; ACCURACY; VALIDITY; FEATURES;
D O I
10.3390/ijms25031473
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
More than 75% of traumatic brain injuries (TBIs) are mild (mTBI) and military service members often experience repeated combat-related mTBI. The chronic comorbidities concomitant with repetitive mTBI (rmTBI) include depression, post-traumatic stress disorder or neurological dysfunction. This study sought to determine a long noncoding RNA (lncRNA) expression signature in serum samples that correlated with rmTBI years after the incidences. Serum samples were obtained from Long-Term Impact of Military-Relevant Brain-Injury Consortium Chronic Effects of Neurotrauma Consortium (LIMBIC CENC) repository, from participants unexposed to TBI or who had rmTBI. Four lncRNAs were identified as consistently present in all samples, as detected via droplet digital PCR and packaged in exosomes enriched for CNS origin. The results, using qPCR, demonstrated that the lncRNA VLDLR-AS1 levels were significantly lower among individuals with rmTBI compared to those with no lifetime TBI. ROC analysis determined an AUC of 0.74 (95% CI: 0.6124 to 0.8741; p = 0.0012). The optimal cutoff for VLDLR-AS1 was <= 153.8 ng. A secondary analysis of clinical data from LIMBIC CENC was conducted to evaluate the psychological symptom burden, and the results show that lncRNAs VLDLR-AS1 and MALAT1 are correlated with symptoms of depression. In conclusion, lncRNA VLDLR-AS1 may serve as a blood biomarker for identifying chronic rmTBI and depression in patients.
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页数:20
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