1.Risk factors and early diagnosis strategies for traumatic intracranial venous sinus occlusion
Fali LI ; Yongyi ZHENG ; Guoxiong ZHENG ; Pei YANG ; Zhian HAN
Chinese Journal of Postgraduates of Medicine 2016;39(12):1091-1094
Objective To analyze the risk factors for traumatic cerebral venous sinus occlusion (CVSO)and to investigate the strategies of early diagnosis of traumatic CVSO. Methods The clinical data of 212 patients with moderate to severe closed traumatic brain injury from January 2012 to December 2015 were analyzed retrospectively. Logistic regression analysis was used to evaluate the risk factors for traumatic CVSO. Results Of the 212 patients with traumatic brain injury, 16.5%(35/212) patients had CVSO. Ten patients had CVSO of thrombotic type (typeⅠ), 16 patients had CVSO of compression type (typeⅡ), and 9 patients had CVSO of mixed type (typeⅢ). Logistic regression analysis showed that skull fracture (OR = 8.141; 95%CI: 3.224-20.840) and epidural hematoma of crossing venous sinus (OR = 3.179; 95%CI: 1.470-7.037) were the risk factors for CVSO, and the former was more significantly correlated with CVSO. Female gender was the risk factor for CVSO typeⅠ(OR =10.425; 95%CI: 1.831-30.053), epidural hematoma of crossing venous sinus was the risk factor for CVSO typeⅡ(OR = 5.766; 95%CI: 1.885-18.197), and skull fracture, epidural hematoma of crossing venous sinus, and the previous history of vein thrombosis was the risk factors for CVSO type Ⅲ(OR =18.005, 4.596, 11.394; 95%CI: 2.021-58.836, 1.144-19.525, 1.436-46.558). Conclusions In the early diagnosis of traumatic CVSO, the crossing venous sinus fracture line and epidural hematoma should be given attention. Attention should be paid to the history of venous thrombosis. MR venography and CT venography contributes to early diagnosis of CVSO.
2.Assessment of nasopharyngeal carcinoma risk by EB virus antibody profile.
Weimin CHENG ; Guoxiong CHEN ; Honglin CHEN ; Ruixian LUO ; Zibo WU ; Yingsi LU ; Bojian ZHENG ; Mingfang JI ; Jinsheng LIANG ; Xintang CEN ; Dekun WANG ; Yongsheng ZONG ; Wenhan WU
Chinese Journal of Oncology 2002;24(6):561-563
OBJECTIVETo evaluate the risk of nasopharyngeal carcinoma (NPC) through EB virus antibody profile by enzyme linked immunosorbent assay (ELISA).
METHODSEBNA 1/IgA, EBNA 1/IgG and zta/IgG by ELISA and VCA/IgA by immmunoenzymatic method were detected in 121 NPC patients and 332 healthy subjects (HS) in the Pearl river estuary.
RESULTSThe sensitivity rates were 85%, 83% and 79% for EBNA 1/IgA, EBNA 1/IgG and zta/IgG, all three of which if combined was the highest 92%. The specificity rates were 86%, 86% and 80% for EBNA 1/IgA, EBNA 1/IgG and zta/IgG, all three of which if combined was also the highest 93%. According to the level of odds ratio, nasopharyngeal carcinoma risk could be divided into 3 groups: low, moderate and high-risk groups. 93% of HS had low risk of NPC with the odds ratio 0.0 to 0.3. 0.4% of HS had high risk of NPC with the odds ratio of 137.9%.
CONCLUSIONELISA is more objective than the traditional immunoenzymatic method in the detection and diagnosis of NPC. The combination of EBNA 1/IgA, EBNA 1/IgG and zta/IgG is able to evaluate the risk of NPC.
Adolescent ; Adult ; Aged ; Aged, 80 and over ; Antibodies, Viral ; analysis ; Enzyme-Linked Immunosorbent Assay ; Epstein-Barr Virus Nuclear Antigens ; analysis ; Female ; Herpesvirus 4, Human ; isolation & purification ; Humans ; Male ; Middle Aged ; Nasopharyngeal Neoplasms ; diagnosis ; virology ; Risk Factors
3.Comparison of cognitive function in patients with treatment-resistant depression and drug-naive first-episode major depressive disorder
Chaodun ZHENG ; Yingmei CHEN ; Jiuwei TAN ; Guoxiong LIU ; Yinglian CAI ; Xiaofeng LAN ; Yanling ZHOU
Sichuan Mental Health 2021;34(5):429-434
ObjectiveTo explore the differences of cognitive function in patients with treatment-resistant depression and drug-naive first-episode major depressive disorder, and to examine the relationship between severity of clinical symptoms and cognitive function, so as to provide references for prognosis improvement. MethodsFrom November 2016 to December 2019, 119 patients with drug-naive first-episode major depressive disorder and 82 patients with treatment-resistant depression in a hospital in Guangzhou were enrolled, meantime, another 71 healthy individuals recruited from the community were set as healthy control group. Clinical symptoms were assessed using Hamilton Depression Scale-17 item (HAMD-17) and Hamilton Anxiety Scale (HAMA). Cognitive domains, including speed of processing, working memory, verbal learning and memory, and visual learning and memory were measured with the MATRICS Consensus Cognitive Battery (MCCB). Multiple covariance analysis was used to compare the differences in cognitive function among three groups. Thereafter, partial correlation analysis was performed within patient groups to explore the relationship of HAMD-17/HAMA score with the four dimensions of MCCB. ResultsThe speed of processing, visual learning and memory scores of treatment-resistant depression group and drug-naive first-episode depression group were lower than those of healthy control group, and the working memory score of the treatment-resistant depression group was lower than that of the healthy control group, with statistical significance (P<0.05 or 0.01). The speed of processing, visual learning and memory scores of treatment-resistant depression group were significantly lower than those of drug-naive first-episode depression group (P<0.05 or 0.01). Partial correlation analysis within patient groups found that HAMD-17/HAMA total score had no correlation with the four dimensions of MCCB (P>0.05). ConclusionCompared with drug-naive first-episode major depressive disorder patients and healthy controls, the impairments of speed of processing, visual learning and memory are more severe in patients with treatment-resistant depression. Moreover, the cognitive function impairment in patients with drug-naive first-episode major depressive disorder and treatment-resistant depression has no correlation with the severity of depressive and anxious symptoms.