Causal relationship between endometriosis with infertility and ankylosing spondylitis.

Retrospective studies have identified an increased risk of ankylosing spondylitis (AS) in endometriosis patients. The purpose of this study was to investigate the causal relationship between clinical phenotypes of endometriosis and AS using mendelian randomized analysis (MR). MR was performed using data from genome-wide association studies (GWASs). Heterogeneity, pleiotropy and sensitivity analyses were performed to evaluate the robustness of the results by MR Egger and inverse variance weighted (IVW), leave-one-out analysis. IVW, IVW-MRE (inverse variance weighted multiplicative random effects), weighted median and MR Egger were used to explore the relationship between endometriosis and AS. The IVW analysis showed a causal relationship between infertile endometriosis and AS (OR = 0.8334, P = 0.02191), and the same result was observed with IVW-MRE (OR = 0.8334, P = 0.0007933). However, further stratified analysis showed that no matter which statistical method was used, ovarian endometriosis (IVW: OR = 0.1662, P = 0.4986; IVW-MRE: OR = 0.1662, P = 0.4986; MR Egger: OR = - 0.9577, P = 0.2798; Weighted median: OR = 0.2628, P = 0.3452), pelvic peritoneum endometriosis (IVW: OR = 0.4363, P = 0.225; IVW-MRE: OR = 0.4363, P = 0.225, MR Egger: OR = 4.159, P = 0.1705; Weighted median: OR = 0.4112, P = 0.2714), rectovaginal endometriosis (IVW: OR = 0.1365, P = 0.805; IVW-MRE: OR = 0.1365, P = 0.805) there was no causal relationship between endometriosis and AS. This study suggested that patients with infertility endometriosis are at increased risk for AS. This study supports clinicians to pay more attention to the occurrence of AS in endometriosis patients with infertility.

A resting-state electroencephalographic microstates study in depressed adolescents with non-suicidal self-injury.

Neuroimaging studies have revealed abnormal brain activities in depressed teenagers who engage in non-suicidal self-injury (NSSI). We used resting-state electroencephalography (EEG) microstate analysis, which indicates the brief overlap of brain network activation for exploring the characteristics of large-scale cortical activities in depressed adolescents engaged with NSSI to clarify the underlying temporal mechanism. A modified k-means cluster algorithm was used to segment 64-channel resting-state EEG data into microstates. Data from 27 healthy adolescents, 37 adolescents with major depressive disorder (MDD), and 53 adolescents with both MDD and NSSI were examined in this study. The resting-state microstate parameters were compared among groups using the one-way ANOVA and Spearman correlation. Then the associations between significantly different microstate parameters and the depressive severity and self-harming data in the patient groups were further analyzed. The MDD group had higher contribution (p < 0.01), occurrence (p < 0.01) of microstate A, and higher microstate E→A transition (p < 0.05) than the HC and the NSSI group. The MDD group showed a distinctly longer duration (p < 0.05) of microstate A and microstate A→C transition than the HC. The transition probability from B to C was increased in the NSSI group compared to the HC. In the MDD group, the HAMD correlated with the duration of microstate A (Spearman's rho = 0.34, p = 0.044), as the PHQ-9 correlated with its occurrence (Spearman's rho = 0.37, p = 0.028). This research revealed that whereas depressive adolescents with NSSI and MDD displayed similar patterns with healthy controls in EEG microstate, the MDD group did not. Additionally, the non-random transition from microstate E→A may protect against recent self-harm in adolescents with MDD.

circRNF20 aggravates the malignancy of retinoblastoma depending on the regulation of miR-132-3p/PAX6 axis.

Circular RNAs (circRNAs) serve as essential players in diverse human cancers, including retinoblastoma (RB). In this study, the function of circRNA Ring Finger Protein 20 (circRNF20) in RB progression was investigated. Quantitative real-time polymerase chain reaction, western blot assay or immunohistochemistry assay was performed to determine the expression of circRNF20, miR-132-3p and Paired Box 6 (PAX6). Dual-luciferase reporter assay, RNA immunoprecipitation assay and RNA pull-down assay were utilized to verify the relationships among circRNF20, miR-132-3p and PAX6. In vivo experiment was done for circRNF20 function in tumor formation. It was found that ircRNF20 level was increased in RB tissues and linked to advanced tumor, nodes, metastases (TNM) stage and poor overall survival rate. Deficiency of circRNF20 suppressed cell proliferation, migration and invasion and induced apoptosis in vitro, as well as blocked tumor growth in vivo. circRNF20 directly targeted miR-132-3p and miR-132-3p overexpression inhibited RB cell progression. PAX6 was the target gene of miR-132-3p. Moreover, miR-132-3p inhibition or PAX6 overexpression reversed circRNF20 deficiency-mediated effects on RB cell malignant behaviors. In addition, exosomal circRNF20 was able to promote RB cell progression. Thus, we concluded that circRNF20 served as an oncogene in RB progression through the circRNF20/miR-132-3p/PAX6 pathway.

LncRNA LINC00673 is Downregulated in Diabetic Retinopathy and Regulates the Apoptosis of Retinal Pigment Epithelial Cells via Negatively Regulating p53.

BACKGROUND: Long noncoding RNA (LncRNA) LINC00673 has been proven to play critical roles in cancer biology, while its role in other diseases is unknown. It has been reported that LINC00673 could interact with p53, a critical player in diabetes and diabetic complications, suggesting that LINC00673 may also participate in diabetic retinopathy (DR). This study aimed to investigate the role of LINC00673 in DR. METHODS: The present study included 3 groups of participants, including DR group, diabetes (DB) group, and healthy control (Control) group. Flow cytometry was utilized to determine cell apoptosis. Proteins and messenger RNAs (mRNAs) were estimated by Western blot and quantitative reverse transcription PCR (qRT-PCR), respectively. RESULTS: LINC00673 was downregulated in plasma samples of DR patients (n=60) in comparison with the healthy controls (n=60) and negatively correlated with p53 only across DR patients but not across the healthy controls. In retinal pigment epithelial cells (RPECs), high glucose treatment downregulated LINC00673. Moreover, LINC00673 overexpression downregulated p53 and decreased RPEC apoptosis, while LINC00673 silencing upregulated p53 and increased RPEC apoptosis. In addition, p53 overexpression reduced the effects of LINC00673 overexpression. CONCLUSION: LINC00673 is downregulated in DR patients and regulates RPEC apoptosis via negatively regulating p53.

Hydrolysis and decomposition of waste activated sludge with combined lysozyme and rhamnolipid treatment: Effect of pH.

Effect of pH on waste activated sludge (WAS) hydrolysis and decomposition treating with lysozyme and rhamnolipid combined (Ly + RL) was investigated in this study. Results showed that Ly + RL system could significantly improve the release of soluble organic matters at the optimal RL dosage of 0.3 g/gSS and lysozyme dosage of 0.15 g/gSS. Alkali conditions showed better effect than that of acid on the release of soluble organics, improvement of WAS biodegradability and reduction of big floc size within Ly + RL treatment system and the optimal pH was 10. And 9591.6 mg/L soluble chemical oxygen demand (SCOD), 1612.0 mg/L protein and 1211.6 mg/L polysaccharide were released at pH10 after 12 h co-digestion. 83.7% bacteria and 92.2% archaea were decomposed at pH10. Class Gammaproteobacteria (82.4%) was the predominant bacteria after treated by Ly + RL system, and the treated WAS was beneficial for the subsequent organics bio-degradation and volatile fatty acids accumulation.

Enhancement of excess sludge hydrolysis and decomposition by combined lysozyme and rhamnolipid pretreatment.

Feasibility of combined lysozyme and rhamolipid (RL) pretreatment on the enhancement of excess sludge (ES) hydrolysis and decomposition was assessed in this study. Results showed lysozyme and RL combined treatment could significantly promote ES hydrolysis and decomposition, an additional 1196.9 mg/L soluble chemical oxygen demand (SCOD), 792.5 mg/L protein and 133.5 mg/L polysaccharide were released compared with the sum of sole RL and sole lysozyme treatment at the optimal RL dosage of 0.3 g/gSS and lysozyme dosage of 0.15 g/gSS after 8 h co-digestion. 45.3% bacteria and 84.5% archaea decomposition degree were gained under the combined treatment at the optimal RL dosage. Class Gammaproteobacteria and genus Methanothrix were the predominant bacteria and archaea with the relative abundance of 72.4% and 60.8%, respectively. After the combined pretreatment, ES was beneficial for volatile fatty acids accumulation and acetic acid dependent methane generating inferred from the results of microbial community composition.

Enhancement of excess sludge hydrolysis and decomposition with different lysozyme dosage.

The performance of the lysozyme catalysis on excess sludge (ES) hydrolysis and decomposition was investigated in this study. For this purpose, the release of soluble organic matters from sludge flocs, extracellular polymeric substances (EPS) changes in composition and distribution and the quantity variations of microorganisms were monitored. Results indicated that lysozyme boosted the ES hydrolysis significantly with approximately 236.5 mg/L soluble chemical oxygen demand (SCOD), 58.6 mg/L polysaccharide and 662.7 mg/L protein release within 240 min at the lysozyme dosage of 150 mg/gSS. Arising lysozyme dosages (from 0 to 150 mg/gSS step by step) could dramatically enhance the efficiency of the enzyme on ES with the concentration of polysaccharide increased from 84.6 mg/L to 143.2 mg/L and protein increased from 325.0 mg/L to 987.7 mg/L in total EPS. The decomposition effect of lysozyme on microorganisms improved with dosage, about 15.4%, 17.5% and 20.2% bacteria and 56.3%, 57.2% and 65.0% archaea were disintegrated at the lysozyme dosages of 50, 100 and 150 mg/gSS, respectively. However, fungi were barely influenced by the enzymatic catalysis. Tryptophan-protein like substances and aromatic protein were the dominant ES lysis compositions in EPS.