[No authors listed]
Postmenopausal osteoporosis (PMOP) is a common skeletal disorder in postmenopausal women. The present study aimed to identify the key long nonâcoding RNAs (lncRNAs) in PMOP through RNA sequencing. RNA sequencing was performed to obtain the expression profile of lncRNAs and mRNAs in blood samples of patients with PMOP and normal controls (NCs). Following the identification of differentially expressed mRNAs (DEmRNAs) and differentially expressed lncRNAs (DElncRNAs), the DElncRNA-DEmRNA coâexpression network was constructed. A search was performed for the DEGs transcribed within a 100âkb window upstream or downstream of DElncRNAs, which served as nearby DEmRNAs of DElncRNAs. Functional annotation of the DEmRNAs coâexpressed with DElncRNAs was performed. The GSE56815 dataset was used to verify the expression of selected DEmRNAs and DElncRNAs. Three blood samples from patients with PMOP and two blood samples from NCs were used for RNA sequencing. Compared with the NC group, a total of 185 DEmRNAs and 51 DElncRNAs were obtained in PMOP. A total of 3,057 coâexpression DElncRNAâDEmRNA pairs and 97 DElncRNAânearby DEmRNA pairs were obtained. Six DEmRNAs [diacylglycerol Oâacyltransferase 2, potassium voltageâgated channel subfamily S member 1, peptidase inhibitor 3, secretory leukocyte peptidase inhibitor, galectinârelated protein and alkaline phosphatase, liver/bone/kidney (ALPL)] were nearby coâexpressed genes of four DElncRNAs, including LOC105376834, LOC101929866, LOC105374771 and LOC100506113. Three PMOP-associated DEmRNAs, including ALPL, suppressor of cytokine signaling 3 and adrenomedullin, were coâexpressed with the hub DElncRNAs (LINC00963, LOC105378415, LOC105377067, HCG27, LOC101928143 and LINC01094) of the positively and negatively coâexpressed DElncRNAâDEmRNA interaction network. The expression of selected DEmRNAs and DElncRNAs was consistent with the RNAâsequencing results. In conclusion, the present study identified the key DEmRNAs and DElncRNAs in PMOP, which may provide clues for understanding the mechanism and developing novel biomarkers for PMOP.
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