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1.
Otolaryngol Head Neck Surg ; 170(2): 309-319, 2024 Feb.
Article in English | MEDLINE | ID: mdl-37727944

ABSTRACT

OBJECTIVE: There is a link between laryngopharyngeal reflux (LPR) and the formation of benign vocal fold lesions (BVFLs). However, previous studies have mainly focused on LPR suggested by symptoms and signs, rather than objectively diagnosed LPR via pharyngeal pH monitoring. We, therefore, conducted a Meta-analysis to evaluate the association between pharyngeal pH monitoring diagnosed LPR and the odds of BVFLs. DATA SOURCES: Relevant observational studies were identified by searching PubMed, Embase, Cochrane Library, and Web of Science. REVIEW METHODS: We evaluated between-study heterogeneity using the Cochrane Q test and estimated the I2 statistic. Random-effects models were used when significant heterogeneity was observed; otherwise, fixed-effects models were used. RESULTS: Thirteen datasets from 9 studies were included. Among them, 493 were diagnosed with LPR and 344 had BVFLs. LPR was related to a higher odds of BVFLs (odds ratio: 3.26, 95% confidence interval: 1.84-5.76, P < .001) with moderate heterogeneity (P for Cochrane Q test = .006, I2 = 57%). Subgroup analyses showed that the association was similar in studies with only pharyngeal pH monitoring (Restech), with double-probe or 3-site pH monitoring, and with 24-hour multichannel intraluminal impedance-pH monitoring (P for subgroup difference = .15). In addition, subgroup analysis showed consistent results in studies from Asia and Europe (P for subgroup analysis = .12), and the association seemed to be consistent for vocal Reinke's edema, nodules, and polyps (P for subgroup difference = .09). CONCLUSION: Pharyngeal pH monitoring diagnosed LPR is associated with the formation of BVFLs.


Subject(s)
Laryngopharyngeal Reflux , Vocal Cords , Humans , Esophageal pH Monitoring , Laryngopharyngeal Reflux/diagnosis , Pharynx , Polyps
3.
J Asian Nat Prod Res ; 12(8): 654-61, 2010 Aug.
Article in English | MEDLINE | ID: mdl-20706900

ABSTRACT

Three new polyoxypregnane glycosides, tenacigenosides F-H (1-3), were isolated from the stems of Marsdenia tenacissima. The structures of these new compounds were elucidated from 1D and 2D NMR spectra, as well as from HR-MS and acid hydrolysis.


Subject(s)
Drugs, Chinese Herbal/isolation & purification , Glycosides/isolation & purification , Marsdenia/chemistry , Pregnanes/isolation & purification , Drugs, Chinese Herbal/chemistry , Glycosides/chemistry , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular , Plant Stems/chemistry , Pregnanes/chemistry
4.
Protein Pept Lett ; 17(5): 547-54, 2010 May.
Article in English | MEDLINE | ID: mdl-19995342

ABSTRACT

The recognition of human leukocyte antigen (HLA) molecules by specific receptors is a crucial step in the regulation of natural killer (NK) cell function. Killer cell immunoglobulin-like receptor (KIR) 3DS1 is one of the activating receptors of NK cell and is implicated in slowing disease progression in HIV infection. KIR3DS1 play an important role in the outcome of multiple diseases associated with viral infections. In contrast to the inhibitory receptor, much less is known about the ligands of KIR3DS1. In order to achieve a better understanding of the biology of KIR3DS1 and its ligand systems, it is necessary to identify the ligands of KIR3DS1. In this work, we utilized recombinant HLA-B2705 molecules and DsbA-KIR3DS1 fusion protein to monitor the interaction between HLA-B2705 complexes and DsbA-KIR3DS1 using BIAcore 3000 SPR sensor and found that the specific binding between KIR3DS1 and HLA-B2705 existed and the affinity was 6.95x10(-6) mol//L. So we concluded that HLA-B2705 is a possible ligand of KIR3DS1.


Subject(s)
HLA-B Antigens/metabolism , Receptors, KIR3DS1/metabolism , Recombinant Fusion Proteins/metabolism , Blotting, Western , Chromatography, Gel , Cloning, Molecular , Electrophoresis, Polyacrylamide Gel , Escherichia coli/genetics , HLA-B Antigens/chemistry , HLA-B Antigens/genetics , Humans , Protein Binding , Protein Folding , Receptors, KIR3DS1/chemistry , Receptors, KIR3DS1/genetics , Recombinant Fusion Proteins/chemistry , Recombinant Fusion Proteins/genetics , Surface Plasmon Resonance , beta 2-Microglobulin/genetics , beta 2-Microglobulin/metabolism
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