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SAL_11925 details
Primary information
SALIDSAL_11925
Biomarker nameCathepsin D
Biomarker TypeDiagnostic
Sampling MethodThe maternal saliva (N=20) collected at enrolment (V1), 18-20 weeks (V2), and 26-29 weeks (V3) of gestation. The collection of saliva at delivery was avoided as the participants wouldnÕt fulfill the preparatory criteria for collection
Collection MethodUnstimulated saliva
Analysis MethodSWATH-MS
Collection SiteWhole Saliva
Disease CategoryPregnancy
Disease/ConditionHuman pregnancy
Disease SubtypeNA
Fold Change/ Concentration>1.5
Up/DownregulatedUpregulated
ExosomalNA
OrganismHomo sapiens
PMID32415095
Year of Publication2020
Biomarker IDP07339
Biomarker CategoryProtein
SequenceMQPSSLLPLALCLLAAPASALVRIPLHKFTSIRRTMSEVGGSVEDLIAKGPVSKYSQAVPAVTEGPIPEVLKNYMDAQYYGEIGIGTPPQCFTVVFDTGSSNLWVPSIHCKLLDIACWIHHKYNSDKSSTYVKNGTSFDIHYGSGSLSGYLSQDTVSVPCQSASSASALGGVKVERQVFGEATKQPGITFIAAKFDGILGMAYPRISVNNVLPVFDNLMQQKLVDQNIFSFYLSRDPDAQPGGELMLGGTDSKYYKGSLSYLNVTRKAYWQVHLDQVEVASGLTLCKEGCEAIVDTGTSLMVGPVDEVRELQKAIGAVPLIQGEYMIPCEKVSTLPAITLKLGGKGYKLSPEDYTLKVSQAGKTLCLSGFMGMDIPPPSGPLWILGDVFIGRYYTVFDRDNNRVGFAEAARL
Title of studySalivary proteome signatures in the early and middle stages of human pregnancy with term birth outcome
Abstract of studyThe establishment and maintenance of pregnancy in humans proceed through a continuous change of biochemical and biophysical processes. It requires a constant interaction between the fetus and the maternal system. The present prospective study aims to elucidate changes in salivary proteome from the early to middle stages of term pregnancy, and establishing an expressional trajectory for modulated proteins. To date, a comprehensive characterization of the longitudinal salivary proteome in pregnancy has not been performed and it is our immediate interest. In the discovery phase, maternal saliva (N = 20) at 6-13, 18-21, and 26-29 weeks of gestation was analyzed using level-free proteomics (SWATH-MS) approach. The expression levels of 65 proteins were found to change significantly with gestational age and distributed into two distinct clusters with a unique expression trajectory. The results revealed that altered proteins are involved in maternal immune modulation, metabolism, and host defense mechanism. Further, verification of 12 proteins was employed using targeted mass spectrometry (MRM-MS) in a separate subset of saliva (N = 14). The MRM results of 12 selected proteins confirmed a similar expression pattern as in SWATH-MS analysis. Overall, the results not only demonstrate the longitudinal maternal saliva proteome for the first time but also set the groundwork for comparative analysis between term birth and adverse pregnancy outcomes.