An effective technique for the processing of saliva for the analysis of leptin and adiponectin

The recovery of protein from saliva has been extensively investigated as a method to monitor health. The aim of this study was to compare filtration and centrifugation as two methods of saliva processing necessary for determining the levels of salivary leptin and adiponectin. Thirty-seven healthy pa...

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Main Authors: S. Thanakun, H. Watanabe, S. Thaweboon, Y. Izumi
Other Authors: Mahidol University
Format: Article
Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/31391
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spelling th-mahidol.313912018-10-19T12:41:27Z An effective technique for the processing of saliva for the analysis of leptin and adiponectin S. Thanakun H. Watanabe S. Thaweboon Y. Izumi Mahidol University Tokyo Medical and Dental University Biochemistry, Genetics and Molecular Biology Neuroscience The recovery of protein from saliva has been extensively investigated as a method to monitor health. The aim of this study was to compare filtration and centrifugation as two methods of saliva processing necessary for determining the levels of salivary leptin and adiponectin. Thirty-seven healthy patients (median age of 45 years; range 35-73) participated in the study. Unstimulated whole saliva was collected by a drooling technique. An aliquot was filtered using a Millex-Millipore® (0.45 μm PVDF Dura Pore membrane) syringe and a second aliquot was centrifuged at 15 000 × g for 15 min at 4 ° C. Leptin and adiponectin levels were analyzed using an ELISAkit for serum (RayBio®, GA, USA) with minor modifications. Leptin and adiponectin levels following the filtration technique yielded comparable results with those after centrifugation. Correlation was observed between filtered and centrifuged salivary leptin levels ((r = 0.9155; 95% CI 0.8362-0.9573; p < 0.0001) with concordance correlation coefficient k 0.9114 (95% CI 0.8332-0.9539)). Less correlation was observed for adiponectin ((r=0.5718; 95% CI 0.3041-0.7558; p = 0.0002) with concordance correlation coefficient k 0.5586 (95% CI 0.2977-0.7419)). Using a Bland-Altman plot, similar measurements for both adipocytokines were observed with mean difference within a 95% CI, and interpreted as no systematic differences between the two processing techniques. This study showed that filtration is an alternative saliva processing technique to retrieve supernatant for protein analysis. Filtered saliva yielded leptin and adiponectin concentrations comparable with those obtained from centrifuged saliva. © 2013 Published by Elsevier Inc. 2018-10-19T04:42:58Z 2018-10-19T04:42:58Z 2013-01-01 Article Peptides. Vol.47, (2013), 60-65 10.1016/j.peptides.2013.06.010 18735169 01969781 2-s2.0-84885133940 https://repository.li.mahidol.ac.th/handle/123456789/31391 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84885133940&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Biochemistry, Genetics and Molecular Biology
Neuroscience
spellingShingle Biochemistry, Genetics and Molecular Biology
Neuroscience
S. Thanakun
H. Watanabe
S. Thaweboon
Y. Izumi
An effective technique for the processing of saliva for the analysis of leptin and adiponectin
description The recovery of protein from saliva has been extensively investigated as a method to monitor health. The aim of this study was to compare filtration and centrifugation as two methods of saliva processing necessary for determining the levels of salivary leptin and adiponectin. Thirty-seven healthy patients (median age of 45 years; range 35-73) participated in the study. Unstimulated whole saliva was collected by a drooling technique. An aliquot was filtered using a Millex-Millipore® (0.45 μm PVDF Dura Pore membrane) syringe and a second aliquot was centrifuged at 15 000 × g for 15 min at 4 ° C. Leptin and adiponectin levels were analyzed using an ELISAkit for serum (RayBio®, GA, USA) with minor modifications. Leptin and adiponectin levels following the filtration technique yielded comparable results with those after centrifugation. Correlation was observed between filtered and centrifuged salivary leptin levels ((r = 0.9155; 95% CI 0.8362-0.9573; p < 0.0001) with concordance correlation coefficient k 0.9114 (95% CI 0.8332-0.9539)). Less correlation was observed for adiponectin ((r=0.5718; 95% CI 0.3041-0.7558; p = 0.0002) with concordance correlation coefficient k 0.5586 (95% CI 0.2977-0.7419)). Using a Bland-Altman plot, similar measurements for both adipocytokines were observed with mean difference within a 95% CI, and interpreted as no systematic differences between the two processing techniques. This study showed that filtration is an alternative saliva processing technique to retrieve supernatant for protein analysis. Filtered saliva yielded leptin and adiponectin concentrations comparable with those obtained from centrifuged saliva. © 2013 Published by Elsevier Inc.
author2 Mahidol University
author_facet Mahidol University
S. Thanakun
H. Watanabe
S. Thaweboon
Y. Izumi
format Article
author S. Thanakun
H. Watanabe
S. Thaweboon
Y. Izumi
author_sort S. Thanakun
title An effective technique for the processing of saliva for the analysis of leptin and adiponectin
title_short An effective technique for the processing of saliva for the analysis of leptin and adiponectin
title_full An effective technique for the processing of saliva for the analysis of leptin and adiponectin
title_fullStr An effective technique for the processing of saliva for the analysis of leptin and adiponectin
title_full_unstemmed An effective technique for the processing of saliva for the analysis of leptin and adiponectin
title_sort effective technique for the processing of saliva for the analysis of leptin and adiponectin
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/31391
_version_ 1763490152083095552