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Article: Proteome-Wide Mendelian Randomisation Identifies Causal Links of Plasma Proteins With Periodontitis

TitleProteome-Wide Mendelian Randomisation Identifies Causal Links of Plasma Proteins With Periodontitis
Authors
KeywordsMendelian randomisation
Periodontitis
Protein
Therapeutic target
Issue Date10-May-2024
PublisherElsevier
Citation
International Dental Journal, 2024 How to Cite?
Abstract

Objective

Periodontitis is a complex and multifactorial disease and it is challenging to decipher its underlying causes and mechanisms. This study attempted to explore potential circulating proteins in connection to periodontitis through proteome-wide Mendelian randomisation (MR).

Methods

We analysed 1722 circulating proteins to identify prospective drug targets for tackling periodontitis, using the genomic dataset from the FinnGen study. Two-sample MR was conducted to evaluate the bidirectional relationship between circulating proteins and periodontitis risk. A dataset from the UK Biobank was used to validate the findings. Single-cell analysis was performed to assess the cellular expression of the identified proteins within gingival tissues.

Results

MR analyses found that genetically predicted circulating levels of von Willebrand factor A domain-containing 1 (von Willebrand factor A domain containing 1 [VWA1], odds ratios: 0.94, 95% CI 0.92-0.97, P = 1.28 × 10−5) were inversely associated with periodontitis. In contrast, the level of growth differentiation factor 15 (growth differentiation factor 15 [GDF15], odds ratios: 1.05, 95% CI 1.02-1.07, P = 2.12 × 10−5) might be associated with an increased risk of periodontitis. Single-cell analysis indicated that VWA1 was primarily expressed in endothelial cells of healthy gingival tissues, while the main source of GDF15 was not derived from periodontal cells.

Conclusions

The present study suggests that certain plasma proteins like VWA1 and GDF15 may be potentially indicative of the risk and susceptibility to periodontitis. These proteins could possibly be the potential therapeutic targets for treating periodontitis, and further investigation is highly warranted.


Persistent Identifierhttp://hdl.handle.net/10722/343644
ISSN
2023 Impact Factor: 3.2
2023 SCImago Journal Rankings: 0.803

 

DC FieldValueLanguage
dc.contributor.authorZhan, Chaoning-
dc.contributor.authorZhu, Yuexin-
dc.contributor.authorFok, Melissa Rachel-
dc.contributor.authorJin, Lijian-
dc.contributor.authorHan, Bing-
dc.contributor.authorLin, Yifan-
dc.date.accessioned2024-05-24T04:12:42Z-
dc.date.available2024-05-24T04:12:42Z-
dc.date.issued2024-05-10-
dc.identifier.citationInternational Dental Journal, 2024-
dc.identifier.issn0020-6539-
dc.identifier.urihttp://hdl.handle.net/10722/343644-
dc.description.abstract<h3>Objective</h3><p>Periodontitis is a complex and multifactorial disease and it is challenging to decipher its underlying causes and mechanisms. This study attempted to explore potential circulating proteins in connection to periodontitis through proteome-wide Mendelian randomisation (MR).</p><h3>Methods</h3><p>We analysed 1722 circulating proteins to identify prospective drug targets for tackling periodontitis, using the genomic dataset from the FinnGen study. Two-sample MR was conducted to evaluate the bidirectional relationship between circulating proteins and periodontitis risk. A dataset from the UK Biobank was used to validate the findings. Single-cell analysis was performed to assess the cellular expression of the identified proteins within gingival tissues.</p><h3>Results</h3><p>MR analyses found that genetically predicted circulating levels of von Willebrand factor A domain-containing 1 (von Willebrand factor A domain containing 1 [VWA1], odds ratios: 0.94, 95% CI 0.92-0.97, <em>P</em> = 1.28 × 10<sup>−5</sup>) were inversely associated with periodontitis. In contrast, the level of growth differentiation factor 15 (growth differentiation factor 15 [GDF15], odds ratios: 1.05, 95% CI 1.02-1.07, <em>P</em> = 2.12 × 10<sup>−5</sup>) might be associated with an increased risk of periodontitis. Single-cell analysis indicated that VWA1 was primarily expressed in endothelial cells of healthy gingival tissues, while the main source of GDF15 was not derived from periodontal cells.</p><h3>Conclusions</h3><p>The present study suggests that certain plasma proteins like VWA1 and GDF15 may be potentially indicative of the risk and susceptibility to periodontitis. These proteins could possibly be the potential therapeutic targets for treating periodontitis, and further investigation is highly warranted.</p>-
dc.languageeng-
dc.publisherElsevier-
dc.relation.ispartofInternational Dental Journal-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectMendelian randomisation-
dc.subjectPeriodontitis-
dc.subjectProtein-
dc.subjectTherapeutic target-
dc.titleProteome-Wide Mendelian Randomisation Identifies Causal Links of Plasma Proteins With Periodontitis-
dc.typeArticle-
dc.identifier.doi10.1016/j.identj.2024.04.019-
dc.identifier.scopuseid_2-s2.0-85192957261-
dc.identifier.eissn1875-595X-
dc.identifier.issnl0020-6539-

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