Oral mucosal lesions and risk of all-cause and cardiovascular mortality in people treated with long-term haemodialysis: The ORAL-D multinational cohort study.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2019
Historique:
received: 15 03 2019
accepted: 06 06 2019
entrez: 22 6 2019
pubmed: 22 6 2019
medline: 3 3 2020
Statut: epublish

Résumé

Chronic kidney disease is a risk factor for oral diseases, which may be associated with premature death. We evaluated the risk of all-cause and cardiovascular mortality associated with oral mucosal lesions in adults with kidney failure treated with long-term haemodialysis. Oral mucosal lesions (herpes, ulceration, neoformation, white lesion, red lesion, oral candidiasis, geographical tongue, petechial lesions, and fissured tongue) were evaluated within the Oral Diseases in Haemodialysis (ORAL-D) study, a multinational cohort study of 4726 haemodialysis adults. We conducted cox regression analyses adjusted for demographic and clinical variables to evaluate the association with all-cause and cardiovascular mortality. Overall, 4205 adults (mean age 61.6 ± 15.6 years) underwent oral mucosal examination with 40% affected by at least one lesion. The prevalence of oral lesions was (in order of frequency): oral herpes 0.5%, mucosal ulceration 1.7%, neoformation 2.0%, white lesion 3.5%, red lesion 4.0%, oral candidiasis 4.6%, geographical tongue 4.9%, petechial lesions 7.9%, and fissured tongue 10.7%. During median follow-up of 3.5 years, 2114 patients died (1013 due to cardiovascular disease). No association was observed between any individual oral lesion and all-cause or cardiovascular mortality when adjusted for comorbidities, except for oral candidiasis, which was associated with all-cause mortality (adjusted hazard ratio 1.37, 95% CI 1.00 to 1.86) and cardiovascular mortality (adjusted hazard ratio 1.64, 95% CI 1.09 to 2.46). Oral mucosal lesions are prevalent in haemodialysis patients. Oral candidiasis appears to be a risk factor for death due to cardiovascular diseases.

Sections du résumé

BACKGROUND
Chronic kidney disease is a risk factor for oral diseases, which may be associated with premature death. We evaluated the risk of all-cause and cardiovascular mortality associated with oral mucosal lesions in adults with kidney failure treated with long-term haemodialysis.
METHODS
Oral mucosal lesions (herpes, ulceration, neoformation, white lesion, red lesion, oral candidiasis, geographical tongue, petechial lesions, and fissured tongue) were evaluated within the Oral Diseases in Haemodialysis (ORAL-D) study, a multinational cohort study of 4726 haemodialysis adults. We conducted cox regression analyses adjusted for demographic and clinical variables to evaluate the association with all-cause and cardiovascular mortality.
RESULTS
Overall, 4205 adults (mean age 61.6 ± 15.6 years) underwent oral mucosal examination with 40% affected by at least one lesion. The prevalence of oral lesions was (in order of frequency): oral herpes 0.5%, mucosal ulceration 1.7%, neoformation 2.0%, white lesion 3.5%, red lesion 4.0%, oral candidiasis 4.6%, geographical tongue 4.9%, petechial lesions 7.9%, and fissured tongue 10.7%. During median follow-up of 3.5 years, 2114 patients died (1013 due to cardiovascular disease). No association was observed between any individual oral lesion and all-cause or cardiovascular mortality when adjusted for comorbidities, except for oral candidiasis, which was associated with all-cause mortality (adjusted hazard ratio 1.37, 95% CI 1.00 to 1.86) and cardiovascular mortality (adjusted hazard ratio 1.64, 95% CI 1.09 to 2.46).
CONCLUSION
Oral mucosal lesions are prevalent in haemodialysis patients. Oral candidiasis appears to be a risk factor for death due to cardiovascular diseases.

Identifiants

pubmed: 31226151
doi: 10.1371/journal.pone.0218684
pii: PONE-D-19-07494
pmc: PMC6588239
doi:

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0218684

Déclaration de conflit d'intérêts

MR, PN, VS, EC, RG, MRL, MT, PS, AB-S, JD, LF, JNF, DC, SS, AGB, JH, CW, LG are employees of Diaverum. GS holds a consultancy with Diaverum Renal Services. JH and GS received unrestricted funding from Diaverum Renal Services, a provider of renal services and LCO (Le Cliniche Odontoiatriche, Italy). Funding was used to assist with the cost of oral examination visits in countries where these required specific funding. Funding was also applied to cover overhead costs for study coordinators in each contributing country, material printing and distribution and procurement of standardized examination kits for all patient assessments. This does not alter our adherence to PLOS ONE policies on sharing data and materials.

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Auteurs

Marinella Ruospo (M)

Diaverum Medical Scientific Office, Lund, Sweden.

Suetonia C Palmer (SC)

University of Otago, Christchurch, New Zealand.

Giusi Graziano (G)

Diaverum Medical Scientific Office, Lund, Sweden.

Patrizia Natale (P)

Diaverum Medical Scientific Office, Lund, Sweden.
University of Bari, Bari, Italy.

Valeria Saglimbene (V)

Diaverum Medical Scientific Office, Lund, Sweden.
University of Sydney, Sydney, Australia.

Massimo Petruzzi (M)

University of Bari, Bari, Italy.

Michele De Benedittis (M)

University of Bari, Bari, Italy.

Jonathan C Craig (JC)

Flinders University, Adelaide, Australia.

David W Johnson (DW)

University of Queensland, Brisbane, Australia.
Translational Research Institute, Brisbane, Australia.

Pauline Ford (P)

University of Queensland, Brisbane, Australia.

Marcello Tonelli (M)

University of Calgary, Calgary, Canada.

Eduardo Celia (E)

Diaverum Medical Scientific Office, Lund, Sweden.

Ruben Gelfman (R)

Diaverum Medical Scientific Office, Lund, Sweden.

Miguel R Leal (MR)

Diaverum Medical Scientific Office, Lund, Sweden.

Marietta Török (M)

Diaverum Medical Scientific Office, Lund, Sweden.

Paul Stroumza (P)

Diaverum Medical Scientific Office, Lund, Sweden.

Luc Frantzen (L)

Diaverum Medical Scientific Office, Lund, Sweden.

Anna Bednarek-Skublewska (A)

Diaverum Medical Scientific Office, Lund, Sweden.
Medical University of Lublin, Lublin, Poland.

Jan Dulawa (J)

Diaverum Medical Scientific Office, Lund, Sweden.
Medical University of Silesia, Silesia, Poland.

Domingo Del Castillo (D)

Diaverum Medical Scientific Office, Lund, Sweden.

Staffan Schön (S)

Diaverum Medical Scientific Office, Lund, Sweden.

Amparo G Bernat (AG)

Diaverum Medical Scientific Office, Lund, Sweden.

Jörgen Hegbrant (J)

Diaverum Medical Scientific Office, Lund, Sweden.

Charlotta Wollheim (C)

Diaverum Medical Scientific Office, Lund, Sweden.

Letizia Gargano (L)

Diaverum Medical Scientific Office, Lund, Sweden.

Giovanni F M Strippoli (GFM)

Diaverum Medical Scientific Office, Lund, Sweden.
University of Bari, Bari, Italy.
University of Sydney, Sydney, Australia.

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Classifications MeSH