Evidence map›Paper›PMID 39806633›Full record

ArticleBMJ open2024

Association between oral microbiome diversity and all-cause mortality: a longitudinal study of NHANES, 2009-2012.

Ju Yu, Bo Lin, Zhanqiang Zhang, Wanna Chen, Weiming Lv, Liang Zheng

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Article in BMJ open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Ju Yu *Department of Thyroid Surgery, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, China.
Bo Lin *Department of Thyroid Surgery, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, China.
Zhanqiang Zhang *Department of Thyroid Surgery, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, China.
Wanna ChenDepartment of Thyroid Surgery, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, China.
Weiming LvDepartment of Thyroid Surgery, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, China.
Liang ZhengDepartment of Thyroid Surgery, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, China zhengliang3@mail.sysu.edu.cn.ORCID http://orcid.org/0000-0001-9676-546X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe study investigates the association between oral microbiome diversity and all-cause mortality.

designPopulation-based cohort study.

settingUS National Health and Nutrition Examination Survey (2009-2010 and 2011-2012).

participantsA total of 8224 participants who had valid data on the oral microbiome diversity and survival through 31 December 2019 were included in this study. PRIMARY AND SECONDARY OUTCOME MEASURES: Oral microbiome diversity was measured using the observed number of amplicon sequence variant (ASV) and grouped into quartiles. Cox proportional hazards regression models were used to estimate the HR and 95% CI for all-cause mortality according to the quartiles of ASV number, adjusted for potential confounders.

resultsAmong the 8224 participants (mean (SD) age: 42.0 (15.1) years; 49.9% male; 37.2% white, 23.8% black, 27.2% Hispanic and 11.8% other race/ethnicity), the median follow-up time was 108 months (IQR, 95-120 months) and 429 (5.2%) deaths were identified. Participants with a higher ASV number were more likely to be poor, non-Hispanic black or Hispanic, uninsured and current smokers, more likely to have poor self-rated oral health and periodontitis and less likely to use dental floss. However, compared with the lowest quartile of the ASV number, a suggestive association was observed for the second quartile (HR=0.80, 95% CI: 0.60 to 1.08), a significant reduction in all-cause mortality was observed for the third (HR=0.55, 95% CI: 0.37 to 0.82) and the fourth (HR=0.58, 95% CI: 0.38 to 0.89) quartile. The dose-response association for all-cause mortality risk was curvilinear; the protective association plateaued when the number of ASVs was larger than 120.

conclusionDespite being linked to greater socioeconomic disadvantages and poorer oral health, higher oral microbiome diversity was significantly associated with a substantial reduction in all-cause mortality.

Indexed as

MicrobiotaMortalityMouthAdultCause of DeathFemaleHumansLongitudinal StudiesMaleMiddle AgedNutrition SurveysProportional Hazards ModelsUnited StatesCognitionMICROBIOLOGYMortalityORAL MEDICINE

Identifiers

PMID39806633
PMCPMC11667316

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.