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. 2022 Aug 25;49(11):1087–1105. doi: 10.1111/joor.13362

Relationship between tongue pressure and handgrip strength: A systematic review and meta‐analysis

Itsuka Arakawa‐Kaneko 1,2,, Yuko Watarai 3, Martin Schimmel 1,4, Samir Abou‐Ayash 1
PMCID: PMC9804501  PMID: 35972300

Abstract

Objectives

Muscle strength decreases with age, causing a decline in physical and oro‐facial function. However, the impact of physiological and pathophysiological factors on tongue pressure (TP) has not been clarified. The purpose of this systematic review and meta‐analysis was to compare and analyse TP and handgrip strength (HGS) between individuals aged <60 and ≥60 years, gender and need for care (independent older adults (IC) and older adults receiving nursing care (NC)). Furthermore, the effect of HGS in physical function on TP was examined.

Methods

Human clinical studies reporting HGS and TP were searched systematically using PubMed and Ichushi‐Web published from 1969 to Nov 2021. Random‐effects meta‐regressions were performed to compare between subgroups and to examine the association between HGS and TP (α < .05).

Results

Forty‐four studies with a total of 10 343 subjects were included. TP and HGS values were significantly higher in people aged <60 years relative to ≥60 years and in IC relative to NC (all p < .001). Regarding gender, there was no significant difference in TP (p = .370). However, a significant gender‐dependent difference in TP was observed in people aged <60 years (p < .001), but not in aged ≥60 years in IC group (p = .118) and aged ≥60 years in NC group (p = .895). There was a significant positive correlation of HGS and TP (p < .001).

Conclusions

Similar to decrease in HGS, age‐related sarcopaenia seems to have an effect on oro‐facial muscles like the tongue. Research on rehabilitation measures for oro‐facial muscle strength, similar to HGS might be beneficial to improve the personally acquired oro‐facial potential.

Keywords: frailty, geriatric dentistry, hand strength, muscle strength, pressure, tongue


This systematic review and meta ‐ analysis focused on muscle strength, hypothesising that age‐related decline in physical muscle strength represented by handgrip strength could equally be found in tongue pressure and analysed the effects of age, gender and the need for care.

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1. INTRODUCTION

As a result of the global trend of an aging population, nursing care needs will grow correspondingly. 1 In this situation, frailty adults are at risk for falls, hospitalisation, disability and death. 2 The most well‐known model of the frailty phenotype was proposed by Fried et al., 2 and their criteria for physical frailty are based on: unintentional weight loss, self‐reported exhaustion, low physical activity, slow walking speed and weakness (handgrip strength (HGS)). Falling into a frailty cycle leads to a vicious circle of sarcopaenia and decreased general function. 2 , 3 Most frail older adults exhibit sarcopaenia, and some older adults with sarcopaenia are frail. 4 Primary sarcopaenia is considered to be age‐related loss of skeletal muscle mass or quantity, muscle strength and physical performance, while secondary sarcopaenia is progressive generalised muscle weakness secondary to disease, malnutrition and inactivity. 5 Sarcopaenia is often assessed with HGS for muscle strength, skeletal muscle mass index (SMI) for muscle mass and gait speed for physical performance. 5 As sarcopaenia progresses, metabolism and consumed energy decrease, and then appetite (food intake) decreases, causing weight loss and malnutrition, further promoting sarcopaenia. Several studies have reported that systemic sarcopaenia and frailty are associated with decreased oro‐facial function in older adults. 6 , 7 , 8

The decline in oral function with aging is predicted to affect the decline in nutritional status and physical function. 6 , 9 A recent study has proposed that in line with the Meikirch model for health, that there is an age‐related decline of the biologically given potential of the oro‐facial system during physiological aging processes. 10 The management of oral hypofunction is expected to delay the need for nursing care and contribute to the extension of healthy life expectancy. Diagnosis of oral hypofunction is necessary prior to management, which allows for a comprehensive assessment of oral function. There are seven criteria for diagnosis of oral hypofunction proposed by the Japanese Society of Gerodontology: oral cleanness, oral dryness, lip and tongue motor function, tongue pressure (TP), occlusal force, masticatory function and swallowing function. 11 Moreover, previous studies have examined the associations between oral health and sarcopaenia, 12 oral function and sarcopaenia, 13 , 14 , 15 , 16 swallowing muscles and sarcopaenic dysphagia, 17 , 18 oral function and physical performance, 19 , 20 , 21 , 22 , 23 oral function and cognitive function 24 and oral function and polypharmacy. 7 Especially, TP and tongue thickness, which are sensitive markers for oral frailty, decrease with age. 25 However, the association between general physiology and pathophysiological factors on TP has not been clarified.

Hence, we focused on muscle strength, hypothesising that age‐related decline in physical muscle strength represented by HGS could equally be found in TP and analysed the effects of age, gender and the need for care. This systematic review and meta‐analysis designed to evaluate the relationship between HGS and TP among aged <60 and ≥60 years. The null hypothesis was that there would be no correlation between HGS and TP in people older and younger than 60 years. Furthermore, the influence of gender, need for care (independent older adults (i.e. without need for care) (IC) vs. older adults receiving nursing care (NC)) and measuring device was analysed as secondary outcomes.

2. MATERIALS AND METHODS

2.1. Protocol and registration

This systematic review was conducted following the Preferred Reporting Items for Systematic Reviews and Meta‐Analyses (PRISMA) guidelines. 26 The PRISMA checklist is provided in the Appendix S1. The focused question was designed based on the PICO format (P: population, I: intervention, C: comparison, O: outcome) as follows: P (general populations), I (physiology), C (pathophysiology) and O (TP). Accordingly, the PICO question was: ‘In patients younger or older than 60 years, is there an association between TP and general physiology and pathophysiology.’ This study protocol for the systematic review and meta‐analysis was registered in PROSPERO (registration number CRD42020187265).

2.2. Eligibility criteria

Studies were eligible if they met the following inclusion criteria: (a) human clinical studies (randomised controlled trials (RCTs), non‐randomised controlled trials (non‐RCTs), cross‐sectional studies, cohort studies, case–control studies), (b) subjects over 18 years of age, (c) studies with more than 10 subjects in study arm or group, (d) studies with TP values assessed with the JMS tongue strength measurement device (JMS) (JM‐TPM; JMS Co., Ltd.) or Iowa Oral Performance Instrument (IOPI; IOPI Medical LLC), (e) studies reporting HGS in kg or kgf, (f) publications in English, German or Japanese.

Studies were excluded if they met the following criteria: (a) in vitro or animal studies, (b) subjects younger than 18 years old or age not reported (c) fewer than 10 subjects in each relevant study arm/group, (d) insufficient documentation of TP and HGS, (e) measurement of TP in units other than kPa, (f) TP during swallowing, (g) publications not written in English, German or Japanese.

2.3. Search strategy

Two reviewers (SAA and IA) searched electronically in the PubMed/MEDLINE and the Japanese database Ichu Shi‐Web for publications in English, German, and Japanese between 1969 and Nov 30th, 2021. In the initial search, the following search terms and combinations were applied: ((patient OR population OR subject OR people OR individuals) AND (condition OR muscle OR body OR capacity OR power OR performance OR physiology OR pathophysiology) AND (‘tongue strength’ OR ‘tongue pressure’ OR ‘tongue force’ OR ‘lingual pressure’)). An additional hand search was carried out on the reference lists of related review articles dealing with similar topics in the following journals: Dysphagia, Journal of Speech, Language, and Hearing Research, Journal of Medical Speech‐language Pathology, Archives of otolaryngology‐head & neck surgery, Seminars in Speech and Language, Perspectives on Swallowing and Swallowing Disorders (Dysphagia), Journal of Motor Behaviour, Journal of the American Geriatrics Society, Archives of Physical Medicine and Rehabilitation. Collecting references and eliminating duplicates were performed using a reference manager software (EndNote X8®).

2.4. Study selection and data extraction

Duplicate articles were removed, and the titles and abstracts of the remaining articles were screened independently by two reviewers (IA, YW) according to the eligibility criteria. Next, the full‐text articles that met eligibility criteria were evaluated by the same reviewers and the reasons for exclusion were noted. Studies with insufficient data, unstable subjects, etc., were finally excluded for meta‐analysis. Disagreements between two reviewers regarding included studies were discussed and resolved by a third reviewer (SAA).

After the full‐text screening, a first reviewer (IA) collected the following extracted data from all applicable studies and recorded them in a spreadsheet software (Excel, Microsoft Office 2017): authors, year of publication, sample size, age, gender, TP and HGS values (mean, minimum, maximum), TP measuring device (JMS or IOPI), need for care (IC or NC) and study design. The second reviewer (YW) checked the extracted data. Discordance in data extraction between these two authors were discussed and decided in consultation with a third reviewer (SAA). Kappa score was calculated to identify the level of agreement between internal reviewers.

2.5. Risk of bias in individual studies

The methodological quality was evaluated individually by two authors (IA, YW) using the Newcastle‐Ottawa‐Scale (NOS) 27 for the included observational studies and the Cochrane risk of bias tool 28 for the included RCTs and non‐RCTs. The NOS was used to assess the quality of observational studies, including case–control studies, cohort studies and cross‐sectional studies, in three major domains: selection (four items), comparability (one item) and exposure (three items for case–control study) or outcome (three items for cohort study and cross‐sectional study). Each item was given a certain number of stars if the study met the criteria. Studies with 7–10 stars corresponded to high quality, 4–6 stars to intermediate quality, and 1–3 stars to low quality. The Cochrane risk of bias tool is a domain‐based assessment comprising the seven domains: random sequence generation, allocation concealment, blinding of participants and personnel, blinding of outcome assessment, incomplete outcome data, selective reporting and other sources of bias. The assigned judgement for each domain is assessed as ‘low risk of bias’, ‘high risk of bias’ or ‘unclear risk of bias’.

2.6. Data synthesis and statistical analysis

All statistical analysis was conducted using Stata/IC 16.0 for Unix (StataCorp LLC), with two‐sided at a significance level of 0.05. For the analysis, the results were sorted and processed into subgroups according to participant age, gender, TP measuring device type and need for care. Unweighted TP and HGS values from each included study were aggregated for each subgroup and calculated as mean, standard deviation (SD), median, minimum and maximum values, respectively. A test of homogeneity was performed for this meta‐analysis. A random‐effects meta‐regression was applied to TP and HGS, respectively, to estimate weighted mean (EWM) with a 95% confidence interval (95% CI) for the various subgroups as well as estimating weighted mean difference (WMD) between subgroups and inter‐subgroup comparison, including age (<60 vs. ≥60 years), device (JMS vs. IOPI), gender (men vs. women) and need for care (IC vs. NC). Additionally, the effect of HGS on TP was analysed using a random‐ effects meta‐regression with TP as dependent variable and HGS as independent variable. The results were presented as coefficients, 95% CIs, p‐values and the adjusted R 2 (%), which indicates the proportion of between study variance of mean TP explained by mean HGS. Individual mean TPs and HGSs, estimated overall mean TPs and HGSs, their 95% CIs and the weights of each study were provided as forest plots.

3. RESULTS

3.1. Study selection

The systematic electronic search found 1376 articles and the hand search found 47 articles, resulting in a total of 1423 articles identified. After removing 71 duplicate articles, 1352 titles were screened independently by two reviewers (IA and YW) to assess their suitability for the inclusion criteria, and 767 abstracts were assessed for further screening. The remaining 116 articles were assessed in full text, and 72 articles were excluded since they did not meet the eligibility criteria due to the following reasons: insufficient data (58 articles), incorrect unit (six articles), no measuring device mentioned (three articles), ineligible subjects (five articles). Finally, a total of 44 articles were eligible and included in the qualitative and quantitative synthesis in this systematic review and meta‐analysis. The Kappa scores indicated high agreement, between the two reviewers (title: κ = .88, abstract: κ = .88, full‐text: κ = .92). The flow diagram of the literature search and screening process is shown in Figure 1. The included and excluded studies during data extraction are listed in the Appendix S2.

FIGURE 1.

FIGURE 1

Flow diagram of screening and selection of publications for systematic review and meta‐analysis.

3.2. Study characteristics

A total of 10 343 subjects' data in 44 studies published between 2013 and 2021 were analysed. Extracted data for subjects <60 years of age (young) were reported in seven studies included 829 subjects with a mean age of 31.4 ± 11.9 [range 19.7–53.5] years, and those for subjects ≥60 years (older adults) were in 41 studies included 9514 subjects with a mean age of 76.9 ± 5.2 [range 66.2–88.0] years. In regard to gender, a total of 5767 data were analysed: 2015 men (17 studies) and 3752 women (23 studies). In regard to the TP measuring device, 549 subjects (three studies) were assessed with the IOPI, and 9794 subjects (41 studies) were assessed with the JMS. In regard to need for care, there were 28 studies included 8270 subjects with IC and 14 studies included 1244 subjects with NC. Table 1a summarise the characteristics of the included studies. An overview of the unweighted synthesis values, separated by age, gender, measuring device, need for care, and the combination of those parameters (JMS data only) is presented in Table 1b for TP and in Table 1c for HGS. The mean TP assessed with JMS of individual studies, their 95% CIs and their weights and the estimated overall mean TP for combinations of age and need for care are described as forest plots, HGS are drawn as well (Figure S1).

TABLE 1.

(a) Study characteristics of included studies (n = 44), (b) Tongue pressure ‐descriptive analysis and (c) Handgrip strength ‐descriptive analysis.

(a)
Author Year Subjects (n) Men (n) Women (n) Mean age ± SD (years) Median age (Q1, Q3) (years) Min age (years) Max age (years) Tongue pressure device Mean tongue pressure ± SD (kPa) Median tongue pressure (Q1, Q3) (kPa) Mean handgrip strength ± SD (kg) Median handgrip strength (Q1, Q3) (kg)
Sugiya 2021 24 20 4 77.5 ± 5.0 NA 65 NA JMS 38.0 ± 5.3 NA 36.0 ± 8.4 NA
Ogawa 2021 45 22 23 84.3 ± 7.8 NA 65 NA JMS 15.8 ± 8.1 NA 9.9 ± 6.5 NA
Miyoshi 2021 22 0 22 67.8 ± 1.4 NA 65 69 JMS 35.3 ± 5.9 NA 24.0 ± 2.8 NA
2021 99 0 99 75.3 ± 2.6 NA 70 79 JMS 35.0 ± 7.9 NA 21.3 ± 3.7 NA
2021 84 0 84 82.9 ± 2.5 NA 80 89 JMS 31.9 ± 7.5 NA 19.7 ± 3.3 NA
Kugimiya 2021 610 0 610 NA 78 (70, 86) 65 NA JMS NA 31.3 (25.8, 35.7) NA 21.0 (17.0, 25.0)
2021 268 268 0 NA 71 (68, 78.8) 65 NA JMS NA 33.4 (27.8, 39) NA 35.0 (30.3, 40.0)
Kim 2021 51 25 26 32.1 ± 7.4 NA 20 45 JMS 38.92 ± 10.93 NA 31.14 ± 10.49 NA
2021 54 26 28 53.5 ± 4.2 NA 46 60 JMS 38.28 ± 10.50 NA 28.22 ± 8.71 NA
2021 45 21 24 66.2 ± 2.8 NA 61 70 JMS 31.68 ± 7.82 NA 27.56 ± 9.29 NA
2021 61 23 38 77.4 ± 5.2 NA 71 NA JMS 26.52 ± 9.74 NA 21.44 ± 8.03 NA
Kato 2021 107 0 107 74.37 ± 4.46 NA 66 84 JMS 32.89 ± 6.41 NA 23.66 ± 3.69 NA
Iyota 2021 42 23 19 73.1 ± 3.1 NA 68 79 JMS 33.8 ± 8.4 NA 31.2 ± 7.4 NA
Hirata 2021 90 55 35 77.2 ± 8.3 NA 65 NA JMS 27.5 ± 9.9 NA 22.4 ± 7.8 NA
Chang 2021 26 9 17 73.53 ± 6.33 NA 65 NA IOPI 34.84 ± 11.57 NA 22.88 ± 6.80 NA
2021 336 140 196 71.61 ± 5.18 NA 65 NA IOPI 38.20 ± 14.01 NA 26.52 ± 7.33 NA
Sakai 2020 30 15 15 NA 88 (79.75, 91.00) 65 NA JMS NA 26.75 (21.43, 31.78) NA 17.4 (12.70, 23.00)
2020 30 15 15 NA 89 (85.00, 90.00) 65 NA JMS NA 18.10 (14.20, 23.075) NA 12.0 (8.40, 13.50)
Nakamori 2020 163 163 0 76.9 ± 5.8 NA 65 NA JMS 37.4 ± 10.2 NA 28.8 ± 6.9 NA
2020 91 0 91 79.5 ± 6.7 NA 65 NA JMS 32.5 ± 10.5 NA 15.9 ± 4.5 NA
Nagano 2020 19 19 0 79.3 ± 7.2 NA 65 NA JMS 27.5 ± 10.1 NA 17.9 ± 6.5 NA
2020 76 0 76 84.3 ± 5.0 NA 65 NA JMS 24.9 ± 8.5 NA 12.7 ± 3.4 NA
Miyoshi 2020 40 0 40 70.4 ± 2.8 NA 65 74 JMS 32.8 ± 7.4 NA 23.4 ± 5.0 NA
2020 123 0 123 80.3 ± 4.1 NA 75 NA JMS 31.4 ± 7.7 NA 20.2 ± 3.4 NA
Kunieda 2020 16 13 3 85.0 ± 6.6 NA NA NA JMS 21.8 ± 5.1 NA 14.5 ± 6.3 NA
Kugimiya 2020 282 282 0 NA 75 (70, 79) 65 NA JMS NA 30.2 (25.1, 34.5) NA 33 (28.8, 38.0)
2020 397 0 282 NA 76 (71, 80) 65 NA JMS NA 28.4 (23.4, 33.1) NA 20 (17.0, 23.2)
Kobuchi 2020 54 16 38 78.8 ± 7.1 NA NA NA JMS 28.5 ± 7.7 NA 22.4 ± 7.1 NA
Hirano 2020 36 0 36 76.2 ± 5.0 NA 65 NA JMS 25.1 ± 9.2 NA 21.9 ± 3.7 NA
Hirata 2020 66 37 29 NA 77.0 (70.0, 84.2) 65 NA JMS NA 28.9 (22.4, 33.5) NA 23.3 (16.9, 27.0)
Higa 2020 42 42 0 72.4 ± 4.7 NA 65 NA JMS 36.8 ± 8.9 NA 35.3 ± 7.2 NA
2020 70 0 70 69.0 ± 4.5 NA 65 NA JMS 34.6 ± 8.4 NA 22.7 ± 4.1 NA
Arakawa 2019 68 29 39 81.5 ± 7.3 NA 65 NA JMS 22.1 ± 8.9 NA 15.8 ± 6.6 NA
2019 99 35 64 79.4 ± 6.5 NA 65 NA JMS 27.1 ± 11.2 NA 17.1 ± 6.9 NA
Wakabayashi 2019 108 72 36 76 ± 7 NA 65 NA JMS 21.4 ± 9.4 NA 17.0 ± 8.0 NA
Morita 2019 52 52 0 77.0 ± 5.3 NA 65 NA JMS 31.8 ± 6.4 NA 33.0 ± 5.6 NA
2019 179 0 179 74.1 ± 4.8 NA 65 NA JMS 30.7 ± 6.4 NA 21.5 ± 3.6 NA
Kugimiya 2019 445 445 0 77.0 ± 4.9 NA 70 NA JMS 30.8 ± 9.0 NA 32.2 ± 6.3 NA
2019 673 0 673 77.0 ± 4.5 NA 70 NA JMS 29.8 ± 7.7 NA 21.5 ± 4.5 NA
Koyama 2019 24 0 24 19.7 ± 1.5 NA 18 NA JMS 36.49 ± 6.29 NA 26.88 ± 3.87 NA
Kito 2019 86 6 80 75.6 ± 5.6 NA 65 NA JMS 32.4 ± 8.0 NA 21.6 ± 4.8 NA
Kaji 2019 82 82 0 72.1 ± 7.2 NA 60 NA JMS 31.6 ± 10.2 NA 30.9 ± 6.2 NA
2019 62 0 62 70.5 ± 5.8 NA 60 NA JMS 27.1 ± 8.5 NA 20.1 ± 3.7 NA
Hara 2019 497 208 289 37.7 ± 10.7 NA 20 59 JMS 37.3 ± 7.7 NA 32.5 ± 9.8 NA
2019 288 97 191 70.6 ± 5.4 NA 60 89 JMS 31.4 ± 8.0 NA 27.2 ± 8.3 NA
Sakai 2018 25 25 0 82.4 ± 7.8 NA 65 NA JMS 19.2 ± 9.7 NA 22.3 ± 6.3 NA
2018 38 0 38 84.2 ± 6.1 NA 65 NA JMS 20.1 ± 10.6 NA 14.3 ± 5.1 NA
Hiroshimaya 2018 18 18 0 84.4 ± 5.0 NA NA NA JMS 21.2 ± 8.3 NA NA 22.6 (19.3, 24.4)
2018 46 0 46 87.2 ± 5.6 NA NA NA JMS 18.9 ± 10.4 NA NA 13.4 (10.9, 16.5)
Yoshimi 2018 37 37 0 NA 72.81 (69.00, 77.00) 65 NA JMS 29.63 ± 9.27 NA NA 35.22 (28.88, 41.25)
2018 81 0 81 NA 69.57 (66.00, 73.00) 65 NA JMS 30.85 ± 7.74 NA NA 23.50 (20.50, 26.38)
Yamanashi 2018 1603 650 953 72.8 ± 7.4 NA 65 95 JMS 30.5 ± 10.1 NA 26.0 ± 8.8 NA
Suzuki 2018 245 0 245 NA 81.0 (75.0, 85.0) 65 NA JMS 28.4 ± 9.5 NA NA 19.1 (15.7, 22.0)
Morita 2018 262 56 206 74.2 ± 5.9 NA 60 89 JMS 30.9 ± 6.4 NA 25.0 ± 6.4 NA
Higashi 2018 241 241 0 NA 71.0 (64.0, 78.0) NA NA JMS 30.5 ± 10.6 NA NA 31.4 (25.8, 36.9)
2018 397 0 397 NA 70.0 (62.0, 77.0) NA NA JMS 28.3 ± 9.9 NA NA 20.5 (16.1, 23.9)
Hashiguchi 2017 15 7 8 21.9 ± 4.0 NA 18 25 JMS 40.4 ± 8.6 NA 34.5 ± 8.5 NA
Sakai 2017 64 64 0 NA 84.5 (78, 89) NA NA JMS NA 25.2 (21.4, 32.3) NA 17.4 (14.2, 23.3)
2017 110 0 110 NA 84.0 (80, 88.3) NA NA JMS NA 26.7 (22.4, 32.6) NA 13.6 (10.6, 17.3)
Sakai 2017 201 70 131 NA 84 (79, 89) 65 NA JMS NA 26.8 (21.8, 32.6) NA 15.1 (11.7, 19.5)
Yasuhara 2016 47 47 0 25.66 ± 6.43 NA 18 46 JMS 45.60 ± 9.23 NA 40.92 ± 6.49 NA
2016 54 0 54 23.48 ± 4.23 NA 18 39 JMS 38.68 ± 7.37 NA 24.42 ± 4.33 NA
Furuya 2016 169 169 0 75.9 ± 6.1 NA NA NA JMS 31.8 ± 7.8 NA 35.2 ± 6.7 NA
2016 195 0 195 75.4 ± 5.6 NA NA NA JMS 29.3 ± 7.1 NA 22.7 ± 4.2 NA
Saito 2015 27 9 18 20.7 ± 0.6 NA 20 22 JMS 32.3 ± 10.4 NA 28.8 ± 7.9 NA
2015 17 11 6 74.1 ± 4.5 NA 65 84 JMS 27.1 ± 5.6 NA 27.8 ± 7.6 NA
Nakahigashi 2015 21 0 21 77.4 ± 6.6 NA 70 89 JMS 29.6 ± 10.3 NA 19.9 ± 3.2 NA
2015 41 0 41 81.0 ± 7.2 NA 70 89 JMS 24.3 ± 9.3 NA 13.5 ± 4.6 NA
Mendes 2015 30 NA NA 30.37 ± 6.75 31.5 (26.00, 36.25) 18 39 IOPI 56.57 ± 14.85 NA 38.20 ± 12.05 NA
2015 30 NA NA 49.13 ± 5.07 50 (45.00, 53.25) 40 58 IOPI 51.97 ± 10.81 NA 32.20 ± 11.05 NA
2015 30 NA NA 69.63 ± 8.06 67.00 (63.00, 74.75) 60 86 IOPI 43.20 ± 13.58 NA 26.93 ± 10.15 NA
Shimada 2014 13 13 0 73.5 ± 5.7 NA NA NA JMS 36.1 ± 8.1 NA 36.2 ± 7.2 NA
2014 27 0 27 74.4 ± 5.0 NA NA NA JMS 32.2 ± 7.0 NA 22.3 ± 4.4 NA
Buehring 2013 48 48 0 81.3 ± 6.3 NA 70 95 IOPI 50.6 ± 12.7 NA 32.4 ± 7.4 NA
2013 49 0 49 80.0 ± 5.5 NA 70 95 IOPI 47.0 ± 10.2 NA 18.3 ± 4.8 NA
(b)
Studies Subgroups Subjects Unweighted mean tongue pressure (kPa)
Mean SD Median Min‐max
Gender
Men 17 (42.5%) 17 (38.6%) 2015 (34.9%) 32.4 7.7 31.6 19.2–50.6
Women 23 (57.5%) 27 (61.4%) 3752 (65.1%) 30.6 5.7 30.9 18.9–47.0
Device
JMS 41 (93.2%) 68 (90.7%) 9794 (94.7%) 30.0 5.7 30.6 15.8–45.6
IOPI 3 (6.8%) 7 (9.3%) 549 (5.3%) 46.1 7.8 47.0 34.8–56.6
Need for care
Independent (ic) 28 (66.7%) 45 (69.2%) 8270 (86.9%) 32.7 4.9 31.7 25.1–50.6
Nursing care (nc) 14 (33.3%) 20 (30.8%) 1244 (13.1%) 23.7 3.9 24.6 15.8–28.5
Age
Older adults (o) 41 (85.4%) 65 (86.7%) 9514 (92.0%) 30.0 6.2 30.5 15.8–50.6
Young adults (y) 7 (14.6%) 10 (13.3%) 829 (8.0%) 41.7 7.5 38.8 32.3–56.6
(c)
Studies Subgroups Subjects Unweighted mean handgrip strength (kg)
Mean SD Median Min‐max
Gender
Men 17 (42.5%) 17 (38.6%) 2015 (34.9%) 30.6 6.6 32.4 17.9–40.9
Women 23 (57.5%) 27 (61.4%) 3752 (65.1%) 20.1 3.8 21.0 12.7–26.9
Device
JMS 41 (93.2%) 68 (90.7%) 9794 (94.7%) 23.8 7.1 22.4 9.9–40.9
IOPI 3 (6.8%) 7 (9.3%) 549 (5.3%) 28.2 6.6 26.9 18.3–38.2
Need for care
Independent (ic) 28 (66.7%) 45 (69.2%) 8270 (86.9%) 25.8 5.8 23.7 15.9–36.2
Nursing care (nc) 14 (33.3%) 20 (30.8%) 1244 (13.1%) 16.7 3.9 16.4 9.9–22.4
Age
Older adults (o) 41 (85.4%) 65 (86.7%) 9514 (92.0%) 23.0 6.7 22.3 9.9–36.2
Young adults (y) 7 (14.6%) 10 (13.3%) 829 (8.0%) 31.8 5.1 31.7 24.4–40.9

Abbreviations: ic, independent group; NA, not applicable; nc, nursing care group; o, older adults; y, young adults.

3.3. Quality assessment

In the quality assessment, 39 cross‐sectional studies, two before and after studies, one prospective cohort study, one RCT and one non‐RCT were evaluated. Forty‐two analytical studies were assessed with NOS (Table 2a); six studies (14.3%) were considered low quality, 27 studies (64.3%) intermediate and nine studies (21.4%) high quality. One RCT was rated as having a low risk of bias or unclear risk of bias and one non‐RCT was rated as having a high risk (Table 2b).

TABLE 2.

Results of quality assessment for (a) analytical study according to NOS, and for (b) included randomised clinical trials (RCTs) according to Cochrane Collaboration's tool for assessing risk of bias.

(a)
Author Year Study design Selection Comparability Outcome Ottawa total stars Quality
Sugiya 2021 Cross‐sectional 3 0 1 4 Intermediate
Ogawa 2021 Cross‐sectional 3 2 2 7 High
Miyoshi 2021 Cross‐sectional 1 2 1 4 Intermediate
Kugimiya 2021 Cross‐sectional 5 2 2 9 High
Kim 2021 Cross‐sectional 2 2 2 6 Intermediate
Kato 2021 Cross‐sectional 3 1 2 6 Intermediate
Hirata 2021 Cross‐sectional 1 2 2 5 Intermediate
Chang 2021 Cross‐sectional 4 2 2 8 High
Sakai 2020 Cross‐sectional 4 0 2 6 Intermediate
Nakamori 2020 Cross‐sectional 1 2 2 5 Intermediate
Nagano 2020 Before and after 1 2 2 5 Intermediate
Miyoshi 2020 Cross‐sectional 2 2 2 6 Intermediate
Kunieda 2020 Cross‐sectional 3 0 1 4 Intermediate
Kugimiya 2020 Cross‐sectional 5 2 1 8 High
Kobuchi 2020 Cross‐sectional 3 2 2 7 High
Hirano 2020 Cross‐sectional 1 0 1 2 Low
Hirata 2020 Cross‐sectional 1 1 2 4 Intermediate
Higa 2020 Before and after 1 1 2 4 Intermediate
Arakawa 2019 Cross‐sectional 2 1 2 5 Intermediate
Wakabayashi 2019 Prospective cohort 3 2 0 5 Intermediate
Morita 2019 Cross‐sectional 3 1 1 5 Intermediate
Kugimiya 2019 Cross‐sectional 4 2 1 7 High
Koyama 2019 Cross‐sectional 1 0 1 2 Low
Kaji 2019 Cross‐sectional 3 2 2 7 High
Hara 2019 Cross‐sectional 3 2 2 7 High
Sakai 2018 Cross‐sectional 3 2 1 6 Intermediate
Hiroshimaya 2018 Cross‐sectional 3 1 2 6 Intermediate
Yoshimi 2018 Cross‐sectional 3 1 2 6 Intermediate
Yamanashi 2018 Cross‐sectional 2 1 2 5 Intermediate
Suzuki 2018 Cross‐sectional 2 1 1 4 Intermediate
Morita 2018 Cross‐sectional 1 2 1 4 Intermediate
Higashi 2018 Cross‐sectional 3 1 3 7 High
Hashiguchi 2017 Cross‐sectional 1 1 1 3 Low
Sakai (Tongue) 2017 Cross‐sectional 2 1 2 5 Intermediate
Sakai (Relationship) 2017 Cross‐sectional 3 1 2 6 Intermediate
Yasuhara 2016 Cross‐sectional 1 1 1 3 Low
Furuya 2016 Cross‐sectional 2 2 1 5 Intermediate
Saito 2015 Cross‐sectional 0 1 1 2 Low
Nakahigashi 2015 Cross‐sectional 0 1 1 2 Low
Mendes 2015 Cross‐sectional 2 1 1 4 Intermediate
Shimada 2014 Cross‐sectional 2 2 1 5 Intermediate
Buehring 2013 Cross‐sectional 3 2 1 6 Intermediate
(b)
Author Year Study design Random sequence generation Allocation concealment Blinding of participants and personnel Blinding of outcome assessment Incomplete outcome data Selective reporting Other bias
Iyota 2021 Non‐RCT High risk High risk Low risk Low risk Low risk Low risk High risk
Kito 2019 RCT Unclear Low risk Low risk Low risk Low risk Low risk Low risk

3.4. Synthesis of results

3.4.1. Tongue pressure

Regarding analysis of age group, the WMD between young and older groups was 11.5 kPa (SE: 2.13 kPa), indicating that TP was significantly higher in subjects <60 years (p < .001). Regarding analysis of measuring device, the TP value assessed with the IOPI was significantly higher than those with the JMS, with a WMD of 15.9 kPa (SE: 2.36 kPa) (p < .001). Analysing the TP values measured with the JMS only among IC for both genders, significantly higher TP values were found in the younger group than in the older adults' group for both men (p < .001) and women (p = .001).

In terms of TP, there was no difference between men and women (WMD: −1.8 kPa; SE: 1.97 kPa; p = .370). However, when the gender differences in TP values measured with the JMS were analysed in combination with age and need for care, a significantly higher TP was found in men than in women in the younger IC (p < .001), whereas there was no significant gender difference in older adults' IC (p = .118) and in older adults' NC (p = .895).

Regarding analysis of need for care, TP was significantly higher in the IC compared to in the NC, with a WMD of −8.8 kPa (SE: 1.2 kPa) (p < .001). When analysing the difference in TP values of older adults measured with JMS between IC and NC, TP was significantly higher in the IC than in the NC for both men and women (both p < .001). Table 3a provides a detailed overview on the EWM TP for each group and the WMD between groups.

TABLE 3.

(a) Tongue pressure and gender, device, need for care, age (estimation by random‐effects meta‐regression a ), (b) Handgrip strength and gender, device, need of care, age (estimation by random‐effects meta‐regression a ).

(a)
No. of studies No. of subgroups (rows) No. of subjects EWM/WMD SE 95% CI p‐value
Gender
Men 17 17 2015 32.4 1.83 28.8–36.0
Women 23 27 3752 30.6 1.06 28.5–32.7 .370
Women versus men WMD −1.8 1.97 −5.6 to 2.1
Device
JMS 41 68 9794 30.0 0.68 28.7–31.4
IOPI 3 7 549 46.0 2.90 40.3–51.7 <.001
IOPI versus JMS WMD 15.9 2.36 11.2–20.5
Need for care
ic 28 45 8270 32.6 0.69 31.3–34.0
nc 14 20 1244 23.8 0.87 22.1–25.5 <.001
ic versus nc WMD −8.8 1.20 −11.2 to −6.5
Age
o 41 65 9514 29.9 0.75 28.5–31.4
y 7 10 829 41.5 2.28 37.0–46.0 <.001
y versus o WMD 11.5 2.13 7.3–15.7
JMS only: Men/women
Men y ic 1 1 47 45.6 1.35 43.0–48.2
Women y ic 2 2 78 37.7 1.09 35.6–39.9 <.001
Women y ic versus men y ic WMD −7.9 2.02 −11.8 to −3.9
Men o ic 11 11 1794 32.5 0.81 31.0–34.1
Women o ic 16 19 3314 31.0 0.59 29.8–32.1 .118
Women o ic versus men o ic WMD −1.5 0.99 −3.5 to 0.4
Men o nc 4 4 126 23.6 1.95 19.8–27.4
Women o nc 5 5 311 23.3 1.56 20.2–26.4 .895
Women o nc versus men o nc WMD −0.3 2.48 −5.2 to 4.5
Young adults/older adults
Men y ic 1 1 47 45.6 1.35 43.0–48.2
Men o ic 11 11 1794 32.5 0.81 31.0–34.1 <.001
Men o ic versus men y ic WMD −13.1 2.95 −18.8 to −7.3
Women y ic 2 2 78 37.7 1.09 35.6–39.9
Women o ic 16 19 3314 31.0 0.59 29.8–32.1 .001
Women o ic versus women y ic WMD −6.6 1.93 −10.4 to −2.9
Independent/nursing care
Men o ic 11 11 1794 32.5 0.81 31.0–34.1
Men o nc 4 4 126 23.6 1.95 19.8–27.4 <.001
Men o nc versus men o ic WMD −8.9 1.83 −12.5 to −5.3
Women o ic 16 19 3314 31.0 0.59 29.8–32.1
Women o nc 5 5 311 23.3 1.56 20.2–26.4 <.001
Women o nc versus women o ic WMD −7.6 1.42 −10.4 to −4.8
(b)
No. of studies No. of subgroups (rows) No. of patients EWM /WMD SE 95% CI p‐value
Gender
Men 17 17 2015 30.6 1.59 27.5–33.7
Women 23 27 3752 20.1 0.73 18.7–21.5 <.001
Women versus men WMD −10.5 1.54 −13.5 to −7.5
Device
JMS 41 68 9794 23.7 0.86 22.0–25.4
IOPI 3 7 549 28.0 2.50 23.2–32.9 .125
IOPI versus JMS WMD 4.3 2.83 −1.2 to 9.9
Need for care
ic 28 45 8270 25.7 0.85 24.1–27.4
nc 14 20 1244 16.7 0.88 14.9–18.4 <.001
nc versus ic WMD −9.0 1.41 −11.8 to −6.3
Age
o 41 65 9514 23.0 0.83 21.4–24.6
y 7 10 829 31.7 1.64 28.4–34.9 <.001
y versus o WMD 8.7 2.24 4.3–13.1
JMS only: Men/women
Men y ic 1 1 47 40.9 0.95 39.1–42.8
Women y ic 2 2 78 25.6 1.23 23.2–28.0 <.001
Women y ic versus men y ic WMD −15.3 2.22 −19.7 to −11.0
Men o ic 11 11 1794 33.1 0.69 31.8–34.5
Women o ic 16 19 3314 21.3 0.44 20.5–22.2 <.001
Women o ic versus men o ic WMD −11.8 0.78 −13.3 to −10.2
Men o nc 4 4 126 20.2 1.18 17.9–22.5
Women o nc 5 5 311 13.4 0.31 12.8–14.1 <.001
Women o nc versus men o nc WMD −6.7 0.90 −8.4 to −4.9
Young adults/older adults
Men y ic 1 1 47 40.9 0.95 39.1–42.8
Men o ic 11 11 1794 33.1 0.69 31.8–34.5 .001
Men o ic versus men y ic WMD −7.8 2.43 −12.6 to −3.1
Women y ic 2 2 78 25.6 1.23 23.2–28.0
Women o ic 16 19 3314 21.3 0.44 20.5–22.2 .003
Women o ic versus women y ic WMD −4.3 1.46 −7.1 to −1.4
Independent/nursing care
Men o ic 11 11 1794 33.1 0.69 31.8–34.5
Men o nc 4 4 126 20.2 1.18 17.9–22.5 <.001
Men o nc versus men o ic WMD −12.9 1.38 −15.6 to −10.2
Women o ic 16 19 3314 21.3 0.44 20.5–22.2
Women o nc 5 5 311 13.4 0.31 12.8–14.1 <.001
Women o nc versus women o ic WMD −7.7 0.90 −9.5 to −6.0

Abbreviations: EWM, estimated weighted mean; ic, independent group; nc, nursing care group; o, older adults; WMD, estimated weighted mean difference between groups; y, young adults.

a

Except for JMS only, women e nc versus men e nc (t‐test for independent group).

3.4.2. Handgrip strength

Regarding age group, the WMD between young and older adults' groups was 8.7 kg (SE: 2.24 kg), indicating that HGS was significantly higher in subjects <60 years (p < .001). Furthermore, a significantly higher HGS values among IC were found in younger group than in older adults' group both for men (p = .001) and women (p = .003).

Regarding gender, the HGS was significantly higher in men than in women (WMD: −10.5 kg; SE: 1.54 kg; p < .001). Analysing the gender differences in combination with age and need for care, a significantly higher HGS was shown in men than in women in the younger IC, in older adults IC and in older adults NC (all p < .001).

Regarding need for care, the HGS was significantly higher in the IC compared to the NC, with a WMD of −9.0 kg (SE: 1.41 kg) (p < .001). When analysing the difference in HGS values between IC and NC in older adults, HGS was significantly higher in the IC than in the NC for both men and women (both p < .001). Table 3b provides a detailed overview on the EWM HGS for each group and the WMD between groups.

3.4.3. Effect of handgrip strength on tongue pressure

The null hypothesis of homogeneity of studies was rejected by statistical test (p < .05 for each analysis) for all forest plots. Therefore, random‐effects models were used for the analysis in this study because this approach allows variation (heterogeneity) of study outcomes, that is heterogeneity of studies is incorporated in the analysis. The random‐effects meta‐regression analysis to evaluate the effect of HGS on TP was performed separately for all studies and for different groups, including age, gender, device and need for care. There is a significant positive correlation between TP and HGS in older adults' group (p < .001), in men (p = .006), in women (p = .002), in the group with TP values measured with JMS (p < .001), in IC (p = .001) and in NC (p = .024), whereas no significant correlation in young group (p = .053) and in the group with TP values measured with IOPI (p = .100; Table 4a; Figure 2) Subsequently, the multivariate analysis based on data from all studies (n = 75), adjusting for age, device and need for care, showed a significant positive effect of HGS and TP (p < .001; Table 4b).

TABLE 4.

(a) Effect of handgrip strength on tongue pressure – analysis of all studies and subgroups (multivariate random‐effects meta‐regression) and (b) Effect of handgrip strength on tongue pressure (multivariate random‐effects meta‐regression adjusted for device, need for care and age) (n = 75).

(a)
No. of subgroups Coeff. [95% CI] p‐value Adj. R 2 (%)
Total 75 0.69 [0.51–0.86] <.001 46.9
Gender
Men 17 0.74 [0.25–1.23] .006 38.9
Women 27 0.83 [0.34–1.33] .002 32.2
Device
JMS 68 0.58 [0.45–0.71] <.001 56.2
IOPI 7 0.79 [−0.22 to 1.79] .100 34.7
Need for care
Independent 55 0.46 [0.20–0.71] .001 19.5
Nursing care 20 0.50 [0.07–0.92] .024 26.1
Age
Older adults 65 0.53 [0.35–0.72] <.001 36.1
Young adults 10 0.90 [−0.01 to 1.80] .053 34.5
(b)
Coeff. [95% CI] p‐value
0.28 [0.14–0.42] <.001

Note: (a): Estimation by random‐effects meta‐regression. (b): Estimation by random‐effects meta‐regression adjusted for device, need for care and age.

FIGURE 2.

FIGURE 2

Linear relationship between mean tongue pressure and mean handgrip strength estimated by random‐effects meta‐regression (straight line) and the scatter plot of mean tongue pressure and mean handgrip strength (circles) for (A) men, (B) women, (C) independent subjects, (D) subjects with nursing care, (E) older adults, (F) young people, (G) subjects who were measured for tongue pressure with JMS, (H) subjects who were measured for tongue pressure with IOPI.

4. DISCUSSION

In this systematic review and meta‐analysis, TP and HGS values were summarised by age groups, gender, need for care and measuring device, and the effect of HGS on TP was analysed. TP and HGS were significantly higher in people <60 years than in those ≥60 years, in men than in women and in people living independently than in people receiving nursing care. In addition, there was a significant difference in TP between measured with IOPI and JMS. A significant correlation between HGS and TP was observed. Therefore, the null hypothesis was rejected.

Tongue pressure increases with age during the growth stage of childhood 29 and decreases with aging. A previous study reported that TP and HGS values in healthy older adults were significantly higher than in older adults receiving nursing care. 30 Regarding the tongue pressure, it was suggested that it may conclude that healthy older people could maintain a value of 30 kPa. 31 In the present study, older adults' groups were classified into those with and without nursing care, and the EWM TP indicated that the independent older adults were 32.5 kPa for men and 31.0 kPa for women, while those requiring nursing care were 23.6 kPa for men and 23.3 kPa for women, supporting the tongue pressure reference value for oral hypofunction. 11 With regard to gender, previous studies found that TP was significantly higher in men than in women among healthy older adults, 32 , 33 whereas no significant gender difference in older adults receiving nursing care 34 , 35 and in healthy older adults 36 as demonstrated in our previous systematic review. 37 The current results similarly indicated a significant gender difference in the healthy young group, while no significant gender difference was found in the older adults' group, either in IC or NC. The proportion of older adults requiring nursing care increases with age, 38 and older adults requiring nursing care have lower potential, ADL and oral function than independent older adults. The first thing to consider is that individual difference might be more influential than gender difference in older adults. The second thing to consider is that there would be less change in tongue pressure with age in women. Among women, aging‐induced decreases in swallowing‐related muscle strength tended to be more gradual than the corresponding decreases in whole‐body strength. 39 In fact, the current study found that WMD between healthy older and younger people was smaller in women with a WMD of −6.6 kPa (SE: 1.93 kPa) than in men with a WMD of −13.1 kPa (SE: 2.95 kPa).

The HGS, one of the criteria for sarcopaenia and frailty, is defined by the Asian Working Group for Sarcopaenia (AWGS) as the threshold for low muscle strength in Asians: <28 kg for men and <18 kg for women. The EWM HGS values in this present meta‐analysis were 33.1 kg for men and 21.3 kg for women in independent older adults, and 20.8 kg for men and 13.8 kg for women in older adults requiring care, which are very reasonable considering the AWGS reference values. HGS is used to assess physical function in the rehabilitation field. 40 One systematic review illustrated that HGS was associated with mobility and ADL in older people. 41 In this present review, adjusting for age, gender, need for care and tongue pressure measuring device, HGS and TP are significantly correlated.

Previous evidence on a correlation between HGS and TP is indecisive. 22 , 30 , 31 , 33 , 42 , 43 , 44 , 45 , 46 , 47 , 48 , 49 , 50 , 51 , 52 , 53 In the present meta‐analysis, TP was used as dependent variable and HGS was used as an independent variable, that is the estimated coefficient shows the influence (effect) of handgrip strength on tongue pressure. Significant correlations between HGS and TP could be shown in independent group (p = .001), in requiring nursing care group (p = .024) and in older adults' group (p < .001), but not in young group (p = .053) as the p‐value was just above the level of significance. This result might be due to the small number of young groups studies (n = 7). Furthermore, the estimated coefficients of men and women are very similar (0.74 [0.25–1.23], 0.83 [0.34–1.33]). Since there was no hint that the effect of HGS on TP does depend on gender, it was estimated without adjusting for gender factors in Table 4b. The results of this present study suggested that HGS can be used to roughly analyse TP. Measuring HGS is an easier approach for non‐dental health‐care professionals, as they do not have to look in the patients' mouths. And if HGS is low, it may predict a decline in oro‐facial function and help to collaborate with dentistry.

An accumulated poor oral status including low TP was reported to significantly predict future physical weakening (new onsets of physical frailty, sarcopaenia and disability), 7 and low TP would significantly hinder food bolus formation and propagation, thus leading to malnourishment following decreased oral intake. 45 , 54 A decrease in the food intake diversity is considered to be a risk to decrease the limb skeletal muscle mass. 55 TP is one of the muscle strength indicators of the swallowing muscles, 56 or predictors of the risk of low nutrition. 57 The swallowing muscles are inevitably affected by malnutrition and disuse. 58 It has also been noted that although the swallowing muscles are strained, it receives constant input stimulation from the respiratory centre and are different from other skeletal muscles, and there is no certainty as to whether the swallowing muscle and other skeletal muscles undergo functional decline in parallel. 58 , 59 TP and HGS have been correlated, but the direct mechanism is not yet clear. In the future, with increasing evidence that poor oral function can lead to a deterioration of general health, it may be effective and important to expand the opportunities for TP measurements as well as HGS measurements. Furthermore, a lot studies have suggested that low nutrition, sarcopaenia and dysphagia are closely related. 60 Further research is needed to prevent the vicious circle of ‘sarcopaenia ‐ dysphagia ‐ low nutrition’ 59 from starting.

This systematic review has some limitations. The number of young people was less than that of older adults. In addition, there were only three study investigated TP and HGS in healthy young people, divided by gender. Data on TP values were taken from studies that measured tongue pressure using either JMS or IOPI. As a result, most of the studies used JMS, and most of the studies were performed in Japan. In the future, it will be necessary to analyse research data not only from Japan but also from around the world. It is expected to contribute to the further development of healthy longevity by examining the differences between countries and new perspectives on the characteristics of older people.

It was proposed that oro‐facial fitness is a state in which the physiological, psychosocial and environmental requirements of life of an individual are met. 10 The loss of oro‐facial function may or may not be restored through dental intervention or training. 10 Reduced neuro‐plastic capacity in older adults might preclude a positive outcome of these strategies that might need to be accompanied by functional training and nutritional counselling. 10 However, a few longitudinal studies reported physical and/or intervention and nutritional management for older adults could be effective to improve oral and physical function. 61 , 62 , 63 , 64 Additionally, another previous study suggested that decrease in overall muscle strength, which may result from bedrest during hospitalisation, is more important as a factor than the actual performance of activities of daily living in the reduction of TP. 53 On the other hand, age‐related decline in TP might be associated with high TP, reflecting decreased reserve. 31 Although many studies have shown that age‐related changes result in a decrease in tongue pressure, a previous study was reported that age‐related decline in tongue function might be different from decline in physical function, 31 suggesting that further longitudinal studies are needed. Additionally analysing the relationship between oral function and muscle mass, nutritional status, cognitive function, level of care and psychosocial function will be essential in examining the factors that influence it.

5. CONCLUSIONS

Based on the results of this systematic review and meta‐analysis, it is concluded that when tongue pressure is measured using the JMS:

  • Tongue pressure and handgrip strength are higher in subjects younger than 60 years relative to subjects 60 years and older in both men and women.

  • Gender differences were found in tongue pressure and handgrip strength in the younger independent subjects. However, in older adults' group, there is significantly gender difference in handgrip strength, but not tongue pressure regardless of the presence or absence of receiving care.

  • In older adults' group, subjects who live independently have significantly higher tongue pressure and handgrip strength compared to those who receive care.

  • Handgrip strength and tongue pressure are significantly correlated.

  • It is suggested further study might be necessary to research on rehabilitation measures for muscle strength, similar to handgrip strength might be beneficial to improve the personally acquired oro‐facial potential according to age‐related sarcopaenia.

AUTHOR CONTRIBUTION

Itsuka Arakawa‐Kaneko initiated the study together with Samir Abou‐Ayash and Martin Schimmel, and conceptualised and designed the study, collected and analysed data, drafted and revised the manuscript. Yuko Watarai contributed to data collection, and analysis during the systematic search. Martin Schimmel contributed to the conception and design of the study and critically revised the manuscript. Samir Abou‐Ayash contributed to the conception and design of the study, analysing data and critically revised the manuscript.

CONFLICT OF INTEREST

The authors have no conflicts of interest to declare.

PEER REVIEW

The peer review history for this article is available at https://publons.com/publon/10.1111/joor.13362.

Supporting information

Figure S1

Appendix S1

Appendix S2

ACKNOWLEDGEMENTS

The authors express their gratitude to biostatistician Mrs. Hiltrud Niggemann for conducting the statistical analysis. The authors declare they received no financial funding for this investigation. Open access funding provided by Universitat Bern.

Arakawa‐Kaneko I, Watarai Y, Schimmel M, Abou‐Ayash S. Relationship between tongue pressure and handgrip strength: A systematic review and meta‐analysis. J Oral Rehabil. 2022;49:1087‐1105. doi: 10.1111/joor.13362

DATA AVAILABILITY STATEMENT

The original data can be made available upon reasonable request.

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Figure S1

Appendix S1

Appendix S2

Data Availability Statement

The original data can be made available upon reasonable request.


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