Next Article in Journal
Virtual Care and the Inverse Care Law: Implications for Policy, Practice, Research, Public and Patients
Next Article in Special Issue
Lateral Cephalometric Analytical Uses for Temporomandibular Joint Disorders: The Importance of Cervical Posture and Hyoid Position
Previous Article in Journal
The Influence on Post-Activation Potentiation Exerted by Different Degrees of Blood Flow Restriction and Multi-Levels of Activation Intensity
Previous Article in Special Issue
Clinical Efficacy of 1% CHX Gluconate Gel and 0.12% CHX Solution: A Randomized Controlled Trial
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Association between Handgrip Strength and Periodontitis in Korean Adults Aged ≥30 Years: Data from the Korea National Health and Nutrition Examination Survey (2014–2015)

1
Department of Dental Hygiene, Graduate School, Gachon University, Incheon 21936, Korea
2
Department of Dental Hygiene, College of Health Science, Gachon University, Incheon 21936, Korea
*
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2022, 19(17), 10598; https://doi.org/10.3390/ijerph191710598
Submission received: 18 July 2022 / Revised: 19 August 2022 / Accepted: 21 August 2022 / Published: 25 August 2022
(This article belongs to the Special Issue Approach to Promoting Oral Health)

Abstract

:
This study used data from the Korea National Health and Nutrition Examination Survey 2014–2015 database to analyze the association between periodontitis and handgrip strength, a representative measure of hand impairment and function, in adults aged ≥30 years. The data of 5926 adults (male: 2766, females: 3160) who underwent handgrip strength and periodontal tissue examination and had neither rheumatoid arthritis nor osteoarthritis were analyzed. Handgrip strength was assessed using a digital grip strength dynamometer. The average values of the right handgrip strength, calculated separately by sex and age group (five 10-year age groups), were used as the cut-off for reduced handgrip strength. Periodontal status was evaluated using the Community Periodontal Index, defining scores ≥ 3 as periodontitis. Chi-square test and multivariate logistic regression analyses were performed to compare the differences in the prevalence of periodontitis according to handgrip strength. In the final regression model adjusted for risk factors for periodontitis, the likelihood of periodontitis decreased as the level of handgrip strength increased (p < 0.05). Therefore, this study suggests that handgrip strength may be a valuable indicator of periodontal health.

1. Introduction

According to the new classification scheme for periodontal and peri-implant diseases set by the European Federation of Periodontology and American Association of Periodontology in 2017, periodontitis has been subdivided into three categories based on pathophysiology: necrotizing periodontal diseases, periodontitis as a manifestation of systemic disease, and periodontitis, a category that combines the diseases previously recognized as “chronic” or “aggressive” [1]. Periodontitis is a chronic multifactorial inflammatory disease wherein periodontal tissues are destroyed by pathogenic bacteria such as Porphyromonas gingivalis and Treponema denticola colonizing in dental biofilm [2].
Periodontitis is mainly characterized by clinical attachment loss, radiographically assessed alveolar bone loss, presence of periodontal pockets, and gingival bleeding [1,3], and it is being monitored in many countries because it is the leading cause of tooth loss [4]. Furthermore, it is well-known that chronic inflammation in periodontal tissues and various systemic diseases, including cardiovascular disease, diabetes, pulmonary disease, and dementia, have a positive bidirectional relationship [5,6]. Hence, controlling inflammatory periodontal disease is essential for both oral and systemic health.
Dental biofilm accumulation on the surface of the teeth is the leading cause of periodontitis [2]. Biofilm is a sticky microbial community with more than 700 different bacterial species attached to salivary glycoproteins [2,7]. The most basic and effective method for the removal of dental biofilm is tooth brushing [2,8]. However, the effectiveness of manual tooth brushing generally depends on several factors, including brushing movements and the motor function of the hand [2,9,10]. In particular, impaired functions of the fingers or joints of the hand reportedly affect the extent of dental biofilm formation [11,12,13]. A cross-sectional study demonstrated that a decrease in handgrip strength and manual dexterity facilitated the accumulation of pathogenic dental biofilm in independent older adults [14].
Although the etiological factors of periodontitis have been elucidated, the disease does not show a significant decrease globally, unlike dental caries [15]. In particular, the prevalence of periodontitis requiring treatment is approximately 35% in Korean adults aged ≥30 years [16]. In addition, gingivitis and periodontitis were the most frequent causes of Korean adults visiting a medical institution between 2019 and 2020 [17]. Furthermore, hand function that can directly or indirectly affect the quality of oral care, especially in-hand manipulation skills, begin to decline in middle age [18]. Handgrip strength, indicating the force with which one can grip an object, peaks in the late 30s and decreases gradually thereafter [19,20,21,22]. Although the decline in hand function begins at a relatively early age, most previous studies that analyzed the correlation between oral health and hand function, including handgrip strength, were conducted only among the elderly. Therefore, there is a need to analyze the influence of hand function on periodontal status in both old and young adults at the age when the decline in hand function sets in. Hence, we analyzed the correlation between periodontitis and handgrip strength, a representative measure of hand impairment and function, in Korean adults aged ≥30 years using the Korea National Health and Nutrition Examination Survey (KNHANES) database.

2. Materials and Methods

2.1. Participants

This study used the KNHANES VI (2014–2015) database. The KNHANES, as a nationally representative survey conducted by the Korea Disease Control and Prevention Agency, is a surveillance system to evaluate the health and nutritional status of Koreans and monitor the prevalence and risk factors of major chronic diseases [16]. The KNHANES comprises health interviews, examinations, and nutrition surveys. Among the participants in KNHANES VI (2014–2015) (a total of 14,144 people), the study analyzed the data of subjects who met the following criteria: (1) age ≥30 years; (2) handgrip strength and periodontal tissue examination performed; (3) the right hand being the dominant hand; and (4) the absence of rheumatoid arthritis or osteoarthritis, which are diseases that affect handgrip strength. The data of 5926 participants (male: 2766, females: 3160) were analyzed. As a result of calculating the minimum sample size using G*power (ver. 3.1; Informer Technologies, Düsseldorf, Germany) [23], the study was confirmed to meet the required sample size (minimum sample size: 133 participants). Written informed consent was obtained from all participants prior to the KNHANES. KNHANES VI was approved by the Institutional Review Board (IRB) of the Korea Disease Control and Prevention Agency (IRB No. 2013–07CON-03–4C and 2013–12EXP-03–5C). The study protocol was approved by the IRB of Gachon University (IRB No.1044396–201910-HR-189–01), and all procedures were performed in accordance with the World Medical Association Declaration of Helsinki.

2.2. Measurements

The study used the data pertaining to sociodemographic characteristics (age, sex, personal income, and education), oral health behaviors (daily cigarette consumption, daily alcohol consumption, frequency of daily tooth brushing, use of interproximal cleaning devices, and dental check-ups in the past year), systemic health conditions (body mass index (BMI), glycated hemoglobin, total cholesterol (TC), triglyceride (TG), high-density lipoprotein cholesterol (HDL-C), and low-density lipoprotein cholesterol (LDL-C)), hand function (handgrip strength), and periodontal status (Community Periodontal Index (CPI)). Oral health behaviors were reclassified as follows based on previous studies [16,24,25]: daily cigarette consumption (non-smoker, light smoker (<10 cigarettes), and moderate/heavy smoker (≥10 cigarettes)), daily alcohol consumption (non-drinker, light drinker (0–6 units for men or 0–2 units for women), moderate/heavy drinker (≥7 units for men or ≥3 units for women); the study only considered the amount of alcohol regardless of the type), frequency of daily tooth brushing (≤2 and ≥3 times), dental check-ups in the past year (yes/no), and use of interproximal cleaning devices (yes/no). BMI was classified as underweight (<18.5 kg/m2), normal (18.5–24.9 kg/m2), and obese (≥25 kg/m2), and glycated hemoglobin was classified as normal (<6.5%) and diabetes (≥6.5%) [26]. TC, TG, HDL-C, and LDL-C were considered normal at levels <200, <150, ≥60, and <130 mg/dL, respectively [27]. Handgrip strength was measured to assess hand function. Low handgrip strength indicates a decline in the overall function [28]. Handgrip strength was measured using a digital grip strength dynamometer (T.K.K 5401; Takei, Tokyo, Japan) that can measure a force of 5.0 kg to 100.0 kg in 0.1 kg increments. The participants were asked to stand upright with their feet hip-width apart and elbows fully extended. The handle of the dynamometer was adjusted such that the second joint of the index finger was flexed at 90°. The participants were instructed to squeeze the grip with the maximum force for at least three seconds and not to shake the hand dynamometer during the measurements.
The normal range of handgrip strength differs greatly according to sex and age [21]. Therefore, to set the cut-off values for defining reduced handgrip strength, the average value of the right handgrip strength was calculated separately by sex and age group (five groups, ranging from 30 years to above 70 years of age). All participants were categorized into two groups based on the average handgrip strength of their respective groups. Participants whose handgrip strength was greater than or equal to the average were classified into the normal group, and those whose handgrip strength was lower than the average were classified into the reduced group. The average values (M ± SD) of handgrip strength by sex and age group were as follows: males (30s: 44.79 ± 0.36 kg, 40s: 43.20 ± 0.30 kg, 50s: 40.08 ± 0.27 kg, 60s: 37.15 ± 0.30 kg, and over 70 years: 30.88 ± 0.35 kg) and females (30s: 26.00 ± 0.20 kg, 40s: 25.89 ± 0.19 kg, 50s: 24.83 ± 0.20 kg, 60s: 22.96 ± 0.23 kg, and over 70 years: 19.03 ± 0.30 kg). Periodontal status was evaluated using the CPI [29]. The mouth was divided into six parts: three parts in the maxillary arch (right posterior (#18–14), anterior (#13–23), and left posterior (#24–28)) and three parts in the mandibular arch (right posterior (#48–44), anterior (#43–33), and left posterior (#34–38)). A dentist who completed the calibration training examined the index teeth (#16, #17, #11, #26, #27, #31, #36, #37, #46, or #47) with a CPI probe. Each index tooth was evaluated for gingival bleeding, calculus, and periodontal pockets and scored on a scale of 0–4: healthy periodontal tissue (CPI 0), gingival bleeding on probing (CPI 1), periodontal tissue with gingival calculus (CPI 2), periodontal tissue with shallow periodontal pockets (4–5 mm) (CPI 3), and periodontal tissue with deep periodontal pockets (≥6 mm) (CPI 4) [16]. Those with a CPI score less than 3 were classified into the non-periodontitis group, whereas those with a CPI score of 3 or higher were classified into the periodontitis group [16].

2.3. Statistical Analysis

The collected data were analyzed using SPSS Statistics software (ver. 23; IBM Co., Armonk, NY, USA). A chi-square test was used to compare the differences in the prevalence of periodontitis according to sociodemographic characteristics, oral health behaviors, systemic health conditions, and handgrip strength. After adjusting for potential confounders, multivariate logistic regression analyses were performed to determine the strength of association between handgrip strength and periodontitis. For the multivariate logistic regression analyses, variables with p-value < 0.05 in the chi-square test were included as independent variables, and periodontitis was the dependent variable. Statistical significance was set at α = 0.05.

3. Results

3.1. Periodontitis According to Sociodemographic Characteristics and Oral Health Behaviors

The prevalence of periodontitis was higher in men (40.8%) than in women (27.9%) and increased with age, with the highest rate in the age group of 60–69 years (50.0%) (p < 0.001). The prevalence of periodontitis was higher in the group with the lowest personal income (39.8%) and in those with an educational level of primary school completion (50.9%) than those in the respective groups when compared (p < 0.001). The prevalence of periodontitis was higher in heavy smokers (47.6%), those who brushed their teeth twice or less per day (39.2%), those who had not undergone dental check-ups in the previous year (36.1%), and those who did not use interproximal cleaning devices (40.5%) than that in subjects in the respective groups when compared (p < 0.01) (Table 1).

3.2. Periodontitis According to Systemic Health Conditions and Handgrip Strength

The prevalence of periodontitis was higher in those with a BMI of ≥25 kg/m2 (42.0%), glycated hemoglobin level of ≥6.5% (55.5%), TC level of ≥240 mg/dL (39.8%), TG level of ≥200 mg/dL (45.0%), and HDL-C level of <40 mg/dL (44.5%) than it was in subjects in the respective groups when compared (p < 0.05). In addition, the prevalence of periodontitis was higher in the reduced handgrip strength group (38.3%) than in the normal handgrip strength group (33.1%) (p = 0.001) (Table 2).

3.3. Strength of Association between Periodontitis and Handgrip Strength

In the crude model in which handgrip strength was input as a continuous variable, handgrip strength and periodontitis showed a negative correlation (confidence interval (CI): 0.984–0.997). Moreover, in the multivariate logistic regression model adjusted for the risk factors of periodontitis, the likelihood of periodontitis decreased as the handgrip strength increased (CI: 0.974–0.999) (Table 3).

4. Discussion

Although bacterial biofilm on dental surfaces is the primary cause of periodontitis, several factors, including systemic health, are involved in its progression [30]. Therefore, for further prevention of periodontitis, various systemic factors other than intraoral factors need to be considered. Hand function has been known to be associated with personal hygiene, especially oral health behaviors in older adults [11,13,31,32]. However, hand function, including in-hand manipulation skills and handgrip strength, peaks in the 30s and then declines continuously with age [18,20,21,22]. Accordingly, it is necessary to determine the effect of hand function on periodontal health and include middle-aged adults in the studies. Hence, this study analyzed the association between periodontitis and handgrip strength in 5926 Korean adults aged ≥30 years who participated in KNHANES VI (2014–2015). Handgrip strength represents not only hand impairment and function but also overall muscle strength [33,34]. More importantly, it is a useful tool that can indirectly evaluate the systemic health status of the adult population, as poor handgrip strength is closely related to diseases that contribute to mortality, such as cardiovascular disease and cancer [35,36].
Bivariate analysis revealed that the proportion of patients with reduced handgrip strength was higher in the periodontitis group than in the normal group (p = 0.001). Moreover, in the final regression model adjusted for the risk factors of periodontitis and considering handgrip strength as a continuous variable, it was confirmed that the higher the handgrip strength, the lower the incidence of periodontitis (p = 0.030). Thus, this study suggests that reduced handgrip strength can be a predictor of periodontitis in adults aged ≥30 years. Several previous studies, which included mostly elderly subjects, have reported the importance of hand function in the quality of oral care [11,32]. One study reported that older adults with decreased manual dexterity or handgrip strength had a higher accumulation of mature dental biofilm, a causative factor of oral diseases [32]. Hashimoto et al. [37] suggested that older adults aged 80 years or above who showed high handgrip strength had more teeth than did those with low handgrip strength. In addition, cross-sectional studies among adults aged ≥19 years reported that people with low handgrip strength showed poorer oral health behaviors, including tooth brushing [38,39]. Therefore, considering previous studies and our findings, we infer that reduced handgrip strength has a direct and indirect adverse effect on the ability to perform daily oral care in adults aged ≥30 years and eventually contributes to developing periodontal inflammation over a prolonged period. Low handgrip strength can cause discomfort and premature fatigue of the hand when manipulating a toothbrush handle. Fatigue, in turn, reduces the brushing time, brushing force, and brushing movements, eventually resulting in less efficient biofilm removal. Therefore, interventional programs for handgrip strength enhancement can improve hand motor skills and periodontal health. Customized oral hygiene care programs should also be provided according to individual handgrip strength. In particular, to perform a rolling stroke that is generally recommended for adults in South Korea, the performer must turn the wrist after holding the toothbrush handle with the palm of the hand [40]. This means that when using the rolling stroke method, biofilm removal may be more affected by hand function than it would when using other brushing techniques. Hence, dental hygienists need to continuously motivate and support adults with low handgrip strength to provide optimal oral hygiene care. In addition, considering previous studies finding that probiotics or paraprobiotics included in chewing gum or toothpaste significantly reduce specific periodontopathogens related to periodontitis and maintain a balanced oral microbiota, ultimately leading to improvement quality of clinical activities performed by professionals and self-oral care performed by patients [41,42], these agents can be recommended to periodontal patients with reduced handgrip strength as a supplement to improve periodontal health. Finally, a collaboration between dental professionals and musculoskeletal specialists is necessary for optimal periodontal health.
This study is of significance, as it is the first publication to demonstrate the association between reduced handgrip strength and periodontitis in adults aged ≥30 years, using the KNHANES database, which represents the health status of the South Korean population. In addition, although reduced handgrip strength was not found to be a predisposing factor for periodontitis, the study has provided an opportunity to understand that handgrip strength should be included among the management items for periodontal health.
However, this study has several limitations. First, as the KNHANES is a cross-sectional survey, it is difficult to explain the causal relationships between the variables used in the study, especially between periodontitis and reduced handgrip strength. Second, we considered the average handgrip strength, which was calculated separately by sex and age group, as the cut-off value for defining reduced handgrip strength, and handgrip strength was used as a continuous variable in the logistic regression model. However, according to several previous studies, the abnormal range of handgrip strength varies depending on various factors, including ethnicity and sex [22]. Consequently, the degree of association between periodontitis and reduced handgrip strength may differ depending on the cut-off value used to define the reduced handgrip strength. Third, the CPI score used to evaluate periodontal status may not accurately reflect the periodontal status of all existing teeth because only the index teeth were examined to represent each sextant [43]. Fourth, although the final regression model was adjusted for the risk factors of periodontitis, variables that we did not consider might have affected our results. In particular, tooth-brushing techniques and duration are important factors for biofilm removal [2,44]; however, these habit-related factors were not considered in this study. Hence, future studies should use a longitudinal design and adjust for multiple confounding variables that affect periodontal status to determine the association between handgrip strength and periodontitis.

5. Conclusions

Analyzing the association between handgrip strength and periodontitis using the KNHANES database that represents the health status of the South Korean population confirmed that reduced handgrip strength was independently associated with periodontitis in adults aged ≥30 years. Therefore, the study’s findings suggest that maintaining stronger handgrip strength may contribute to improving periodontal health. Additionally, customized oral hygiene care programs should be provided depending on the individual’s handgrip strength.

Author Contributions

Conceptualization, H.-R.A. and J.-S.C.; methodology, H.-R.A. and J.-S.C.; software, H.-R.A.; formal analysis, H.-R.A. and J.-S.C.; investigation, H.-R.A. and J.-S.C.; data curation, H.-R.A.; writing—original draft preparation, H.-R.A. and J.-S.C.; writing—review and editing, H.-R.A. and J.-S.C.; visualization, H.-R.A.; supervision, J.-S.C.; project administration, J.-S.C. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The KNHANES VI was approved by the Korea Disease Control and Prevention Agency Institutional Review Board (IRB No. 2013–07CON-03–4C and 2013–12EXP-03–5C), and all involved procedures were performed in accordance with the World Medical Association Declaration of Helsinki. In addition, the protocol for this study was approved by the IRB of Gachon University (IRB NO. 1044396–201910-HR-189–01).

Informed Consent Statement

Written informed consent was obtained from all participants prior to inclusion in the KNHANES.

Data Availability Statement

The findings of this study were analyzed using a publicly available database. The data are located at: https://knhanes.kdca.go.kr/knhanes/sub03/sub03_02_05.do. (accessed on 2 May 2021).

Acknowledgments

We thank the Korea Disease Control and Prevention Agency, which conducted the Korea National Health and Nutrition Examination Survey, and all of the participants and investigators involved in the survey.

Conflicts of Interest

The authors declare that they have no conflict of interest.

References

  1. Papapanou, P.N.; Sanz, M.; Buduneli, N.; Dietrich, T.; Feres, M.; Fine, D.H.; Flemmig, T.F.; Garcia, R.; Giannobile, W.V.; Graziani, F.; et al. Periodontitis: Consensus report of workgroup 2 of the 2017 World Workshop on the Classification of Periodontal and Peri-Implant Diseases and Conditions. J. Periodontol. 2018, 89, S173–S182. [Google Scholar] [CrossRef]
  2. Eaton, K.; Ower, P. Practical Periodontics, 1st ed.; Elsevier: St. Louis, MO, USA, 2015; pp. 13–26, 67–79, 217–231. [Google Scholar]
  3. Ndjidda Bakari, W.; Thiam, D.; Mbow, N.L.; Samb, A.; Guirassy, M.L.; Diallo, A.M.; Diouf, A.; Diallo, A.S.; Benoist, H.M. New classification of periodontal diseases (NCPD): An application in a sub-Saharan country. BDJ. Open. 2021, 7, 16. [Google Scholar] [CrossRef] [PubMed]
  4. Pihlstrom, B.L.; Michalowicz, B.S.; Johnson, N.W. Periodontal diseases. Lancet 2005, 366, 1809–1820. [Google Scholar] [CrossRef]
  5. Preshaw, P.M.; Alba, A.L.; Herrera, D.; Jepsen, S.; Konstantinidis, A.; Makrilakis, K.; Taylor, R. Periodontitis and diabetes: A two-way relationship. Diabetologia 2012, 55, 21–31. [Google Scholar] [CrossRef]
  6. Lee, Y.T.; Lee, H.C.; Hu, C.J.; Huang, L.K.; Chao, S.P.; Lin, C.P.; Su, E.C.; Lee, Y.C.; Chen, C.C. Periodontitis as a modifiable risk factor for dementia: A nationwide population-based cohort study. J. Am. Geriatr. Soc. 2017, 65, 301–305. [Google Scholar] [CrossRef] [PubMed]
  7. Dewhirst, F.E.; Chen, T.; Izard, J.; Paster, B.J.; Tanner, A.C.; Yu, W.H.; Lakshmanan, A.; Wade, W.G. The human oral microbiome. J. Bacteriol. 2010, 192, 5002–5017. [Google Scholar] [CrossRef]
  8. Darby, M.L.; Walsh, M. Dental Hygiene: Theory and Practice, 4th ed.; Elsevier: St. Louis, MO, USA, 2015; pp. 397–405. [Google Scholar]
  9. Digel, I.; Kern, I.; Geenen, E.M.; Akimbekov, N. Dental plaque removal by ultrasonic toothbrushes. Dent. J. 2020, 8, 28. [Google Scholar] [CrossRef] [PubMed]
  10. Arweiler, N.B.; Auschill, T.M.; Sculean, A. Patient self-care of periodontal pocket infections. Periodontology 2000 2018, 76, 164–179. [Google Scholar] [CrossRef]
  11. Felder, R.; James, K.; Brown, C.; Lemon, S.; Reveal, M. Dexterity testing as a predictor of oral care ability. J. Am. Geriatr. Soc. 1994, 42, 1081–1086. [Google Scholar] [CrossRef]
  12. Poole, J.L.; Brewer, C.; Rossie, K.; Good, C.C.; Conte, C.; Steen, V. Factors related to oral hygiene in persons with scleroderma. Int. J. Dent. Hyg. 2005, 3, 13–17. [Google Scholar] [CrossRef]
  13. Padilha, D.M.; Hugo, F.N.; Hilgert, J.B.; Dal Moro, R.G. Hand function and oral hygiene in older institutionalized Brazilians. J. Am. Geriatr. Soc. 2007, 55, 1333–1338. [Google Scholar] [CrossRef] [PubMed]
  14. Shin, N.R.; Choi, J.S. Manual dexterity and dental biofilm accumulation in independent older adults without hand disabilities: A cross-sectional study. Photodiagn. Photodyn. Ther. 2019, 25, 74–83. [Google Scholar] [CrossRef] [PubMed]
  15. Frencken, J.E.; Sharma, P.; Stenhouse, L.; Green, D.; Laverty, D.; Dietrich, T. Global epidemiology of dental caries and severe periodontitis—A comprehensive review. J. Clin. Periodontol. 2017, 44, S94–S105. [Google Scholar] [CrossRef]
  16. Ministry of Health & Welfare. 2015 Korea Health Statistics: Korea National Health and Nutrition Examination Survey (KNHANES VI-3); Ministry of Health & Welfare: Sejong, Korea, 2016; pp. 3–5, 54–55, 296–297.
  17. Health Insurance Review and Assessment Service and National Health Insurance Service. 2018 National Health Insurance Statistical Yearbook; Health Insurance Review and Assessment Service and National Health Insurance Service: Wonju, Korea, 2019; pp. 620–622. [Google Scholar]
  18. Dayanidhi, S.; Valero-Cuevas, F.J. Dexterous manipulation is poorer at older ages and is dissociated from decline of hand strength. J. Gerontol. A. Biol. Sci. Med. Sci. 2014, 69, 1139–1145. [Google Scholar] [CrossRef]
  19. Massy-Westropp, N.M.; Gill, T.K.; Taylor, A.W.; Bohannon, R.W.; Hill, C.L. Hand grip strength: Age and gender stratified normative data in a population-based study. BMC. Res. Notes 2011, 4, 127. [Google Scholar] [CrossRef]
  20. Kim, C.R.; Jeon, Y.J.; Kim, M.C.; Jeong, T.; Koo, W.R. Reference values for hand grip strength in the South Korean population. PLoS ONE 2018, 13, e0195485. [Google Scholar] [CrossRef]
  21. Lee, Y.L.; Lee, B.H.; Lee, S.Y. Handgrip strength in the Korean population: Normative data and cutoff values. Ann. Geriatr. Med. Res. 2019, 23, 183–189. [Google Scholar] [CrossRef]
  22. McGrath, R.; Hackney, K.J.; Ratamess, N.A.; Vincent, B.M.; Clark, B.C.; Kraemer, W.J. Absolute and Body Mass Index normalized handgrip strength percentiles by gender, ethnicity, and hand dominance in Americans. Adv. Geriatr. Med. Res. 2020, 2, e200005. [Google Scholar] [CrossRef]
  23. Faul, F.; Erdfelder, E.; Buchner, A.; Lang, A.G. Statistical power analyses using G* Power 3.1: Tests for correlation and regression analyses. Behav. Res. Methods. 2009, 41, 1149–1160. [Google Scholar] [CrossRef]
  24. Okuyemi, K.S.; Ahluwalia, J.S.; Richter, K.P.; Mayo, M.S.; Resnicow, K. Differences among African American light, moderate, and heavy smokers. Nicotine Tob. Res. 2001, 3, 45–50. [Google Scholar] [CrossRef] [PubMed]
  25. Wang, J.; Lv, J.; Wang, W.; Jiang, X. Alcohol consumption and risk of periodontitis: A meta-analysis. J. Clin. Periodontol. 2016, 43, 572–583. [Google Scholar] [CrossRef] [PubMed]
  26. International Expert Committee. International Expert Committee report on the role of the A1C assay in the diagnosis of diabetes. Diabetes Care 2009, 32, 1327–1334. [Google Scholar] [CrossRef] [PubMed]
  27. Committee for the Korean Guidelines for the Management of Dyslipidemia. 2015 Korean guidelines for the management of dyslipidemia. Korean Circ. J. 2016, 46, 275–306. [Google Scholar] [CrossRef] [PubMed]
  28. Muehldorfer-Fodor, M.; Ziegler, S.; Harms, C.; Neumann, J.; Kundt, G.; Mittlmeier, T.; Prommersberger, K.J. Load distribution of the hand during cylinder grip analyzed by Manugraphy. J. Hand Ther. 2017, 30, 529–537. [Google Scholar] [CrossRef] [PubMed]
  29. World Health Organization. Oral Health Surveys: Basic Methods, 5th ed.; World Health Organization: Geneva, Switzerland, 2013.
  30. Kaur, G.; Grover, V.; Bhaskar, N.; Kaur, R.K.; Jain, A. Periodontal infectogenomics. Inflamm. Regen. 2018, 38, 8. [Google Scholar] [CrossRef] [PubMed]
  31. Liu, C.J.; Marie, D.; Fredrick, A.; Bertram, J.; Utley, K.; Fess, E.E. Predicting hand function in older adults: Evaluations of grip strength, arm curl strength, and manual dexterity. Aging Clin. Exp. Res. 2017, 29, 753–760. [Google Scholar] [CrossRef]
  32. Shin, N.R.; Yi, Y.J.; Choi, J.S. Hand motor functions on the presence of red fluorescent dental biofilm in older community-dwelling Koreans. Photodiagn. Photodyn. Ther. 2019, 28, 120–124. [Google Scholar] [CrossRef]
  33. Tyler, H.; Adams, J.; Ellis, B. What can handgrip strength tell the therapist about hand function? Hand Ther. 2005, 10, 4–9. [Google Scholar] [CrossRef]
  34. Sayer, A.A.; Syddall, H.E.; Martin, H.J.; Dennison, E.M.; Roberts, H.C.; Cooper, C. Is grip strength associated with health-related quality of life? Findings from the Hertfordshire cohort study. Age Ageing 2006, 35, 409–415. [Google Scholar] [CrossRef]
  35. Celis-Morales, C.A.; Welsh, P.; Lyall, D.M.; Steell, L.; Petermann, F.; Anderson, J.; Iliodromiti, S.; Sillars, A.; Graham, N.; Mackay, D.F.; et al. Associations of grip strength with cardiovascular, respiratory, and cancer outcomes and all cause mortality: Prospective cohort study of half a million UK Biobank participants. BMJ 2018, 361, k1651. [Google Scholar] [CrossRef]
  36. Bohannon, R.W. Grip strength: An indispensable biomarker for older adults. Clin. Interv. Aging 2019, 14, 1681–1691. [Google Scholar] [CrossRef] [PubMed]
  37. Hashimoto, M.; Yamanaka, K.; Shimosato, T.; Ozawa, A.; Takigawa, T.; Hidaka, S.; Sakai, T.; Noguchi, T. Oral condition and health status of elderly 8020 achievers in Aichi Prefecture. Bull. Tokyo Dent. Coll. 2006, 47, 37–43. [Google Scholar] [CrossRef] [PubMed]
  38. Lee, J.H.; Lee, S.Y.; Han, K.; Han, J.S. Relationship between oral health behaviour and handgrip strength: A cross-sectional study with 7589 Korean adults. Acta. Odontol. Scand. 2020, 78, 438–444. [Google Scholar] [CrossRef] [PubMed]
  39. Kim, J.E.; Kim, N.Y.; Choi, C.H.; Chung, K.H. Association between oral health status and relative handgrip strength in 11,337 Korean. J. Clin. Med. 2021, 10, 5425. [Google Scholar] [CrossRef]
  40. Blue, C.M. Darby’s Comprehensive Review of Dental Hygiene, 8th ed.; Elsevier: St. Louis, MO, USA, 2016; pp. 494–495. [Google Scholar]
  41. Scribante, A.; Butera, A.; Alovisi, M. Customized minimally invasive protocols for the clinical and microbiological management of the oral microbiota. Microorganisms 2022, 10, 675. [Google Scholar] [CrossRef]
  42. Butera, A.; Gallo, S.; Pascadopoli, M.; Maiorani, C.; Milone, A.; Alovisi, M.; Scribante, A. Paraprobiotics in non-surgical periodontal therapy: Clinical and microbiological aspects in a 6-month follow-up domiciliary protocol for oral hygiene. Microorganisms 2022, 10, 337. [Google Scholar] [CrossRef]
  43. Yen, A.M.F.; Lai, H.; Fann, J.C.Y.; Chiu, S.Y.H.; Chen, S.L.S. Relationship between community periodontal index and fecal hemoglobin concentration, an indicator for colorectal neoplasm. J. Dent. Res. 2014, 93, 760–766. [Google Scholar] [CrossRef]
  44. Petker-Jung, W.; Weik, U.; Margraf-Stiksrud, J.; Deinzer, R. What characterizes effective tooth brushing of daily users of powered versus manual toothbrushes? BMC Oral Health 2022, 22, 10. [Google Scholar] [CrossRef]
Table 1. Association between sociodemographic characteristics or oral health behaviors and periodontitis.
Table 1. Association between sociodemographic characteristics or oral health behaviors and periodontitis.
CharacteristicsDivisionNPeriodontal Statusχ2 (p)
Non-
Periodontitis
Periodontitis
Socio-demographic characteristics
SexMale27661550 (59.2)1216 (40.8)107.770
(<0.001)
Female31602228 (72.1)932 (27.9)
Age (years)30–3912711070 (84.4)201 (15.6)488.095
(<0.001)
40–491345956 (69.2)389 (30.8)
50–591404752 (52.1)652 (47.9)
60–691095560 (50.0)535 (50.0)
≥70811440 (53.2)371 (46.8)
Personal incomeLowest (<25%)1325787 (60.2)538 (39.8)37.989
(<0.001)
Middle low (25–50%)1464891 (63.0)573 (37.0)
Middle high (50–75%)15541039 (68.1)515 (31.9)
Highest (>75%)15601049 (69.8)511 (30.2)
EducationPrimary school1114563 (49.1)551 (50.9)258.044
(<0.001)
Middle school689363 (51.6)326 (48.4)
High school19221215 (63.8)707 (36.2)
≥College21651615 (75.5)550 (24.5)
Oral health behaviors
Daily cigarette Non-smoker47283158 (69.0)1570 (31.0)111.428
(<0.001)
Consumption Light smoker229133 (60.4)96 (39.6)
Heavy smoker905450 (52.4)455 (47.6)
Daily alcohol Non-drinker1608995 (63.7)613 (36.3)3.672
Consumption ††Light drinker26091687 (66.6)922 (33.4)(0.247)
Moderate/heavy drinker16481061 (65.1)587 (34.9)
Frequency of daily tooth brushing≤227371619 (60.8)1118 (39.2)50.251
≥330602091 (69.7)969 (30.3)(<0.001)
Dental check-ups in the past yearYes18971278 (68.7)619 (31.3)13.200
No39622463 (63.9)1499 (36.1)(0.002)
Use of interproximal cleaning devicesYes21251567 (75.1)558 (24.9)149.812
No37362175 (59.5)1561 (40.5)(<0.001)
%, weighted. Light smokers (<10 cigarettes); moderate/heavy smokers (≥10 cigarettes). †† Light drinkers (<7 units for men or <3 units for women); moderate/heavy drinkers (≥7 units for men or ≥3 units for women).
Table 2. Association between systemic health conditions or handgrip strength and periodontitis.
Table 2. Association between systemic health conditions or handgrip strength and periodontitis.
CharacteristicsDivisionNPeriodontal Statusχ2 (p)
Non-
Periodontitis
Periodontitis
BMIUnderweight (<18.5 kg/m2)194145 (78.9)49 (21.1)75.008
(<0.001)
Normal (18.5–24.9 kg/m2)37822513 (68.2)1269 (31.8)
Obese (≥25 kg/m2)19131086 (58.0)827 (42.0)
GlycatedNormal (<6.5%)50183305 (67.5)1713 (32.5)103.632
(<0.001)
hemoglobinDiabetes (≥6.5%)559261 (44.5)298 (55.5)
TCOptimal/normal (<200 mg/dL)34662239 (66.9)1227 (33.1)10.408
(0.015)
Borderline high (200–239 mg/dL)16351041 (64.3)594 (35.7)
Abnormal/high (≥240 mg/dL)499297 (60.2)202 (39.8)
TGOptimal/normal (<150 mg/dL)38492596 (69.7)1253 (30.3)93.061
(<0.001)
Borderline high (150–199 mg/dL)780453 (59.3)327 (40.7)
Abnormal/high (≥200 mg/dL) 971528 (55.0)443 (45.0)
HDL-CReasonably good (≥60 mg/dL)1210888 (75.5)322 (24.5)108.906
(<0.001)
Normal (40–59 mg/dL)31662025 (65.5)1141 (34.5)
Abnormal/low (<40 mg/dL)1224664 (55.5)560 (44.5)
LDL-CNormal (<130 mg/dL)22681419 (65.1)849 (34.9)3.291
(0.292)
Borderline high (130–159 mg/dL)738462 (63.7)276 (36.3)
Abnormal high (≥160 mg/dL)300179 (59.9)121 (40.1)
Handgrip Normal39982616 (66.9)1382 (33.1)15.083
strengthReduced/poor 19281162 (61.7)766 (38.3)(0.001)
%, weighted. BMI, body mass index; TC, total cholesterol; TG, triglyceride; HDL-C, high-density lipoprotein cholesterol; LDL-C, low-density lipoprotein cholesterol.
Table 3. Factors associated with periodontitis based on multiple logistic regression analysis.
Table 3. Factors associated with periodontitis based on multiple logistic regression analysis.
CharacteristicsCrudeAdjusted
OR (95% CI)pOR (95% CI)p
Handgrip strength
(continuous)
0.990 (0.984–0.997)0.0020.986 (0.974–0.999)0.030
CI, confidence interval. p-values were obtained from multivariate logistic regression analyses. Adjusted for sociodemographic characteristics (age, sex, personal income, education), oral health behaviors (daily cigarette consumption, frequency of tooth brushing, dental check-ups in the past year, use of interproximal cleaning devices), and systemic health conditions (glycated hemoglobin, BMI, TC, TG, HDL-C).
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

An, H.-R.; Choi, J.-S. Association between Handgrip Strength and Periodontitis in Korean Adults Aged ≥30 Years: Data from the Korea National Health and Nutrition Examination Survey (2014–2015). Int. J. Environ. Res. Public Health 2022, 19, 10598. https://doi.org/10.3390/ijerph191710598

AMA Style

An H-R, Choi J-S. Association between Handgrip Strength and Periodontitis in Korean Adults Aged ≥30 Years: Data from the Korea National Health and Nutrition Examination Survey (2014–2015). International Journal of Environmental Research and Public Health. 2022; 19(17):10598. https://doi.org/10.3390/ijerph191710598

Chicago/Turabian Style

An, Hye-Ryeong, and Jun-Seon Choi. 2022. "Association between Handgrip Strength and Periodontitis in Korean Adults Aged ≥30 Years: Data from the Korea National Health and Nutrition Examination Survey (2014–2015)" International Journal of Environmental Research and Public Health 19, no. 17: 10598. https://doi.org/10.3390/ijerph191710598

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop