1. Introduction
The oral cavity contains diverse microbial communities, consisting of bacteria, fungi, and viruses. Recent research has shown that oral diseases (e.g., periodontitis) are associated with high serum HbA1c levels and low serum vitamin C levels, suggesting an important relationship between oral health and general health condition [
1,
2]. Therefore, maintenance of good oral hygiene is vital for ensuring oral and general health at all stages of life. Notably, poor oral hygiene is associated with risks of aspiration pneumonia and oral candidiasis in older people [
3,
4]. Aspiration pneumonia occurs due to swallowing difficulties (i.e., dysphagia) and the aspiration of oral resident bacteria in older people. In addition, oral candidiasis is a common fungal infection in older people [
5]. Oral candidiasis is caused by an impaired immune mechanism, medication use, xerostomia, and denture use in older people [
5,
6]. Common clinical features of chronic atrophic candidiasis (i.e., denture-related stomatitis due to the presence of
Candida) are erythema and edema of the mucosa. The long-term use of dentures and poor oral hygiene presumably contributes to the risk of oral candidiasis by producing an environment ideal for growth of
Candida. In addition, decline in activities of daily living may be associated with oral candidiasis due to poor oral health care in older people.
Thus far, the prevalence of oral Candida in older Japanese people has not been fully investigated. The aim of this study was to clarify the association between oral Candida detection and the dependency status of older people. Therefore, the present study investigated the rate of Candida detection in the oral cavity in dependent older people who had a certified need for long-term care or support, as well as in independent older people. In addition, the study investigated the relationship between the rate of oral Candida detection and clinical factors, such as medical history and oral health status.
2. Materials and Methods
2.1. Participants
This study included 31 dependent older people aged ≥70 years (nine men, 22 women; mean age, 85.1 years) who had a certified need for long-term support or nursing care, from October 2018 to October 2019. Of the 31 older people, nine required long-term support and 22 required nursing care. These individuals typically lived at home and regularly received support and care at a local day care center in Hiroshima City. In addition, this study included 27 independent older patients aged ≥70 years (six men, 21 women; mean age, 82.8 years) who visited Hiroshima University Hospital from March 2019 to December 2019. Of these 27 patients, none had a certified need for long-term support or nursing care. The study protocol was approved by the Ethical Committee of Hiroshima University, and all participants provided written informed consent.
2.2. Oral Examination
Oral samples were collected a few hours after participants had eaten breakfast, following tooth brushing. Therefore, most participants exhibited good oral hygiene before the oral examination and sample collection. Oral moisture was evaluated by an oral moisture-checking device (Moisture Checker Mucus
®, Scalar Corporation, Tokyo, Japan), as previously described [
7]. This device can measure the percentage of water at the surface of the oral mucosa by means of measuring the dielectric constant. The sensor of the device, protected by a disposable polyethylene cover, was applied to the measurement site at a pressure of approximately 200 g. The oral moisture level was measured at the tongue dorsum, with median values calculated from three independent measurements. A Bacterial Counter (Panasonic Healthcare Co., Ltd., Tokyo, Japan) was used to count the number of oral bacteria on the tongue surface, in accordance with the manufacturer’s instructions.
2.3. Oral Sample Processing and DNA Extraction
An Orcellex
® Brush (Rovers Medical Devices, NL, Netherlands) was used to collect samples from the tongue surface, in accordance with the method used in a prior study [
8]. The tongue surface was swabbed softly 10 times, using an Orcellex
® Brush. Then, the brush was placed in a 1.5 mL tube containing lysis buffer (Invitrogen, Carlsbad, CA, USA). After removal of the brush, samples were centrifuged at 3000×
g for 10 min; the supernatant was then decanted. DNA was extracted and purified using a PureLink™ Microbiome DNA Purification Kit (Invitrogen), in accordance with the manufacturer’s protocol. This kit enables purification of high-quality microbial DNA from a wide variety of sample types.
2.4. Detection of Candida Species by PCR
Each mixture was amplified with 1.0 µL DNA, GoTaq
® Green Master Mix (Promega, Madison, WI, USA), and primers. We used the following previously described PCR primer sets [
9]:
Candida albicans, 5′-TTTATCAACTTGTCACACCAGA-3′ (sense) and 5′-ATCCCGCCTTACCACTACCG-3′ (antisense);
Candida glabrata, 5′-TTATCACACGACTCGACACT-3′ (sense) and 5′-CCCACATACTGATATGGCCTACAA-3′ (antisense); and
Candida tropicalis, 5′-CAATCCTACCGCCAGAGGTTAT-3′ (sense) and 5′-TGGCCACTAGCAAAATAAGCGT-3′ (antisense). The PCR program consisted of initial melting at 95 °C for 5 min, followed by 35 cycles of 95 °C for 1 min, 58 °C for 1 min, and 72 °C for 1 min. After the reaction, 10 µL of PCR product was electrophoresed on a 2% agarose gel and stained with ethidium bromide. The universal 16S rRNA gene was used as control; its primer sequences were 5′-CGTTAGTAATCGTGGATCAGAATG-3′ (sense) and 5′-TGTGACGGGCGGTGTGTA-3′ (antisense).
2.5. Statistical Analysis
SPSS Statistics, version 24.0 (IBM Corp., Armonk, NY, USA) was used for statistical analysis. The χ2 test or Fisher’s exact test were used to examine significant differences between participant groups, with respect to clinical factors. Student’s t-test or the Mann–Whitney U test were used to evaluate significant differences in age, remaining teeth, degree of oral moisture, and number of oral bacteria between the two groups. Spearman’s rank correlation coefficient was used to examine the correlation between the degree of oral moisture and number of oral bacteria. p-values < 0.05 were considered statistically significant.
4. Discussion
In this study, dependent older people exhibited a significantly higher rate of detection of
C. albicans, compared with independent older people. Thiyahuddin et al. have reported that older people living in aged care facilities showed increased rates of detection of both
C. albicans and
C. glabrata in the oral cavity, compared with similarly aged people living at home [
10]. Therefore, dependent older people are more likely to experience oral candidiasis, compared with independent older people. In the present study, dependent older people more commonly wore dentures, compared with independent older people. The fitting surface of denture resin acts as a reservoir for microorganisms (i.e.,
Candida species) [
11]. Thus, poor denture hygiene and prolonged denture use increase the risk of oral candidiasis. Denture use may be associated with high prevalence of oral
Candida detection in dependent older people.
Histological changes in the salivary gland due to aging (i.e., decrease in number of acinar cells and increase in amount of fibrous tissue) lead to reductions in salivary flow [
12]. This reduced salivary secretion attenuates immunologic and non-immunologic defenses in the oral cavity [
12]. In the present study, we examined the degrees of oral moisture in dependent and independent older people of similar age. Dependent older people exhibited significantly lower levels of oral moisture, compared with independent older people. Thus, the salivary secretion capacity may be reduced in many dependent older people. Importantly, we found a significant negative correlation between the degree of oral moisture and the number of oral bacteria in older people. Sue et al. have also described a correlation between the level of moisture and the number of bacteria on the tongue surface in middle-aged and older people [
8]. Therefore, we speculate that dry mouth due to aging leads to an elevated number of oral bacteria. Dependent older people are likely to exhibit an increased risk of oral candidiasis because of reduced saliva secretion and poor oral hygiene.
C. albicans is the predominant pathogenic yeast among
Candida species [
13]. Biofilm formation by
C. albicans is involved in its resistance to conventional antifungal drugs [
13]. The rate of oral
C. glabrata infections has been increasing recently, and these infections have shown potent resistance to azole antifungal agents [
14,
15]. In addition, mixed infection by
C. albicans and
C. glabrata has been commonly observed in the oral cavity [
16,
17]. Both
C. albicans and
C. glabrata were frequently detected concurrently in dependent older people in the present study. Moreover, both
C. albicans and
C. glabrata were detected concurrently more frequently in people who required nursing care than in people who required long-term support. Both
C. glabrata and
C. tropicalis were detected concurrently in people who required nursing care alone. These results suggest that older people who experienced decline in activities of daily living are more susceptible to mixed oral
Candida infection. Furthermore, mixed infection by
C. albicans and
C. glabrata has been shown to induce invasion of epithelium by
C. glabrata [
18]. Mixed
Candida infection may contribute to persistent
Candida infection in oral mucosa, which results in chronic oral candidiasis in older people. However, the exact mechanism by which
C. albicans induces invasion of the epithelium by
C. glabrata remains unclear.
We did not investigate the periodontal health of the older people in this study. Importantly, periodontal disease has been associated with systemic disease (e.g., diabetes, cardiovascular disease, and metabolic syndrome) [
19,
20]. In addition, several studies have shown that periodontitis is involved in poor oral health-related quality of life [
21,
22,
23]. Periodontitis and tooth loss may be associated with changes in cognitive function among older adults [
21]. Therefore, prevention and treatment of periodontal disease are necessary to maintain good quality of life among older people.
A previous systematic review demonstrated that patients with dementia had significantly fewer teeth and worse oral hygiene, compared with people who did not have dementia [
24]. We were unable to determine the oral hygiene statuses of participants in this study. Therefore, it is unclear whether cognitive function influenced their oral hygiene status. Additional studies are needed to clarify the relationship between cognitive function and oral hygiene in older people.