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Background: Physio-Cognitive Decline Syndrome (PCDs) is characterized by the coexistence of MIND (mobility impairment, no disability) and CIND (cognitive impairment, no dementia), which predicts dementia risk. Deteriorating oral health can contribute to malnutrition, cognitive decline, and physical frailty, all of which may exacerbate PCDs symptoms. This study investigates the association between oral health and PCDs, exploring sex differences in this relationship. Method: A cross-sectional analysis of the baseline data from the Nanjing Brain Health Cohort included 252 participants aged 60 and older, assessing physical mobility (6-meter walk test, grip strength), cognitive function (MoCA), and oral health (natural teeth count, denture use, tongue and lip motor function, masticatory and swallowing ability, Oral Frailty Index). Logistic regression models were used to examine associations between oral health and PCDs. Results: Among participants, 15.5% were classified as having PCDs. The odds of having PCDs were lower with a higher number of teeth (OR = 0.939, 95% CI: 0.890–0.991, p = 0.021), while impaired tongue and lip motor function increased the odds of PCDs (OR = 3.811, 95% CI: 1.059–13.717, p = 0.041). In females, the odds of MIND and CIND were lower with a greater number of teeth and denture use. For males, the odds of PCDs were higher with oral frailty (OR = 5.202, 95% CI: 1.429–18.940, p = 0.012). Conclusions: Findings underscore the significant association between oral health and the odds of PCDs among older adults, with sex-specific effects. For women, maintaining natural teeth and proper denture use are associated with lower odds of MIND and CIND, while for men, oral frailty is linked to higher odds of PCDs. Healthcare providers should consider oral health and incorporate sex-specific strategies. [ABSTRACT FROM AUTHOR]

Background: Behavioral and Psychological Symptoms of Dementia (BPSD) are core and highly detrimental symptoms of dementia. Previous research has suggested a potential association between pain and BPSD, but pieces of evidence are lacking. Objective: This study aimed to investigate the association between pain and BPSD in patients with dementia. Methods: Seven databases were searched from inception to February 2024, including PubMed, Web of Science, Embase, CINAHL, Cochrane Library, China National Knowledge Infrastructure (CNKI), and WanFang Data. Cross-sectional and longitudinal studies were included. We included studies that involved older adults with dementia and assessed the pain and BPSD by using validated tools. The quality of cohort studies was assessed using the Newcastle–Ottawa Scale, and the quality of cross-sectional studies was evaluated using AHRQ criteria. Two researchers independently screened the articles, extracted the data, and assessed the quality of the studies. A meta-analysis was conducted using Stata 15.0. Data not suitable for meta-analysis was analyzed through a qualitative synthesis to provide a comprehensive overview of the findings. Results: A total of 12 studies were included, comprising nine cross-sectional studies and three longitudinal studies. All studies were of medium to high quality. Studies reported that pain was associated with 13 different types of BPSD, including agitation, aggression, abnormal thought process, anxiety, care refusal, delirium, depression, delusions, hallucinations, sexual disinhibition, sleep disturbances, socially inappropriate behavior, and wandering. A pooled odds ratio (OR) of 1.25 (95%CI [1.17,1.33], p < 0.001) indicated a significant positive association between pain and BPSD. Specifically, pain was positively associated with aggression (OR = 1.07, 95%CI [1.00,1.13], p = 0.035), agitation (OR = 1.17, 95%CI [1.14, 1.21], p < 0.001), and depression (OR = 2.11, 95%CI [1.76,2.52], p < 0.001). However, pain was significantly negatively associated with wandering (OR = 0.77, 95%CI [0.73, 0.81], p < 0.001). Conclusions: Pain was significantly positively associated with BPSD in patients with dementia, specifically with aggression, depression, and agitation. However, pain was negatively associated with wandering. This emphasizes the importance of further research in this area and improved interventions for pain and BPSD management. Trial registration: www.crd.york.ac.uk CRD42023432320, registered 08/08/2024. [ABSTRACT FROM AUTHOR]