A snapshot of the prevalence of physical activity amongst older, community dwelling people in Victoria, Australia: patterns across the 'young-old' and 'old-old'

BACKGROUND: Physical activity has a range of health benefits for older people. The aim of this study was to determine physical activity prevalence and attitudes amongst respondents to a trial screening survey. METHODS: A cross-sectional survey was conducted. Subjects were community dwelling older people aged ≥ 65 years, recruited via general practices in Victoria, Australia. Participants completed a mailed screening tool containing the Geriatric Depression Scale, the Active Australia survey and the Physical Activity Readiness Questionnaire. RESULTS: Of 330 participants, 20% were ≥ 80 years. Activity levels were similar to those reported in population studies. The proportion of participants reporting physical activity was greatest for the walking category, but decreased across categories of physical activity intensity. The oldest-old were represented at all physical activity intensity levels. Over half reported exercising at levels that, according to national criteria are, 'sufficient to attain health benefit'. A greater proportion of participants aged 85 years and older were unaware of key physical activity messages, compared to participants aged less than 85 years. CONCLUSION: Most population surveys do not provide details of older people across age categories. This survey provided information on the physical activity of people up to 91 years old. Physical activity promotion strategies should be tailored according to the individual's needs. A better understanding of the determinants of physical activity behaviour amongst older sub-groups is needed to tailor and target physical activity promotion strategies and programs to maximise physical activity related health outcomes for older people

Molecular indicators of methane metabolisms at cold seeps along the United States Atlantic Margin

Anaerobic oxidation of methane (AOM) and the environmental conditions supporting AOM on continental margins is an essential component to global methane budgets. Diagnostic lipid biomarkers and their compound specific isotope analysis preserved in authigenic carbonates at cold seeps can serve as “fingerprints” to archaeal−bacterial consortia involved in AOM. However, despite the discovery of several hundreds of seeps along the United States Atlantic Margin (USAM), there are relatively few biomarker investigations of cold seep carbonates along this passive margin. A lipid biomarker, carbon isotope, and DNA marker gene study was therefore undertaken to determine the microbial origins of authigenic carbonates from two USAM seeps, Norfolk and the Baltimore Canyon seep fields. Results from this study capture a distinct archaeal lipid signature from putative methanotrophic archaea, including archaeol (I), sn-2-hydroxyarchaeol, 2,6,10,15,19-pentamethylicosane (PMI), and crocetane. The 13C-depleted AOM-related archaeal lipid samples (i.e., archaeol: −91.6‰, sn-2-hydroxyarchaeol: −129.2‰, PMI −92.8‰, and crocetane: −70.9‰) confirm the dominance of methane assimilation and isotope fractionation during AOM. These results are consistent with the detection of archaeal anaerobic methanotrophs (ANMEs) based on 16S rRNA gene sequencing. The Norfolk authigenic carbonate contained ANME-1a, -1b, 2a-2b, and 2c whereas only the ANME-2 clade was detected at Baltimore and present as the subclusters 2a-2b and -2b. The ANME-2d clade may also be present, particularly at the Baltimore seep site, given the high abundance of Candidatus Methanoperedens nitroreducens detected in the mcrA gene sequencing. The presence of terminally branched fatty acids, antesio- and iso-C15:0 components, as well as C16:1ω7 with δ13C values as low as −107.6‰, are indicative of sulfate-reducing bacteria (SRB) at the Norfolk seep site and supports syntrophy of SRB with methane-oxidizing archaea. In contrast, nitrate-driven AOM in syntrophy M. nitroreducens at the Baltimore seep site is consistent with elevated fatty acid δ13C values and lack of Deltaproteobacteria at the Baltimore seep site. Taken together, the range in lipid composition, distribution, and carbon isotopic composition observed at the Norfolk and Baltimore seep sites suggests AOM is performed by multiple archaea instead of a single species and may be paired with either or both nitrate- and sulfate-reduction. Given the heterogeneous nature of cold seep ecosystems, this study fills a critical spatial gap in our knowledge of AOM activity at two seep sites along a passive margin. •AOM is performed by multiple archaeal sources, instead of a single archaeal species.•Heterogeneity in the lipid δ13C values reflects diverse metabolic pathways•AOM is linked to both nitrate and sulfate reduction•Different ANME clades at the Norfolk and Baltimore seeps suggest spatial variability between seep

Social Engagement and Amyloid-β-Related Cognitive Decline in Cognitively Normal Older Adults

Objective: Public health recommendations promote social engagement to reduce risk of cognitive decline and dementia. The objective of this study was to evaluate the longitudinal associations of social engagement and cognition in cognitively normal older adults with varying levels of neocortical amyloid-beta, the Alzheimer's disease (AD) pathologic marker. Methods: Two hundred seventeen men and women, age 63-89 underwent assessments for social engagement and cognitive performance at baseline and 3 years later using the Community Healthy Activities Model Program for Seniors questionnaire and the Preclinical Alzheimer Cognitive Composite (PACC). Amyloid-beta was measured using Pittsburgh compound B-PET. Multivariable regression models estimated main and interactive effects of baseline social engagement and amyloid-beta on cognitive change. Reciprocal models estimated main and interactive effects of baseline cognitive performance and amyloid-beta on change in social engagement. Results: Baseline social engagement was associated with PACC change as a modifier but not as a main effect. Lower baseline social engagement was associated with greater amyloid-beta-related PACC decline, while higher baseline social engagement was associated with relative preservation of PACC scores (beta = 0.05, p = 0.03). Reciprocally, lower baseline PACC score was associated with decline in social engagement score (beta = 1.1, p = 0.02). This association was not modified by amyloid-beta, and there was no direct association of amyloid-beta with change in social engagement. Conclusions: Low social engagement may be a marker of neurocognitive vulnerability in older adults who are cognitively normal but have evidence of AD pathophysiologic change. Understanding changes in social engagement in older adults may lead to earlier diagnosis of AD and advances in evidence-based prevention and treatment.</p

Regional tau pathology and loneliness in cognitively normal older adults.

Loneliness is a perception of social and emotional isolation that increases in prevalence among older adults during the eighth decade of life. Loneliness has been associated with higher brain amyloid-β deposition, a biologic marker of Alzheimer's disease, in cognitively normal older adults, suggesting a link with preclinical Alzheimer's disease pathophysiology. This study examined whether greater loneliness was associated with tau pathology, the other defining feature of Alzheimer's disease, in 117 cognitively normal older adults. Using flortaucipir positron emission tomography, we measured tau pathology in the entorhinal cortex, a region of initial accumulation in aging adults with or without elevated amyloid-β, and in the inferior temporal cortex, a region of early accumulation typically associated with elevated amyloid-β and memory impairment. Loneliness was measured by self-report using the 3-item UCLA-loneliness scale. We found that higher tau pathology in the right entorhinal cortex was associated with greater loneliness, controlling for age, sex, and apolipoprotein E ε4, the Alzheimer's disease genetic risk marker. This association remained significant after further adjustment for socioeconomic status, social network, depression and anxiety scores, and memory performance. There was no association of inferior temporal cortical or left entorhinal tau pathology with loneliness. Exploratory whole-brain surface maps supported these findings and identified additional clusters correlating loneliness and tau in the right fusiform gyrus. These results provide further support for loneliness as a socioemotional symptom in preclinical Alzheimer's disease