PhD ThesisThe number of those aged over 80 years-old (the “very-old”) will increase from 5% of the
population in European countries in 2010, to more than 10% of the population by 2050
(OECD, 2013). Very little is known about the nutritional intake, nutritional status and its
association with health and wellbeing in the very-old. Due to its diverse biological effects,
vitamin D has gained immense interest recently as a potential modifier for a range of health
outcomes This PhD systematically reviewed the available literature to provide an accurate
snapshot of vitamin D status in the very-old. It also used a unique dataset from the
Newcastle 85+ Study, a longitudinal community-dwelling study of health trajectory and
outcomes conducted in over 800 people from the North-East of England aged 85 years.
The overall aim of using this data were to explore vitamin D association with a range of
functional and ageing biomarkers in the very-old. Vitamin D status [25(OH)D] was
available for 775 participants, and measured by immunoassays at baseline only and divided
to the following concentration: 50 nmol/l
(high). Disability was measured using a questionnaire on the difficulty of performing 17
Activities of Daily Living at baseline, 1.5, 3 and 5 years. NTproBNP was measured using
an electrochemiluminescent sandwich immunoassay. The HbA1c was measured using a
Tosoh Eurogenetics automated HLC-723G7 HPLC analyser. Telomere Length was
measured as an abundance of telomeric template vs. a single gene by quantitative real-time
PCR. Spirometry and peak flow measurements were to obtain three technically satisfactory
maximal effort ‘blows’ to generate reproducible FEV1and FVC. Results of the systematic
review showed that prevalence of deficiency varies by latitude and living conditions of the
participants, and that vitamin D deficiency is widespread in many regions, particularly in
Europe. Using the Newcastle 85+ Study data also showed a high prevalence of vitamin D
deficiency (>30%) was found amongst very-old adults. Findings of this thesis indicate that
participants with low 25(OH)D concentration (<25 nmol/l) were more likely to have a
poorer disability trajectory over 5 years compared with those with moderate concentration
(25–50 nmol/l) (OR= 3.12, 95% CI= 1.6–5.8, p= 0.001), although physical activity was the
strongest predictor of disability trajectories. However, this thesis could not prove the
protective effect of vitamin D in regards to metabolic and cardiopulmonary health
biomarkers (NT-proBNP, HbA1c, FEV1, FVC and diastolic blood pressure) in fully
adjusted models at baseline or over 18 and 36 months. Finally, high 25(OH)D
concentration is positively associated with Telomere Length (95%CI= 12.0-110.3, B=
61.2+25.0, p=0.015) but does not have protective effects over 18 and 36 months. In
conclusion, this thesis highlights that vitamin D deficiency is very common in very-old
adults and that low vitamin D status is associated with at least some functional and ageing
biomarkers in this under studied age group.Saudi Arabian
Government and to Umm Al Qura Universit
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