scholarly journals The Influence of Serum Uric Acid on Bone Mineral Density, Hip Geometry, and Fracture Risk: The Rotterdam Study

2016 ◽  
Vol 101 (3) ◽  
pp. 1113-1122 ◽  
Author(s):  
Taulant Muka ◽  
Ester A. L de Jonge ◽  
Jessica C. Kiefte-de Jong ◽  
André G. Uitterlinden ◽  
Albert Hofman ◽  
...  

Abstract Context: The role of uric acid (UA) in skeletal metabolism remains to be unraveled. Objective: We prospectively investigated the association between UA, bone mineral density at the femoral neck (FN-BMD), hip bone geometry parameters, and incident fracture risk and examined whether the associations were modified by age and vitamin C intake. Participants and Setting: Data of 5074 participants of The Rotterdam Study, a prospective population-based cohort. Exposure: Serum UA was assessed at baseline. Main Outcomes and Measures: FN-BMD was measured at baseline, and at second, third, and fourth visits of the Rotterdam Study. Hip bone geometry parameters were measured at baseline and at the second and third visits. Results: Serum UA levels (per SD increase) were positively associated with FN-BMD (β = 0.007 g/cm2; 95% confidence interval [CI] = 0.002–0.01), thicker cortices (β = 0.002 cm; 95% CI = 0.0003–0.002), lower bone width (β = −0.013 cm; 95% CI = −0.23 to −0.003), and lower cortical buckling ratio (β = −0.19; 95% CI = −0.33 to −0.06). The effects of UA on FN-BMD and cortical buckling ratio tended to become stronger over time. Hazard ratios and 95% CIs per SD increase of baseline UA levels for the development of any type of incident fractures, nonvertebral fractures, and osteoporotic fractures were 0.932 (0.86–0.995), 0.924 (0.856–0.998), and 0.905 (0.849–0.982), respectively. These associations were more prominent in older individuals (age, >65 y) and in participants with high intakes of vitamin C (> median). Conclusions: Higher levels of serum UA are associated with higher BMD (at the expense of thicker cortices and narrower bone diameters) and may be a protective factor in bone metabolism. However, interactions with age and vitamin C may be present.

PLoS ONE ◽  
2015 ◽  
Vol 10 (6) ◽  
pp. e0129116 ◽  
Author(s):  
Taulant Muka ◽  
Katerina Trajanoska ◽  
Jessica C. Kiefte-de Jong ◽  
Ling Oei ◽  
André G Uitterlinden ◽  
...  

Bone ◽  
2008 ◽  
Vol 42 (2) ◽  
pp. 286-293 ◽  
Author(s):  
Lisette Stolk ◽  
Joyce B.J. van Meurs ◽  
Pascal P. Arp ◽  
Albert Hofman ◽  
Huibert A.P. Pols ◽  
...  

2005 ◽  
Vol 16 (12) ◽  
pp. 1713-1720 ◽  
Author(s):  
I. I. de Liefde ◽  
M. van der Klift ◽  
C. E. D. H. de Laet ◽  
P. L. A. van Daele ◽  
A. Hofman ◽  
...  

2013 ◽  
Author(s):  
Julie Pasco ◽  
Stephen Lane ◽  
Sharon Brennan ◽  
Elizabeth Timney ◽  
Gosia Bucki-Smith ◽  
...  

2019 ◽  
Vol 19 (3) ◽  
pp. 259-273 ◽  
Author(s):  
Neelam Kaushal ◽  
Divya Vohora ◽  
Rajinder K Jalali ◽  
Sujeet Jha

Background And Objective:Osteoporosis is a common bone disorder that increases susceptibility to fragility bone fractures. The clinical and public health repercussions of osteoporosis are huge due to the morbidity, mortality, and cost of medical care linked with fragility fractures. Clinical assessment of osteoporotic risk factors can help to identify candidates at an early stage that will benefit from medical intervention and potentially lowering the morbidity and mortality seen with fractures and complications. Given this, research is ongoing to evaluate the association of osteoporosis with some novel or less well-studied risk factors/bio-markers such as uric acid (UA).Discussion:Uric acid’s antioxidant activity has been proposed to be one of the factors responsible for increasing longevity and lowering rates of age-related cancers during primate evolution, the level of which increased markedly due to loss of uricase enzyme activity (mutational silencing). Accumulated evidence shows that oxidative stress is the fundamental mechanism of age-related bone loss and acts via enhancing osteoclastic activity and increasing bone resorption. Antioxidant substances such as ascorbic acid scavenge free radicals are positively related to bone health. Thus, it is hypothesized that uric acid holds bone-protective potential owing to its potent antioxidative property. Several correlation studies have been conducted globally to investigate the relationship between serum uric acid with bone mineral density and osteoporosis. Few pre-clinical studies have tried to investigate the interaction between uric acid and bone mineral density and reported important role played via Runt-related transcription factor 2 (RUNX2)/core-binding factor subunit alpha-1 (CBF-alpha-1), Wingless-related integration site (Wnt)-3a/β-catenin signaling pathway and 11β Hydroxysteroid Dehydrogenase type 1.Conclusion:In this review, the authors provided a comprehensive summary of the literature related to association studies reported in humans as well work done until date to understand the potential cellular and molecular mechanisms that interplay between uric acid and bone metabolism.


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