The Effects of Obesity on Bone Structure and Strength

Obesity Clinical Trial

Official title:

The Effects of Obesity on Bone Structure and Strength

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02629185
• Other study ID #: STH15688
• Status: Completed
• Phase: N/A
• First received: December 7, 2015
• Last updated: December 9, 2015
• Start date: September 2010
• Est. completion date: December 2013

Study information

• Verified date: December 2015
• Source: Sheffield Teaching Hospitals NHS Foundation Trust
• Contact: n/a
• Is FDA regulated: No
• Health authority: United Kingdom: Department of Health
• Study type: Observational

Clinical Trial Summary

High body weight is protective against hip and spine fracture, but has been found to increase the risk of humerus, foot and ankle fracture. Increasing understanding of the actions of adipokines on bone suggests that there may be complex effects on different aspects of bone geometry and microarchitecture and that these effects may vary depending on whether adipokines act directly on bone cells or through the central nervous system and between cortical and trabecular compartments. Previous research is limited by the use of areal dual-energy x-ray absorptiometry (DXA) scans which may be inaccurate in obese populations due to increased body thickness.

The aim of this study is to investigate the effect of obesity on bone mineral density, bone geometry, bone microarchitecture and bone strength of the hip, lumbar spine, distal radius and tibia.

This is an observational, cross-sectional study of normal weight and obese individuals matched by age, gender, height, postcode and smoking. The total number of subjects will be 240; men and premenopausal women ages 25 to 40 years and men and postmenopausal women ages 55 to 75 years. DXA, high-resolution peripheral computed tomography (HR-pQCT), quantitative computed tomography (QCT) and finite element analysis will be used to assess bone structure and strength. Biochemical markers of bone turnover and hormones related to bone metabolism will also be measured in order to identify potential mediators of the effects of obesity on bone structure and strength.

A sub-study has been included to evaluate the interaction of fracture risk and cardiovascular risk in obese and non-obese individuals. There is evidence of an interaction between bone mineral density (BMD) and cardiovascular risk and test the hypothesis that there are common pathways linking BMD and cardiovascular risk, including fat secretion of inflammatory cytokines e.g. interleukin-1 and adipokines e.g. leptin and adiponectin. Ultrasound based assessments of vascular function will be used to assess cardiac risk and relate these measures to bone density.

Obese individuals have lower circulating levels of 25OHD. This may be due to poor nutritional intake, reduced sunlight exposure or the vitamin D being stored in fat tissue. The investigators will measure levels of 25OHD in lean, overweight and obese men and women to examine whether 25(OH)D is related to age or gender and whether low 25OHD in obesity affects bone health in subsets of lean, overweight and obese participants of different ages.

Description:

This is a single centre, observational, cross-sectional, case-controlled study to determine the effects of obesity on bone structure and strength. Cases will be obese individuals and controls will be lean individuals. Overweight individuals will increase the applicability of the vitamin D sub-study to the general population. Cases will be individually matched to controls by gender, age, height, first part of postcode (e.g. S5, S10) and smoking, listed in order of priority. Individually matched controls will reduce the influence of potential confounding factors on the data collected. Blinding is not applicable to this study design.

Participants aged 25-40 years will attend for two visits:

Visit 1 - Consent, questionnaire, anthropometric measurements (height, weight, waist-to-hip ratio (WHR), triceps skinfold), tympanic temperature, blood sampling, neuromuscular function tests (chair stand test, narrow walk test and grip strength) Visit 2 - Anthropometric measurements (height, weight), pregnancy test, measurement of supine abdominal thickness, hip width measurement, DXA (whole body, spine, hip), HR-pQCT (tibia, radius), QCT (spine and hip).

Participants aged 55-75 years will attend for three visits; visits 1 and 2 as for the younger participants, and an additional visit to form the cardiovascular sub-study:

Visit 3 - Anthropometric measurements (height, weight), blood pressure, cardiovascular risk measurements (abdominal aortic calcification (AAC), flow mediated dilatation (FMD), carotid intima-media thickness (CIMT), pulse wave velocity (PWV) and ABPI).

Due to the seasonality of vitamin D levels, the vitamin D sub-study must be completed in the summer months. Participants who have completed the main study prior to August 2012 and have given their consent to be contacted regarding future research will be invited to participate in the vitamin D sub-study by telephone and subsequently sent written information about the vitamin D sub-study. Volunteers will be invited to attend for one additional visit between August 2012 and October 2012.

Future participants (those yet to consent to taking part in the main study) will be invited to participate in the vitamin D sub-study prior to consenting to the main study. As vitamin D levels are affected by seasonality, the substudy components can be completed at visit 1 of the main study for participants who attend for their first study visit between August 2012 and October 2012. However, participants attending for visit 1 of the main study between October 2012 and April 2013 will be invited to attend for an additional visit to complete the vitamin D sub-study in summer/autumn 2013.

Participation in the vitamin D sub-study will require a small blood sample to be taken and the completion of diet and sun exposure questionnaires.

The effect of obesity on bone structure will be determined by comparing the measures of BMD, bone microarchitecture and geometry in the obese study group with the lean group. The effects of obesity on bone strength will be determined using Finite element analysis (FEA). Outcomes from the neuromuscular function tests will be compared between the lean and obese groups to determine the effect of obesity on lower extremity strength, balance, coordination and flexibility. Hormones and bone turnover markers will be compared in lean and obese participants and any associations between hormones and bone turnover markers and measures of bone structure and strength will be identified.

The relationship between cardiovascular risk and BMD will be assessed by comparing the measures of FMD, CIMT, PWV, AAC and ABPI in the obese sub-study group with the lean sub-study group. The interactions between cardiovascular risk and fracture risk will be studies using the surrogate imaging for atherosclerosis risk.

Comparisons of the levels of hormones, inflammatory markers and other biochemical factors will be made between the lean and obese participants and tests will be made for associations between these measures and measures of cardiovascular risk.

The primary outcome in the main study will be mean difference in hip BMD between obese and lean individuals.

Secondary outcomes will be mean difference in cross-sectional moment of inertia, cortical and trabecular BMD, bone microarchitecture and geometry and neuromuscular function between lean and obese individuals, association between BMD and cardiovascular risk and association between body weight and circulating 25(OH)D.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 258
• Est. completion date: December 2013
• Est. primary completion date: December 2013
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 25 Years to 75 Years

Eligibility

Inclusion criteria:

Caucasian

BMI of 18.5 kg/m2 or above

Ages 25 to 40 years (and premenopausal if female) or 55 to 75 years (and postmenopausal (at least 5 years since last menstrual period) if female)

Sufficiently mobile to undergo scanning

Able to remain motionless for the duration of the scans

Able and willing to participate in the study and provide written informed consent

Exclusion criteria:

Previous orthopaedic surgery or fractures which preclude imaging at all sites

History of any long term immobilization (duration greater than three months)

High trauma fracture or low trauma fracture less than one year prior to recruitment

Current pregnancy or trying to conceive

Delivery of last child less than one year prior to recruitment

Breast feeding less than one year prior to recruitment

Pre-diagnosed diabetes mellitus

History of or current conditions known to affect bone metabolism including:

• Diagnosed skeletal disease

• Osteoarthritis at study measurement sites

• Chronic renal disease

• Malabsorption syndromes

• Diagnosed endocrine disorders

• Hypocalcemia or hypercalcemia

• Diagnosed restrictive eating disorder

Conditions which prevent the analysis of the DXA scans or the interpretation of their result

Use of medications or treatment known to affect bone metabolism including Depot medroxyprogesterone or the combined oral contraceptive pill

Alcohol intake of greater than 21 units per week

Competitive athlete, defined as participating in competitive sport at amateur or professional level

Markedly abnormal clinical laboratory parameters that are assessed as clinically significant by the PI.

Study Design

Observational Model: Ecologic or Community, Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

• Obesity
• Osteoporosis

Locations

Country	Name	City	State
United Kingdom	University of Sheffield	Sheffield

Sponsors (4)

Lead Sponsor	Collaborator
Sheffield Teaching Hospitals NHS Foundation Trust	National Osteoporosis Society, Orthopaedic Research UK, University of Sheffield

Country where clinical trial is conducted

United Kingdom, 

References & Publications (1)

Evans AL, Paggiosi MA, Eastell R, Walsh JS. Bone density, microstructure and strength in obese and normal weight men and women in younger and older adulthood. J Bone Miner Res. 2015 May;30(5):920-8. doi: 10.1002/jbmr.2407. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	mean difference in DXA hip BMD between normal weight and obese		one measurement at study entry (cross-sectional study)	No
Secondary	mean difference in other BMD measures between normal weight and obese	DXA spine and hip, QCT spine and hip, HR-pQCT radius and tibia	one measurement at study entry (cross-sectional study)	No
Secondary	mean difference in bone microarchitecture measures between normal weight and obese	HR-pQCT radius and tibia	one measurement at study entry (cross-sectional study)	No
Secondary	mean difference in biochemical bone turnover markers between normal weight and obese	serum C-terminal crosslink of type I collagen (CTX), n-teminal telopeptide of type I procoallgen (PINP), osteocalcin, bone alkaline phosphatase (BAP)	one measurement at study entry (cross-sectional study)	No
Secondary	mean difference in hormones between normal weight and obese	sex steroids, insulin-like growth hormone -1 (IGF-1), adipocyte hormones	one measurement at study entry (cross-sectional study)	No
Secondary	mean difference in cardiovascular risk measures between normal weight and obese	lipids, CIMT, PWV, AAC, FMD	one measurement at study entry (cross-sectional study)	No
Secondary	mean difference in vitamin D measures between normal weight and obese	25OHD, 1,25OHD, DBP, free 25OHD, vitamin D binding protein (DBP), DBP genotype	one measurement at study entry (cross-sectional study)	No