Achilles Tendon Rupture Clinical Trial
Official title:
Metabolic Complications Following Achilles Tendon Rupture - A Cohort Study
Introduction This study will evaluate the effect on glucose, lipid and bone metabolism
following conservative orthopaedic procedures in patients who suffered from acute Achilles
tendon rupture. The sedentary rehabilitation period following these procedures may impact
negatively upon glucose, lipid and bone metabolic pathways whereas the more physically active
rehabilitation period instituted 8 weeks after the injury is hypothesized to impose positive
metabolic effects.
The study is addition to the on-going clinical trial, Non-operative Treatment of Acute
Achilles Tendon Rupture: Early Controlled Mobilization Compared With Immobilization,
ClinicalTrials.gov Identifier: NCT02015364.
Perspective This study will establish whether the well-known effects on glucose, lipid and
bone metabolism of a sedentary lifestyle can be observed already following 8 weeks of almost
total abstain from physical activity in non-diabetic individuals, who suffered an acute
Achilles tendon rupture. Thereby, we will add knowledge to the previous findings following
strict bed-rest in healthy individuals on glucose and lipid metabolism and bone turnover. In
a clinical perspective it is important to examine the extent to which individuals deteriorate
in various metabolic pathways to better understand the pathophysiology behind these defects
both in healthy individuals and in patients, who undergo bed rest or an equal reduction in
physical activity as part of their rehabilitation.
Study design The present study includes 50 cases, who are examined early following injury (<
2 weeks) (baseline), 8 weeks (6 - 10 weeks) after injury and 52 weeks (40 - 64 weeks) after
injury, respectively.
Oral glucose tolerance test (OGTT) with ingestion of 75 g of glucose during a maximum of 3
min from baseline (0 min). Plasma for glucose, insulin, C-peptide, NEFA will be drawn.
The individual will bring in morning spot urine for measurement of suPAR, creatinine, albumin
and orosomucoid.
The individual will have drawn blood for measurement of HbA1c, total cholesterol, LDL
cholesterol, HDL cholesterol, triglyceride, Na, K, creatinine, HgB, CRP, leukocytes, ALAT,
alkaline phosphatase, Ca++, D vitamin, TSH, albumine and amylase. Also blood for BTM and
plasma suPAR, IL6, TNFa and hsCRP will be drawn. Finally blood for lipid density profiling
and lipid particle size will be drawn DXA of hip and lumbar spine including abdominal
visceral and subcutaneous fat is done on a Hologic Discovery scanner.
Introduction This study will evaluate the effect on glucose, lipid and bone metabolism
following conservative orthopaedic procedures in patients who suffered from acute Achilles
tendon rupture. The sedentary rehabilitation period following these procedures may impact
negatively upon glucose, lipid and bone metabolic pathways whereas the more physically active
rehabilitation period instituted 8 weeks after the injury is hypothesized to impose positive
metabolic effects.
An on-going clinical trial, Non-operative Treatment of Acute Achilles Tendon Rupture: Early
Controlled Mobilization Compared With Immobilization, ClinicalTrials.gov Identifier:
NCT02015364 is already addressing as primary endpoints the Achilles tendon total rupture
score and patient reported validation score developed to assess symptoms and physical
activity after treatment for Achilles tendon rupture. The present study is an
amendment/extension of that ongoing clinical trial.
An oral glucose tolerance test (OGTT) with frequent measurements of glucose, insulin,
C-peptide and plasma free fatty acids can provide detailed information on insulin
sensitivity, glucose tolerance, beta cell function, lipolysis and lipid oxidation as well as
metabolic clearance of insulin(11-13).
Modern DXA scanners exhibit high performance and sensitivity to distinguish small changes in
BMD. Also sensitive markers of changes in bone metabolism have recently been available. In
particular two bone mass turnover markers (BTM) have been suggested to monitor bone
resorption (CTX, carboxy-terminal cross-linked telopeptides of type 1 collagen) and bone
formation ( P1NP, procollagen type 1 amino-terminal propeptide(14), but also osteocalcin (OC)
is suggested as a marker of bone formation. DXA scanners have recently been validated to
measure visceral adiposity, which is strongly associated with insulin sensitivity(15). A DXA
scan exposes the individual to an X-ray radiation equal to only one day of background
radiation, which makes this scanning modality much less harmful in terms of radiation dose
compared to traditional CT scans (a 100-fold less radiation).
Traditional markers of low grade inflammation (LGI) include TNFa and IL6 and hsCRP. New
promising markers include suPAR in plasma and urine and urine orosomucoid. suPAR has shown to
predict CVD in non-diabetic community resting individuals(16). Urine orosomucoid is a strong
predictor of major events in T2D and might be an early marker of glucose metabolic
derangement(17). Low density lipoprotein (LDL) particles and especially those with a low
particle size are atherogenic(18). Thus increased levels of LGI markers and immune markers
including small LDL particles exhibit a particular at herogenic cocktail. A sedentary
lifestyle is associated with an increase in these markers of LGI, impaired immune response
and dyslipidaemia.
In the present setting we want to investigate the putative negative impact on glucose, lipid,
and bone metabolism during a period of restrain from exercise secondary to immobilization
following Achilles tendon rupture. We also want to study these patients during their physical
active rehabilitation (at week 8 - 52), to establish whether they succeed in improving the
metabolic impairments they suffered during the early post-injury period, during which period
strong limitations in physical activity is prescribed (week 0 - 8).
Perspective This study will establish whether the well-known effects on glucose, lipid and
bone metabolism of a sedentary lifestyle can be observed already following 8 weeks of almost
total abstain from physical activity in non-diabetic individuals, who suffered an acute
Achilles tendon rupture. Thereby, we will add knowledge to the previous findings following
strict bed-rest in healthy individuals on glucose and lipid metabolism and bone turnover. In
a clinical perspective it is important to examine the extent to which individuals deteriorate
in various metabolic pathways to better understand the pathophysiology behind these defects
both in healthy individuals and in patients, who undergo bed rest or an equal reduction in
physical activity as part of their rehabilitation.
Hypothesis Implementation of a sedentary lifestyle with almost no physical activity in
non-diabetic individuals undergoing non-operative treatment of acute Achilles tendon rupture
will during 8 weeks
- impair insulin sensitivity and glucose effectiveness
- decrease disposition index
- compensatory decrease in insulin clearance
- decrease lipid oxidation
- increase visceral adipose tissue
- increase number of low density lipoprotein particles and a decrease the particle size
- increase immune and low grade inflammatory response as measured in plasma and urine
- induce bone loss in hip as measured by BMD
- increase bone resorption and decrease bone formation as measured by selected bone
turnover markers.
During the following physical active rehabilitation from week 8 to week 52 the above proposed
negative impact upon glucose, lipid and bone metabolism is thought to reverse at least partly
so.
The relative positive effect on metabolic performance is hypothesized to be associated with
duration from immobilization to full mobilization, which will be monitored by use of
validated tools.
Study design Fifty non-diabetic individuals of age 18 to 70 years who should undergo
non-operative treatment of acute Achilles tendon rupture and who are included to the
randomized clinical trial: Non-operative Treatment of Acute Achilles Tendon Rupture: Early
Controlled Mobilization Compared With Immobilization, ClinicalTrials.gov Identifier:
NCT02015364 at the department of orthopaedics, Hvidovre Hospital are recruited as cases for
this study. That study examines the effect on functional outcome measures of early controlled
mobilization of the ankle from the beginning of week 3 following injury versus full
immobilization during the initial 8 weeks post injury. Both groups are allowed full
weight-bearing from the beginning of week 3 and physical activity level is expected to be the
same in the two groups. As such randomization regime is unlikely to influence metabolism.
The present study includes 50 cases, who are examined early following injury (< 2 weeks)
(baseline), 8 weeks (6 - 10 weeks) after injury and 52 weeks (40 - 64 weeks) after injury,
respectively.
Examinations Oral glucose tolerance test (OGTT) with ingestion of 75 g of glucose during a
maximum of 3 min from baseline (0 min). Plasma for glucose, insulin, C-peptide, NEFA will be
drawn at time -10, -5, -1, 10, 15, 20, 30, 45, 60, 75, 90, 105, 120, 150, 180, 240 min. This
test will be performed in the morning starting at approximately 8 am. The tests are done
after an overnight fast of at least 10 hours.
The individual will bring in morning spot urine for measurement of suPAR, creatinine, albumin
and orosomucoid.
Before the OGTT the individual will have drawn blood for measurement of HbA1c, total
cholesterol, LDL cholesterol, HDL cholesterol, triglyceride, Na, K, creatinine, HgB, CRP,
leukocytes, ALAT, alkaline phosphatase, Ca++, D vitamin, TSH, albumine and amylase. Also
blood for BTM and plasma suPAR, IL6, TNFa and hsCRP will be drawn. Finally blood for lipid
density profiling and lipid particle size will be drawn before the OGTT.
Body weight and height and waist and hip circumference will be measured. DXA of hip and
lumbar columna including abdominal visceral and subcutaneous fat is done on a Hologic
Discovery scanner by use of updated software. DXA will be carried out approximately at 12 am.
Acquisition of glucose and lipid metabolism will be done by use of the MinModel and the NEFA
MinModel as described (11;12) All blood and urine samples will be destroyed after analysis.
However a research biobank will be established since the period of time from most blood and
urine sampling until analysis exceeds 1 week. This study will store all urine and blood
samples in a freezer until all case subjects and controls have finished examinations. The
duration of this period will be maximum 2 years from last patient last visit. Thus the
research biobank will be established for storage only.
The urine and blood samples will be destroyed after analysis at Hvidovre and Glostrup
Hospitals. Analysis results will all be anonymous and some will be sent abroad to our
researcher Prof. Raymond Boston in USA, who will perform statistical calculations from
analysis data. Permission for establishment of a research biobank is obtained from the Danish
Data protection Agency.
Measurements of physical activity are acquired from the Primary Investigators ongoing trial
"Non-operative Treatment of Acute Achilles Tendon Rupture: Early Controlled Mobilization
Compared With Immobilization".
Statistics Ten days of bed rest in 13 healthy young individuals showed a 20% (P<0.05)
significant decrease in insulin sensitivity and a 50% (P<0.05) reduction in lipid
oxidation(2). Thirty-one days of bed rest in 8 healthy women was significantly associated
with bone loss in total hip (2.07%, P<0.001)(7).
The present study does not imply strict bed rest but exhibits a longer sedentary period of
following up compared to the above studies and include a larger number of participants, also.
During the initial 8 weeks of strictly sedentary immobilization following the injury of the
Achilles tendon we suggest that the patients will decrease their insulin sensitivity by at
least 20%, the estimate of SD of the endpoint is 20%. Thus, using the MIREDIF statistics
(Douglas Altman, Practical statistics for Medical research, Chapman & Hall, 1999), we can
calculate that a population of 22 patients will generate a power >90% at significance level
P<0.05 to investigate that primary endpoint. Similarly, the SD on lipidoxidation is 30% and
the estimate is that the change during the sedentary period is at least 30%, thus by n=22
patients the power will be > 90%. Finally the change in BMD is likely 1% and the SD is 1%,
thus n=22 patients will provide a statistical power of at least 90%. During the period of
physical restitution we estimate a fully reversion of the deficit in endpoints during the
sedentary period, i.e. similar calculation on power is valid during the restitution period.
The participants in the present study are included from the randomized clinical trial:
Non-operative Treatment of Acute Achilles Tendon Rupture: Early Controlled Mobilization
Compared with Immobilization. Randomization regime is unlikely to influence metabolism,
however, it will be considered as a variable in the statistical analyses of the endpoints.
Ethical issues The study adheres to the Danish Act on Processing of Personal Data and, Danish
Act on Health and the Helsinki II convention of clinical trials. All participants are
informed about the purpose of the study and all ethical issues and a written consent is
obtained before participation. At any given time, the participants can withdraw their
acceptant for participation in the study. Personal data concerning demographic relations such
as gender and age will be accessed as well to ensure the case subjects meet the inclusion
criteria and for statistically use. To make assessments on study participation, the principal
investigator will also gain access to relevant data from the patients medical files
concerning illnesses or conditions the case subject might report.
The amount of blood drawn during the 52 weeks of participation in the study is less than 500
ml, which is the standard amount of blood drawn at a single donation of blood from a blood
donor. The use of intravenous cannula can cause irritation or infection of vein or insertion
site. All procedures will be performed as described in SOP.
The X-ray radiation from DXA during the study period equals 3 days of background radiation in
Denmark and this amount of radiation is 30-fold less than that of a standard CT-scan of
abdomen. In other words the dose of radiation is so low that a calculation of risk is not
possible.
;
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