Microcirculation and Bone Metabolism in Patients With Type 2 Diabetes Mellitus and Charcot Foot - A Pilot Study

Bone Diseases, Metabolic Clinical Trial

Official title:

Bone Metabolism and Endothelial Function in Patients With Type 2 Diabetes Mellitus and Charcot Foot - an Observational Comparative Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02435329
• Other study ID #: Charcodiab13
• Secondary ID: 15/NI/0043
• Status: Completed
• Start date: June 2015
• Est. completion date: November 2016

Study information

• Verified date: September 2019
• Source: Tameside General Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

This study is part of a research project for a University MD Program. This is an observational study aimed at comparing the differences in bone metabolism and microcirculation in patients with type 2 diabetes mellitus (with and without diabetic neuropathy and Charcot foot) with healthy subjects.

Diabetes is gradually becoming a global epidemic along with its associated complications. Diabetes can affect several systems in our body particularly the eyes, nerves and the kidneys. The damaging effects occur at the level of the small blood vessels (microcirculation) that supply these vital structures. Normally, the inner lining of these blood vessels (endothelium) plays a very important role in maintaining adequate blood flow. The endothelium releases a chemical substance called nitric oxide, which relaxes these small blood vessels thereby ensuring sufficient blood supply to these key structures. Nitric oxide also prevents blockage of these vessels. Any form of metabolic stress like hyperglycaemia (raised blood sugar as seen in diabetes) can cause abnormal changes in the normal behaviour of the endothelium (endothelial dysfunction). Therefore hyperglycaemia promotes endothelial dysfunction by lowering nitric oxide levels, which may lead to diabetic complications like diabetic retinopathy (eye damage), nephropathy (kidney damage) or neuropathy (nerve damage).

In addition, patients with diabetes also suffer from osteoporosis (thinning of bones). Osteoporosis is a bone disorder characterised by a reduction in bone mineral content leading to an increased risk of developing fractures. The increased risk of fractures in patients with type 2 diabetes is attributed to poor bone quality resulting from the harmful effects of high blood glucose. Studies have also shown that nitric oxide has a bone protective effect as demonstrated by its ability to prevent bone fragmentation and improve bone strength.

Study of markers of endothelial function and bone metabolism will facilitate a better understanding about the origin of diabetic complications. This will aid in the development of novel therapeutic agents that target the harmful triggers in diabetes and eventually may prevent and retard the onset of the debilitating diabetic complications.

Description:

This is an observational study aimed at observing and comparing differences in bone metabolism and microcirculation in patients with type 2 diabetes and healthy controls.

In this study, 50 participants will be recruited and then categorised into the following groups:

1. Control group: 10 healthy volunteers (Hospital staff and spouses/ partners of patients will volunteer as healthy subjects)

2. Type 2 diabetic patients without neuropathy: 10

3. Type 2 diabetic patients with neuropathy:

• 10 patients with painless neuropathy

• 10 patients with painful neuropathy

4. Type 2 diabetic patients with unilateral Charcot foot: 10

Visit Schedule The estimated time for enrollment of patients will be within 3 months. The duration of the study is 5 months.

Screening (-2 Weeks): To assess for eligibility. This will include informed consent process, medical history and physical examination, screening for neuropathy and routine bloods. Laboratory work-up done at screening will be considered for data analysis.

Visit 1 - Baseline visit

• Anthropometric measures: Height, weight, BMI, waist circumference

• Vital parameters: supine and standing blood pressure, pulse, respiratory rate and temperature

• Laboratory assessment that includes markers of endothelial activation, inflammation and bone metabolism.

• Markers of endothelial activation will be investigated using systemic protein suspension array technology. For e.g. adhesion molecules like ICAM, VCAM and inflammatory molecules.

• Nitric oxide will be analysed using Griess assay

• Bone turnover markers [e.g., P1NP (Procollagen type 1 amino terminal propeptide), CTX (C-terminal cross-linked telopeptide of type-I collagen), Sclerostin, RANKL (receptor activator for nuclear factor (NF)-kB (RANK) ligand), OPG (osteoprotegerin), OPN (osteopontin), OCN (osteocalcin), BMP4 (Bone morphogenetic protein 4) and TGF-1β(Transforming growth factor-1β) - using ELISA (enzyme-linked immunosorbent assay).

• IL-6 - Interleukin-6, an inflammatory cytokine implicated in osteoporosis (using ELISA)

• Assessment of skin microcirculation with Laser Doppler Iontophoresis

• Assessment of calcaneal bone mineral density (BMD) with Bone Sonometer (ultrasound)

• Advanced glycation end-products will be assessed by an AGE reader which uses the technique of skin autofluorescence

Clinical Procedures

Assessment of the microcirculation with Laser Doppler Iontophoresis:

A standard measurement of microcirculation is laser Doppler iontophoresis, which is used by several research institutes. In this trial the skin microcirculation will be measured on the dorsum of the foot using a Perimed Laser Doppler imager and iontophoresis system.

Endothelial-mediated vasodilation will be measured by the iontophoresis of acetylcholine, while sodium nitroprusside will be used to measure endothelium-independent vasodilation. The iontophoresis system consists of an ION chamber (iontophoresis delivery vehicle device) that sticks firmly to the skin and a reference electrode. The response in blood flow will be imaged and quantified using the Perimed Laser Doppler Imager (PeriScan PIMII; Perimed, Sweden).

Analysis of AGE:

An AGE reader, which utilizes the principle of skin autofluorescence, will measure the accumulation of AGE in the skin. This validated device provides a real-time, non-invasive assessment of cardiovascular risk for chronic diseases like Diabetes, renal failure, cardiovascular disease, etc. AGE-modified proteins have autofluorescent properties and when excited by ultraviolet (UV) light they emit fluorescence in particular wavelengths. The levels of AGE in skin correlate with AGE levels in blood.

The volar aspect of the forearm will be placed on the AGE reader, which is equipped with a UV light source. The UV light triggers AGE in skin, after penetrating 1mm of the dermis, to emit autofluorescence that is then detected by the AGE reader. The intensity of fluorescence correlates with the quantity of AGE in the skin.

Assessment of calcaneal BMD:

This is a simple and convenient method to assess peripheral BMD and assess fracture risk. The device used is a quantitative ultrasound called Sahara Clinical Bone Sonometer (Sahara Clinical Bone Sonometer; Hologic, Waltham, MA). The calcaneus is the preferred peripheral site to assess fracture risk. This device uses ultrasound waves to determine the BMD of the calcaneus. In this procedure, once the bare heel is placed in the device, the BMD is calculated within 30 seconds and the results are then generated on paper by the device.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 31
• Est. completion date: November 2016
• Est. primary completion date: November 2016
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 40 Years to 75 Years

Eligibility

Inclusion Criteria:

• • Subjects aged between 40-75 years

• Healthy subjects or non-diabetic subjects for the control group.

• A diagnosis of type 2 DM based on one of the following criteria (ADA - 2010):

• Fasting plasma glucose (FPG) = 126 mg/dL (7.0 mmol/L) or

• 2-h plasma glucose = 200 mg/dl (11.1 mmol/L) during an OGTT or

• Classic symptoms of hyperglycaemia or hyperglycaemic crisis with a random plasma glucose = 200 mg/dL (11.1 mmol/L).

• Patients on treatment for type 2 diabetes mellitus

• Presence of diabetic neuropathy will be confirmed when 2 of the following neurological tests are positive on examination (vibration perception threshold, 10 gm. monofilament, 128 Hz tuning fork, ankle reflex, pin-prick)

• Painful diabetic neuropathy diagnosed according to LANSS (Leeds Assessment of Neuropathic Symptoms and Signs) scoring

• For patients with chronic Charcot foot, the diagnosis should be confirmed by clinical judgment and by radiologic examination - X-ray, technetium-labeled bisphosphonate bone scan or MRI)

Exclusion Criteria:

• • At screening, age below 40 years and above 75 years.

• Type 1 diabetes mellitus (patients with a history of ketoacidosis, age of onset of DM before 25 years of age, BMI <21 kg/m2 and use of insulin without a concomitant oral hypoglycemic agent)

• Major cardiovascular complications within 3 months prior to screening

• Recent history of smoking within the last 6 months

• Scars, tattoos or rashes over the forearm

• Recent or current oral steroid therapy or topical steroids applied to the forearm

• Patients with uncontrolled hypertension (systolic blood pressure [SBP] > 160/90 mmHg) or hypotension (SBP = 100 mm Hg or a diastolic BP of =60 mm Hg) at screening.

• History of general systemic illness including cardiac, hepatic or renal insufficiency

• Patients with renal insufficiency characterized by a creatinine clearance of less than 60 ml/min or a serum creatinine of more than 130 µmol/l

• Receiving treatment for inflammatory disease or malignancy

• Other non-diabetic causes of neuropathy

• History of chronic alcohol consumption

• History of metabolic bone disorders (Osteoporosis, Paget's disease, etc.) or treatment for bone disorders (past or current treatment for osteoporosis, bisphosphonate therapy within the last 3 years)

• History of malignancy

• History of active foot ulcers

• History of concomitant therapy that may interfere with bone metabolism e.g. glucocorticoids (within the last 3 months), hormone replacement therapy (in the last 12 months), SERM (selective oestrogen receptor modulator), thiazolidinedione, anticonvulsant use

• Receiving drugs that fluoresce (e.g., Doxorubicin, Daunomycin, Camptothecin, Protoporphyrin, Fluoroquinolones, Tetracycline, Hydroxychloroquine or Quinidine)

• History of photosensitivity reactions (e.g., sensitive to ultraviolet light, or taking medication known to cause photosensitivity

• Simultaneous participation in other clinical trials or involvement in another research trial involving an investigational product in the past 12 weeks.

Related Conditions & MeSH terms

• Bone Diseases
• Bone Diseases, Metabolic
• Diabetes Mellitus
• Diabetes Mellitus, Type 2
• Diabetic Angiopathies
• Metabolic Diseases

Intervention

Other:
• Baseline comparison of microcirculation and bone metabolism
Baseline comparison of microcirculation and bone metabolism among the 5 different groups

Locations

Country	Name	City	State
United Kingdom	Tameside Hospital NHS Foundation Trust	Ashton-under-Lyne	Greater Manchester

Sponsors (2)

Lead Sponsor	Collaborator
Tameside General Hospital	Manchester Metropolitan University

Country where clinical trial is conducted

United Kingdom, 

References & Publications (6)

Hofbauer LC, Brueck CC, Singh SK, Dobnig H. Osteoporosis in patients with diabetes mellitus. J Bone Miner Res. 2007 Sep;22(9):1317-28. Review. — View Citation

Mascarenhas JV, Jude EB. Pathogenesis and medical management of diabetic Charcot neuroarthropathy. Med Clin North Am. 2013 Sep;97(5):857-72. doi: 10.1016/j.mcna.2013.05.002. — View Citation

Pacher P, Beckman JS, Liaudet L. Nitric oxide and peroxynitrite in health and disease. Physiol Rev. 2007 Jan;87(1):315-424. Review. — View Citation

Roberts AC, Porter KE. Cellular and molecular mechanisms of endothelial dysfunction in diabetes. Diab Vasc Dis Res. 2013 Nov;10(6):472-82. doi: 10.1177/1479164113500680. Epub 2013 Sep 3. Review. — View Citation

Vestergaard P. Discrepancies in bone mineral density and fracture risk in patients with type 1 and type 2 diabetes--a meta-analysis. Osteoporos Int. 2007 Apr;18(4):427-44. Epub 2006 Oct 27. Review. — View Citation

Wimalawansa SJ. Nitric oxide: new evidence for novel therapeutic indications. Expert Opin Pharmacother. 2008 Aug;9(11):1935-54. doi: 10.1517/14656566.9.11.1935 . Review. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Impaired endothelial function in patients with type 2 DM with/ without diabetic neuropathy and Charcot foot compared to their healthy counterparts as measured by:	Endothelial-dependent and independent vasodilatations	At baseline
Primary	Impaired endothelial function in patients with type 2 DM with/ without diabetic neuropathy and Charcot foot compared to their healthy counterparts as measured by:	Markers of endothelial activation, which include adhesion molecules like ICAM, VCAM and inflammatory molecules.	at baseline
Primary	Impaired endothelial function in patients with type 2 DM with/ without diabetic neuropathy and Charcot foot compared to their healthy counterparts as measured by:	Serum Nitric oxide	at baseline
Primary	Impaired endothelial function in patients with type 2 DM with/ without diabetic neuropathy and Charcot foot compared to their healthy counterparts as measured by:	Advanced glycation end-products	at baseline
Secondary	Impaired bone metabolism in patients with type 2 DM with/ without diabetic neuropathy and Charcot foot compared to their healthy counterparts as assessed by:	Bone turnover markers like P1NP, CTX, Sclerostin, RANKL, OPG, OPN, OCN, BMP4 and TGF-1ß.	At baseline
Secondary	Impaired bone metabolism in patients with type 2 DM with/ without diabetic neuropathy and Charcot foot compared to their healthy counterparts as assessed by:	Calcaneal bone mineral density (BMD)	At baseline