Type2 Diabetes
Conditions
Brief summary
Type 2 diabetes mellitus (T2DM) is a metabolic condition characterized by chronic hyperglycemia and progressive insulin resistance, which progressively lead to macro- and microvascular damage and subsequent impairments in blood pressure (BP) control. Therapeutic approaches to manage T2DM focus on improving glycaemic control and BP and include pharmaceutical treatments (e.g. Metformin and insulin), physical activity and exercise, and calorie restriction. However, pharmaceutical interventions can be expensive and are associated with low adherence. Although exercise and diet programs have been shown to be effective, like pharmaceutical interventions, they often have poor adherence in people with T2DM. With the number of people with T2DM (464 million) continuing to rise and expected to reach 700 million by 2045, the costs associated with the clinical management of this condition are likely to become unsustainable. There is, therefore, a need to explore the potential of alternative interventions. In particular, interventions which may be cheaper than clinical management and have better adherence than exercise, and hypoglycemic agents, to improve glycemic control and deleterious cardiovascular manifestations of this condition. Passive heating may be one such intervention with therapeutic potential.
Detailed description
Current estimates suggest 422 million people worldwide live with a form of diabetes, of which \ 90% have type 2 diabetes mellitus (T2DM). The total direct and indirect cost of care for individuals with diabetes in the UK is £23.7 billion, equating to \ 20% of the annual NHS budget, this figure is expected to rise to \ £39.8 billion by the year 2035. Approximately 85-90% of cases of T2DM arise from a poor lifestyle and obesity, with the remaining 10-15% resulting from genetic predispositions. Current interventions include pharmaceutical treatments, exercise and calorie restrictive diets, which aim to improve glycaemic control. However, pharmaceutical interventions carry a high financial cost, while exercise and diet programmes have a low adherence rate in individuals with T2DM. With the prevalence of T2DM continuing to increase, the costs associated with the clinical care of these individuals are likely to become unsustainable. Simple, inexpensive interventions to improve the clinical profile of this group are therefore needed. One emerging potential therapy to improve glucose homoeostasis is passive heating. Preliminary evidence suggests passive heating may have beneficial effects for metabolic health in animal models and in humans. In 1999, the use of hot tubs (38-41°C , 30 mins / day for 3 weeks) was shown to reduce fasting plasma glucose concentrations by \ 14% (1.3 mmol.L-1) and decrease HbA1c by \ 10-11 mmol/mol in 8 individuals with T2DM. Given the rate of turnover in haemoglobin this reduction is surprising as the treatment period was run over 3 weeks and the total haemoglobin turnover takes \ 115 days. While more recent work has been conducted into the effects of a single bout of passive heating in healthy adults and individuals with T2DM (including ourselves, under review), none have been done on chronic heating since Hooper. Hooper postulated that an increase in skeletal muscle blood flow may be responsible for this increased glucose clearance, citing evidence that this can modulate insulin mediated glucose uptake. Other mechanisms have also been purported, but have yet to be elucidated, including; increased insulin sensitivity, altered inflammatory response, activation of heat shock proteins (HSP), altered gut microbiome and butyrate. Repeated passive heating results in transient increases in deep body temperature and may improve glucose homeostasis via similar mechanisms to exercise. Regular aerobic exercise also improves macro- and microvascular function, muscle oxygenation, autonomic function, cardiorespiratory fitness, lung function and delays age related muscle loss. Acute exercise studies show that insulin sensitivity after 1h of moderate exercise does not change, however, insulin sensitivity appears to be improved following bouts longer than an hour or performed at greater intensity. Increases in insulin sensitivity have a curvilinear relationship with energy expenditure and could also be due to greater HSP expression. However, it is unrealistic for people with T2DM to perform this level of activity. Passive heating may be one supplemental exercise mimetic to augment improvements in insulin sensitivity, cardiorespiratory fitness and muscle strength, and function. The investigators recently provided evidence that acute passive heating in poeple with T2DM (currently under review for publication) is well tolerated and increases extracellualr \[HSP70\], and energy expenditure, and reduce diabstolic blood pressure. There is a growing body of evdience that suggests passive heating may improve many facets of human physiology, however, the mechanisms that underpin these benefits have yet to be established and future research needs to explore these further.
Interventions
8-12 x1 h water immersion (to the clavicle, @40 °C, rectal temperature \ 38.5 °C and \<39 °C) sessions over a period of 14 days.
Sponsors
Study design
Intervention model description
We plan to run a within-subject, pre-, post-intervention study
Eligibility
Inclusion criteria
* Male or female (post-menopausal) aged 35 years or above. * Diagnosed with T2DM as defined by the WHO (≥48 mmol/mol). * Participant is willing and able to give informed consent for participation in the study. * Participant is able to understand and fully cooperate with the study protocol.
Exclusion criteria
Severe peripheral neuropathy (to the point to which they cannot sense temperature) * Uncontrolled hypertension (≥180 systolic / 100 diastolic mmHg) * Taking any medication which may interfere with data interpretation or safety * Who have had a myocardial infarction or cerebro-vascular event * Any cardiac abnormalities which restrict hard exercise * Current smokers or who have stopped within 3 months * Participant is unable to understand and/or fully cooperate with the study protocol * Any other serious medical condition which would interfere with data interpretation or safety will be excluded from participation. * Skin ulcerations * Eczema * Pre-existing postural hypertension * Existing cardiac diseases (identified during screening)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Insulin Sensitivity | Change from pre (day 1) - post 8-12 days of 1 hour of passive heating | Does chronic passive heating improve insulin sensitivity? Calculated using the QUICKI for fasting and Gutt for post-prandial, with glucose and insulin concentrations. A higher value means they have better insulin sensitivity. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Plasma eHSP70 Concentration | pre - post following 8-12 days of 1 hour of passive heating | Does chronic passive heating increase plasma \[eHSP70\]? |
| Plasma IL-6 Concentration | pre - post following 8-12 days of 1 hour of passive heating | Does chronic passive heating reduce plasma \[IL-6\]? |
| Plasma IL-10 Concentration | pre - post following 8-12 days of 1 hour of passive heating | Does chronic passive heating increase plasma \[IL-10\]? |
| Resting Metabolic Rate | pre - post following 8-12 days of 1 hour of passive heating | Does chronic passive heating reduce plasma resting metabolic rate? |
| Flow Mediated Dilation | pre - post following 8-12 days of 1 hour of passive heating | Does chronic passive heating improve macrovascular function? Measured via ultrasound |
| Cutaneous Vascular Conductance | pre - post following 8-12 days of 1 hour of passive heating | Does chronic passive heating improve microvascular function? Assessed via iontophoresis or the forearm with ACh and Insulin, Area under the curve is the unit. (CVC = skin flux/MAP; flux/mmHg-1) |
| Resting Heart Rate | pre - post following 8-12 days of 1 hour of passive heating | Does chronic passive heating reduce resting heart rate? |
| Plasma Glucose Concentration | pre - post following 8-12 days of 1 hour of passive heating | Does chronic passive heating reduce plasma \[glucose\]? |
| NOX | Pre- v post 8-12 1 h hot water immersions | Nitrates + nitrites |
| Cardiac Output Index | pre - post following 8-12 days of 1 hour of passive heating | Does chronic passive heating increase cardiac output? Measured noninvasively via thoracic impedance. L/min/m2 is the unit. |
| TNF-alpha | Pre- v post 8-12 1 h hot water immersions | TNF-alpha |
| Butyric Acid | Pre- v post 8-12 1 h hot water immersions | Butyric acid |
| SBP | Pre- v post 8-12 1 h hot water immersions | Systolic blood pressure |
| DBP | Pre- v post 8-12 1 h hot water immersions | Diastolic blood pressure |
| MAP | Pre- v post 8-12 1 h hot water immersions | Mean arterial pressure |
| Stroke Volume Index | pre - post following 8-12 days of 1 hour of passive heating | Does chronic passive heating increase stroke volume? Measured noninvasively via thoracic impedance |
Countries
United Kingdom
Participant flow
Pre-assignment details
Pre-post design, not an RCT. Therefore no assignment details.
Participants by arm
| Arm | Count |
|---|---|
| Passive Heating 8-12 x1 h water immersion (to the clavicle, @40 °C, rectal temperature \
38.5 °C and \<39 °C) sessions over a period of 14 days.
Passive heating: 8-12 x1 h water immersion (to the clavicle, @40 °C, rectal temperature \
38.5 °C and \<39 °C) sessions over a period of 14 days. | 14 |
| Total | 14 |
Withdrawals & dropouts
| Period | Reason | FG000 |
|---|---|---|
| Overall Study | Withdrawal by Subject | 3 |
Baseline characteristics
| Characteristic | Passive Heating | — |
|---|---|---|
| Age, Continuous | 65 years STANDARD_DEVIATION 8 | — |
| BMI | 30 kg/m2 STANDARD_DEVIATION 5.2 | — |
| DBP | 81 mmHg STANDARD_DEVIATION 11 | — |
| HbA1c | 66 mmol/mol STANDARD_DEVIATION 27 | — |
| Height | 1.68 meters STANDARD_DEVIATION 0.1 | — |
| History of microvascular disease | 21 % of cohort | — |
| Mass | 85 kg STANDARD_DEVIATION 19 | — |
| Race and Ethnicity Not Collected | — | — Participants |
| Region of Enrollment United Kingdom | 14 Participants | — |
| SBP | 136 mmHg STANDARD_DEVIATION 19 | — |
| Sex: Female, Male Female | 6 Participants | — |
| Sex: Female, Male Male | 8 Participants | — |
| T2DM duration | 10 years STANDARD_DEVIATION 8 | — |
Adverse events
| Event type | EG000 affected / at risk |
|---|---|
| deaths Total, all-cause mortality | 0 / 14 |
| other Total, other adverse events | 0 / 14 |
| serious Total, serious adverse events | 0 / 14 |
Outcome results
Insulin Sensitivity
Does chronic passive heating improve insulin sensitivity? Calculated using the QUICKI for fasting and Gutt for post-prandial, with glucose and insulin concentrations. A higher value means they have better insulin sensitivity.
Time frame: Change from pre (day 1) - post 8-12 days of 1 hour of passive heating
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Passive Heating | Insulin Sensitivity | Fasting - pre | 0.31 AU | Standard Deviation 0.03 |
| Passive Heating | Insulin Sensitivity | Fasting - post | 0.33 AU | Standard Deviation 0.04 |
| Passive Heating | Insulin Sensitivity | Post-prandial - pre | 0.10 AU | Standard Deviation 0.04 |
| Passive Heating | Insulin Sensitivity | Post-prandial - post | 0.10 AU | Standard Deviation 0.05 |
Butyric Acid
Butyric acid
Time frame: Pre- v post 8-12 1 h hot water immersions
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Passive Heating | Butyric Acid | Pre | 285 pg/mL | Standard Deviation 294 |
| Passive Heating | Butyric Acid | Post | 405 pg/mL | Standard Deviation 458 |
Cardiac Output Index
Does chronic passive heating increase cardiac output? Measured noninvasively via thoracic impedance. L/min/m2 is the unit.
Time frame: pre - post following 8-12 days of 1 hour of passive heating
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Passive Heating | Cardiac Output Index | Pre | 3.57 L/min/m2 | Standard Deviation 0.74 |
| Passive Heating | Cardiac Output Index | Post | 3.05 L/min/m2 | Standard Deviation 0.54 |
Cutaneous Vascular Conductance
Does chronic passive heating improve microvascular function? Assessed via iontophoresis or the forearm with ACh and Insulin, Area under the curve is the unit. (CVC = skin flux/MAP; flux/mmHg-1)
Time frame: pre - post following 8-12 days of 1 hour of passive heating
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Passive Heating | Cutaneous Vascular Conductance | Insulin AUC - pre | 1.11 flux/mmHg | Standard Deviation 2.1 |
| Passive Heating | Cutaneous Vascular Conductance | Insulin AUC - post | 0.81 flux/mmHg | Standard Deviation 0.99 |
| Passive Heating | Cutaneous Vascular Conductance | ACh AUC - pre | 1.52 flux/mmHg | Standard Deviation 1.6 |
| Passive Heating | Cutaneous Vascular Conductance | ACh AUC - post | 2.06 flux/mmHg | Standard Deviation 2.77 |
DBP
Diastolic blood pressure
Time frame: Pre- v post 8-12 1 h hot water immersions
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Passive Heating | DBP | Pre | 81 mmHg | Standard Deviation 11 |
| Passive Heating | DBP | Post | 80 mmHg | Standard Deviation 10 |
Flow Mediated Dilation
Does chronic passive heating improve macrovascular function? Measured via ultrasound
Time frame: pre - post following 8-12 days of 1 hour of passive heating
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Passive Heating | Flow Mediated Dilation | Pre | 2.88 % increase from baseline diameter | Standard Deviation 1.81 |
| Passive Heating | Flow Mediated Dilation | Post | 2.45 % increase from baseline diameter | Standard Deviation 1.56 |
MAP
Mean arterial pressure
Time frame: Pre- v post 8-12 1 h hot water immersions
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Passive Heating | MAP | Pre | 99 mmHg | Standard Deviation 11 |
| Passive Heating | MAP | Post | 95 mmHg | Standard Deviation 11 |
NOX
Nitrates + nitrites
Time frame: Pre- v post 8-12 1 h hot water immersions
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Passive Heating | NOX | Pre | 74.5 micromolar | Standard Deviation 23.7 |
| Passive Heating | NOX | Post | 67.3 micromolar | Standard Deviation 22 |
Plasma eHSP70 Concentration
Does chronic passive heating increase plasma \[eHSP70\]?
Time frame: pre - post following 8-12 days of 1 hour of passive heating
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Passive Heating | Plasma eHSP70 Concentration | Pre | 2435 pg/mL | Standard Deviation 984 |
| Passive Heating | Plasma eHSP70 Concentration | Post | 2524 pg/mL | Standard Deviation 790 |
Plasma Glucose Concentration
Does chronic passive heating reduce plasma \[glucose\]?
Time frame: pre - post following 8-12 days of 1 hour of passive heating
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Passive Heating | Plasma Glucose Concentration | Fasting - pre | 10.06 mmol/L | Standard Deviation 4.51 |
| Passive Heating | Plasma Glucose Concentration | Fasting - post | 9.95 mmol/L | Standard Deviation 4.58 |
| Passive Heating | Plasma Glucose Concentration | Post-prandial - pre | 17.34 mmol/L | Standard Deviation 7.34 |
| Passive Heating | Plasma Glucose Concentration | Post-prandial - post | 16.84 mmol/L | Standard Deviation 6.49 |
Plasma IL-10 Concentration
Does chronic passive heating increase plasma \[IL-10\]?
Time frame: pre - post following 8-12 days of 1 hour of passive heating
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Passive Heating | Plasma IL-10 Concentration | Pre | 13.55 pg/mL | Standard Deviation 35.88 |
| Passive Heating | Plasma IL-10 Concentration | Post | 12.50 pg/mL | Standard Deviation 31.47 |
Plasma IL-6 Concentration
Does chronic passive heating reduce plasma \[IL-6\]?
Time frame: pre - post following 8-12 days of 1 hour of passive heating
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Passive Heating | Plasma IL-6 Concentration | Pre | 5.60 pg/mL | Standard Deviation 10.46 |
| Passive Heating | Plasma IL-6 Concentration | Post | 5.46 pg/mL | Standard Deviation 8.47 |
Resting Heart Rate
Does chronic passive heating reduce resting heart rate?
Time frame: pre - post following 8-12 days of 1 hour of passive heating
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Passive Heating | Resting Heart Rate | Pre | 67 beats/min | Standard Deviation 12 |
| Passive Heating | Resting Heart Rate | Post | 64 beats/min | Standard Deviation 11 |
Resting Metabolic Rate
Does chronic passive heating reduce plasma resting metabolic rate?
Time frame: pre - post following 8-12 days of 1 hour of passive heating
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Passive Heating | Resting Metabolic Rate | Pre | 1987 kcal/day | Standard Deviation 512 |
| Passive Heating | Resting Metabolic Rate | Post | 1855 kcal/day | Standard Deviation 380 |
SBP
Systolic blood pressure
Time frame: Pre- v post 8-12 1 h hot water immersions
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Passive Heating | SBP | Post | 127 mmHg | Standard Deviation 15 |
| Passive Heating | SBP | Pre | 136 mmHg | Standard Deviation 19 |
Stroke Volume Index
Does chronic passive heating increase stroke volume? Measured noninvasively via thoracic impedance
Time frame: pre - post following 8-12 days of 1 hour of passive heating
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Passive Heating | Stroke Volume Index | Pre | 54.6 mL/m2 | Standard Deviation 13.3 |
| Passive Heating | Stroke Volume Index | Post | 49.4 mL/m2 | Standard Deviation 11.3 |
TNF-alpha
TNF-alpha
Time frame: Pre- v post 8-12 1 h hot water immersions
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Passive Heating | TNF-alpha | Pre | 10.51 pg/mL | Standard Deviation 18.65 |
| Passive Heating | TNF-alpha | Post | 10.15 pg/mL | Standard Deviation 18.14 |