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Cut Down on Carbohydrate Usage in the Diet of Type 2 Diabetes. The Hypo-energetic Study (CutDM-Hypo)

Primary Purpose

Diabetes Mellitus, Type 2, Overweight and Obesity

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
CRHP Diet
CD Diet
Sponsored by
Bispebjerg Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus, Type 2 focused on measuring Weight Loss, Diet, Carbohydrate-Restricted, Diet, High-Protein, Insulin Resistance, Non-alcoholic Fatty Liver Disease, Metabolic Syndrome

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Type 2 diabetes with HbA1c between 48 mmol/mol and 97 mmol/mol with or without metformin and dipeptidyl peptidase-4 (DPP-4) inhibitors
  • Overweight or obesity with BMI ≥ 25 kg/m2 and desired weight loss
  • Non-smokers for > 1 year
  • Willingness to abstain from alcohol for 6 weeks
  • Hemoglobin > 7 mmol/L for men and > 6 mmol/L for women
  • Estimated glomerular filtration rate (eGFR) > 30 mL/min/1.73 m2

Exclusion Criteria:

  • Critical illness as evaluated by the principal investigator
  • Systemic corticosteroid treatment, e.g. prednisolone
  • Reported or journalized severe food allergy or intolerance
  • Reported or journalized severe gut disease e.g. Crohn's disease, Coeliac disease etc.
  • Reported or journalized alcohol dependence syndrome
  • Injectable diabetes medication, including insulin and GLP-1 analogues
  • Sulfonylureas (SUs) and sodium-glucose cotransporter 2 (SGLT-2) inhibitors, unless discontinuation is possible, in which case a 2-month wash-out is mandatory
  • Repeated fasting plasma glucose > 13.3 mmol/L
  • Urine albumin / creatinine ratio > 300 mg/g
  • Lactation, pregnancy or planning of pregnancy during the study
  • Inability, physically or mentally, to comply with the procedures required by the study protocol, as evaluated by the principal investigator
  • Presently participating in other clinical trials

Sites / Locations

  • Bispebjerg Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

CRHP Diet

CD Diet

Arm Description

Hypo-energetic carbohydrate-reduced high-protein (CRHP) dietary intervention with a controlled 5-7% loss in body weight.

Hypo-energetic conventional diabetes (CD) dietary intervention with a controlled 5-7% loss in body weight.

Outcomes

Primary Outcome Measures

Change in glycated hemoglobin (HbA1c) during 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
The change in HbA1c will be assessed during 6 weeks of fully provisioned hypo-energetic CRHP diet compared with hypo-energetic CD diet, while achieving concurrent body weight loss of 5-7 percent in both groups. Levels of HbA1c will be measured at baseline, week 2, 4, 5 and 6. HbA1c will be expressed in mmol/mol.

Secondary Outcome Measures

Change in hepatic fat content after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Hepatic fat content will be assessed by magnetic resonance spectroscopy (MRs) at baseline and week 6.
Change in fasting plasma triglycerides during 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Levels of triglycerides will be measured from fasting at baseline, week 2, 4, 5 and 6. Triglycerides will be expressed in mmol/L.

Full Information

First Posted
January 8, 2019
Last Updated
January 26, 2021
Sponsor
Bispebjerg Hospital
Collaborators
University of Copenhagen, University of Aarhus, The Danish Dairy Research Foundation, Denmark, Arla Foods
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1. Study Identification

Unique Protocol Identification Number
NCT03814694
Brief Title
Cut Down on Carbohydrate Usage in the Diet of Type 2 Diabetes. The Hypo-energetic Study
Acronym
CutDM-Hypo
Official Title
Cut Down on Carbohydrate Usage in the Diet of Type 2 Diabetes; Mechanisms of Effective Therapy of Diabetes by Selective Choice of Macronutrients. The Hypo-energetic Study.
Study Type
Interventional

2. Study Status

Record Verification Date
January 2021
Overall Recruitment Status
Completed
Study Start Date
January 29, 2019 (Actual)
Primary Completion Date
July 22, 2020 (Actual)
Study Completion Date
December 30, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Bispebjerg Hospital
Collaborators
University of Copenhagen, University of Aarhus, The Danish Dairy Research Foundation, Denmark, Arla Foods

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Scientific evidence for the dietary treatment of type 2 diabetes (T2D) is insufficient, which is why the investigators aim to reform dietary recommendation to the overweight or obese patient with type 2 diabetes. This clinical study will examine the effect of a highly controlled hypo-energetic carbohydrate-reduced high-protein (CRHP) diet intervention under caloric restriction-induced body weight loss as a treatment modality in T2D. The investigators hypothesize that this intervention compared to the conventional diabetes (CD) diet with similar loss in body weight improves metabolic control and cardiovascular risk profile in T2D by: Reducing diurnal and postprandial glycaemia, thereby facilitating a significant reduction in HbA1c Reducing ectopic lipid deposits in liver, muscle and pancreas Improving lipid profile towards a less atherogenic profile Improving metabolic actions of insulin, through increased sensitivity and β-cell function Reducing diurnal blood pressure with no adverse effect on heart rate variability
Detailed Description
The present study will be performed as a 6-week randomized fully controlled feeding study, which will address the effect of the hypo-energetic CRHP diet compared with the hypo-energetic CD diet with the macronutrient composition currently recommended to patients with T2D combined with a caloric restriction-induced 5-7% body weight loss on T2D. The study includes n=80 T2D patients. Measurements include fasting blood samples every 2 weeks during the 6 weeks of the study. Additionally, larger measurement programs will be undertaken at baseline and after 6 weeks, including MRi/s for liver, pancreas and muscle fat content and visceral and subcutaneous adipose tissue; DXA scans for body composition; oral glucose tolerance tests (OGTT); continuous glucose monitoring (CGM); diurnal blood pressure and holter recording. Questionnaires of health-related quality of life, level of physical activity and satiety by visual analogue scale will be performed at baseline and week 6 as well as fecal and diurnal urine sampling. To ensure a similar body weight loss between intervention groups as well as participants, aimed at 5-7%, caloric intake during the 6 weeks of the study will be hypo-energetic adjusted for each participant according to estimated daily total energy expenditure (TEE). A calculation requiring sex, age, weight and height will be performed to estimate resting energy expenditure (REE), which multiplied with the participant's physical activity level (PAL) will estimate TEE, and thus with an initial caloric deficit of 5% determine the caloric content in the hypo-energetic diet for each participant. Additionally, participants will be weighed twice a week and caloric content adjusted accordingly to ensure a controlled body weight loss. It is important to recognize that the CRHP diet and the CD diet principally do not differ in the quality of carbohydrate and protein. Thus, this study is unable to address a potential benefit of changes in quality of carbohydrate; however, both diet interventions exhibit a relatively low glycemic index of maximum 55. Until week 6 diets will be prepared and distributed from the research kitchen of the Department of Nutrition, Exercise and Sports, Faculty of Science, University of Copenhagen, Denmark, to optimize compliance and adherence to the prescribed diet. Following this period and again after approximately 3 months participants will be invited to group sessions with dietician guidance on how to sustain their body weight loss and continue with their assigned diet. A follow-up visit at week 30 will include a blood sample, a spot urine sample and body weight measurement.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 2, Overweight and Obesity
Keywords
Weight Loss, Diet, Carbohydrate-Restricted, Diet, High-Protein, Insulin Resistance, Non-alcoholic Fatty Liver Disease, Metabolic Syndrome

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
72 (Actual)

8. Arms, Groups, and Interventions

Arm Title
CRHP Diet
Arm Type
Experimental
Arm Description
Hypo-energetic carbohydrate-reduced high-protein (CRHP) dietary intervention with a controlled 5-7% loss in body weight.
Arm Title
CD Diet
Arm Type
Active Comparator
Arm Description
Hypo-energetic conventional diabetes (CD) dietary intervention with a controlled 5-7% loss in body weight.
Intervention Type
Dietary Supplement
Intervention Name(s)
CRHP Diet
Intervention Description
Dietary macronutrient composition of 30 E% from carbohydrate, 30 E% from protein and 40 E% from fat
Intervention Type
Dietary Supplement
Intervention Name(s)
CD Diet
Intervention Description
Dietary macronutrient composition of 50 E% from carbohydrate, 17 E% from protein and 33 E% from fat
Primary Outcome Measure Information:
Title
Change in glycated hemoglobin (HbA1c) during 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
The change in HbA1c will be assessed during 6 weeks of fully provisioned hypo-energetic CRHP diet compared with hypo-energetic CD diet, while achieving concurrent body weight loss of 5-7 percent in both groups. Levels of HbA1c will be measured at baseline, week 2, 4, 5 and 6. HbA1c will be expressed in mmol/mol.
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
Change in hepatic fat content after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
Hepatic fat content will be assessed by magnetic resonance spectroscopy (MRs) at baseline and week 6.
Time Frame
6 weeks
Title
Change in fasting plasma triglycerides during 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
Levels of triglycerides will be measured from fasting at baseline, week 2, 4, 5 and 6. Triglycerides will be expressed in mmol/L.
Time Frame
6 weeks
Other Pre-specified Outcome Measures:
Title
Change in fat content subcutaneously, viscerally and ectopically in pancreas and skeletal muscle after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
Subcutaneous, visceral and ectopic fat in pancreas and skeletal muscle will be assessed by magnetic resonance imaging/spectroscopy (MRi/s) at baseline and week 6.
Time Frame
6 weeks
Title
Change in lean body mass (LBM) after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
LBM will be assessed by dual-energy X-ray absorptiometry (DXA) at baseline and week 6. Changes will be expressed in kilograms (kg).
Time Frame
6 weeks
Title
Change in fat mass (FM) after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
FM will be assessed by dual-energy X-ray absorptiometry (DXA) at baseline and week 6. Changes will be expressed in kilograms (kg).
Time Frame
6 weeks
Title
Change in diurnal blood pressure (DBP) after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
DBP will be assessed over 24 hours by a blood pressure monitor (Ontrak 90227 from Spacelabs Healthcare) at baseline and week 6. DBP will be expressed in mmHg.
Time Frame
6 weeks
Title
Change in heart rate variability (HRV) after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
HRV will be assessed by 48-hour Holter-monitoring (Faros 360 from Bittium) at baseline and week 6.
Time Frame
6 weeks
Title
Change in diurnal glycemia after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
Glycemia will be assessed using 7-day continuous glucose monitoring (CGM) (FreeStyle Libre Pro from Abbott) at baseline and week 6.
Time Frame
6 weeks
Title
Change in glycemic variability after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
Glycemic variability will be assessed using 7-day continuous glucose monitoring (CGM) (FreeStyle Libre Pro from Abbott) at baseline and week 6.
Time Frame
6 weeks
Title
Change in insulin sensitivity after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
Insulin sensitivity will be assessed based on a 4-hour oral glucose tolerance test (OGTT) at baseline and week 6 and expressed by the Matsuda Index.
Time Frame
6 weeks
Title
Change in beta-cell function after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
Beta-cell function will be assessed based on a 4-hour oral glucose tolerance test (OGTT) at baseline and week 6 and expressed by the Insulinogenic Index and Disposition Index.
Time Frame
6 weeks
Title
Change in Homeostasis Model Assessment (HOMA) of insulin resistance and beta-cell function after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
HOMA will be performed at baseline and week 6 and expressed by HOMA-IR and HOMA-beta.
Time Frame
6 weeks
Title
Change in lipid profile after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
Lipid profile, including lipoproteins will be assessed from fasting at baseline and week 6.
Time Frame
6 weeks
Title
Change in glucose after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
Glucose will be measured during a 4-hour oral glucose tolerance test (OGTT) at baseline and week 6. Glucose will be expressed in mmol/L.
Time Frame
6 weeks
Title
Change in insulin after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
Insulin will be measured during a 4-hour oral glucose tolerance test (OGTT) at baseline and week 6. Insulin will be expressed in pmol/L.
Time Frame
6 weeks
Title
Change in C-peptide after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
C-peptide will be measured during a 4-hour oral glucose tolerance test (OGTT) at baseline and week 6. C-peptide will be expressed in pmol/L.
Time Frame
6 weeks
Title
Change in non-esterified fatty acids (NEFA) after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
NEFA metabolism will be assessed using the minimal model technique based on an oral glucose tolerance test (OGTT) at baseline and week 6. NEFA will be expressed in micromol/L.
Time Frame
6 weeks
Title
Change in triglycerides after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
Triglycerides will be measured during a 4-hour oral glucose tolerance test (OGTT) at baseline and week 6. Triglycerides will be expressed in mmol/L.
Time Frame
6 weeks
Title
Change in glucagon after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
Glucagon will be measured during a 4-hour oral glucose tolerance test (OGTT) at baseline and week 6. Glucagon will be expressed in pmol/L.
Time Frame
6 weeks
Title
Change in glucagon-like-peptide-1 (GLP-1) after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
GLP-1 will be measured during a 4-hour oral glucose tolerance test (OGTT) at baseline and week 6. GLP-1 will be expressed in pmol/L.
Time Frame
6 weeks
Title
Change in glucose-dependent insulinotropic polypeptide (GIP) after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
GIP will be measured during a 4-hour oral glucose tolerance test (OGTT) at baseline and week 6. GIP will be expressed in pmol/L.
Time Frame
6 weeks
Title
Change in peptide YY (PYY) after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
PYY will be measured during a 4-hour oral glucose tolerance test (OGTT) at baseline and week 6. PYY will be expressed in pmol/L.
Time Frame
6 weeks
Title
Change in ghrelin after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
Ghrelin will be measured during a 4-hour oral glucose tolerance test (OGTT) at baseline and week 6. Ghrelin will be expressed in pmol/L.
Time Frame
6 weeks
Title
Change in cholecystokinin (CCK) after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
CCK will be measured during a 4-hour oral glucose tolerance test (OGTT) at baseline and week 6. CCK will be expressed in pmol/L.
Time Frame
6 weeks
Title
Change in gastrin after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
Gastrin will be measured during a 4-hour oral glucose tolerance test (OGTT) at baseline and week 6. Gastrin will be expressed in pmol/L.
Time Frame
6 weeks
Title
Change in growth hormone (GH) after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
GH will be measured during a 4-hour oral glucose tolerance test (OGTT) at baseline and week 6. GH will be expressed in ng/mL.
Time Frame
6 weeks
Title
Change in insulin-like growth factor-1 (IGF-1) after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
IGF-1 will be measured from fasting at baseline and week 6. IGF-1 will be expressed in ng/mL.
Time Frame
6 weeks
Title
Change in insulin-like growth factor-binding protein 1 (IGFBP-1) after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
IGFBP-1 will be measured during a 4-hour oral glucose tolerance test (OGTT) at baseline and week 6. IGFBP-1 will be expressed in ng/mL.
Time Frame
6 weeks
Title
Change in leptin after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
Leptin will be measured from fasting at baseline and week 6. Leptin will be expressed in ng/mL.
Time Frame
6 weeks
Title
Change in adiponectin after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
Adiponectin will be measured from fasting at baseline and week 6. Adiponectin will be expressed in microg/mL.
Time Frame
6 weeks
Title
Change in tumor necrosis factor alpha (TNF-alpha) after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
TNF-alpha will be measured from fasting at baseline and week 6 and expressed in pg/mL.
Time Frame
6 weeks
Title
Change in interleukin-6 (IL-6) after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
IL-6 will be measured from fasting at baseline and week 6 and expressed in pg/mL.
Time Frame
6 weeks
Title
Change in high-sensitive C-reactive protein (hsCRP) after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
hsCRP will be measured from fasting at baseline and week 6 and expressed in mg/L.
Time Frame
6 weeks
Title
Change in renal function assessed from eGFR and diurnal excretion of albumin after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
eGFR and diurnal excretion of albumin will be assessed at baseline and week 6.
Time Frame
6 weeks
Title
Change in urinary excretion of urea and glucose after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
Urinary excretion of urea and glucose will be assessed at baseline and week 6.
Time Frame
6 weeks
Title
Change in urinary oxidative DNA and RNA modifications after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
Urinary oxidative DNA and RNA modifications will be assessed at baseline and week 6.
Time Frame
6 weeks
Title
Change in subjective satiety after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
Subjective satiety will be assessed by a self-reported visual analog scale (VAS) questionnaire with four questions regarding experienced satiety (range 0-100 mm) integrated into one composite satiety score at baseline and week 6.
Time Frame
6 weeks
Title
Change in health-related quality of life (HRQoL) after 6 weeks of hypo-energetic CRHP diet compared with hypo-energetic CD diet.
Description
HRQoL will be assessed using a self-reported 36-item Short-Form (SF-36) health survey with 36 questions regarding different domains of HRQoL (each scoring from 0-100 points) at baseline and week 6. HRQoL will be reported as composite scores; a physical and mental component summary (PCS/MCS) score.
Time Frame
6 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Type 2 diabetes with HbA1c between 48 mmol/mol and 97 mmol/mol with or without metformin and dipeptidyl peptidase-4 (DPP-4) inhibitors Overweight or obesity with BMI ≥ 25 kg/m2 and desired weight loss Non-smokers for > 1 year Willingness to abstain from alcohol for 6 weeks Hemoglobin > 7 mmol/L for men and > 6 mmol/L for women Estimated glomerular filtration rate (eGFR) > 30 mL/min/1.73 m2 Exclusion Criteria: Critical illness as evaluated by the principal investigator Systemic corticosteroid treatment, e.g. prednisolone Reported or journalized severe food allergy or intolerance Reported or journalized severe gut disease e.g. Crohn's disease, Coeliac disease etc. Reported or journalized alcohol dependence syndrome Injectable diabetes medication, including insulin and GLP-1 analogues Sulfonylureas (SUs) and sodium-glucose cotransporter 2 (SGLT-2) inhibitors, unless discontinuation is possible, in which case a 2-month wash-out is mandatory Repeated fasting plasma glucose > 13.3 mmol/L Urine albumin / creatinine ratio > 300 mg/g Lactation, pregnancy or planning of pregnancy during the study Inability, physically or mentally, to comply with the procedures required by the study protocol, as evaluated by the principal investigator Presently participating in other clinical trials
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Steen B Haugaard, Professor
Organizational Affiliation
Dept. of Endocrinology, Copenhagen University Hospital Bispebjerg
Official's Role
Principal Investigator
Facility Information:
Facility Name
Bispebjerg Hospital
City
Copenhagen
State/Province
Copenhagen NV
ZIP/Postal Code
2400
Country
Denmark

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Individual participant data (IPD) may be shared by request to the corresponding author in accordance with the Danish Data Protection Agency.
Citations:
PubMed Identifier
35679680
Citation
Jensen NJ, Wodschow HZ, Skytte MJ, Samkani A, Astrup A, Frystyk J, Hartmann B, Holst JJ, Larsen TM, Madsbad S, Magkos F, Miskowiak KW, Haugaard SB, Krarup T, Rungby J, Thomsen MN. Weight-loss induced by carbohydrate restriction does not negatively affect health-related quality of life and cognition in people with type 2 diabetes: A randomised controlled trial. Clin Nutr. 2022 Jul;41(7):1605-1612. doi: 10.1016/j.clnu.2022.05.005. Epub 2022 May 18.
Results Reference
derived
PubMed Identifier
34993571
Citation
Thomsen MN, Skytte MJ, Samkani A, Carl MH, Weber P, Astrup A, Chabanova E, Fenger M, Frystyk J, Hartmann B, Holst JJ, Larsen TM, Madsbad S, Magkos F, Thomsen HS, Haugaard SB, Krarup T. Dietary carbohydrate restriction augments weight loss-induced improvements in glycaemic control and liver fat in individuals with type 2 diabetes: a randomised controlled trial. Diabetologia. 2022 Mar;65(3):506-517. doi: 10.1007/s00125-021-05628-8. Epub 2022 Jan 7.
Results Reference
derived

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Cut Down on Carbohydrate Usage in the Diet of Type 2 Diabetes. The Hypo-energetic Study

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