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Long-Term Effects of a Novel Continuous Remote Care Intervention Including Nutritional Ketosis for the Management of Type 2 Diabetes: A 2-year Non-randomized Clinical Trial

Shaminie J. Athinarayanan, Rebecca N. Adams, Sarah J. Hallberg, Amy L. McKenzie, Nasir H. Bhanpuri, Wayne W. Campbell, Jeff S. Volek, Stephen D. Phinney, James P. McCarter
doi: https://doi.org/10.1101/476275
Shaminie J. Athinarayanan
1Virta Health, 501 Folsom Street, San Francisco, CA 94105, USA
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Rebecca N. Adams
1Virta Health, 501 Folsom Street, San Francisco, CA 94105, USA
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Sarah J. Hallberg
1Virta Health, 501 Folsom Street, San Francisco, CA 94105, USA
2Indiana University Health Arnett, Lafayette, IN, USA
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Amy L. McKenzie
1Virta Health, 501 Folsom Street, San Francisco, CA 94105, USA
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Nasir H. Bhanpuri
1Virta Health, 501 Folsom Street, San Francisco, CA 94105, USA
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Wayne W. Campbell
3Department of Nutrition Science, Purdue University, West Lafayette, IN, USA
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Jeff S. Volek
1Virta Health, 501 Folsom Street, San Francisco, CA 94105, USA
4Department of Human Sciences, The Ohio State University, Columbus, OH, USA
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Stephen D. Phinney
1Virta Health, 501 Folsom Street, San Francisco, CA 94105, USA
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James P. McCarter
1Virta Health, 501 Folsom Street, San Francisco, CA 94105, USA
5Department of Genetics, Washington University School of Medicine, St. Louis, MO, USA
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ABSTRACT

OBJECTIVE Studies on long-term sustainability of low-carbohydrate approaches to treat diabetes are limited. We aim to assess the effects of a continuous care intervention (CCI) on retention, glycemic control, weight, body composition, cardiovascular, liver, kidney, thyroid, inflammatory markers, diabetes medication usage and disease outcomes at 2 years in adults with type 2 diabetes (T2D).

RESEARCH DESIGN AND METHODS An open label, non-randomized, controlled study with 262 and 87 participants with T2D were enrolled in the CCI and usual care (UC) groups, respectively.

RESULTS Significant changes from baseline to 2 years in the CCI group included: HbA1c (−12% from 7.7±0.1%); fasting glucose (−18% from 163.67±3.90 mg/dL); fasting insulin (−42% from 27.73±1.26 pmol L-1); weight (−10% from 114.56±0.60 kg); systolic blood pressure (−4% from 131.7±0.9 mmHg); diastolic blood pressure (−4% from 81.8±0.5 mmHg); triglycerides (−22% from 197.2±9.1 mg/dL); HDL-C (+19% from 41.8±0.9 mg/dL), and liver alanine transaminase (−21% from 29.16±0.97 U/L). Spine bone mineral density in the CCI group was unchanged. Glycemic control medication use (excluding metformin) among CCI participants declined (from 56.9% to 26.8%, P=1.3×10-11) including prescribed insulin (−62%) and sulfonylureas (−100%). The UC group had no significant changes in these parameters (except uric acid and anion gap) or diabetes medication use. There was also significant resolution of diabetes (reversal, 53.5%; remission, 17.6%) in the CCI group but not in UC. All the reported improvements had p-values <0.00012.

CONCLUSIONS The CCI sustained long-term beneficial effects on multiple clinical markers of diabetes and cardiometabolic health at 2 years while utilizing less medication. The intervention was also effective in the resolution of diabetes and visceral obesity, with no adverse effect on bone health.

TRIAL REGISTRATION Clinicaltrials.gov NCT02519309

Author contributions

S.J.A, R.N.A, and J.P.M drafted the manuscript. S.J.A, R.N.A, A.L.M, N.H.B, and S.J.H participated in data acquisition and compiling. R.N.A and S.J.A analyzed the data. J.P.M, A.L.M, N.H.B, W.W.C, R.N.A, S.J.A, S.J.H, S.D.P and J.S.V edited the manuscript. All authors approved the final version of the manuscript.

Abbreviations
CCI
continuous care intervention;
UC
usual care;
T2D
type 2 diabetes;
HbA1c
hemoglobin A1c;
CVD
cardiovascular disease;
VLCD
very low calorie diet;
BMI
body mass index;
BHB
beta-hydroxybutryrate;
BMD
bone mineral density;
CAF
central abdominal fat;
A/G
android:gynoid ratio;
LELM
lower extremities lean mass;
HDL
high density lipoprotein;
LDL
low density lipoprotein;
ALT
alanine aminotransferase;
AST
aspartate aminotransferase;
ALP
alkaline phosphatase;
NAFLD
nonalcoholic fatty liver disease;
NLF
NAFLD liver fat score;
NFS
NAFLD fibrosis score;
TSH
thyroid stimulating hormone;
BUN
blood urea nitrogen;
eGFR
estimated glomerular filtration rate;
hsCRP
high sensitive C-reactive protein;
WBC
white blood cells;
HOMA-IR
Homeostatic Model Assessment of Insulin Resistance;
SGLT-2
sodium-glucose cotransporter-2 inhibitors;
DPP-4
dipeptidyl peptidase-4 inhibitors;
GLP-1
glucagon-like-peptide 1 receptor agonists;
FFM
fat-free mass;
VAT
visceral adipose tissue;
GLM
generalized linear model;
LMM
linear mixed-effect model;
ADA
American Diabetes Association;
CLIA
Clinical Laboratory Improvement Amendments;
IRB
Institutional Review Board;
DXA
dual-energy X-ray absorptiometry

Footnotes

  • DATA SHARING: The complete data and statistical codes are available upon reasonable request.

  • Conflicts of Interests: SJA, RNA, SJH, ALM, NHB, SDP and JPM are employed by Virta Health Corp and were offered stock options. SDP and JSV are founders of Virta Health Corp. WWC has no conflict of interest to declare.

  • Financial support: Virta Health Corp. is the study sponsor.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission.
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Posted December 06, 2018.
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Long-Term Effects of a Novel Continuous Remote Care Intervention Including Nutritional Ketosis for the Management of Type 2 Diabetes: A 2-year Non-randomized Clinical Trial
Shaminie J. Athinarayanan, Rebecca N. Adams, Sarah J. Hallberg, Amy L. McKenzie, Nasir H. Bhanpuri, Wayne W. Campbell, Jeff S. Volek, Stephen D. Phinney, James P. McCarter
bioRxiv 476275; doi: https://doi.org/10.1101/476275
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Long-Term Effects of a Novel Continuous Remote Care Intervention Including Nutritional Ketosis for the Management of Type 2 Diabetes: A 2-year Non-randomized Clinical Trial
Shaminie J. Athinarayanan, Rebecca N. Adams, Sarah J. Hallberg, Amy L. McKenzie, Nasir H. Bhanpuri, Wayne W. Campbell, Jeff S. Volek, Stephen D. Phinney, James P. McCarter
bioRxiv 476275; doi: https://doi.org/10.1101/476275

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