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Meditations on First Philosophy, in The Philosophical Writings of René Descartes,
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Mind and body: how the health of the body impacts on neuropsychiatric
Thibault Renoir, Kyoko Hasebe, and Laura GrayFront Pharmacol (2013). 2013; 4: 158. . doi: 10.3389/fphar.2013.00158
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Connecting the Mind–Body Split: Understanding the Relationship between Symptoms and Emotional Well-Being in Chronic Pain and Functional Gastrointestinal Disorders
Line Caes, Alex Orchard, and Deborah Christie
Healthcare (Basel). 2017 Dec; 5(4): 93. doi: 10.3390/healthcare5040093
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Along roads less traveled: complementary, alternative, and integrative treatments.
Muskin P. R., Gerbarg P. L., Brown R. P.
The Psychiatric Clinics of North America. 2013;36(1):13–15. doi: 10.1016/j.psc.2013.01.009.

Mindfulness meditation training alters cortical representations of interoceptive attention.
Farb N. A. S., Segal Z. V., Anderson A. K.
Social Cognitive and Affective Neuroscience. 2013;8(1):15–26. doi: 10.1093/scan/nss066

The polyvagal theory: new insights into adaptive reactions of the autonomic nervous system.
Porges S. W.
Cleveland Clinic Journal of Medicine. 2009;76(supplement 2):S86–S90. doi: 10.3949/ccjm.76.s2.17.

Heart rate variability, prefrontal neural function, and cognitive performance: the neurovisceral integration perspective on self-regulation, adaptation, and health.
Thayer J. F., Hansen A. L., Saus-Rose E., Johnsen B. H.
Annals of Behavioral Medicine. 2009;37(2):141–153. doi: 10.1007/s12160-009-9101-z.

Potential self-regulatory mechanisms of yoga for psychological health.
Gard T., Noggle J. J., Park C. L., Vago D. R., Wilson A.
Frontiers in Human Neuroscience. 2014;8(article 770) doi: 10.3389/fnhum.2014.00770

Breathing practices for treatment of psychiatric and stress-related medical conditions.
Brown R. P., Gerbarg P. L., Muench F.
The Psychiatric Clinics of North America. 2013;36(1):121–140. doi: 10.1016/j.psc.2013.01.001

Effects of yoga on the autonomic nervous system, gamma-aminobutyric-acid, and allostasis in epilepsy, depression, and post-traumatic stress disorder.
Streeter C. C., Gerbarg P. L., Saper R. B., Ciraulo D. A., Brown R. P.
Medical Hypotheses. 2012;78(5):571–579. doi: 10.1016/j.mehy.2012.01.021.

Physiological Effects of Mind and Body Practices
Shirley Telles,  Patricia Gerbarg, and Elisa H. Kozasa
Biomed Res Int. 2015; 2015: 983086. doi: 10.1155/2015/983086
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The mind-body relationship in psychotherapy: grounded cognition as an explanatory framework
Nuwan D. Leitan and Greg Murray
Front Psychol. 2014; 5: 472. doi: 10.3389/fpsyg.2014.00472
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Responding to mental health’s mind-body problem.
Thomas N.
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Physiological implications of the immune-neuro-endocrine network.
Besedovsky HO, del Rey A. Ader R, Felten DL, Cohen N,
Psychoneuroimmunology (1991). 2nd ed. New York: Academic Press; pp. 589–608.

How Mind-Body Practice Works—Integration or Separation?
Yi-Yuan Tang, Changhao Jiang, and Rongxiang Tang
Front Psychol. 2017; 8: 866. doi: 10.3389/fpsyg.2017.00866
PMID: 28603513

Mindfulness-Based Movement: A Polyvagal Perspective
Alexander R. Lucas, Heidi D. Klepin, Stephen W. Porges, W. Jack Rejeski
Integr Cancer Ther. 2018 Mar; 17(1): 5–15. doi: 10.1177/1534735416682087
PMCID: PMC5482784

Top-Down and Bottom-Up Mechanisms in Mind-Body Medicine: Development of an Integrative Framework for Psychophysiological Research
Ann Gill Taylor, Lisa E. Goehler, Daniel I. Galper, Kim E. Innes, Cheryl Bourguignon
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Gut/brain axis and the microbiota
EA Mayer, K Tillisch, A Gupta – The Journal of clinical …, 2015 – Am Soc Clin Investig … PDF Advertisement. Review Series Free access | 10.1172/JCI76304. Gut/brain axis and the microbiota …

The gut-brain axis: interactions between enteric microbiota, central and enteric nervous systems
M Carabotti, A Scirocco, MA Maselli… – … : quarterly publication of …, 2015 – ncbi.nlm.nih.gov
The gut–brain axis (GBA) consists of bidirectional communication between the central and  the enteric nervous system, linking emotional and cognitive centers of the brain with peripheral intestinal functions. Recent advances in research have described the importance …

The microbiome‐gut‐brain axis: from bowel to behavior
JF Cryan, SM O’mahony – Neurogastroenterology & Motility, 2011 – Wiley Online Library The ability of gut microbiota to communicate with the brain and thus modulate behavior is emerging as an exciting concept in health and disease. The enteric microbiota interacts with the host to form essential relationships that govern homeostasis. Despite the unique enteric …

Neuropeptides and the microbiota-gut-brain axis
P Holzer, A Farzi – Microbial endocrinology: The microbiota-gut–brain axis …, 2014 – Springer Neuropeptides are important mediators both within the nervous system and between neurons and other cell types. Neuropeptides such as substance P, calcitonin gene-related peptide and neuropeptide Y (NPY), vasoactive intestinal polypeptide, somatostatin and …

Microbial genes, brain & behaviour–epigenetic regulation of the gut–brain axis
RM Stilling, TG Dinan, JF Cryan – Genes, Brain and Behavior, 2014 – Wiley Online Library To date, there is rapidly increasing evidence for host–microbe interaction at virtually all  levels of complexity, ranging from direct cell‐to‐cell communication to extensive systemic  signalling, and involving various organs and organ systems, including the central nervous …

Microbes and the gut‐brain axis
P Bercik, SM Collins, EF Verdu – Neurogastroenterology & …, 2012 – Wiley Online Library Background The ‘gut‐brain‘or ‘brain‐gut axis‘, depending on whether we emphasize bottom‐ up or top‐bottom pathways, is a bi‐directional communication system, comprised of neural  pathways, such as the enteric nervous system (ENS), vagus, sympathetic and spinal nerves …

The microbiome-gut-brain axis during early life regulates the hippocampal serotonergic system in a sex-dependent manner
G Clarke, S Grenham, P Scully, P Fitzgerald… – Molecular …, 2013 – nature.comBacterial colonisation of the intestine has a major role in the post-natal development and maturation of the immune and endocrine systems. These processes are key factors underpinning central nervous system (CNS) signalling. Regulation of the microbiome–gut …

Neuropeptide Y, peptide YY and pancreatic polypeptide in the gut–brain axis
P Holzer, F Reichmann, A Farzi – Neuropeptides, 2012 – Elsevier
The gut–brain axis refers to the bidirectional communication between the gut and the brain. Four information carriers (vagal and spinal afferent neurons, immune mediators such as cytokines, gut hormones and gut microbiota-derived signalling molecules) transmit …

Stress & the gut-brain axis: regulation by the microbiome
JA Foster, L Rinaman, JF Cryan – Neurobiology of stress, 2017 – Elsevier
The importance of the gut–brain axis in regulating stress-related responses has long been appreciated. More recently, the microbiota has emerged as a key player in the control of this axis, especially during conditions of stress provoked by real or perceived homeostatic …

Ingestion of Lactobacillus strain regulates emotional behavior and central GABA receptor expression in a mouse via the vagus nerve
JA Bravo, P Forsythe, MV Chew… – Proceedings of the …, 2011 – National Acad Sciences
There is increasing, but largely indirect, evidence pointing to an effect of commensal gut microbiota on the central nervous system (CNS). However, it is unknown whether lactic acid bacteria such as Lactobacillus rhamnosus could have a direct effect on neurotransmitter …

Mind-altering microorganisms: the impact of the gut microbiota on brain and behaviour
JF Cryan, TG Dinan – Nature reviews neuroscience, 2012 – nature.com
Recent years have witnessed the rise of the gut microbiota as a major topic of research
interest in biology. Studies are revealing how variations and changes in the composition of the gut microbiota influence normal physiology and contribute to diseases ranging from …

The First Microbial Colonizers of the Human Gut: Composition, Activities, and Health Implications of the Infant Gut Microbiota.
Milani C, Duranti S, Bottacini F, Casey E, Turroni F, Mahony J, Belzer C, Delgado Palacio S, Arboleya Montes S, Mancabelli L, Lugli GA, Rodriguez JM, Bode L, de Vos W, Gueimonde M, Margolles A, van Sinderen D, Ventura M.
Microbiol Mol Biol Rev. 2017 Nov 8;81(4). pii: e00036-17. doi: 10.1128/MMBR.00036-17. Print 2017 Dec.

 

Mother-to-Infant Microbial Transmission from Different Body Sites Shapes the Developing Infant Gut Microbiome.
Ferretti P, Pasolli E, Tett A, Asnicar F, Gorfer V, Fedi S, Armanini F, Truong DT, Manara S, Zolfo M, Beghini F, Bertorelli R, De Sanctis V, Bariletti I, Canto R, Clementi R, Cologna M, Crifò T, Cusumano G, Gottardi S, Innamorati C, Masè C, Postai D, Savoi D, Duranti S, Lugli GA, Mancabelli L, Turroni F, Ferrario C, Milani C, Mangifesta M, Anzalone R, Viappiani A, Yassour M, Vlamakis H, Xavier R, Collado CM, Koren O, Tateo S, Soffiati M, Pedrotti A, Ventura M, Huttenhower C, Bork P, Segata N.
Cell Host Microbe. 2018 Jul 11;24(1):133-145.e5. doi: 10.1016/j.chom.2018.06.005.

More than just a gut instinct-the potential interplay between a baby’s nutrition, its gut microbiome, and the epigenome.
Mischke M, Plösch T.
Am J Physiol Regul Integr Comp Physiol. 2013 Jun 15;304(12):R1065-9. doi: 10.1152/ ajpregu.00551.2012. Epub 2013 Apr 17.

Intestinal Dysbiosis and the Developing Lung: The Role of Toll-Like Receptor 4 in the Gut-Lung Axis.
Wedgwood S, Gerard K, Halloran K, Hanhauser A, Monacelli S, Warford C, Thai PN, Chiamvimonvat N, Lakshminrusimha S, Steinhorn RH, Underwood MA.
Front Immunol. 2020 Mar 5;11:357. doi: 10.3389/fimmu.2020.00357.
eCollection 2020.PMID:32194566

Investigating bifidobacteria and human milk oligosaccharide composition of lactating mothers.
Lugli GA, Duranti S, Milani C, Mancabelli L, Turroni F, Alessandri G, Longhi G, Anzalone R, Viappinai A, Tarrachini C, Bernasconi S, Yonemitsu C, Bode L, Goran MI, Ossiprandi MC, van Sinderen D, Ventura M.
FEMS Microbiol Ecol. 2020 Mar 19. pii: fiaa049. doi: 10.1093/femsec/fiaa049.
PMID:32188978

Infant respiratory syncytial virus prophylaxis and nasopharyngeal microbiota until 6 years of life: a subanalysis of the MAKI randomised controlled trial.
Man WH, Scheltema NM, Clerc M, van Houten MA, Nibbelke EE, Achten NB, Arp K, Sanders EAM, Bont LJ, Bogaert D.
Lancet Respir Med. 2020 Mar 20. pii: S2213-2600(19)30470-9. doi: 10.1016/S2213-2600(19)30470-9.
PMID:32203712

Distinct maternal microbiota clusters are associated with diet during pregnancy: impact on neonatal microbiota and infant growth during the first 18 months of life.
García-Mantrana I, Selma-Royo M, González S, Parra-Llorca A, Martínez-Costa C, Collado MC. Gut Microbes. 2020 Mar 13:1-17. doi: 10.1080/19490976.2020.1730294. [Epub ahead of print]
PMID:32167021

Timing of complementary feeding is associated with gut microbiota diversity and composition and short chain fatty acid concentrations over the first year of life.
Differding MK, Benjamin-Neelon SE, Hoyo C, Østbye T, Mueller NT.
BMC Microbiol. 2020 Mar 11;20(1):56. doi: 10.1186/s12866-020-01723-9. PMID:32160858

Infant Gut Microbiome Associated With Cognitive Development.
Carlson AL, Xia K, Azcarate-Peril MA, Goldman BD, Ahn M, Styner MA, Thompson AL, Geng X, Gilmore JH, Knickmeyer RC.
Biol Psychiatry. 2018 Jan 15;83(2):148-159. doi: 10.1016/j.biopsych.2017.06.021.
Epub 2017 Jun 27.

Visceral Fat Is Associated With Mucosal Healing of Infliximab Treatment in Crohn’s Disease.
Shen W, Cao L, Li Y, Cai X, Ge Y, Zhu W.
Dis Colon Rectum. 2018 Jun;61(6):706-712. doi: 10.1097/DCR.0000000000001074.

Subcutaneous Abdominal Fat and Thigh Muscle Composition Predict Insulin Sensitivity Independently of Visceral Fat
Bret H Goodpaster, F Leland Thaete, Jean-Aimé Simoneau and David E Kelley
Diabetes 1997 Oct; 46(10): 1579-1585. https://doi.org/10.2337/diacare.46.10.1579

Visceral Adiposity Index

A reliable indicator of visceral fat function associated with cardiometabolic risk
Marco C. Amato, MD, Carla Giordano, MD, Massimo Galia, MD, Angela Criscimanna, MD
Salvatore Vitabile, BSC, MSC, Massimo Midiri, MD, Aldo Galluzzo, MD
Diabetes Care 2010 Apr; 33(4): 920-922. https://doi.org/10.2337/dc09-1825

Ablation of PRDM16 and Beige Adipose Causes Metabolic Dysfunction and a Subcutaneous to Visceral Fat Switch
PaulCohen12Julia D.Levy1YingyingZhang1AndreaFrontini3Dmitriy P.Kolodin4Katrin J.Svensson1James C.Lo12XingZeng1LiYe1Melin J.Khandekar1JunWu1Subhadra C.Gunawardana5Alexander S.Banks1João Paulo G.Camporez6Michael J.Jurczak6ShingoKajimura8David W.Piston5DianeMathis4…Bruce M.Spiegelman1
Cell Volume 156, Issues 1–2, 16 January 2014, Pages 304-316
https://doi.org/10.1016/j.cell.2013.12.021

The clinical importance of visceral adiposity: a critical review of methods for visceral adipose tissue analysis.
Shuster, A., Patlas, M., Pinthus, J. H., & Mourtzakis, M.
The British journal of radiology (2012), 85(1009), 1-10.

Sagittal abdominal diameter is an independent predictor of all-cause and cardiovascular mortality in incident peritoneal dialysis patients.
Lee MJ, Shin DH, Kim SJ, Yoo DE, Ko KI, Koo HM, Kim CH, Doh FM, Oh HJ, Park JT, Han SH, Yoo TH, Choi KH, Kang SW.
PLoS One. 2013 Oct 22;8(10):e77082. doi: 10.1371/journal.pone.0077082. eCollection 2013.
PMID:24167560

Why visceral fat is bad: mechanisms of the metabolic syndrome.
Bergman, R. N., Kim, S. P., Catalano, K. J., Hsu, I. R., Chiu, J. D., Kabir, M., … & Ader, M.
Obesity (2006), 14(S2), 16S-19S.

Visceral fat is an independent predictor of all-cause mortality in men.
Kuk JL, Katzmarzyk PT, Nichaman MZ, Church TS, Blair SN, Ross R.
Obesity (Silver Spring). 2006 Feb;14(2):336-41.
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Normal-weight central obesity: implications for total and cardiovascular mortality.
Sahakyan, K. R., Somers, V. K., Rodriguez-Escudero, J. P., Hodge, D. O., Carter, R. E., Sochor, O., Lopez-Jimenez, F.
Annals of internal medicine (2015), 163(11), 827-835.

Abdominal visceral and subcutaneous adipose tissue compartments: association with metabolic risk factors in the Framingham Heart Study.
Fox, C. S., Massaro, J. M., Hoffmann, U., Pou, K. M., Maurovich-Horvat, P., Liu, C. Y.,& D’Agostino, R. B.
Circulation (2007), 116(1), 39-48.

Metabolic obesity: the paradox between visceral and subcutaneous fat.
Hamdy, O., Porramatikul, S., & Al-Ozairi, E.
Current diabetes reviews (2006), 2(4), 367-373.

Fructose consumption: considerations for future research on its effects on adipose distribution, lipid metabolism, and insulin sensitivity in humans.
Stanhope, K. L., & Havel, P. J.
The Journal of nutrition (2009), 139(6), 1236S-1241S.

Dietary omega-3 fatty acids aid in the modulation of inflammation and metabolic health.
Zivkovic, A. M., Telis, N., German, J. B., & Hammock, B. D.
California agriculture (2011), 65(3), 106.

Effects of supplemental fish oil on resting metabolic rate, body composition, and salivary cortisol in healthy adults.
Noreen, E. E., Sass, M. J., Crowe, M. L., Pabon, V. A., Brandauer, J., & Averill, L. K.
Journal of the International Society of Sports Nutrition (2010) 7(1), 31.

Does fish oil have an anti-obesity effect in overweight/obese adults? A meta-analysis of randomized controlled trials.
Du, S., Jin, J., Fang, W., & Su, Q.
PLoS One (2015), 10(11), e0142652.

Lifestyle factors and 5‐year abdominal fat accumulation in a minority cohort: the IRAS family study.
Hairston, K. G., Vitolins, M. Z., Norris, J. M., Anderson, A. M., Hanley, A. J., & Wagenknecht, L. E.
Obesity (2012), 20(2), 421-427.

Normal Protein Intake Is Required for Body Weight Loss and Weight Maintenance, and Elevated Protein Intake for Additional Preservation of Resting Energy Expenditure and Fat Free Mass, 2.
Soenen, S., Martens, E. A., Hochstenbach-Waelen, A., Lemmens, S. G., & Westerterp-Plantenga, M. S.
The Journal of nutrition (2013), 143(5), 591-596.

A high-protein diet for reducing body fat: mechanisms and possible caveats.
Pesta, D. H., & Samuel, V. T.
Nutrition & metabolism (2014), 11(1), 53.

Intake of macronutrients as predictors of 5-y changes in waist circumference.
Halkjær, J., Tjønneland, A., Thomsen, B. L., Overvad, K., & Sørensen, T. I.
The American journal of clinical nutrition (2006), 84(4), 789-797.

Higher-Protein Diets Are Associated with Higher HDL Cholesterol and Lower BMI and Waist Circumference in US Adults1–4.
Pasiakos, S. M., Lieberman, H. R., & Fulgoni III, V. L.
The Journal of nutrition (2015), 145(3), 605-614.

Metabolic implications of dietary trans‐fatty acids.
Dorfman, S. E., Laurent, D., Gounarides, J. S., Li, X., Mullarkey, T. L., Rocheford, E. C., … & Commerford, S. R.
Obesity 2009, 17(6), 1200-1207.

Trans fat diet induces abdominal obesity and changes in insulin sensitivity in monkeys.
Kavanagh, K., Jones, K. L., Sawyer, J., Kelley, K., Carr, J. J., Wagner, J. D., & Rudel, L. L.
Obesity 2007, 15(7), 1675-1684.

Consuming fructose-sweetened, not glucose-sweetened, beverages increases visceral adiposity and lipids and decreases insulin sensitivity in overweight/obese humans.
Stanhope, K. L., Schwarz, J. M., Keim, N. L., Griffen, S. C., Bremer, A. A., Graham, J. L., … & McGahan, J.
The Journal of clinical investigation 2009, 119(5), 1322-1334.

Fruit and vegetable intakes, C-reactive protein, and the metabolic syndrome.
Esmaillzadeh, A., Kimiagar, M., Mehrabi, Y., Azadbakht, L., Hu, F. B., & Willett, W. C.
The American journal of clinical nutrition 2006, 84(6), 1489-1497.

Comparison of energy-restricted very low-carbohydrate and low-fat diets on weight loss and body composition in overweight men and women.
Volek, J. S., Sharman, M. J., Gómez, A. L., Judelson, D. A., Rubin, M. R., Watson, G., … & Kraemer, W. J.
Nutrition & metabolism 2004, 1(1), 13.

A Lower-Carbohydrate, Higher-Fat Diet Reduces Abdominal and Intermuscular Fat and Increases Insulin Sensitivity in Adults at Risk of Type 2 Diabetes–3.
Gower, B. A., & Goss, A. M.
The Journal of nutrition 2014, 145(1), 177S-183S.

Short-term weight loss and hepatic triglyceride reduction: evidence of a metabolic advantage with dietary carbohydrate restriction.
Browning, J. D., Baker, J. A., Rogers, T., Davis, J., Satapati, S., & Burgess, S. C.
The American journal of clinical nutrition 2011, 93(5), 1048-1052.

A dose–response relation between aerobic exercise and visceral fat reduction: systematic review of clinical trials.
Ohkawara, K., Tanaka, S., Miyachi, M., Ishikawa-Takata, K., & Tabata, I.
International journal of obesity (2007), 31(12), 1786.

Dose–response effect of walking exercise on weight loss. How much is enough?.
Brill, J. B., Perry, A. C., Parker, L., Robinson, A., & Burnett, K.
International journal of obesity (2002), 26(11), 1484.

High intensity interval exercise training in overweight young women.
Sijie, T., Hainai, Y., Fengying, Y., & Jianxiong, W.
The Journal of sports medicine and physical fitness (2012), 52(3), 255-262.

Physical activity and central adiposity in a cohort of African-American adults.
McGrath S, Brazel D, Dugas L, Cao G, Durazo-Arvizu R, Luke A.
BMC Obes. 2017 Nov 7;4:34. doi: 10.1186/s40608-017-0170-4. eCollection 2017.
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The effect of abdominal exercise on abdominal fat.
Vispute, S. S., Smith, J. D., LeCheminant, J. D., & Hurley, K. S.
The Journal of Strength & Conditioning Research (2011), 25(9), 2559-2564.

Beccuti, G., & Pannain, S. (2011). Sleep and obesity. Current opinion in clinical nutrition and metabolic care, 14(4), 402.

Sleep apnea and daytime sleepiness and fatigue: relation to visceral obesity, insulin resistance, and hypercytokinemia.
Vgontzas, A. N., Papanicolaou, D. A., Bixler, E. O., Hopper, K., Lotsikas, A., Lin, H. M., … & Chrousos, G. P.
The Journal of Clinical Endocrinology & Metabolism (2000), 85(3), 1151-1158.

http://www.kenniscentrumsuiker.nl/images/pdf/brochures/De_menselijke_motor_2012_online_03.pdf
van Kemenade, M.C. & Vugt, Jeroen & Riemslag Baas, S & Metselaar, H.J. & Man, Robert & Ijzermans, Jan. (2017). SUN-P214: Bedside Nutritional Assessment Tools Compared with CT Based Skeletal Muscle Mass Analysis in Patients Awaiting Liver Transplantation. Clinical Nutrition. 36. S133. 10.1016/S0261-5614(17)30414-4.