NIH: "Ketogenic Diet Is Preventive & Supportive Care for COVID-19 Patients"

This is an official article by NIH, which we are publishing as a PUBLIC SERVICE. According to NIH, the aim of this work is to highlight the potential role of Ketogenic Diets in the management and prevention of COVID-19, focusing on the beneficial effects that may exert on inflammation, immune system and respiratory function.

Our (Comfort Keto) purpose of publishing this work in its entirety is to make sure that the original document is always available to the general public, even if NIH may someday decide to remove it from the NLM (National Library of Medicine) website for any reason.

The original document titled "Ketogenic Diet as a Preventive and Supportive Care for COVID-19 Patients" has been published on March 20, 2021 by the "National Library of Medicine; National Center for Biotechnology Information" - a fully integral branch of NIH, National Institute for Health. The url address for the original article is https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC8003632/

We thank our website member "e39dinan" for bringing this article to our attention.

Published online 2021 Mar 20. doi: 10.3390/nu13031004 PMCID: PMC8003632 PMID: 33804603 Ketogenic Diet as a Preventive and Supportive Care for COVID-19 Patients

Elena Gangitano,1,*† Rossella Tozzi,2,† Orietta Gandini,2 Mikiko Watanabe,1 Sabrina Basciani,1 Stefania Mariani,1 Andrea Lenzi,1 Lucio Gnessi,1 and Carla Lubrano1,* Dimitrios T. Karayiannis, Academic Editor and Zafeiria Mastora, Academic Editor Author information Article notes Copyright and License information Disclaimer This article has been cited by other articles in PMC. Associated Data Data Availability Statement Go to:

Abstract Severe obesity is associated with an increased risk of admission to intensive care units and need for invasive mechanical ventilation in patients with COVID-19. The association of obesity and COVID-19 prognosis may be related to many different factors, such as chronic systemic inflammation, the predisposition to severe respiratory conditions and viral infections. The ketogenic diet is an approach that can be extremely effective in reducing body weight and visceral fat in the short term, preserving the lean mass and reducing systemic inflammation. Therefore, it is a precious preventive measure for severely obese people and may be considered as an adjuvant therapy for patients with respiratory compromise.

Keywords: SARS-CoV-2, COVID-19, obesity, ketogenic diet, VLCKD, inflammation, viral infections, respiratory failure

Go to: 1. Introduction Coronavirus 2019 disease (COVID-19), caused by SARS-CoV-2 virus, has spread worldwide causing a pandemic since March 2020, now leading to new waves of infection. Overall fatality rate reached 2.3% [1] and, to date, 2,343,069 cases of COVID-19 and 80,253 (3.4%) deaths have been registered in Italy [2].

In most cases the clinical presentation is characterized by fever, dry cough, fatigue and mild pneumonia, although critical forms with desaturation and respiratory failure, septic shock, and/or multiple organ dysfunction can also occur; it has been estimated that moderate and severe forms can affect 14% and 5% of patients, respectively [1]. COVID-19 management consists of supportive therapy and preventing respiratory insufficiency through oxygen therapy or positive ventilation. The most widely adopted therapeutic protocol is based on the use of antibiotic prophylaxis, steroids and anticoagulant therapy, although there is no conclusive evidence supporting their role [3]. In order to limit the typical coagulative hyperactivation and the well-known condition of thrombosis susceptibility [4,5], heparin is now used in early stage COVID-19 patients; however, intensive care units are gradually filling up again, fearing the national health system collapse.

COVID-19 mortality is highly correlated to the severity of the inflammation-related cytokine storm and to the presence of multiple comorbidities (obesity, type 2 diabetes, hypertension, chronic obstructive pulmonary disease) increasing the risk of developing critical forms of infection [6]. In light of these considerations, it is therefore mandatory to pursue new strategies to reduce risk factors and to limit the development of the cytokine storm syndrome (CSS) in order to prevent patients’ worsening and access to emergency rooms.

The nutritional approach to COVID-19 patients is extremely important to ensure the correct amount of nutrients, necessary to face the infection and the body’s capacity to face and fight the virus. Current European Society for Clinical Nutrition and Metabolism (ESPEN) expert statements for COVID-19 patients recommend considering energy needs of 27–30 kcal per kg body weight and day, and 1–1.3 g per Kg of proteins, depending on disease status. Fat and carbohydrate ratio are currently suggested to be 30:70 for patients without respiratory deficiency and 50:50 for ventilated patients [7].

The ketogenic diet (KD), reducing carbohydrates oral intake, allows the hepatic production of ketone bodies and the onset of nutritional ketosis as a result of an increased utilization of fat as metabolic fuel when the availability of glucose is low. Ketone bodies are attracting more and more attention for their anti-inflammatory role and immune metabolism modulation [8]. Besides the well-known metabolic advantages (better hyperglycemia control, reduction of insulin resistance, improvement of hepatic steatosis), several “non-classical” beneficial effects have been attributed to KDs, including growth factors, leptin or IGF-1 modulation [9], together with the protection of renal, brain function and anti-viral effects [10].

KDs provide for a deprivation of carbohydrate content equal to 5–10% of total kcal daily intake, although the specific macronutrient composition may vary. As reported by Watanabe et al. [11], ketogenic diets differ mainly in calorie intake and protein content. High Fat Ketogenic Diets (HFKD) are characterized by a restriction of carbohydrates (CHO) < 50 g per day with unrestricted intake of fat, a relative increase of protein (0.8–1.2 g per day), and ad libitum caloric intake; very low-calorie ketogenic diets (VLCKD) are characterized by approximately the same amount of CHO and protein as in HFKDs, but significantly lower fat and therefore calorie intake, which goes as low as 600 kcal/daily. Very low-calorie diets (VLCD), providing a marked restriction of daily calorie intake, are characterized instead by a variable amount of carbohydrate intake which may or may not be able to induce ketosis [12] (Table 1).

Main differences between ketogenic and low-carbohydrate diets (with the kind permission of Watanabe et al. [11]).

While HFKDs are still used in refractory epilepsy in children, VLCKD are now recommended in severe or sarcopenic obesity, prior to bariatric surgery, to improve glycemic control, dyslipidemia and for a rapid reduction of cardiovascular risk factors in obese patients, not responsive to standard diets [12].

Current contraindications to the VLCKD include type 1 diabetes mellitus, kidney or liver failure, heart failure, cardiac arrhythmias, recent stroke, myocardial infarction, pregnancy and breastfeeding. Of note, active/severe infections and respiratory failure are currently among the conditions not recommended for implementing a VLCKD regimen for a hypothesized immunosuppression and acidosis risk, respectively [13]. Nevertheless, studies conducted in the past have reported good results, also highlighting some benefits derived from ketosis [13]. As per HFKDs, patients with CVD, heart, liver or kidney disease need close medical supervision in order to safely undergo such regimen, and those with severe dyslipidemia or a history of hypertriglyceridemia associated pancreatitis are recommended against undergoing this dietary regimen [14].

The aim of this work is to highlight the potential role of KDs in the management and prevention of COVID-19, focusing on the beneficial effects that may exert on inflammation, immune system and respiratory function.

Go to: 2. Low Chronic Inflammation, COVID-19 and Ketogenic Diet As described above, severe forms of COVID-19 are characterized by an ineffective adaptive immune response that leads to a persistence in C-reactive protein (CRP) and interleukin (IL) -6 elevation [15]. This pattern falls within the so-called chronic low-grade inflammatory phenotype (CLIP), a phenomenon that underlies many of the diseases associated with more critical forms of COVID-19, such as diabetes, obesity, insulin-resistance, hypertension and atherosclerosis [16]. All these metabolic derangements are closely related to inflammation triggered by the abnormal expansion of visceral adipose tissue, which has been shown to predict poor COVID-19 prognosis as well as respiratory indicators [17]. Specifically, the white adipose tissue M1 macrophages secretion of pro-inflammatory cytokines including tumor necrosis factor (TNF) alpha, IL-6, CRP, IL-1, is increased, whereas a steep decline occurs in the production of anti-inflammatory cytokines like IL-10, the interleukin-1 receptor antagonist (IL-1RA), and adiponectin. Not only the adipose tissue, but also the immune cells, liver, brain, muscles and pancreas suffer from the inflammatory insult in subjects with obesity. Macrophage-like Kupffer cells initiate the inflammatory process in the liver preceding the inflammatory signals produced by the white adipose tissue, which may further lead to hepatic-necro-inflammation [18]. Moreover, role of P-loop domain belonging to the STAND class of NTPases with homology to the oligomerization module found in AAA+ ATPases (NACHT), Leucine-rich repeat (LRR), and NOD-like receptors (NLRs) Pyrin Domain-Containing 3 Protein (NLRP3) for maintenance of chronic inflammation is crucial. In fact, in response to activation of innate immune receptors by stimuli such as microbial ligands, transcription of pro-inflammatory genes, including those encoding NLRP3 and pro-IL1β, is induced [19].

KDs inhibit aerobic glycolysis, which has been proven to occur following inflammatory activation of cells from both myeloid and lymphoid lineage; in particular, KDs prevent the differentiation and effector functions of inflammatory cells, while promoting the differentiation of regulatory subsets. Moreover, the ketone body β- hydroxybutyrate blocks NLRP3 inflammasome activation [20].

Go to: 3. Immune System, COVID-19 and Ketogenic Diet SARS-CoV-2 infects lung cells and enters host epithelial cells through Transmembrane Serine Protease 2 (TMPRSS2) action and spike protein binding Angiotensin Converting Enzyme 2 (ACE-2) receptor. After alveolar epithelial cells pyroptosis-induced death and damage-associated molecular patterns (DAMPs) release, macrophages and monocytes are recruited and cytokines secreted. More specifically, in case of a dysfunctional immune response, we observe an abnormal monocytes, macrophages and T-cells infiltration favored by vascular permeability, a systemic cytokine storm (IL-6, IFN gamma, IL-2, IL-10, Granulocyte colony-stimulating factor G-CSF, TNF), clinical worsening (pulmonary oedema and pneumonia) and widespread inflammation and/or multiorgan damage due to excessive TNF and reactive oxygen species (ROS) production. On the contrary, in a healthy immune system, initial inflammation attracts virus specific T-cells to the site of infection, where they can eliminate the infected cells before the virus spreads. Neutralizing antibodies in these individuals can block viral infection resulting in early recovery [15]. Noteworthy, viral infection can also result in an aberrant cytokine production by the immune cells such as monocytes and macrophages. Elderly people seem to be more susceptible to critical forms of COVID-19 due to an ageing lung microenvironment causing altered dendritic cell maturation and migration to the lymphoid organs and to an inefficient IFN response [21].

Karagiannis et al. [22] demonstrated that restricting dietary glucose by feeding mice a HFKD (72% fat, 2.4% sugar) largely ablates lung-resident type 2 Innate Lymphoid Cells (ILC-2) and reduces airway inflammation by impairing fatty acid metabolism and the formation of lipid droplets. Chronic activation of ILCs, typical of allergenic airway inflammation, needs exogenous fatty acids which are transiently stored in lipid droplets and therefore converted into phospholipids to promote ILCs proliferation. This metabolic program, imprinted by IL-33 and regulated by the genes Peroxisome proliferator-activated receptor gamma (PPAR-γ) and Diacylglycerol O-Acyltransferase 1 (Dgat1), is controlled by glucose availability as well as mammalian target of rapamycin (mTOR) signaling. Moreover, Goldberg et al. reported that a HFKD allows for better survival and increased protective IL-17-secreting γδ T cells in the lungs of mice with influenza virus [10], while Ryu et al. have recently provided preclinical evidence that a HFKD is capable of providing a protective effect against the animal equivalent of COVID-19 in aged mice, with the maintenance of a better oxygen saturation and an increase in γδ T cells [23].

Go to: 4. Obesity, Viral Infections and Respiratory Function Weight excess is associated with a higher susceptibility to viral infections [3], as seasonal and H1N1 influenza [24,25], and a higher risk of hospitalization for these conditions [26,27,28,29]. In recent years, during the H1N1 influenza pandemic, obesity has been shown to be associated with hospitalization and death [29] and critically ill patients were frequently morbidly obese [25]. Similarly to other viral infections, severe obesity is associated with a high risk of COVID-19 complications [30]. Among obesity comorbidities, hypertension, dyslipidemia, prediabetes and insulin resistance might predispose individuals to cardiovascular events and increased susceptibility to infection via atherosclerosis. Resulting cardiac dysfunction and kidney failure can more easily lead to pneumonia-associated organ failures [31]. Moreover, visceral adipose tissue—a reliable and specific marker of insulin resistance—has been independently associated with the need of intensive care unit (ICU) resulting as the strongest predictor of worse prognosis in patients with COVID-19 [17]. Considered this, a nutritional approach that can break down insulin resistance such a HFKD, might have beneficial implications in COVID-19 prognosis likely without any detrimental effects.

Obese patients are predisposed to the development of chronic and acute respiratory illnesses [32,33], including respiratory tract infections [34]. The reasons for this susceptibility to respiratory disease are many and not completely elucidated yet [35,36]. Obese people have alterations in respiratory physiology [37] and immune response [24,33] and, consequently, develop a lower response to antiviral therapies and vaccinations [24]. The alterations in respiratory physiology consist in a decreased functional residual capacity and reduced expiratory reserve volume, hypoxemia and ventilation perfusion abnormalities [28,37]. The presence of Obstructive Sleep Apnea Syndrome (OSAS), which is common in obese people, may predispose the patients to COVID-19 complications [38].

Obesity is characterized by low-grade systemic inflammation, that may be related to the pathogenesis of respiratory conditions [33]. Fat tissue may accumulate within the lungs, as observed in the airways of obese humans [39] and in the alveolar interstitium of obese diabetic rats [40]. Adipose tissue accumulation in the outer wall of large airways positively correlated with inflammatory infiltrate of eosinophils and neutrophils in patients with fatal asthma [39].

Animal models of obesity showed that during influenza infection there is increased lung permeability, leading to protein leakage into the bronchoalveolar lavage fluid. For the resolution of the infection, the repair of the damaged epithelial surface is required, but wound repair is impaired. Increased lung oedema and oxidative stress have been observed as well [24]. There is evidence that immune system functioning is altered in obesity. T-cells diversity is reduced and this may be related to the T-cells poor response to influenza virus [24]. CD8+ T memory cells has been shown to be impaired, with consequent exacerbates lung complications and mortality [33]. These cells are responsible for an efficient immune response to vaccination [33], with consequent reduced response to vaccination in obese people [24]. Moreover, obesity may be a factor that exacerbates the aging of the immune system [24].

In addition, the high ACE-2 expression in adipose tissue may play a role in obese patients’ susceptibility to COVID-19 infection, since SARS-CoV-2 shows high affinity for this enzyme [41].

Therefore, interventions aimed to weight loss in obese patients are warranted to prevent viral infection susceptibility and their complications and theoretically may ameliorate respiratory function.

Go to: 5. Low-Carbohydrate Ketogenic Diets and Respiratory Function VLCKDs are, to date, contraindicated for obese patients with respiratory failure [12]. However, some studies reported some beneficial effects from high-fat low-carbohydrate diets and detrimental effects of carbohydrate loads on respiratory parameters. These studies, anyway, often did not specify if patients were in ketosis, but used low amount of CHO, possibly leading to ketosis.

Two studies on a total of 40 healthy patients [42,43] reported that a VLCKD (848 kcal/day; protein: carbohydrate: fat = 43:14:43%) and a HFKD (10% calories from carbohydrate) diet reduced CO2 output without modifying oxygen uptake. Moreover, Rubini et al. compared a VLCKD regimen to a hypocaloric Mediterranean diet showing that only the VLCKD significantly decreased respiratory exchange ratio (p < 0.05) in addition to higher fat mass loss in healthy patients. Therefore, these diets may be helpful in respiratory patients for reducing CO2 body stores levels and dyspnea at rest. On the other hand, a study on 17 healthy women who were administered a HFKD (2400 kcal/day), reported earlier muscle fatigue during daily life activities [44].

Chronic Obstructive Pulmonary Disease (COPD) is often accompanied with hypercapnia and hypoxemia. A reduction in carbon dioxide production would reduce the workload of respiratory muscles and therefore be beneficial for these patients. Some studies focused on the administration of HFKD in COPD patients, and beneficial or, at least, neutral results were observed.

In twelve clinically stable COPD patients, the administration of a high-fat meal had a small effect on gas exchange parameters compared to 12 healthy controls, whereas a high-carbohydrate diet was detrimental on gas exchange parameters, especially in COPD patients [45]. No differences in pulmonary function were detected in 36 COPD patients comparing the administration of a moderate-fat meal with a high-fat meal [46]. On the other hand, the administration of a HFKD in COPD patients with hypercapnia led to an amelioration of respiratory parameters in an overall sample of 74 underweight patients [47,48].

In patients with respiratory failure, providing an adequate protein intake is extremely important to preserve skeletal muscle mass and function [7]. A high-fat low-carbohydrate diet has been reported as a potential useful tool to ameliorate respiratory failure [49,50,51].

In the literature, there are some evidences of a beneficial effect of a high-fat low-carbohydrate diet in mechanically ventilated patients [52,53,54], since it was able to reduce PaCO2 levels [52,53,55] and the time of mechanical ventilation [52,53].

Go to: 6. COVID-19, Lockdown and KDs Both HFKD and VLCKD represent valuable treatments despite being characterized by the presence of contraindications and capable of causing side effects. Therefore, they should be followed under strict medical supervision and be considered similar to pharmacologic treatment. A concern may be that during the isolation imposed during the pandemic, it is difficult to monitor a patient on the ketogenic diet undergoing rehabilitation. Just a few studies reporting the administration of a ketogenic diet during this pandemic have been published, and to the best of our knowledge none published results on its use in COVID-19 infected and/or respiratory patients yet.

Kossof et al. [56] administered a HFKD to patients with uncontrolled seizures, mainly children, during the pandemic, using a combined approach with in person meetings and telemedicine. The authors and the other members of the International Ketogenic Diet Study Group, pediatric consensus group, reported no issues regarding the maintenance of ketosis and seizure control in their group, and raised no questions about the safety of the ketogenic diet in case of respiratory infection. A similar approach in similar setting was used by Ferraris et al. [57] and no major issues were reported, but they did not specify if any of their patients was infected by COVID-19.

Soliman et al. [58] proposed the use of a ketogenic diet and intermittent fasting, with administration of medium-chain triglycerides, as a prophylactic measure and an adjuvant therapy for COVID-19. In fact many viruses, as the varicella-zoster [59], the cytomegalovirus [60] and the hepatitis C [61], need the fatty acid metabolism pathway for their replication, therefore the diet-induced metabolic switch leading to a reduction in the fatty acid synthesis pathways may help in reducing viral replication [58].

Go to: 7. Conclusion and Future Perspective 7.1. KDs in COVID-19 Prevention Obesity, and in particular visceral abdominal fat, has been indicated as an independent risk factor for worse prognosis in COVID-19, often associated with the need for intensive care [17,30,41,62]. These may be due to the impaired respiratory mechanics, increased airway resistance and impaired gas exchange [25,28,54], as well as obesity-related comorbidities [63], which appear to be directly related to the onset of complications and severe course of COVID-19. In particular, OSAS [38], metabolic syndrome, hypertension, Non-Alcoholic Fatty Liver Disease (NAFLD) and diabetes or insulin resistance have all shown to affect COVID-19 outcome negatively [55,56,57,58]. Finally, it should not be overlooked that obesity is associated with low chronic inflammation within a state of immunological dysfunction that can lead to increased risk of allergies [64] or ineffective response against infections [35] and vaccines [65].

KDs, and specifically VLCKDs, demonstrated to induce weight loss and diabetes remission. VLCKDs are currently used in bariatric surgery preparation [12] thanks to the ability in reducing hepatic volume [11] with a subsequent improvement in intra and post-operative care. Recent findings underlined immune advantages derived from ketone bodies, such as blockage NLRP3 inflammasome [20], reduction in chronic activation of ILCs and induction of protective γδ T-cells against infections [10]. Taken together, in addition to the benefit of airway inflammation prevention by impairing the formation of lipid droplets [22], KDs could be an excellent tool to prevent the infection and stem the damage induced by COVID-19 in the fragile population affected from obesity.

7.2. KDs in Supportive Care of COVID-19 Studies conducted in mice highlighted the beneficial effect of HFD- induced ketone bodies in COVID-19 models [10,23]. In humans, HFKDs has been experimented in Intensive Care Units (ICU) and good results have been reported in mechanically ventilated patients [52,55]. Moreover, telemedicine achieved good results in pediatric epileptic patients under HFKDs, either for safety and compliance, proving that it can be a valid tool to be adopted even in the event of quarantine and fiduciary isolation. On the basis of these considerations, several authors proposed KDs in COVID-19 management and some clinical trials are ongoing [66,67].

7.3. KDs during Rehabilitation Post SARS-CoV-2 Infection Patients affected from COVID-19, especially elderly ones, often require ICU for a longer period (up to 20 days) than other more typical uses of ICU. Among Post Intensive Care Syndrome (PICS), impaired exercise tolerance, neuropathies, muscle weakness/paresis, severe fatigue are responsible for decreased exercise capacity, disability and compromised quality of life for months, even years after intensive care [68]. Muscle atrophy, as well as obesity and immune dysregulation, is associated with Growth Hormone/Insulin-like Growth Factor 1 (GH/IGF-1) impaired axis and might be a link between IGF-1 downregulation and COVID-19 severity [69]. Preserving muscle mass is essential in order to improve rehabilitation and to reduce costs for recovering people.

VLCKDs preserved muscle mass in obese patients [70,71] when a protein intake of at least 1.2 gr of protein/Kg was ensured; the same results have been confirmed when isocaloric KDs have been used in patients affected from multiple sclerosis, reporting a superiority compared to Mediterranean diet [72]. Furthermore, HFKD (75–80% calories from fat, carbohydrates <50 g per day and <10 g per meal) improves quality of life, lean mass and metabolic parameters (included IGF-1) in oncologic patients, compared to standard diet [73].

In conclusion, VLCKDs administration might be considered in severely obese patients as an effective adjuvant therapy for COVID-19, first of all as a preventive measure, to achieve a fast weight loss [67], and secondly as an adjuvant therapy during rehabilitation (see Figure 1). More challenging is the hypothesis of administering HFKD during hospitalization or even more in delicate settings such as an intensive care unit or during positive ventilation; although several data support the evidence that limiting carbohydrate intake and promoting ketone formation may be helpful in ameliorating respiratory parameters. Furthermore, as extensively discussed, HFKDs show a strong anti-inflammatory effect and some data suggest that they may be useful for reducing viral replication. However, many studies are old, the samples small, and the ketosis not specifically addressed, therefore new clinical trials are needed. Hoping that the promising results observed in animal studies can be passed on to humans, we herein suggest considering KDs as an option to be considered for COVID-19 management within the current indications.

Figure 1: Mechanisms through which VLCKD with its consequent weight loss may reduce the susceptibility to severe SARS-CoV-2 infection and stem the damage induced by the virus.

Go to: Author Contributions Conceptualization, L.G., A.L. and C.L.; writing—original draft preparation, E.G., R.T., M.W. and S.B.; writing—review and editing, O.G., S.M., L.G. and C.L.; supervision, L.G. and C.L. All authors have read and agreed to the published version of the manuscript.

Go to: Funding This research received no external funding.

Go to: Data Availability Statement Data sharing not applicable

Go to: Conflicts of Interest The authors declare no conflict of interest.

Go to: Footnotes Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. Go to: References 1. Wu Z., McGoogan J.M. Characteristics of and Important Lessons from the Coronavirus Disease 2019 (COVID-19) Outbreak in China: Summary of a Report of 72314 Cases from the Chinese Center for Disease Control and Prevention. JAMA J. Am. Med. Assoc. 2020;323:1239–1242. doi: 10.1001/jama.2020.2648. [PubMed] [CrossRef] [Google Scholar] 2. Epicentro, Epidemiology for Public Health, Istituto Superiore di Sanità . COVID-19 Integrated Surveillance Data in Italy. Epicentro, Epidemiology for Public Health, Istituto Superiore di Sanità; Rome, Italy: 2021. [Google Scholar] 3. Pascarella G., Strumia A., Piliego C., Bruno F., del Buono R., Costa F., Scarlata S., Agrò F.E. COVID-19 Diagnosis and Management: A Comprehensive Review. J. Intern. Med. 2020;288:192–206. doi: 10.1111/joim.13091. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 4. Levi M., Thachil J., Iba T., Levy J.H. Coagulation Abnormalities and Thrombosis in Patients with COVID-19. Lancet Haematol. 2020;7:e438–e440. doi: 10.1016/S2352-3026(20)30145-9. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 5. Spiezia L., Boscolo A., Poletto F., Cerruti L., Tiberio I., Campello E., Navalesi P., Simioni P. COVID-19-Related Severe Hypercoagulability in Patients Admitted to Intensive Care Unit for Acute Respiratory Failure. Thromb. Haemost. 2020;120:998–1000. doi: 10.1055/s-0040-1714350. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 6. Yang J., Zheng Y., Gou X., Pu K., Chen Z. Prevalence of Comorbidities and Its Effects in Patients Infected with SARS-CoV-2: A Systematic Review and Meta-Analysis. Int. J. Infect. Dis. 2020;94:91–95. doi: 10.1016/j.ijid.2020.03.017. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 7. Barazzoni R., Bischoff S.C., Breda J., Wickramasinghe K., Krznaric Z., Nitzan D., Pirlich M., Singer P. ESPEN Expert Statements and Practical Guidance for Nutritional Management of Individuals with SARS-CoV-2 Infection. Clin. Nutr. 2020;39:1631–1638. doi: 10.1016/j.clnu.2020.03.022. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 8. Lee A.K., Kim D.H., Bang E., Choi Y.J., Chung H.Y. β-Hydroxybutyrate Suppresses Lipid Accumulation in Aged Liver through GPR109A-mediated Signaling. Aging Dis. 2020;11:777–790. doi: 10.14336/AD.2019.0926. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 9. Vidali S., Aminzadeh S., Lambert B., Rutherford T., Sperl W., Kofler B., Feichtinger R.G. Mitochondria: The Ketogenic Diet—A Metabolism-Based Therapy. Int. J. Biochem. Cell Biol. 2015;63:55–59. doi: 10.1016/j.biocel.2015.01.022. [PubMed] [CrossRef] [Google Scholar] 10. Goldberg E.L., Molony R.D., Kudo E., Sidorov S., Kong Y., Dixit V.D., Iwasaki A. Ketogenic Diet Activates Protective γδ T Cell Responses against Influenza Virus Infection. Sci. Immunol. 2019;4:eaav2026. doi: 10.1126/sciimmunol.aav2026. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 11. Watanabe M., Tozzi R., Risi R., Tuccinardi D., Mariani S., Basciani S., Spera G., Lubrano C., Gnessi L. Beneficial Effects of the Ketogenic Diet on Nonalcoholic Fatty Liver Disease: A Comprehensive Review of the Literature. Obes. Rev. 2020;21:e13024. doi: 10.1111/obr.13024. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 12. Caprio M., Infante M., Moriconi E., Armani A., Fabbri A., Mantovani G., Mariani S., Lubrano C., Poggiogalle E., Migliaccio S., et al. Very-Low-Calorie Ketogenic Diet (VLCKD) in the Management of Metabolic Diseases: Systematic Review and Consensus Statement from the Italian Society of Endocrinology (SIE) J. Endocrinol. Investig. 2019;42:1365–1386. doi: 10.1007/s40618-019-01061-2. [PubMed] [CrossRef] [Google Scholar] 13. Watanabe M., Tuccinardi D., Ernesti I., Basciani S., Mariani S., Genco A., Manfrini S., Lubrano C., Gnessi L. Scientific Evidence Underlying Contraindications to the Ketogenic Diet: An Update. Obes. Rev. 2020;21:e13053. doi: 10.1111/obr.13053. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 14. Kirkpatrick C.F., Bolick J.P., Kris-Etherton P.M., Sikand G., Aspry K.E., Soffer D.E., Willard K.-E., Maki K.C. Review of Current Evidence and Clinical Recommendations on the Effects of Low-Carbohydrate and Very-Low-Carbohydrate (Including Ketogenic) Diets for the Management of Body Weight and Other Cardiometabolic Risk Factors: A Scientific Statement from the National Lipid Association Nutrition and Lifestyle Task Force. J. Clin. Lipidol. 2019;13:689–711.e1. doi: 10.1016/j.jacl.2019.08.003. [PubMed] [CrossRef] [Google Scholar] 15. Tay M.Z., Poh C.M., Rénia L., MacAry P.A., Ng L.F.P. The Trinity of COVID-19: Immunity, Inflammation and Intervention. Nat. Rev. Immunol. 2020;20:363–374. doi: 10.1038/s41577-020-0311-8. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 16. Chen Y., Liu S., Leng S.X. Chronic Low-Grade Inflammatory Phenotype (CLIP) and Senescent Immune Dysregulation. Clin. Ther. 2019;41:400–409. doi: 10.1016/j.clinthera.2019.02.001. [PubMed] [CrossRef] [Google Scholar] 17. Watanabe M., Caruso D., Tuccinardi D., Risi R., Zerunian M., Polici M., Pucciarelli F., Tarallo M., Strigari L., Manfrini S., et al. Visceral Fat Shows the Strongest Association with the Need of Intensive Care in Patients with COVID-19. Metab. Clin. Exp. 2020;111:1–8. doi: 10.1016/j.metabol.2020.154319. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 18. Debnath M., Agrawal S., Agrawal A., Dubey G.P. Metaflammatory Responses during Obesity: Pathomechanism and Treatment. Obes. Res. Clin. Pract. 2016;10:103–113. doi: 10.1016/j.orcp.2015.10.012. [PubMed] [CrossRef] [Google Scholar] 19. Levy M., Thaiss C.A., Elinav E. Taming the Inflammasome. Nat. Med. 2015;21:213–215. doi: 10.1038/nm.3808. [PubMed] [CrossRef] [Google Scholar] 20. Kornberg M.D. The Immunologic Warburg Effect: Evidence and Therapeutic Opportunities in Autoimmunity. Wiley Interdiscip. Rev. Syst. Biol. Med. 2020;12:1–17. doi: 10.1002/wsbm.1486. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 21. Pillai P.S., Molony R.D., Martinod K., Dong H., Pang I.K., Tal M.C., Solis A.G., Bielecki P., Mohanty S., Trentalange M., et al. Mx1 Reveals Innate Pathways to Antiviral Resistance and Lethal Influenza Disease. Science. 2017;352:463–466. doi: 10.1126/science.aaf3926. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 22. Karagiannis F., Masouleh S.K., Wunderling K., Surendar J., Schmitt V., Kazakov A., Michla M., Hölzel M., Thiele C., Wilhelm C. Lipid-Droplet Formation Drives Pathogenic Group 2 Innate Lymphoid Cells in Airway Inflammation. Immunity. 2020;52:620–634.e6. doi: 10.1016/j.immuni.2020.03.003. [PubMed] [CrossRef] [Google Scholar] 23. Ryu S., Shchukina I., Youm Y.-H., Qing H., Hilliard B.K., Dlugos T., Zhang X., Yasumoto Y., Booth C.J., Fernández-Hernando C., et al. Ketogenesis Restrains Aging-Induced Exacerbation of COVID in a Mouse Model. bioRxiv. 2020 doi: 10.1101/2020.09.11.294363. [CrossRef] [Google Scholar] 24. Honce R., Schultz-Cherry S. Impact of Obesity on Influenza A Virus Pathogenesis, Immune Response, and Evolution. Front. Immunol. 2019;10:1071. doi: 10.3389/fimmu.2019.01071. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 25. Kumar A., Zarychanski R., Pinto R., Cook D.J., Marshall J., Lacroix J., Stelfox T., Bagshaw S., Choong K., Lamontagne F., et al. Critically Ill Patients with 2009 Influenza A(H1N1) Infection in Canada. JAMA. 2009;302:1872–1879. doi: 10.1001/jama.2009.1496. [PubMed] [CrossRef] [Google Scholar] 26. Kwong J.C., Campitelli M.A., Rosella L.C. Obesity and Respiratory Hospitalizations During Influenza Seasons in Ontario, Canada: A Cohort Study. Clin. Infect. Dis. 2011;53:413–421. doi: 10.1093/cid/cir442. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 27. Moser J.S., Galindo-Fraga A., Ortiz-Hernández A.A., Gu W., Hunsberger S., Galán-Herrera J., Guerrero M.L., Ruiz-Palacios G.M., Beigel J.H. The La Red ILI 002 Study Group Underweight, overweight, and obesity as independent risk factors for hospitalization in adults and children from influenza and other respiratory viruses. Influenza Other Respir. Viruses. 2019;13:3–9. doi: 10.1111/irv.12618. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 28. Kalligeros M., Shehadeh F., Mylona E.K., Benitez G., Beckwith C.G., Chan P.A., Mylonakis E. Association of Obesity with Disease Severity Among Patients with Coronavirus Disease 2019. Obesity. 2020;28:1200–1204. doi: 10.1002/oby.22859. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 29. Morgan O.W., Bramley A., Fowlkes A., Freedman D.S., Taylor T.H., Belay B., Jain S., Cox C., Kamimoto L., Fiore A., et al. Morbid Obesity as a Risk Factor for Hospitalization and Death Due to 2009 Pandemic Influenza A (H1N1) Disease. PLoS ONE. 2010;5:1–6. doi: 10.1371/journal.pone.0009694. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 30. Simonnet A., Chetboun M., Poissy J., Raverdy V., Noulette J., Duhamel A., Labreuche J., Mathieu D., Pattou F., Jourdain M., et al. High Prevalence of Obesity in Severe Acute Respiratory Syndrome Coronavirus-2 ( SARS-CoV-2) Requiring Invasive Mechanical Ventilation. Obesity. 2020;28:1195–1199. doi: 10.1002/oby.22831. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 31. Li B., Yang J., Zhao F., Zhi L., Wang X., Liu L., Bi Z., Zhao Y. Prevalence and Impact of Cardiovascular Metabolic Diseases on COVID-19 in China. Clin. Res. Cardiol. 2020;109:531–538. doi: 10.1007/s00392-020-01626-9. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 32. Franssen F.M.E., Donnell D.E.O., Goossens G.H., Blaak E.E., Schols A.M.W.J. Obesity and the Lung-Obesity and COPD. Thorax. 2008;63:1110–1117. doi: 10.1136/thx.2007.086827. [PubMed] [CrossRef] [Google Scholar] 33. Mancuso P. Obesity and lung inflammation. J. Appl. Physiol. 2010;108:722–728. doi: 10.1152/japplphysiol.00781.2009. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 34. Maccioni L., Weber S., Elgizouli M., Stoehlker A., Geist I., Peter H., Vach W., Nieters A. Obesity and Risk of Respiratory Tract Infections: Results of an Infection-Diary Based Cohort Study. BMC Public Health. 2018;18:1–13. doi: 10.1186/s12889-018-5172-8. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 35. Huttunen R., Syrja J. Obesity and the Risk and Outcome of Infection. Int. J. Obes. 2013;37:333–340. doi: 10.1038/ijo.2012.62. [PubMed] [CrossRef] [Google Scholar] 36. Watanabe M., Risi R., Tuccinardi D., Baquero C.J., Manfrini S., Gnessi L. Obesity and SARS-CoV-2: A Population to Safeguard. Diabetes Metab. Res. Rev. 2020;36:e3325. doi: 10.1002/dmrr.3325. [PubMed] [CrossRef] [Google Scholar] 37. Parameswaran K., Ctodd D., Soth M. Altered Respiratory Physiology in Obesity. Can. Respir. J. 2006;13:203–210. doi: 10.1155/2006/834786. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 38. Memtsoudis S.G., Ivascu N.S., Pryor K.O., Goldstein P.A. Obesity as a Risk Factor for Poor Outcome in COVID-19-Induced Lung Injury: The Potential Role of Undiagnosed Obstructive Sleep Apnoea. Br. J. Anaesth. 2020;125:e262–e263. doi: 10.1016/j.bja.2020.04.078. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 39. Elliot J.G., Donovan G.M., Wang K.C.W., Green F.H.Y., James A.L., Noble P.B. Fatty Airways: Implications for Obstructive Disease. Eur. Respir. J. 2019;54:1900857. doi: 10.1183/13993003.00857-2019. [PubMed] [CrossRef] [Google Scholar] 40. Foster D.J., Ravikumar P., Bellotto D.J., Unger R.H., Hsia C.C.W. Fatty Diabetic Lung: Altered Alveolar Structure and Surfactant Protein Expression. Am. J. Physiol. 2010;298:L392–L403. doi: 10.1152/ajplung.00041.2009. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 41. Kassir R. Risk of COVID-19 for Patients with Obesity. Obes. Rev. 2020;21:e13034. doi: 10.1111/obr.13034. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 42. Rubini A., Bosco G., Lodi A., Cenci L., Parmagnani A., Grimaldi K., Zhongjin Y., Paoli A. Effects of Twenty Days of the Ketogenic Diet on Metabolic and Respiratory Parameters in Healthy Subjects. Lung. 2015;193:939–945. doi: 10.1007/s00408-016-9958-0. [PubMed] [CrossRef] [Google Scholar] 43. Sue Y.D., Chung M.M., Grosvenor M., Wasserman K. Effect of Altering the Proportion of Dietary Fat and Carbohydrate on Excercise Gas Exchange in Normal Subjects. Am. Rev. Respir. Dis. 1989;139:1430–1434. doi: 10.1164/ajrccm/139.6.1430. [PubMed] [CrossRef] [Google Scholar] 44. Sjödin A., Hellström F., Sehlstedt E., Svensson M., Burén J. Effects of a Ketogenic Diet on Muscle Fatigue in Healthy, Young, Normal-Weight Women: A Randomized Controlled Feeding Trial. Nutrients. 2020;12:955. doi: 10.3390/nu12040955. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 45. Kuo C.D., Shiao G.M., Lee J.D. The Effects of High-Fat and High-Carbohydrate Diet Loads on Gas Exchange and Ventilation in COPD Patients and Normal Subjects. Chest. 1993;104:189–196. doi: 10.1378/chest.104.1.189. [PubMed] [CrossRef] [Google Scholar] 46. Akrabawi S.S., Mobarhan S., Stoltz R.R., Ferguson P.W. Gastric Emptying, Pulmonary Function, Gas Exchange, and Respiratory Quotient after Feeding a Moderate versus High Fat Enteral Formula Meal in Chronic Obstructive Pulmonary Disease Patients. Nutrition. 1996;12:366. doi: 10.1016/S0899-9007(96)90853-9. [PubMed] [CrossRef] [Google Scholar] 47. Angelillo A.V., Sukhdarshan B., Durfee D., Dahl J., Patterson A.J., O’Donohue W.J. Effects of Low and High Carbohydrate Feedings in Ambulatory Patients with Chronic Obstructive Pulmonary Disease and Chronic Hypercapnia. Ann. Intern. Med. 1985;103:883–885. doi: 10.7326/0003-4819-103-6-883. [PubMed] [CrossRef] [Google Scholar] 48. Cai B., Zhu Y., Ma Y., Xu Z., Zao Y., Wang J., Lin Y., Comer G.M. Effect of Supplementing a High-Fat, Low-Carbohydrate Enteral Formula in COPD Patients. Nutrition. 2003;19:229–232. doi: 10.1016/S0899-9007(02)01064-X. [PubMed] [CrossRef] [Google Scholar] 49. Kwan R.M.F., Thomas S., Mir M.A. Effects of a Low Carbohydrate Isoenergetic Diet on Sleep Behavior and Pulmonary Functions in Healthy Female Adult Humans. J. Nutr. 1986;116:2393–2402. doi: 10.1093/jn/116.12.2393. [PubMed] [CrossRef] [Google Scholar] 50. Tirlapur V.G., Mir M.A. Effect of Low Calorie Intake on Abnormal Pulmonary Physiology in Patients with Chronic Hypercapneic Respiratory Failure. Am. J. Med. 1984;77:987–994. doi: 10.1016/0002-9343(84)90177-3. [PubMed] [CrossRef] [Google Scholar] 51. Kwan R., Mir A. Beneficial Effects of Dietary Carbohydrate Restriction in Chronic Cor Pulmonale. Am. J. Med. 1987;82:751–758. doi: 10.1016/0002-9343(87)90011-8. [PubMed] [CrossRef] [Google Scholar] 52. Al-Saady N.M., Blackmore C.M., Bennett E.D. High Fat, Low Carbohydrate, Enteral Feeding Lowers PaCO2 and Reduces the Period of Ventilation in Artificially Ventilated Patients. Intensive Care Med. 1989;15:290–295. doi: 10.1007/BF00263863. [PubMed] [CrossRef] [Google Scholar] 53. Faramawy M.A.E.S., Allah A.A., El Batrawy S., Amer H. Impact of High Fat Low Carbohydrate Enteral Feeding on Weaning from Mechanical Ventilation. Egypt. J. Chest Dis. Tuberc. 2014;63:931–938. doi: 10.1016/j.ejcdt.2014.07.004. [CrossRef] [Google Scholar] 54. Cook D., Meade M., Guyatt G., Butler R., Aldawood A., Epstein S. Trials of Miscellaneous Interventions to Wean from Mechanical Ventilation. Chest. 2001;120:438S–444S. doi: 10.1016/S0012-3692(15)50001-9. [PubMed] [CrossRef] [Google Scholar] 55. Mohamed N., Koofy E., Rady H.I., Abdallah S.M., Bazaraa H.M., Rabie A., El-ayadi A.A. The Effect of High Fat Dietary Modification and Nutritional Status on the Outcome of Critically Ill Ventilated Children: Single-Center Study. Korean J. Pediatr. 2019;62:344–352. doi: 10.3345/kjp.2018.06835. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 56. Kossoff E.H., Turner Z., Adams J., Bessone S.K., Avallone J., Mcdonald T.J.W., Diaz-arias L., Barron B.J., Vizthum D., Cervenka M.C. Ketogenic Diet Therapy Provision in the COVID-19 Pandemic: Dual-Center Experience and Recommendations. Epilepsy Behav. 2020;111:1–6. doi: 10.1016/j.yebeh.2020.107181. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 57. Ferraris C., Pasca L., Guglielmetti M., Marazzi C., Trentani C., Varesio C., Tagliabue A., de Giorgis V. Comment on: Ketogenic Diet Therapy Provision in the COVID-19 Pandemic: Dual-Center Experience and Recommendations. Epilepsy Behav. 2020;112:1–2. doi: 10.1016/j.yebeh.2020.107399. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 58. Soliman S., Faris M.A.I.E., Ratemi Z., Halwani R. Switching Host Metabolism as an Approach to Dampen SARS-CoV-2 Infection. Ann. Nutr. Metab. 2020;76:297–303. doi: 10.1159/000510508. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 59. Namazue J., Kato T., Okuno T., Shiraki K., Yamanishi K. Evidence for Attachment of Fatty Acid to Varicella-Zoster Virus Glycoproteins and Effect of Cerulenin on the Maturation of Varicella-Zoster Virus Glycoproteins. Intervirology. 1989;30:268–277. doi: 10.1159/000150102. [PubMed] [CrossRef] [Google Scholar] 60. Koyuncu E., Purdy J.G., Rabinowitz J.D., Shenk T. Saturated Very Long Chain Fatty Acids Are Required for the Production of Infectious Human Cytomegalovirus Progeny. PLoS Pathog. 2013;9:1–15. doi: 10.1371/journal.ppat.1003333. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 61. Herker E., Ott M. Unique Ties between Hepatitis C Virus Replication and Intracellular Lipids. Trends Endocrinol. Metab. 2011;22:241–248. doi: 10.1016/j.tem.2011.03.004. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 62. Stefan N., Birkenfeld A.L., Schulze M.B., Ludwig D.S. Obesity and Impaired Metabolic Health in Patients with COVID-19. Nat. Rev. Endocrinol. 2020;16:341–342. doi: 10.1038/s41574-020-0364-6. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 63. Campia U., Tesauro M., Di Daniele N., Cardillo C. The Vascular Endothelin System in Obesity and Type 2 Diabetes: Pathophysiology and Therapeutic Implications. Life Sci. 2014;118:149–155. doi: 10.1016/j.lfs.2014.02.028. [PubMed] [CrossRef] [Google Scholar] 64. Watanabe M., Masieri S., Costantini D., Tozzi R., de Giorgi F., Gangitano E., Tuccinardi D., Poggiogalle E., Mariani S., Basciani S., et al. Overweight and Obese Patients with Nickel Allergy Have a Worse Metabolic Profile Compared to Weight Matched Non-Allergic Individuals. PLoS ONE. 2018;13:e0202683. doi: 10.1371/journal.pone.0202683. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 65. Ledford H. How Obesity Could Create Problems for a COVID Vaccine. Nature. 2020;586:488–489. doi: 10.1038/d41586-020-02946-6. [PubMed] [CrossRef] [Google Scholar] 66. Sukkar S.G., Bassetti M. Induction of Ketosis as a Potential Therapeutic Option to Limit Hyperglycemia and Prevent Cytokine Storm in COVID-19. Nutrition. 2020;79–80:110967. doi: 10.1016/j.nut.2020.110967. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 67. Paoli A., Gorini S., Caprio M. The Dark Side of the Spoon—Glucose, Ketones and COVID-19: A Possible Role for Ketogenic Diet? J. Transl. Med. 2020;18:1–9. doi: 10.1186/s12967-020-02600-9. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 68. Stam H.J., Stucki G., Bickenbach J. European Academy of Rehabilitation Medicine Covid-19 and Post Intensive Care Syndrome: A Call for Action. J. Rehabil. Med. 2020;52:jrm00044. doi: 10.2340/16501977-2677. [PubMed] [CrossRef] [Google Scholar] 69. Lubrano C., Masi D., Risi R., Balena A., Watanabe M., Mariani S., Gnessi L. Is Growth Hormone Insufficiency the Missing Link Between Obesity, Male Gender, Age, and COVID-19 Severity? Obesity. 2020;28:2038–2039. doi: 10.1002/oby.23000. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 70. Basciani S., Camajani E., Contini S., Persichetti A., Risi R., Bertoldi L., Strigari L., Prossomariti G., Watanabe M., Mariani S., et al. Very-Low-Calorie Ketogenic Diets With Whey, Vegetable, or Animal Protein in Patients With Obesity: A Randomized Pilot Study. J. Clin. Endocrinol. Metab. 2020;105:2939–2949. doi: 10.1210/clinem/dgaa336. [PubMed] [CrossRef] [Google Scholar] 71. Bruci A., Tuccinardi D., Tozzi R., Balena A., Santucci S., Frontani R., Mariani S., Basciani S., Spera G., Gnessi L., et al. Very Low-Calorie Ketogenic Diet: A Safe and Effective Tool for Weight Loss in Patients With Obesity and Mild Kidney Failure. Nutrients. 2020;12:333. doi: 10.3390/nu12020333. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 72. Benlloch M., López-Rodríguez M.M., Cuerda-Ballester M., Drehmer E., Carrera S., Ceron J.J., Tvarijonaviciute A., Chirivella J., Fernández-García D., de La Rubia Ortí J.E. Satiating Effect of a Ketogenic Diet and Its Impact on Muscle Improvement and Oxidation State in Multiple Sclerosis Patients. Nutrients. 2019;11:1156. doi: 10.3390/nu11051156. [PMC free article] [PubMed] [CrossRef] [Google Scholar] 73. Klement R.J., Weigel M.M., Sweeney R.A. A Ketogenic Diet Consumed during Radiotherapy Improves Several Aspects of Quality of Life and Metabolic Health in Women with Breast Cancer. Clin. Nutr. 2021 doi: 10.1016/j.clnu.2021.01.023. in press. [PubMed] [CrossRef] [Google Scholar]

Articles from Nutrients are provided here courtesy of Multidisciplinary Digital Publishing Institute (MDPI)