Short-Term Preoperative Calorie and Protein Restriction Is Feasible in Healthy Kidney Donors and Morbidly Obese Patients Scheduled for Surgery

Franny Jongbloed, Ron W F de Bruin, René A Klaassen, Piet Beekhof, Harry van Steeg, Frank J M F Dor, Erwin van der Harst, Martijn E T Dollé, Jan N M IJzermans, Franny Jongbloed, Ron W F de Bruin, René A Klaassen, Piet Beekhof, Harry van Steeg, Frank J M F Dor, Erwin van der Harst, Martijn E T Dollé, Jan N M IJzermans

Abstract

Introduction: Surgery-induced oxidative stress increases the risk of perioperative complications and delay in postoperative recovery. In mice, short-term preoperative dietary and protein restriction protect against oxidative stress. We investigated the feasibility of a calorie- and protein-restricted diet in two patient populations.

Methods: In this pilot study, 30 live kidney donors and 38 morbidly obese patients awaiting surgery were randomized into three groups: a restricted diet group, who received a synthetic liquid diet with 30% fewer calories and 80% less protein for five consecutive days; a group who received a synthetic diet containing the daily energy requirements (DER); and a control group. Feasibility was assessed using self-reported discomfort, body weight changes, and metabolic parameters in blood samples.

Results: Twenty patients (71%) complied with the restricted and 13 (65%) with the DER-diet. In total, 68% of the patients reported minor discomfort that resolved after normal eating resumed. The mean weight loss on the restricted diet was significantly greater (2.4 kg) than in the control group (0 kg, p = 0.002), but not in the DER-diet (1.5 kg). The restricted diet significantly reduced levels of serum urea and plasma prealbumin (PAB) and retinol binding protein (RBP).

Conclusions: A short-term preoperative calorie- and protein-restricted diet is feasible in kidney donors and morbidly obese patients. Compliance is high and can be objectively measured via changes in urea, PAB, and RBP levels. These results demonstrate that this diet can be used to study the effects of dietary restriction on surgery-induced oxidative stress in a clinical setting.

Keywords: compliance; dietary restriction; feasibility; preoperative diet; protein restriction.

Figures

Figure 1
Figure 1
The number of side effects as percentages of participants in groups consuming a restricted diet and a daily energy requirements diet (DER-diet). (A) Side effects of the dietary restriction and protein restriction diet in the kidney donors were mostly related to nutritional intake and to the gastrointestinal tract; (B) Morbidly obese patients showed relatively more gastrointestinal discomfort; (C) A total of 90% of the kidney donors reported gastrointestinal discomfort during the DER-diet; (D) This percentage was lower in the morbidly obese patients and was the same as discomfort related to nutritional intake. Effects are clustered based on the origin of the symptoms. Within each cluster, each side effect is depicted in a different shade of color.
Figure 2
Figure 2
Visual Analogue Scores (VAS) for nausea, pain, and wellbeing before, during, and after each dietary intervention. (A) The nausea scores increased significantly for patients on the restricted diet and the DER-diet but normalized to baseline levels directly after the intervention period was over; (B) The pain scores did not change significantly during the dietary interventions; (C) The restricted diet resulted in significant decreased VAS wellbeing scores during the diet compared to before, but normalized again directly after the intervention period was over; * p < 0.05. Bars represent the standard error of the mean; DER = daily energy requirements.
Figure 3
Figure 3
Body weight changes in the three dietary intervention groups. Patients on the restricted diet lost an average of 2.5% of their body weight, corresponding to 2.4 ± 1.4 kg; This body weight loss was significantly greater than in the control group, which showed no change; The DER-diet resulted in a 1.7% loss in body weight (1.5 ± 1.4 kg), which was not significantly different than the two other groups; Changes are shown as percentages compared to the body weight at baseline; ** p < 0.01. Bars represent the standard error of the mean. DER = daily energy requirements.
Figure 4
Figure 4
Serum levels of albumin, urea, valine and leucine after the three dietary interventions. (A) Serum albumin did not significantly change in any of the groups; (B) serum urea was decreased significantly after the restricted diet, while it did not change after the DER diet or in the control group; both serum valine (C) and leucine (D) did not differ between groups, but did show a trend towards a decrease after the restricted diet; red symbols = kidney donors, as opposed to morbidly obese individuals (black or gray symbols); DER = daily energy requirements.
Figure 5
Figure 5
Plasma levels of prealbumin (PAB) and retinol binding protein (RBP) after the three dietary interventions. (A) Prealbumin (PAB) and (B) retinol binding protein (RBP) both decreased significantly after the restricted diet, with no changes seen in the DER-diet group or in the control group; (C) PAB and (D) RBP did not change in patients who did not complete the restricted diet. The two corresponding values for the individual patients are connected with a line. * p ≤ 0.002. Red symbols = kidney donors in the restricted diet group. DER = daily energy requirements.

References

    1. Blackburn G.L. Metabolic considerations in management of surgical patients. Surg. Clin N. Am. 2011;91:467–480. doi: 10.1016/j.suc.2011.03.001.
    1. Lushchak V.I. Free radicals, reactive oxygen species, oxidative stress and its classification. Chem. Biol. Interact. 2014;224C:164–175. doi: 10.1016/j.cbi.2014.10.016.
    1. Kucukakin B., Gogenur I., Reiter R.J., Rosenberg J. Oxidative stress in relation to surgery: Is there a role for the antioxidant melatonin? J. Surg. Res. 2009;152:338–347. doi: 10.1016/j.jss.2007.12.753.
    1. Calder P.C., Ahluwalia N., Brouns F., Buetler T., Clement K., Cunningham K., Esposito K., Jonsson L.S., Kolb H., Lansink M., et al. Dietary factors and low-grade inflammation in relation to overweight and obesity. Br. J. Nutr. 2011;106(Suppl. S3):S5–S78. doi: 10.1017/S0007114511005460.
    1. Snoeijs M.G., van Heurn L.W., Buurman W.A. Biological modulation of renal ischemia-reperfusion injury. Curr. Opin. Organ Transplant. 2010;15:190–199. doi: 10.1097/MOT.0b013e32833593eb.
    1. Bonventre J.V., Yang L. Cellular pathophysiology of ischemic acute kidney injury. J. Clin. Investig. 2011;121:4210–4221. doi: 10.1172/JCI45161.
    1. Mitchell J.R., Verweij M., Brand K., van de Ven M., Goemaere N., van den Engel S., Chu T., Forrer F., Muller C., de Jong M., et al. Short-term dietary restriction and fasting precondition against ischemia reperfusion injury in mice. Aging Cell. 2010;9:40–53. doi: 10.1111/j.1474-9726.2009.00532.x.
    1. Van Ginhoven T.M., Huisman T.M., van den Berg J.W., Ijzermans J.N., Delhanty P.J., de Bruin R.W. Preoperative fasting induced protection against renal ischemia/reperfusion injury is independent of ghrelin in mice. Nutr. Res. 2010;30:865–869. doi: 10.1016/j.nutres.2010.09.014.
    1. Van Ginhoven T.M., van den Berg J.W., Dik W.A., Ijzermans J.N., de Bruin R.W. Preoperative fasting induces protection against renal ischemia/reperfusion injury by a corticosterone-independent mechanism. Transpl. Int. 2010;23:1171–1178. doi: 10.1111/j.1432-2277.2010.01116.x.
    1. Verweij M., van Ginhoven T.M., Mitchell J.R., Sluiter W., van den Engel S., Roest H.P., Torabi E., Ijzermans J.N., Hoeijmakers J.H., de Bruin R.W. Preoperative fasting protects mice against hepatic ischemia/reperfusion injury: Mechanisms and effects on liver regeneration. Liver Transpl. 2011;17:695–704. doi: 10.1002/lt.22243.
    1. Jongbloed F., de Bruin R.W., Pennings J.L., Payan-Gomez C., van den Engel S., van Oostrom C.T., de Bruin A., Hoeijmakers J.H., van Steeg H., IJzermans J.N., et al. Preoperative fasting protects against renal ischemia-reperfusion injury in aged and overweight mice. PLoS ONE. 2014;9:306. doi: 10.1371/journal.pone.0100853.
    1. Mitchell J.R., Beckman J.A., Nguyen L.L., Ozaki C.K. Reducing elective vascular surgery perioperative risk with brief preoperative dietary restriction. Surgery. 2013;153:594–598. doi: 10.1016/j.surg.2012.09.007.
    1. Van Nieuwenhove Y., Dambrauskas Z., Campillo-Soto A., van Dielen F., Wiezer R., Janssen I., Kramer M., Thorell A. Preoperative very low-calorie diet and operative outcome after laparoscopic gastric bypass: A randomized multicenter study. Arch. Surg. 2011;146:1300–1305. doi: 10.1001/archsurg.2011.273.
    1. Carbajo M.A., Castro M.J., Kleinfinger S., Gomez-Arenas S., Ortiz-Solorzano J., Wellman R., Garcia-Ianza C., Luque E. Effects of a balanced energy and high protein formula diet (vegestart complet(r)) vs. Low-calorie regular diet in morbid obese patients prior to bariatric surgery (laparoscopic single anastomosis gastric bypass): A prospective, double-blind randomized study. Nutr. Hosp. 2010;25:939–948.
    1. Van Ginhoven T.M., de Bruin R.W., Timmermans M., Mitchell J.R., Hoeijmakers J.H., IJzermans J.N. Pre-operative dietary restriction is feasible in live-kidney donors. Clin. Transplant. 2011;25:486–494. doi: 10.1111/j.1399-0012.2010.01313.x.
    1. Van Ginhoven T.M., Dik W.A., Mitchell J.R., Smits-te Nijenhuis M.A., van Holten-Neelen C., Hooijkaas H., Hoeijmakers J.H., de Bruin R.W., IJzermans J.N. Dietary restriction modifies certain aspects of the postoperative acute phase response. J. Surg. Res. 2011;171:582–589. doi: 10.1016/j.jss.2010.03.038.
    1. Solon-Biet S.M., McMahon A.C., Ballard J.W., Ruohonen K., Wu L.E., Cogger V.C., Warren A., Huang X., Pichaud N., Melvin R.G., et al. The ratio of macronutrients, not caloric intake, dictates cardiometabolic health, aging, and longevity in ad libitum-fed mice. Cell Metab. 2014;19:418–430. doi: 10.1016/j.cmet.2014.02.009.
    1. Schulz K.F., Altman D.G., Moher D., Group C. Consort 2010 statement: Updated guidelines for reporting parallel group randomised trials. BMJ. 2010;340:c332. doi: 10.1136/bmj.c332.
    1. De Klerk M., Kal-van Gestel J.A., Haase-Kromwijk B.J., Claas F.H., Weimar W., Living Donor Kidney Exchange Program Eight years of outcomes of the dutch living donor kidney exchange program. Clin. Transpl. 2011:287–290.
    1. Roza A.M., Shizgal H.M. The harris benedict equation reevaluated: Resting energy requirements and the body cell mass. Am. J. Clin. Nutr. 1984;40:168–182.
    1. Wewers M.E., Lowe N.K. A critical review of visual analogue scales in the measurement of clinical phenomena. Res. Nurs. Health. 1990;13:227–236. doi: 10.1002/nur.4770130405.
    1. Schulz K.F., Altman D.G., Moher D., CONSORT Group CONSORT 2010 Statement: Updated guidelines for reporting parallel group randomised trials. Int. J. Surg. 2011;9:672–677. doi: 10.1016/j.ijsu.2011.09.004.
    1. Harputlugil E., Hine C., Vargas D., Robertson L., Manning B.D., Mitchell J.R. The tsc complex is required for the benefits of dietary protein restriction on stress resistance in vivo. Cell Rep. 2014;8:1160–1170. doi: 10.1016/j.celrep.2014.07.018.
    1. Pamplona R., Barja G. Mitochondrial oxidative stress, aging and caloric restriction: The protein and methionine connection. Biochim. Biophys. Acta. 2006;1757:496–508. doi: 10.1016/j.bbabio.2006.01.009.
    1. Verweij M., Sluiter W., van den Engel S., Jansen E., Ijzermans J.N., de Bruin R.W. Altered mitochondrial functioning induced by preoperative fasting may underlie protection against renal ischemia/reperfusion injury. J. Cell Biochem. 2013;114:230–237. doi: 10.1002/jcb.24360.
    1. Reeves J.G., Suriawinata A.A., Ng D.P., Holubar S.D., Mills J.B., Barth R.J. Short-term preoperative diet modification reduces steatosis and blood loss in patients undergoing liver resection. Surgery. 2013;154:1031–1037. doi: 10.1016/j.surg.2013.04.012.
    1. Osterberg L., Blaschke T. Adherence to medication. N. Engl. J. Med. 2005;353:487–497. doi: 10.1056/NEJMra050100.
    1. Ho W., Spiegel B.M.R. The relationship between obesity and functional gastrointestinal disorders: Causation, association, or neither? Gastroenterol. Hepatol. 2008;4:572–578.
    1. Bauer P., Charpentier C., Bouchet C., Nace L., Raffy F., Gaconnet N. Parenteral with enteral nutrition in the critically ill. Intensive Care Med. 2000;26:893–900. doi: 10.1007/s001340051278.
    1. Tempel Z., Grandhi R., Maserati M., Panczykowski D., Ochoa J., Russavage J., Okonkwo D. Prealbumin as a serum biomarker of impaired perioperative nutritional status and risk for surgical site infection after spine surgery. J. Neurol. Surg. A Cent. Eur. Neurosurg. 2015;76:139–143.
    1. Addis T., Barrett E., Poo L.J., Yuen D.W. The relation between the serum urea concentration and the protein consumption of normal individuals. J. Clin. Investig. 1947;26:869–874. doi: 10.1172/JCI101878.

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