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High BMI among adult haemodialysis patients at a UK hospital: an indicator of poor or adequate nutritional status?

Published online by Cambridge University Press:  22 January 2016

N.A Gityamwi
Affiliation:
School of Biosciences and Medicine, University of Surrey, Guildford, GU2 7XH
M.A Hellyer
Affiliation:
Department of Nutrition and Dietetics, Queen Alexandra Hospital, Portsmouth, PO6 3LY
K.H. Hart
Affiliation:
School of Biosciences and Medicine, University of Surrey, Guildford, GU2 7XH
B Engel
Affiliation:
School of Biosciences and Medicine, University of Surrey, Guildford, GU2 7XH
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Abstract

Type
Abstract
Copyright
Copyright © The Authors 2016 

In the general population obesity is associated with increased risk of morbidity and mortality. In contrast, studies indicate better survival among overweight/obese HD patientsReference Glanton, Hypolite and Hshieh 1 , Reference Kalantar-Zadeh, Kopple and Kilpatrick 2 . However, it should not be forgotten that obesity (excess weight) does not necessarily imply good nutritional status as muscle wasting can occur, concealed by fat accumulation, a condition called “sarcopenic obesity” (SO)Reference Honda, Qureshi and Axelsson 3 . SO has several metabolic implications including inflammationReference Witasp, Carrero and Heimburger 4 and increased risk of cardiovascular eventsReference Kamimura, Carrero and Canziani 5 which are also known to be the leading causes of mortality in chronic kidney disease (CKD) patients. This study aimed to audit the nutritional status and biochemical parameters of UK haemodialysis (HD) patients and to compare these parameters between dialysis settings.

Current patients who had been receiving treatment for at least 6 months at one hospital (via home or satellite unit HD) were eligible for inclusion. Parameters under observation were BMI, serum albumin (Alb), CRP, Adjusted Calcium, Phosphate, iPTH, Urea, Creatinine, Haemoglobin and Ferritin levels with data extracted retrospectively from patient records. Data were analysed using SPSS version 22 and for each biochemical parameter the proportion of patients achieving, exceeding or below the K/DOQI (2006) reference range standards was calculated.

One hundred and forty seven patients were included in the audit (46 receiving home and 101 satellite HD). BMI, Alb and CRP levels raised concern in the sample as a whole (see Table). Only Alb was significantly associated with HD setting with status being better in home HD patients (BMI: X2 = 3·33, p = 0·18; Alb: X2 = 3·68, p = 0·03; CRP: X2 = 0·57, p = 0·45).

The majority of patients had a BMI above the healthy range (overweight or obese (>25 kg/m2 BMI)). High CRP (>5 mg/l) and low albumin levels (<40 g/l) were also observed in the majority of the sample.

Although high BMI as a marker of good nutritional status has been positively associated with improved survival in HD patientsReference Glanton, Hypolite and Hshieh 1 , Reference Kalantar-Zadeh, Kopple and Kilpatrick 2 an increased CRP and decreased albumin indicate an inflammatory state and have been associated with loss of lean muscle mass and increased cardiovascular mortality (defined as the ‘malnutrition, inflammation syndrome’)Reference Kalantar-Zadeh, Kopple and Kilpatrick 2 , Reference Honda, Qureshi and Axelsson 3 , Reference Witasp, Carrero and Heimburger 4 , Reference Reijnierse, Trappenburg and Leter 6 . This raises concern as to whether the BMI levels observed in this sample of HD patients indicate better nutrition or increased health risk and whether there is indeed no significant difference in nutritional status between the two settings regardless of differences in albumin status. Further research to investigate this via appropriate measures for muscle mass, strength and physical performance are requiredReference Reijnierse, Trappenburg and Leter 6 to ascertain the impact of the inflammatory state on body composition and nutritional status of these patients in order to inform appropriate nutritional intervention.

References

1. Glanton, CW, Hypolite, IO, Hshieh, PB et al. (2003) Ann Epidemiol, 13(2), 136143.Google Scholar
2. Kalantar-Zadeh, K, Kopple, JD, Kilpatrick, RD et al. (2005) Am J Kidney Dis, 46(3), 489500.Google Scholar
3. Honda, H, Qureshi, AR, Axelsson, J et al. (2007) Am J Clin Nutr, 86(3), 633638.Google Scholar
4. Witasp, A, Carrero, JJ, Heimburger, O et al. (2011) J Intern Med, 269(4), 410419.CrossRefGoogle Scholar
5. Kamimura, MA, Carrero, JJ, Canziani, ME et al. (2013) Nutr Metab Cardiovasc Dis, 23(9), 891897.Google Scholar
6. Reijnierse, EM, Trappenburg, MC, Leter, MJ et al. (2015) PLoS ONE, 10(8), e0135933.CrossRefGoogle Scholar