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Part 4: Metabolic Syndrome and Nutrition in PD |
Division of Baxter Novum and Renal Medicine, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden
Correspondence to: B. Lindholm, Division of Baxter Novum and Renal Medicine, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, K-56, Karolinska University Hospital, Huddinge, Stockholm S-141 86 Sweden. bengt.lindholm{at}ki.se
Metabolic syndrome (MetS) is defined as a cluster of risk factors for
type 2 diabetes and cardiovascular disease; it is also an independent risk
factor for developing chronic kidney disease (CKD) in the general population.
Therefore, CKD has many similarities and associations with MetS, and the
individual risk factors constituting MetS—especially insulin resistance
and glucose intolerance, hypertension, dyslipidemia, and obesity—are
also common features of the early stages of CKD. In the later stages of CKD,
uremia per se and uremic complications such as fluid retention,
protein–energy wasting, inflammation, and oxidative stress further
contribute to an increase in the prevalence of MetS in CKD patients. In
addition, PD patients exposed to glucose-based PD fluids have an increased
risk of developing metabolic complications. The broad use of MetS in clinical
research has raised the awareness of the public and of individual patients
concerning the value of lifestyle interventions. However, the definition and
pathogenesis of MetS are still debated, and no standardized definition nor
proven prognostic value has been established for MetS as a cluster of risk
factors for diabetes or cardiovascular disease in PD patients. Furthermore,
considering the paradoxical associations of some of the risk factors in MetS
with decreased mortality, another set of risk factors—those specific to
patients with uremia (for example, inflammation and malnutrition)—and
the appropriate cut-off levels to individual MetS risk factors should be taken
account at the same time. Also, the benefit of interventions targeting these
risk factors should be clarified in further clinical studies.
KEY WORDS: Metabolic syndrome; chronic kidney disease.
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