American Journal of Kidney Diseases
Volume 50, Issue 6 , Pages 1001-1008, December 2007

Neuropeptide Y and Markers of Osteoblast Activity in Dialysis Patients: A Cross-Sectional Study

CNR–IBIM, National Research Council-Institute of Biomedicine, Clinical Epidemiology and Physiopathology of Renal Diseases and Hypertension, Reggio Calabria, Italy.

Received 17 April 2007; accepted 6 September 2007. published online 31 October 2007.

Background

In mice, neuropeptide Y (NPY) decreases bone turnover by means of a parathyroid hormone-independent effect on osteoblast activity.

Study Design

Cross-sectional study.

Setting & Participants

We studied the relationship between levels of NPY and biomarkers of osteoblast activity in 161 nondiabetic patients with end-stage renal disease (131 patients, hemodialysis; 30 patients, continuous ambulatory peritoneal dialysis).

Predictors & Outcomes

We performed an analysis of demographic and clinical variables associated with NPY as a dependent variable and a second analysis testing the association of NPY (as an independent variable) with markers of osteoblast activity.

Results

Peritoneal dialysis as treatment modality (β = 0.37; P < 0.001) and longer duration of dialysis therapy (β = 0.24; P < 0.01) were independently related to plasma NPY. NPY level was related inversely (P < 0.001) to serum alkaline phosphatase and bone alkaline phosphatase levels (P = 0.01). The NPY-alkaline phosphatase link was confirmed in a multiple regression analysis adjusting for a series of potential confounders, including parathyroid hormone. In a categorical analysis in which the study population was divided according to NPY quartiles, the proportion of patients with low alkaline phosphatase levels was lowest in the first 2 NPY quartiles (26%) and highest in NPY quartile 4 (80%; P < 0.001), and this association held true in a multiple logistic regression analysis, indicating that the risk of low alkaline phosphatase level increases in parallel with NPY level.

Limitations

The hypothesis generated by this cross-sectional study needs to be confirmed in cohort studies.

Conclusions

The inverse relationships between levels of NPY and biomarkers of bone turnover support the hypothesis that NPY may be implicated in low bone turnover in dialysis patients by a central parathyroid-independent mechanism.

Index Words: Alkaline phosphatase, bone alkaline phosphatase isoenzyme, low bone turnover, neuropeptide Y, osteoblast activity

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 Originally published online as doi:10.1053/j.ajkd.2007.09.001 on October 30, 2007.

PII: S0272-6386(07)01238-3

doi:10.1053/j.ajkd.2007.09.001

American Journal of Kidney Diseases
Volume 50, Issue 6 , Pages 1001-1008, December 2007