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Updated: Jun 29, 2026

Scanning Skeletal Remains for Bone Mineral Density in Forensic Contexts
Published on: January 29, 2018
Bone turnover in malnourished children
F Branca1, S P Robins, A Ferro-Luzzi
1Istituto Nazionale della Nutrizione, Rome, Italy.
Insights
Urinary pyridinoline (PYD) and deoxypyridinoline (DPD) are collagen cross-links that indicate bone and cartilage turnover. Malnourished children showed significantly lower excretion rates, which increased after recovery, correlating with height gain.
Area of Science:
- Biochemistry
- Pediatrics
- Nutrition Science
Background:
- Pyridinoline (PYD) and deoxypyridinoline (DPD) are collagen cross-links found in bone and cartilage.
- Urinary excretion of PYD and DPD serves as a specific marker for skeletal turnover due to bone matrix resorption.
Purpose of the Study:
- To assess skeletal turnover in severely malnourished boys using PYD and DPD excretion.
- To investigate the relationship between skeletal turnover and subsequent growth rate during recovery.
Main Methods:
- Measurement of urinary PYD and DPD excretion rates in 46 severely malnourished boys.
- Assessment of anthropometric data (height-for-age, weight-for-height) and height gain during recovery.
Main Results:
- Urinary PYD and DPD excretion rates were significantly lower in malnourished boys compared to post-recovery.
- Skeletal turnover markers increased substantially after nutritional rehabilitation.
- The rate of height gain during recovery was significantly correlated with initial cross-link excretion, age, and weight-for-height.
Conclusions:
- Urinary PYD and DPD levels reflect skeletal turnover in malnourished children.
- These markers can be utilized to monitor therapeutic interventions aimed at improving growth and alleviating stunting.
Abstract:
Pyridinoline (PYD) and deoxypyridinoline (DPD) are cross-linking aminoacids of collagen that are located mainly in bone and cartilage. When bone matrix is resorbed these cross-links are quantitatively excreted in the urine and therefore represent specific markers. We have measured the urinary excretion rate of PYD and DPD in 46 severely malnourished boys to assess their skeletal turnover and to relate this to their subsequent rate of growth. The children were aged 13 months (SD 6), and height-for-age was -3.6 (1.6) Z-score, and weight-for-height was -2.4 (0.8) Z-score. PYD excretion when malnourished and after "recovery" was 11.2 (4.6) nmol h-1m-2 and 32.2 (10.8) nmol h-1m-2 and DPD excretion was 2.6 (1.3) nmol h-1m-2 and 7.5 (3.0) nmol h-1m-2, respectively. The ratio of the two cross-links did not change with recovery. These data show that cartilage and bone turnover is much lower in the malnourished than in the recovered child. There was no difference in the degree of depression of turnover between the children with marasmus, marasmic-kwashiorkor, or kwashiorkor. The rate of height gain during recovery was significantly related to cross-link excretion, age, and weight-for-height on admission. These three factors accounted for 44% of the variance in the height velocity of the children. PYD and DPD excretion rate could be used to assess therapeutic interventions designed to alleviate stunting.
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