Tactile/kinesthetic stimulation (TKS) increases tibial speed of sound and urinary osteocalcin (U-MidOC and unOC) in premature infants (29–32 weeks PMA)

• Published in: Bone (New York, N.Y.) N.Y.), 2012-10, Vol.51 (4), p.661-666
• Main Authors: Haley, S, Beachy, J, Ivaska, K.K, Slater, H, Smith, S, Moyer-Mileur, L.J
• Format: Article
• Language: English
• Subjects: Acoustics; Biological and medical sciences; Diseases of mother, fetus and pregnancy; Female; Fundamental and applied biological sciences. Psychology; Gynecology. Andrology. Obstetrics; Humans; Infant massage; Infant, Newborn; Infant, Premature; Kinesthesis; Longitudinal Studies; Male; Massage; Medical sciences; Orthopedics; Osteocalcin; Osteocalcin - urine; Pregnancy. Fetus. Placenta; Preterm; Prospective Studies; Pyridinium crosslinks; Speed of Sound (SOS); Tibia - diagnostic imaging; Tibia - physiology; Ultrasonography; Vertebrates: anatomy and physiology, studies on body, several organs or systems
• ISSN: 8756-3282; 1873-2763
• DOI: 10.1016/j.bone.2012.07.016

Abstract Preterm delivery (< 37 weeks post-menstrual age) is associated with suboptimal bone mass. We hypothesized that tactile/kinesthetic stimulation (TKS), a form of infant massage that incorporates kinesthetic movement, would increase bone strength and markers of bone accretion in preterm infants. Preterm, AGA infants (29–32 weeks) were randomly assigned to TKS ( N = 20) or Control ( N = 20). Twice daily TKS was provided 6 days per week for 2 weeks. Control infants received the same care without TKS treatment. Treatment was masked to parents, health care providers, and study personnel. Baseline and week two measures were collected for tibial speed of sound (tSOS, m/sec), a surrogate for bone strength, by quantitative ultrasound (Sunlight8000) and urine markers of bone metabolism, pyridinium crosslinks and osteocalcin (U-MidOC and unOC). Infant characteristics at birth and study entry as well as energy/nutrient intake were similar between TKS and Control. TKS intervention attenuated the decrease in tSOS observed in Control infants ( p < 0.05). Urinary pyridinium crosslinks decreased over time in both TKS and CTL ( p < 0.005). TKS infants experienced greater increases in urinary osteocalcin (U-MidOC, p < 0.001 and unOC, p < 0.05). We conclude that TKS improves bone strength in premature infants by attenuating the decrease that normally follows preterm birth. Further, biomarkers of bone metabolism suggest a modification in bone turnover in TKS infants in favor of bone accretion. Taken together, we speculate that TKS improves bone mineralization.