4.6 Article

Ghrelin and bone: Is there an association in older adults?: The Rancho Bernardo study

Journal

JOURNAL OF BONE AND MINERAL RESEARCH
Volume 21, Issue 5, Pages 752-757

Publisher

WILEY-BLACKWELL
DOI: 10.1359/JBMR.060209

Keywords

ghrelin; BMD; bone turnover; osteoporosis; aging

Funding

  1. Medical Research Council [G106/1133] Funding Source: Medline
  2. NIA NIH HHS [AG 07181] Funding Source: Medline
  3. NIDDK NIH HHS [DK 31801] Funding Source: Medline
  4. Medical Research Council [G106/1133] Funding Source: researchfish
  5. MRC [G106/1133] Funding Source: UKRI

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Introduction: Ghrelin is a gastric hormone recently shown to be associated with bone metabolism in animal and in vitro studies. Studies in humans are limited. We investigated the association of ghrelin with BMD, the bone resorption marker N-telopeptide (NTX), and bone loss in older men and women. Materials and Methods: Participants were 977 community-dwelling men and non-estrogen-using postmenopausal women, 50-91 years of age. Plasma ghrelin was measured by radioimmunoassay from blood obtained between 1984 and 1987. Between 1988 and 1991, BMD was measured at the midshaft radius by single photon absorptiometry and at the femoral neck, total hip, and lumbar spine by DXA. Axial BMD measurements were repeated an average of 4 years later in 544 participants. Bone turnover was assessed by NTX in urine obtained at the same time as the initial BMD. Multiple regression analyses were used to test sex-specific associations of ghrelin with BNM, NTX, and bone loss in both sexes. Results: No significant ghrelin-BMD or ghrelin-bone loss associations were observed in either sex, after adjusting for age and body mass index (BMI). Ghrelin was inversely associated with NTX in men and positively associated with NTX in women, independent of age. After adjusting for both age and BMI, this association reached statistical significance in men and was weakened in women. Conclusions: Ghrelin may be associated with bone turnover, but there is no evidence for an association with BMD or short-term change in BMD in older adults.

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