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. 2018 Jan;46(1):492-503.
doi: 10.1177/0300060517725660. Epub 2017 Aug 29.

Effect of hypercortisolism on bone mineral density and bone metabolism: A potential protective effect of adrenocorticotropic hormone in patients with Cushing's disease

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Effect of hypercortisolism on bone mineral density and bone metabolism: A potential protective effect of adrenocorticotropic hormone in patients with Cushing's disease

Weihong Guo et al. J Int Med Res. 2018 Jan.

Abstract

Objective To investigate the effects of Cushing's disease (CD) and adrenal-dependent Cushing's syndrome (ACS) on bone mineral density (BMD) and bone metabolism. Methods Data were retrospectively collected for 55 patients with hypercortisolism (CD, n = 34; ACS n = 21) from January 1997 to June 2014. BMD was examined in all patients, and bone turnover markers were tested in some patients. Healthy controls (n = 18) were also recruited. Results The lumbar spine and femoral neck BMD were significantly lower in the ACS and CD groups than in the control group. Lumbar BMD was significantly lower in the ACS than CD group. The collagen breakdown product (CTX) concentrations were significantly higher while the osteocalcin and procollagen type I N-terminal propeptide (PINP) concentrations were significantly lower in the ACS and CD groups than in the control group. The PINP concentration was significantly lower while the CTX concentration was significantly higher in the ACS than CD group. In the CD group only, lumbar BMD and serum adrenocorticotropic hormone had a significant positive correlation. Conclusions Bone turnover markers indicated suppressed osteoblast and enhanced osteoclast activities. PINP and CTX changes might indicate bone mass deterioration. Adrenocorticotropic hormone might be protective for lumbar BMD in patients with CD.

Keywords: Bone mineral density; Cushing’s disease; adrenal-dependent Cushing’s syndrome; bone turnover markers; hypercortisolism; osteoporosis.

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Figures

Figure 1.
Figure 1.
Comparison of adrenal cortex function between the adrenal-dependent Cushing’s syndrome (ACS), Cushing’s disease (CD), and healthy control (N) groups Values are expressed as mean ± standard deviation. *P < 0.05 compared with the N group; ΔP < 0.05 compared with the CD group ACTH, adrenocorticotropic hormone; Cor, serum cortisol; UCor, urinary cortisol
Figure 2.
Figure 2.
Comparison of bone mineral density (BMD) between the adrenal-dependent Cushing’s syndrome (ACS), Cushing’s disease (CD), and healthy control (N) groups Values are expressed as mean ± standard deviation. *P < 0.05 compared with the N group; ΔP < 0.05 compared with the CD group
Figure 3.
Figure 3.
Comparison of bone turnover markers between the adrenal-dependent Cushing’s syndrome (ACS), Cushing’s disease (CD), and healthy control (N) groups Values are expressed as mean ± standard deviation. *P < 0.05 compared with the N group; ΔP < 0.05 compared with the CD group Ca, calcium; P, phosphorus; UCa, urinary calcium; ALP, alkaline phosphatase; PTH, parathyroid hormone; OC, osteocalcin; PINP, procollagen type I N-terminal propeptide; CTX, collagen type I cross-linked C-telopeptide
Figure 4.
Figure 4.
Correlation between bone turnover markers and lumbar bone mineral density (BMD) in patients with hypercortisolism OC, osteocalcin; PINP, procollagen type I N-terminal propeptide; CTX, collagen type I cross-linked C-telopeptide
Figure 5.
Figure 5.
Correlation between adrenocorticotropic hormone (ACTH) concentrations and lumbar bone mineral density (BMD) in patients with adrenal-dependent Cushing’s syndrome (ACS) or Cushing’s disease (CD)

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