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Authors Xing WM, Lv XL, Gao WY, Wang JR, Wang ZX, Wang SY, Zhang J, Yan J
Received 17 October 2017
Accepted for publication 8 December 2017
Published 27 February 2018 Volume 2018:13 Pages 343—353
DOI https://doi.org/10.2147/CIA.S154356
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Lucy Goodman
Peer reviewer comments 3
Editor who approved publication: Dr Wu
Objective: This study aimed to verify the existing relationship between bone
mineral density (BMD) and chronic heart failure (CHF) by meta-analysis.
Methods: Databases, including PubMed, Web of Science, and
Chinese National Knowledge Infrastructure, published in English or Chinese up
to February 28, 2017, were searched for studies on the association between CHF
and BMD. Two independent reviewers collected the relevant articles. The
standard mean deviation (SMD) and 95% confidence interval were calculated for
BMD with fixed- and random-effect models. Subgroup and sensitivity analyses
were also conducted.
Results: A total of six studies (552 CHF and 243 non-CHF
patients) were included. The results indicated that the patients with CHF had a lower total
BMD compared with the non-CHF patients. Similar effects were also observed for
femoral neck, arm, leg, and trunk BMD. However, no difference was observed in
the lumbar spine BMD. The SMD of total BMD in New York Heart Association
classes I or II (NYHA I or II) patients was -0.62, while that in NYHA III or IV
patients was -0.87, and the SMD of femoral bone mineral density in NYHA I or II
patients was -0.47, while that in NYHA III or IV patients was -1.07. Moreover,
vitamin D and parathyroid hormone (PTH) were also found to be associated with
CHF.
Conclusion: Patients with CHF had a lower total BMD and
femoral neck, arm, leg, or trochanter BMD than patients with non-CHF. Vitamin D
reduced, whereas PTH increased, with the severity of CHF. The clinical
significance of the present findings remains uncertain and should be confirmed
by future studies.
Keywords: bone mineral
density, chronic heart failure, meta-analysis