Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/37145
Title: Reply to: The Association Between Cognitive Decline and Bone Loss and Fracture Risk Is Not Affected by Medication With Anticholinergic Effect
Authors: Bliuc, Dana
Tran , Thach
Adachi, Jonathan D.
Atkins, Gerald J.
Berger, Claudie
VAN DEN BERGH, Joop 
Cappai , Roberto
Eisman, John A.
van Geel , Tineke
GEUSENS, Piet 
Goltzman, David
Hanley, David A.
Josse, Robert
Kaiser, Stephanie
Kovacs, Christopher S.
Langsetmo, Lisa
Prior, Jerilynn C.
Nguyen, Tuan, V
Solomon, Lucian B.
Stapledon, Catherine
Center, Jacqueline R.
Issue Date: 2022
Publisher: WILEY
Source: JOURNAL OF BONE AND MINERAL RESEARCH,
Status: Early view
Abstract: To the Editors: We are grateful to Dr. Naharci for the interest in our study reporting the association between cognitive decline and bone loss and fracture risk. (1) We agree that bisphosphonates (BPs) have a proven effect on reducing bone loss and fracture risk. (2) Medication with anticholinergic (ACH) side effects may also affect cogni-tive function as well as propensity to fall and fracture, although these effects have not been demonstrated in all studies. (3) We did not include these medication classes in our models because in observational studies the relationship between medication and outcomes is likely driven by factors associated with medication use. This bias by indication can only be avoided by specific study design (ie, propensity score matching), which was beyond the scope of our study. (4) However, we have conducted additional analyses to determine the prevalence of BP and ACH medication in our cohort, the association between these medication classes and our study outcomes and the impact of the addition of these medication classes to our findings. BP and ACH use were self-reported and obtained by questionnaire at baseline, and years 5 and 10. Bone mineral density (BMD) was assessed by dual-energy X-ray absorptiometry (DXA) and cognitive function using the Mini Mental State Examination (MMSE) test during all clinical visits. Follow-up time for BMD
Notes: Bliuc, D (corresponding author), Garvan Inst Med Res, 384 Victoria St, Darlinghurst, NSW 2010, Australia.
d.bliuc@garvan.org.au
Document URI: http://hdl.handle.net/1942/37145
ISSN: 0884-0431
e-ISSN: 1523-4681
DOI: 10.1002/jbmr.4530
ISI #: WOS:000768547700001
Rights: 2022 American Society for Bone and Mineral Research (ASBMR).
Category: A1
Type: Journal Contribution
Validations: ecoom 2023
Appears in Collections:Research publications

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