A variability in response of osteoclasts to zoledronic acid is mediated by smoking associated modifcation in the DNA methylome

A variability in response of osteoclasts to zoledronic acid is mediated by smoking associated modifcation in the DNA methylome

Qihua TanAnaïs Marie Julie MøllerChuan QiuJonna Skov MadsenHui ShenTroels BechmannJean-Marie DelaisseBjarne Winther KristensenHong-Wen DengDavid Karasik & Kent Søe

A variability in response of osteoclasts to zoledronic acid is mediated by smoking-associated modification in the DNA methylome | Clinical Epigenetics | Full Text (biomedcentral.com)

Background Clinical trials have shown zoledronic acid as a potent bisphosphonate in preventing bone loss, but with varying potency between patients. Human osteoclasts ex vivo reportedly displayed a variable sensitivity to zoledronic acid>200-fold, determined by the half-maximal inhibitory concentration (IC50), with cigarette smoking as one of the reported contributors to this variation. To reveal the molecular basis of the smoking-mediated variation on treatment sensitivity, we performed a DNA methylome profling on whole blood cells from 34 healthy female blood donors. Multiple regression models were ftted to associate DNA methylation with ex vivo determined IC50 values, smoking,
and their interaction adjusting for age and cell compositions.
Results We identifed 59 CpGs displaying genome-wide signifcance (p<1e−08) with a false discovery rate
(FDR)<0.05 for the smoking-dependent association with IC50. Among them, 3 CpGs have p<1e−08 and
FDR<2e−03. By comparing with genome-wide association studies, 15 signifcant CpGs were locally enriched (within<50,000 bp) by SNPs associated with bone and body size measures. Furthermore, through a replication analysis using data from a published multi-omics association study on bone mineral density (BMD), we could validate that 29 out of the 59 CpGs were in close vicinity of genomic sites signifcantly associated with BMD. Gene Ontology (GO) analysis on genes linked to the 59 CpGs displaying smoking-dependent association with IC50, detected 18 signifcant GO terms including cation:cation antiporter activity, extracellular matrix conferring tensile strength, ligand–gated ion channel activity, etc.
Conclusions Our results suggest that smoking mediates individual sensitivity to zoledronic acid treatment through epigenetic regulation. Our novel fndings could have important clinical implications since DNA methylation analysis may enable personalized zoledronic acid treatment.

Recent News

 In the last grant period of GEMSTONE, a STSM took place with the main aim of creating a detailed survey for all GEMSTONE members, which will map their expertise and...
During all grant periods of GEMSTONE, 18 short-scientific missions, 6 virtual mobility grants, 1 dissemination conference grant, and 1 ITC conference grant took place. The grantees had the opportunity to...
The Gemstone “Principles of Data Science to Propel MSK Genomic Investigations and Gene Discovery from Omics Data” training school took place at the European University of Cyprus in July 2023....
After the successful GEMSTONE training school in Malta, UM newspoint publishes an interesting article on the training school.
Dr Melissa Formosa and her team present their study on ‘Variants in STAT4 and TMEM151B identified as potential causal factors in Early-Onset Familial Osteoporosis’ at the 49th European Calcified Tissue...
With Gemstone coming to an end, WG2 has released a press release to provide a short overview of their achievements during these four fruitful years. You can read the press...