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No genetic loci reached genome-wide significance for inpatient opioid exposure after joint arthroplastyGenetic Research Looks at Opioid Use After Joint Replacement Surgery

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Key Takeaway
Note that no genetic variants reached genome-wide significance for predicting inpatient opioid use after joint arthroplasty.

This meta-analysis evaluates a genome-wide association study (GWAS) involving 27,896 patients undergoing knee or hip arthroplasty to identify genetic variants associated with average daily opioid exposure during the inpatient postoperative period. The analysis included diverse ancestry groups: 4,676 African, 2,126 African American, and 21,094 European participants.

The primary finding is that no loci reached genome-wide significance in either within-ancestry or cross-ancestry analyses. While some variants showed nominal significance (p < 5 x 10^-6) across different ancestries, these did not meet the threshold for genome-wide significance. Specifically, 5 loci were nominally significant in cross-ancestry analysis, with additional nominal hits in specific ancestral groups (9 in AFR, 4 in AMR, and 3 in EUR).

The authors note that the study is limited by the need for larger sample sizes and more precise phenotyping of opioid exposure. Clinical application is currently limited as no definitive genetic predictors were identified. The study provides a framework for using electronic health record data to investigate the genetics of postoperative opioid use, but results are not yet sufficient to inform clinical practice.

How this fits prior evidence

This finding addresses a gap in understanding the genetic drivers of individual differences in opioid exposure following joint arthroplasty. While other evidence highlights that ERAS pathways may reduce opioid exposure and that EOIPB can reduce postoperative opioid consumption by 19.55 mg, this study does not identify specific genetic markers to predict which patients might require higher doses or different management strategies.

Researchers looked at the genetic information and medical records of nearly 28,000 people who underwent hip or knee replacement surgeries. The goal was to find out if certain genetic markers could predict how much opioid pain medication a patient would need during their stay in the hospital.

The study found that while some small groups of genetic markers showed minor patterns, none reached the level of significance needed to be considered reliable across different populations. This means the researchers did not find clear genetic predictors for how much opioid medicine patients receive after surgery.

Because the results were not statistically strong and the sample sizes need to be larger, these findings are not yet ready to change how doctors treat pain. The study is currently a way to help researchers use electronic health records to better understand the link between genetics and medication needs.

What this means for you:
The study did not find clear genetic markers that predict how much opioid medicine patients need after surgery.

Common questions

Did researchers find specific genes that predict opioid use?

The study did not find any genetic locations that reached genome-wide significance. While a few markers showed nominal significance in small groups, they were not strong enough to be considered reliable across different ancestries or for general use.

Who was included in this study?

The study included 27,896 patients who underwent hip or knee replacement surgery. This group included participants from various backgrounds, including 4,676 African Americans, 2,126 mixed-race individuals, and 21,094 individuals of European descent.

Will these findings change how doctors prescribe pain medicine?

The study is not currently used to change medical practice. Because the results were not genome-wide significant and the researchers noted a need for larger samples, the findings are still in the early stages of research.

Study Details

Study typeMeta analysis
Sample sizen = 27,896
EvidenceLevel 1
PublishedJul 2026
View Original Abstract ↓
Opioids are commonly prescribed to manage acute postoperative pain. However, there is considerable variability in opioid administration patterns and practices, which is partially attributable to patient characteristics. We used electronic health record (EHR) and genotype data from the Million Veteran Program sample to investigate genetic predictors of individual differences in inpatient opioid analgesic exposure following knee or hip arthroplasty (n = 27,896). We extracted data from pharmacy records of administered inpatient opioid medications to derive a measure of average daily opioid exposure during the inpatient postoperative period. We then conducted genome-wide association studies (GWAS) to identify associated genetic variants in individuals of African-like (AFR; nAFR = 4,676), Admixed American-like (AMR; nAMR = 2,126), and European-like (EUR; nEUR = 21,094) genetically inferred ancestries. Models controlled for age, sex, pre-procedure opioid use disorder status, procedure type (knee or hip), length of stay, and the first 10 genetic ancestry principal components. The within-ancestry GWAS were followed by a cross-ancestry GWAS meta-analysis using fixed-effects inverse variance weighting in METAL. No loci reached genome-wide significance in the within- or cross-ancestry GWAS. Five loci were nominally significant (p <5 x 10-6) in the cross-ancestry GWAS, 9 in the AFR GWAS, 4 in the AMR GWAS, and 3 in the EUR GWAS. This study provides a framework for the use of EHR data to examine the genetics of opioid exposure in postoperative care and indicates the need for larger samples and more precise phenotyping to better understand genetic contributors to individual variation in analgesic requirements.
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