# Mitochondria-DNA copy-number in osteoporosis and osteoarthritis among middle-aged women - A population-based cohort study

**Authors:** Christian Anker-Hansen, MirNabi Pirouzifard, Ashfaque Memon, Jan Sundquist, Kristina Sundquist, Bengt Zöller

PMC · DOI: 10.1016/j.ocarto.2024.100501 · Osteoarthritis and Cartilage Open · 2024-07-05

## TL;DR

This study found no significant link between mitochondrial DNA copy number and the risk of osteoarthritis or osteoporosis in middle-aged women.

## Contribution

The novel contribution is a population-based investigation of mitochondrial DNA copy number as a potential predictor of osteoporosis and osteoarthritis.

## Key findings

- Low mtDNA-CN was not associated with incident osteoarthritis or osteoporosis.
- Incident osteoporosis was significantly linked to bone density, smoking, diabetes, and COPD.
- Osteoarthritis was associated with BMI and COPD, but not mtDNA-CN.

## Abstract

Mitochondrial DNA copy number (mtDNA-CN) is associated with aging. A relationship between mtDNA-CN and degenerative disorders, e.g. osteoarthritis (OA) and osteoporosis (OP), has been suggested. We aimed to investigate the relationship of mtDNA-CN and incident OA and OP.

MtDNA-CN was studied in relationship to incident OA and OP in a population-based cohort study of 6916 middle-aged women (52–63 years). Totally 2521 women with sufficient quality of mtDNA were analyzed. After exclusions, 1978 women remained in the study population. Four different endpoints obtained from the National Patient register were studied: 1) OA, 2) OP 3) OA surgery, and 4) OP fracture. In the multivariate model adjustments were made for potential OA and OP risk factors.

Women with low mtDNA-CN were older and had more activity at work. 125 women (6.32%) were affected by incident OP and 254 women (12.84%) had an OP fracture. Incident OA affected 451 women (22.80%) and 175 women (8.85%) had OA surgery. There were no associations between mtDNA-CN and incident risk of OA (Hazard ratio ​= ​1.00, 95% confidence interval 0.83–1.20), OA surgery (0.79, 0.58–1.07), OP (0.89, 0.62–1.27), or OP fracture (1.00, 0.78–1.29). However, incident OP was significantly associated with T-score (bone density), smoking, diabetes mellitus, and chronic obstructive bronchitis (COPD). OA was associated with body mass index and COPD.

The present study suggests that mtDNA-CN, reflecting mitochondrial dysfunction, is not a major predictor for incident OA or OP. However, due to the limited study size minor associations cannot be excluded.

## Linked entities

- **Diseases:** osteoporosis (MONDO:0005298), osteoarthritis (MONDO:0005178), diabetes mellitus (MONDO:0005015)

## Full-text entities

- **Diseases:** diabetes mellitus (MESH:D003920), COPD (MESH:D029424), mitochondrial dysfunction (MESH:D028361), chronic obstructive bronchitis (MESH:D029481), OP (MESH:D010024), degenerative disorders (MESH:D019636), OA (MESH:D010003)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC11295846/full.md

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Source: https://tomesphere.com/paper/PMC11295846