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Fluoroquinolone-induced tendinopathy: etiology and preventive measures
Ferda Kaleagasioglu1, Ercan Olcay
1Department of Pharmacology, Yeditepe University, Faculty of Medicine, Istanbul, Turkey. sfk19@superposta.com
Abstract:
Tendinopathy is a serious health problem and its etiology is not fully elucidated. Among intrinsic and extrinsic predisposing factors of tendinopathy, the impact of therapeutic agents, especially fluoroquinolone (FQ) group antibiotics, is recently being recognized. FQs are potent bactericidal agents widely used in various infectious diseases, including community acquired pneumonia and bronchitis, chronic osteomyelitis, traveler's diarrhea, typhoid fever, shigellosis, chronic bacterial prostatitis, uncomplicated cervical and urethral gonorrhea and prophylaxis of anthrax. FQs have an acceptable tolerability range. However, many lines of evidence for developing tendinitis and tendon rupture during FQ use have resulted in the addition of a warning in patient information leaflets. FQ-induced tendinopathy presents a challenge for the clinician because healing response is poor due to low metabolic rate in mature tendon tissue and tendinopathy is more likely to develop in patients who are already at high risk, such as elderly, solid organ transplant recipients and concomitant corticosteroid users. FQs become photo-activated under exposure to ultraviolet light, and this process results in formation and accumulation of intracellular reactive oxygen species (ROS). The subsequent FQ-related oxidative stress disturbs mitochondrial functions, leading to apoptosis. ROS overproduction also has direct cytotoxic effects on extracellular matrix components. Understanding the mechanisms of the FQ-associated tendinopathy may enable designing safer therapeutic strategies, hence optimization of clinical response. In this review, we evaluate multi-factorial etiology of the FQ-induced tendinopathy and discuss proposed preventive measures such as antioxidant use and protection from natural sunlight and artificial ultraviolet exposure.
Insights
Fluoroquinolone (FQ) antibiotics can cause tendinopathy and tendon rupture, particularly in high-risk patients. Understanding FQ-induced oxidative stress mechanisms may lead to better prevention strategies.
Area of Science:
- Pharmacology
- Orthopedics
- Toxicology
Background:
- Tendinopathy is a significant health issue with incompletely understood causes.
- Fluoroquinolone (FQ) antibiotics are increasingly recognized as a risk factor for tendinopathy.
- FQ-associated tendinopathy is challenging due to poor healing and increased risk in vulnerable populations.
Purpose of the Study:
- To review the multifactorial etiology of fluoroquinolone-induced tendinopathy.
- To discuss the mechanisms underlying FQ-associated tendon damage.
- To explore potential preventive measures against FQ-induced tendinopathy.
Main Methods:
- Literature review of existing studies on fluoroquinolone antibiotics and tendinopathy.
- Analysis of the molecular mechanisms of FQ-induced oxidative stress and apoptosis in tendon tissue.
- Evaluation of patient factors contributing to FQ-related tendinopathy risk.
Main Results:
- Fluoroquinolones can induce tendinopathy and rupture through photo-activation and reactive oxygen species (ROS) generation.
- Oxidative stress from FQs disrupts mitochondrial function, leading to apoptosis and extracellular matrix damage.
- Elderly patients, transplant recipients, and corticosteroid users are at higher risk for FQ-induced tendinopathy.
Conclusions:
- FQ-induced tendinopathy involves complex mechanisms including oxidative stress and apoptosis.
- Preventive strategies may involve antioxidant use and protection from UV light exposure.
- Further research into FQ-induced tendinopathy mechanisms is crucial for developing safer treatments.
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