Minocycline for Controlling Neuropathic Pain: A Systematic Narrative Review of Studies in Humans
Authors Shin DA, Kim TU, Chang MC
Received 18 November 2020
Accepted for publication 13 January 2021
Published 26 January 2021 Volume 2021:14 Pages 139—145
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 4
Editor who approved publication: Dr Michael A Überall
Dong Ah Shin,1 Tae Uk Kim,2 Min Cheol Chang3
1Department of Neurosurgery, Yonsei University, College of Medicine, Seoul, Republic of Korea; 2Department of Physical Medicine and Rehabilitation, College of Medicine, Dankook University, Cheonan, Republic of Korea; 3Department of Physical Medicine and Rehabilitation, College of Medicine, Yeungnam University, Taegu, Republic of Korea
Correspondence: Min Cheol Chang
Department of Physical Medicine and Rehabilitation, College of Medicine, Yeungnam University, 317-1, Daemyungdong, Namku, Taegu 705-717, Republic of Korea
Objective: Minocycline is known to reduce microglial activation, suggesting that it may reduce neuropathic pain. We reviewed studies in humans that evaluated the effectiveness of minocycline in alleviating neuropathic pain.
Methods: We searched the PubMed, Embase, Cochrane library, and SCOPUS databases for papers published before January 06, 2021, using the search words minocycline and pain. The inclusion criteria for the selection of articles were (1) minocycline administered to humans and (2) minocycline administered to control neuropathic pain.
Results: The primary literature search yielded 2299 relevant papers. Based on the assessment of the titles, abstracts, and full-text, nine publications were selected for this review. Only four of the nine studies showed a positive pain-reducing outcome after minocycline administration. Two of the three studies on chemotherapy-induced neuropathic pain showed a positive pain-reducing effect. Minocycline was effective in controlling pain from diabetic and leprotic neuropathies. However, minocycline was not effective in controlling lumbar radicular pain and pain resolution after carpal tunnel release.
Conclusion: Our review provides evidence that minocycline may have some potential for reducing neuropathic pain. Further high-quality studies need to be conducted to validate this potential.
Keywords: minocycline, microglia, neuropathic pain, pain, review
Chronic pain is characterized by enhanced sensory neurotransmission that increases sensitivity to noxious stimuli and the perception of non-noxious stimuli as pain.1 Neuropathic pain is one of the most common and debilitating chronic pain conditions that considerably deteriorates patients’ activities of daily living and quality of life.2 Neuropathic pain is caused by several diseases, including metabolic (eg, diabetic neuropathy), autoimmune (eg, multiple sclerosis), and vascular (eg, stroke and spinal cord infarct) diseases and infection (eg, postherpetic neuralgia), trauma, and cancer. The mechanism underlying neuropathic pain is not clearly understood; however, several likely mechanisms have been suggested, including sensitization of the central and peripheral nervous systems, deafferentation, neurogenic inflammation, and wind-up.3 In clinical practice, several therapeutic methods such as medications, modalities, and procedures are being applied.4,5 However, many cases of chronic pain are refractory to these treatments. Therefore, researchers are attempting to develop novel treatments for alleviating chronic pain.
Regarding medications for reducing neuropathic pain, anticonvulsants (gabapentin or pregabalin), tricyclic antidepressants, and opioids are usually prescribed.1 These drugs primarily target neurons including axons and dendrites.6 Various adverse effects related to the restraint of neuronal activity, such as somnolence or dizziness, are unavoidable. Additionally, these drugs are not sufficient to control neuropathic pain.
Recently, glial cells, especially microglia, have been considered to play an essential role in central sensitization, one of the main mechanisms for the development and persistence of neuropathic pain.7 When the nerve is injured, microglia in the dorsal horn are activated and enhance the release of pro-nociceptive neurotransmitters such as glutamate, cytokines, and chemokines.8 This process enhances neuron-glia communication and results in the sensation of persistent pain despite the absence of continuous noxious stimuli to the tissue. Once microglia are activated, the process related to chronic pain continues, and it is difficult to break this process.9 With the recognition of microglia as prime modulators of progress to chronic pain, considerable effort has been spent in developing drugs to inhibit microglial activation.
Minocycline is a second-generation, semi-synthetic tetracycline that is used as a broad-spectrum antibiotic against a wide range of microorganisms.10 It is also known to have several anti-inflammatory properties, including the reduction in microglial activation, inhibition of T-lymphocytes, suppression of phospholipase A2 activation, and decrease in interleukin (IL)-6 and IL-8.11–13 Minocycline is lipophilic and can penetrate the blood-brain barrier and act on the central nervous system.14 Several animal studies have shown that minocycline attenuates neuropathic pain after injury of peripheral and central nerves via microglial inhibition.11–13,15 Minocycline is known to inhibit the expression of toll-like receptor 4, which is a crucial receptor for microglia-mediated neuroinflammation.16 Consequently, inhibition of microglial cell activity inhibits the production of inflammatory cytokines and the expression of brain-derived neurotrophic factor.15,17,18 Recently, the effect of minocycline on neuropathic pain has been evaluated in patients with various types of neuropathic pain. In addition, minocycline has neuroprotective properties via antioxidant activity.19,20 This is related to the ability to chelate mitochondrial iron, which catalyzes toxic hydroxyl radical formation. Accordingly, minocycline attenuates neuronal cell death.
In the current study, we systematically reviewed previous studies that evaluated the effectiveness of minocycline in alleviating neuropathic pain in humans.
The PubMed, Embase, Cochrane library, and SCOPUS databases were searched for articles published before January 06, 2021 using the search terms minocycline AND pain. Articles related to minocycline administered to humans to control neuropathic pain were selected. Research on all types of neuropathic pain was included in our review. Animal studies and review articles were excluded. In addition, we only included articles published in English.
The primary literature search yielded a total of 3243 potentially relevant papers, among which 944 duplicate articles were removed (Figure 1). After screening for eligibility, based on a review of the title and abstract, 20 articles were identified for full-text reading. After a detailed assessment, 11 articles were excluded. Accordingly, nine publications were selected for this review.21–29 In these selected studies, minocycline was administered in a total of 232 cases. Among the included studies (Table 1), the effectiveness of minocycline in treating chemotherapy-induced neuropathic pain was evaluated in three studies24,28,29 and lumbar radicular pain in two studies.22,27 Its effectiveness was also evaluated in diabetic neuropathy,26 leprosy,23 and carpal tunnel syndrome.21 One study was not classified according to any disease indication.25 Seven studies were randomized controlled trials (RCTs), and the other two were prospective observational studies. In all the included studies, minocycline was administered orally.
Table 1 Summary of the Included Studies
Figure 1 Flow chart showing the study design and selection of eligible studies.
Among the studies evaluating the pain-reducing effects on chemotherapy-induced neuropathic pain, two studies showed a positive effect,24,29 and the other28 presented negative results. Pachman et al24 performed an RCT involving 45 patients with breast cancer receiving weekly paclitaxel chemotherapy. Twenty-two patients received minocycline 100 mg twice daily until 12 weeks of chemotherapy were completed, and 23 patients received a placebo. The degree of neuropathic pain was evaluated by asking patients to maintain a daily symptom questionnaire during chemotherapy comprising 10 items regarding pain symptoms and the use of pain medications. The patients in the minocycline group reported less pain and less use of opioid pain medication than the placebo group. Wang et al29 evaluated minocycline for controlling chemoradiation-related symptoms. They recruited 40 patients with non-small cell lung cancer who were scheduled to receive chemoradiation treatment. Patients were randomly assigned to either the minocycline group (100 mg twice daily) (19 patients) or placebo group (21 patients) over 6–7 weeks of chemoradiation therapy. Pain, fatigue, and shortness of breath were significantly reduced in the minocycline group. However, another study performed by the same research group (Wang et al)28 reported no beneficial effect of minocycline. They recruited 66 patients with locally advanced or metastatic colorectal cancer who were scheduled for oxaliplatin-based chemotherapy. Patients were randomly allocated to receive either minocycline (100 mg twice daily) (32 patients) or placebo (34 patients) over 4 months from the initiation of chemotherapy. The degrees of fatigue and neuropathic pain, and the levels of serum inflammatory markers, including IL receptors, tumor necrosis factor-α receptor, and C-reactive protein, were not significantly different between the two groups.
Martinez et al22 performed an RCT on lumbar radicular pain. Minocycline (100 mg twice daily) was administered to patients scheduled to undergo lumbar discectomy. Forty-three patients received minocycline for 8 days from the evening before surgery, and 42 patients received a placebo. At 3 months after the surgery, the severity of lumbar radicular pain between the two groups was not different. Vanelderen et al27 performed an RCT involving patients with subacute lumbar radicular pain owing to disc herniation, spinal stenosis, and failed back surgery syndrome. For 2 weeks, either minocycline (100 mg), amitriptyline (25 mg), or placebo were administered, and 17 patients in each group completed the study. After 14 days, patients who had taken the minocycline and amitriptyline reported a reduction of 1.47 and 1.41, respectively, in the score on the numeric rating scale. Although the score on the numeric rating scale was significantly reduced compared with that in the placebo group, the magnitude of the reduction was small. The authors concluded that “the effect of minocycline in reducing lumbar radicular pain was not likely to be clinically meaningful.”
The effect of minocycline on diabetic neuropathy was evaluated by Syngle et al.26 Fifty patients with diabetic neuropathy were equally allocated to either the minocycline or placebo group. The scores on the visual analogue scale were reduced considerably after using minocycline (100 mg twice daily) for 6 weeks compared with those with the placebo (minocycline: 6.7 → 2.9, placebo: 5.6 → 4.6). The symptoms related to diabetic neuropathy were measured using the Leeds Assessment of Neuropathic Symptoms and Signs Pain Scale and the Pain Disability Index, both of which were significantly reduced in the minocycline group.
Narang et al23 conducted a prospective pilot study to evaluate whether minocycline could improve the symptoms of leprotic neuropathy. They administered minocycline (100 mg) daily to 11 patients for 3 months and found that all six patients with neuritis showed a reduction in pain with a more than a 75% reduction in the score on the visual analogue scale at 3 months after the initiation of minocycline administration. Additionally, functional improvement was seen in 9 of 11 patients.
Curtin et al21 evaluated whether perioperative administration of minocycline would help reduce the time to pain resolution after carpal tunnel release. Minocycline (200 mg) or placebo was administered to patients with carpal tunnel syndrome (43 patients in the minocycline group, 40 patients in the placebo group) 2 h before the operation, and then 100 mg of minocycline or placebo twice a day for 5 days. They reported that the perioperative administration of minocycline did not reduce the time to pain resolution (minocycline group: 3 weeks vs placebo group: 2 weeks).
Sumitani et al25 prospectively recruited 20 patients with neuropathic pain of various etiologies. They administered 100 mg minocycline daily for 1 week and then 200 mg daily for 3 weeks. At 4 weeks of therapy, the mean score on the numeric rating scale changed from 5.6 at baseline to 5.3; however, the degree of reduction was not significant. The limitation of this study was that the authors did not state what disorders caused the neuropathic pain.
No significant side effects were reported in any of the included studies.
We reviewed nine studies that examined the effect of minocycline on neuropathic pain. Among these, four studies reported a positive pain-reduction effect.
Two of the three studies on chemotherapy-induced neuropathic pain showed a pain-reducing effect. Minocycline was also effective in controlling pain in diabetic and leprotic neuropathies. However, minocycline was not effective in controlling lumbar radicular pain and pain resolution after carpal tunnel release. Lumbar radicular pain is induced by a herniated lumbar disc or spinal stenosis, indicating that pain is in part attributable to nerve-root compression. The pain mechanism of carpal tunnel syndrome also involves the compression of the median nerve beneath the transverse carpal ligament. Based on the results of the reviewed studies, we speculate that when patients’ disorders include a component of nerve compression, the effect of minocycline may not be sufficient to control neuropathic pain. In contrast, chemotherapy-induced, diabetic, and leprotic neuropathies have no component of mechanical nerve compression, and the causes of neuropathic pain are largely owing to nerve inflammation.30–32 In particular, in the leprotic neuropathy study, all patients with neuritis showed excellent outcomes in pain reduction after administration of minocycline.23 We believe that minocycline affects the inflammatory factor in neuropathic pain. The anti-inflammatory effect of minocycline is related to its ability to inhibit the activation of microglia, thereby reducing the production of pro-inflammatory cytokines.11–13,15 Because microglia in the spinal dorsal horn contribute to the persistence of neuropathic pain by releasing several cytokines that mediate pain signaling, downregulation of microglia by minocycline may alleviate neuropathic pain.33
Regarding the side effects of minocycline, although no significant adverse effects were observed in any of the included studies, various side effects, such as dizziness, fatigue, headache, and tooth discoloration toxicities, are known to occur after the use of minocycline.24 Therefore, clinicians or researchers should be aware of the potential of the occurrence of side effects with minocycline and observe their development closely during use.
We found that only four studies showed a positive pain-reducing outcome of minocycline, whereas the other five studies did not show significant positive results. In addition, despite the positive pain-reduction effect of minocycline in some previous studies, a successful outcome in a Phase III RCT evaluating the effectiveness of minocycline for alleviating neuropathic pain has not yet been reported. Therefore, we cannot conclude that the effect of minocycline on reducing neuropathic pain is of general utility; however, it can be said that minocycline has the potential to reduce neuropathic pain. To clarify this issue, further high-quality studies need to be conducted to establish the effect of minocycline according to the type of neuropathic disorder. In addition, to clearly elucidate the pain-reducing effect of minocycline, studies with a large number of subjects should be conducted in the future.
This research was supported by the 2020 Joint Research Project of Institutes of Science and Technology.
The authors report no conflicts of interest for this work.
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