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Abstract

According to the US Centers for Disease Control and Prevention (CDC), an estimated 14% of adults in the United States have either been diagnosed with osteoarthritis (OA) or have symptoms suggestive of the disease. The CDC also points out that the incidence of OA has been gradually increasing over the past 30 years. What is more worrisome is that this trend is going to accelerate due to the aging demographics of the United States and the increasing prevalence of obesity seen in the country. The need for better preventive treatments and efficacious therapeutics are direly needed to combat this public health crisis. Among the possible treatments being hypothesized, antioxidant supplementation has become one of the most widely studied over the past decade due to its ability to attenuate reactive oxygen species (ROS) formation within chondrocytes, a critical step in the pathogenesis of this disease. Vitamin C has emerged as among the most promising of the antioxidant group, with many animal and human studies having been conducted in recent years. Although many of the studies have shown encouraging results in terms of preventing OA, others have reached opposite conclusions, thus making the data controversial. However, after reviewing several of these studies, we hypothesize that certain parameters may not have been properly considered during data collection. In the end, more randomized placebo-controlled trials in humans are desperately needed in order to fully understand whether vitamin C therapy is efficacious in treating and/or preventing OA.

Keywords

antioxidant ascorbic acid nutritional supplementation osteoarthritis vitamin C

Introduction

Osteoarthritis (OA) is one of the most prevalent degenerative diseases affecting over 50 million Americans currently and continues to be the leading cause of disability in the elderly population.¹ A study performed in 2000 found that in individuals over 80 years of age, nearly half of all women and a third of all men experience some degree of symptoms associated with OA.² Individuals with OA might experience symptoms of pain, stiffness, loss of function, and movement, all causing difficulty with everyday activities. The debilitating nature of the disease process not only leads to significant psychological suffering due to a devalued self-worth but also contributes to substantial economic losses from decreased productivity and associated medical care.³ Unfortunately, clinicians expect the number of patients with OA in the United States to continue to increase dramatically over the coming years, largely due to countries rapidly aging demographic and the ever-increasing prevalence of obesity within the country.^4,5 Therefore, researchers and clinicians alike are beginning to explore therapeutic options for in the treatment for OA. Although the exact pathogenesis of the disease has yet to be fully elucidated, several factors including age, history of joint injury, weight, genetics, and gender have been shown to increase individual risk of developing OA.^6,7 The aforementioned risk factors are predominantly non-modifiable; consequently, current therapy has been limited to symptomatic relief. Therefore, attaining a more thorough understanding of the disease process is necessary to develop an effective, disease-modifying option for OA therapy.

Current treatments for OA primarily provide symptomatic relief with the hopes of controlling the common clinical manifestations of pain, swelling, and loss of function/movement.⁸ Oftentimes, conservative measures such as weight loss, muscle stretching, low-impact exercises, and NSAID are used as first-line treatments.⁹ Once these approaches fail, more invasive options such as joint injections and joint replacement surgery can be explored.⁹ However, these options have significant side effects as well as issues regarding the effectiveness in preventing the progression of the disease.^10,11 Overall, symptomatic relief achieved through the use of current approaches does indeed serve a therapeutic role, but only transiently. Therefore, finding more lasting treatment options focusing on disease modification and prevention should be the ultimate goal. Previous research has made it clear that balanced nutrition is an essential factor for maintaining healthy bone and joint structures while also dampening inflammation. Several key nutrients have been closely studied, taking a look at whether supplementation can reduce the progression of OA, as well as prevent it altogether. It is believed that free radical accumulation within human cells is a contributing factor to degenerative changes associated with aging. Specific to musculoskeletal health, reactive oxygen species induced oxidative stress can cause chondrocyte cell death.¹² With that in mind, it would make sense that the presence of anti-oxidants would oppose this joint destructive influence.

In general, antioxidants have demonstrated a protective role in musculoskeletal health in the elderly population.¹³ However, studies looking at the efficacy of antioxidant supplementation in reducing the prevalence and progression of OA have produced varied and sometimes conflicting results. Some effectiveness has been demonstrated with the supplementation of glycosaminoglycans (chondroitin sulfate and glucosamine).¹⁴ These substances, along with their antioxidant properties, were shown to help lubricate and alleviate forces translated across joints by promoting cartilaginous repair and regeneration, thus limiting the incidence of OA.^15,16 Other well-known antioxidants, such as B vitamins and L-carnitine, have shown no substantial benefit to the patient in terms of OA prevention,^17,18 whereas curcumin and L-glutathione have demonstrated some ability to modulate inflammation via downregulating mRNA levels of inflammatory mediators such as IL-1 and matrix metalloproteinase-3 (MMP-3).^19–21 Finally, the link between vitamin D levels and the associated risk of developing OA has been studied on multiple occasions.²² Although previous data indicated that low levels of 25-OH vitamin D were associated with a greater risk of OA progression,¹⁷ Felson et al. contradicted this in his 2007 article. The results demonstrated serum vitamin D levels do not correlate with cartilage loss and developing OA.²² As seen in the studies mentioned above, some nutritional antioxidant supplements can help prevent, manage, and slow the progression of age-related diseases, while others do not affect it at all. Perhaps, the substance with the most promise in serving a therapeutic role in treating and preventing OA has been centered around the administration of the potent, yet widely available antioxidant, vitamin C.

Vitamin C

Vitamin C, also known as L-ascorbic acid, is a water-soluble essential nutrient that is not synthesized by most mammals, including humans. Most mammalian species cannot perform the crucial last step of vitamin C biosynthesis, the conversion of L-gulono-G-lactone into the vitamin, due to inactivation of the gene coding for the enzyme gulonolactone oxidase (GULO).^16,18 Due to this evolutionary mutation, vitamin C is considered an essential vitamin and thus requires daily supplementation. The clinical manifestations of vitamin C dietary deficiency are known as scurvy and have been thoroughly documented in history, most notably during long ship voyages across the ocean. The sailors that happened to avoid developing scurvy had diets predominantly of fruits and vegetables, thus fulfilling their daily vitamin C requirements.²³ Aside from green vegetables, other dietary sources of vitamin C include citrus fruits and potatoes, with daily recommended doses dependent upon factors such as age, gender, and smoking status.²⁴

The molecular structure of vitamin C is similar to that of glucose. It can be oxidized to form dehydroascorbic acid (DHA), the preferred form for use by certain cells in the body.²⁵ The absorption takes place in the ileum of the small intestine via an energy-dependent sodium-dependent transporter, while the transfer of DHA utilizes an energy-independent process of facilitated diffusion.²⁶ Depending on the amount of vitamin C intake, the kidneys will regulate its excretion and reabsorption rates.²⁷ Vitamin C’s most important functions include being a key cofactor in many metabolic pathways, of which several promote proper musculoskeletal development and repair in humans.²⁷ For instance, intracellular vitamin C acts as an essential cofactor for both prolyl hydroxylase and lysyl hydroxylase, two enzymes crucial for collagen synthesis. The vitamin has also been found to play key roles in chondrogenic differentiation and extracellular matrix synthesis. Furthermore, the vitamin acts to promote cell growth through increasing DNA synthesis and differentiation of mesenchymal stem cells to various cell types such as adipocytes, osteoblasts, myoblasts, and chondrocytes.^28,29 In addition, studies have illustrated that vitamin C enhances iron absorption in the gut.^27,30 Iron is a known cofactor necessary for use in collagen synthesis, further contributing to maintaining musculoskeletal health.

Vitamin C and its transporter

Vitamin C is a highly water-soluble vitamin, which cannot diffuse across the hydrophobic plasma membranes. A specific transport system, sodium-dependent vitamin C transporters (SVCT) exists in the plasma membrane to mediate the entry process. Two subtypes of the sodium-dependent vitamin C transporter (SVCT1 and SVCT2) have been discovered.^28,31–33 SVCT1 is expressed in tissues such as liver, kidney, and intestinal epithelial cells, whereas SVCT2 is seen predominantly in tissues such as the brain, heart, and muscles.^28,31,32 Our lab has extensively studied these transporters and their essential role in musculoskeletal tissue engineering over the past decade.^33–36 We previously demonstrated the expression of SVCT2 in chondrocytes, bone marrow stromal cells, osteoblast, and articular cartilage.^33–36 Our laboratory previously reported that the SVCT2 transporter is negatively regulated in human OA tissues and mice aging bones.^28,33–36 In addition, it is known that aging, oxidative stress, and inflammation can negatively alter the SVCT2 expression in these tissues.^28,37,38 Therefore, we speculate that down-regulation of SVCT2 transport might be an important contributing factor in the pathophysiology of OA.

Vitamin C supplementation for OA

The most important inherent property of vitamin C is its ability to act as a strong antioxidant, with the capability to reduce and stabilize potentially damaging free radical compounds. It is known that a major contributing factor to age-induced cartilage degeneration (OA) occurs due to the formation and accumulation of free radicals (superoxide, hydrogen peroxide, peroxynitrite) within chondrocytes.³⁹ More specifically, these reactive oxygen species induce genomic instability in human chondrocytes leading to a reduction in viable cartilage.⁴⁰ Given this fact, it suggests that antioxidants such as vitamin C could serve a protective function in preventing oxidative stress-induced chondrocyte dysfunction from occurring. To gain a better insight into recently published data, we summarize animal studies, human clinical trials, and in-vitro studies involving vitamin C in the setting of treating and/or preventing OA. This information was obtained by searching for primary literature through PubMed with the search criteria; “Vitamin C,” “Osteoarthritis,” “Treatment,” “Prevention.”

Animal studies

Vitamin C supplementation on prevention and progression of OA

Overall, the clinical studies included in Table 1 show mixed results, thus providing a cloudy picture of the vitamin’s ability to serve a therapeutic role in treating and preventing OA. In the 1990 study, Meacock et al. demonstrated that supplementation with vitamin C was associated with less spontaneous cases of OA in guinea pigs due to the chondroprotective effect of the antioxidant. However, the group did note that excess vitamin treatment failed to show any significant difference in disease progression after meniscectomy, a procedure used to mimic OA.⁴¹ Another study examining the progression of mechanically induced OA in mice following supplementation of multiple antioxidants, including vitamin C, showed promising results. The data illustrated that mice in the experimental group consistently had grade 2 osteoarthritic changes, while those receiving the control diet lacking in antioxidants showed more progressed grade 3 and grade 4 osteoarthritic changes.⁴² Similar findings were obtained in a 2020 study investigating how a high vitamin C diet affected chondrocyte proliferation in AA-deficient KO mice. Lindsey et al. showed a substantial increase in chondrocyte proliferation in those mice receiving an enriched vitamin C diet when compared to the control group receiving a diet absent of the vitamin. Although the exact mechanism by which this occurred was not elucidated, the group concluded that vitamin C had a beneficial effect on chondrocyte proliferation; with the possibility of it being used as a novel therapeutic approach to treat OA prevention.⁴³ Nonetheless, not all animal studies involving vitamin C have demonstrated a clear indication of benefit. Kraus et al. showed that drastically elevated serum levels of vitamin C in guinea pigs caused an increased expression of the inflammatory marker, TGF-β, within marginal osteophytes. In addition, synovial fluid levels of cartilage oligomeric matrix protein, a biomarker of cartilage turnover, was drastically increased following prolonged exposure to vitamin C. Thus, it was concluded that the increase in OA-like changes seen with excess serum vitamin C levels was mediated in part by the increased expression of TGF-β.⁴⁴

Table 1.

Complete list of animal studies involving vitamin C and osteoarthritis used for analysis and commentary.

Animal studies
Title of study	Study type	Patient population	Significant findings	Citation
Experimental OA in guinea-pigs	In vivo animal trial	Male guinea-pigs, meniscectomized	Supplementation association with a decrease in developing spontaneous OA, but no significant difference preventing lesions after inducing OA	Meacock et al.⁴¹
Dietary vitamins and selenium diminish development of mechanically induced OA . . .	In vivo animal trial	72 male STR/1 N mice, 44 male Balb/c mice	Antioxidant diet associated with grade 2 OA when compared to control diet associated with grade 3 & 4 OA	Kurz et al.⁴²
The effects of ascorbic acid on cartilage metabolism in guinea pig articular cartilage explants	In vivo animal trial	30 male Hartley guinea pigs, aged 6–10 months	AA supplementation associated with greater SVCT2 gene transcription and mRNA stability	Clark et al.⁴⁵
Ascorbic acid increases the severity of spontaneous knee osteoarthritis in a guinea pig model	In vivo animal trial	46 male Hartley guinea pigs, age 2 months	AA activates TGF-beta—which actively causes osteophyte formation	Kraus et al.⁴⁴
Vitamin C Protects Chondrocytes against Monosodium Iodoacetate-Induced Osteoarthritis by Multiple Pathways.	In vivo animal trial	80 male Wistar rats at 5 weeks of age. Treated with MIA to induce OA-like state.	Vitamin C inhibits OA progress via decreasing apoptosis and pro-inflammatory cytokine expression. There is an optimal dose that is not recommended to surpass.	Chiu et al.⁴⁶
Combination of Magnesium ions and vitamin C alleviates synovitis and osteophyte formation in osteoarthritis of mice	Randomized control trial	Twenty-four male 3-month old mice, meniscectomized	Intra-articular administration of Mg2+ and VC additively alleviates joint destruction and pain in OA	Yao et al.⁴⁷
Vitamin C effects on 5-hydroxumethylcytosine and gene expression in osteoblasts and chondrocytes: Potential involvement of PHD2	Longitudinal study *	Guloncolactone oxidase deficient mice	AA-deficient sfx mice had decreased articular cartilage and trabecular bone, in vitro AA treatment increased chondrocyte proliferation but had no significant effect on osteoblast proliferation	Lindsey et al.⁴³
Intra-articular injection of ascorbic acid/ferric chloride relieves cartilage degradation in rates with osteoarthritis	Randomized control trial	Thirty male Wistar rats with surgically induced osteoarthritis	OARSI scores and content of type 2 collagen were significantly lower in experimental group at 9 and 12 weeks	Liao et al.⁴⁸
Mechanical overloading causes mitochondrial superoxide and SOD2 imbalance in chondrocytes resulting in cartilage degeneration	Control trial	SOD2 KO mice with Surgically-induced OA	Vitamin C-permeable derivative significantly suppressed mitochondrial superoxide level and mitigated cartilage degeneration	Koike et al.⁴⁹

AA, Ascorbic Acid; KO, Knockout; MIA, Monosodium iodoacetate; OA, osteoarthritis; OARSI, Osteoarthritis Research Society International; PHD, prolyl hydroxylase domain-containing protein; SOD, superoxide dismutase; STR, Strain of mice; SVCT, sodium-dependent vitamin C transporters; VC, vitamin C.

Vitamin C injections on the reduction of oxidative stress parameters

More recently, studies looking at the efficacy behind intra-articular injections of vitamin C in conjunction with other inflammatory mediating compounds have been performed. In 2018, a study investigating whether injections of vitamin C and ferric chloride affected OA progression in surgically induced osteoarthritic mice was performed.⁴⁸ Two key features, osteophyte formation, and joint space narrowing, were monitored to quantify the progression of OA in the mice. After 12 weeks of injections, data showed substantial reductions in OA progression within the experimental group mice when compared to the control mice. This allowed the authors to reach the conclusion that intra-articular injections of vitamin C/FeCl₃ effectively delayed OA progression in mice.⁴⁸ Yao et al. found similar results during trial looking at injections with the combination of magnesium ions and vitamin C. Twenty-four male mice, meniscectomized to induce OA, were given injections of either Mg²⁺ alone, a combination of Mg²⁺ and vitamin C, or saline (control). After 2 weeks of injections, significant reduction of joint destruction and pain were noted in the experimental group, most notably in the combined vitamin C and Mg^{2 +} cohort. Researchers quantified this data by looking at osteophyte formation and the amount of inflammatory markers found in the synovium.⁴⁷ The efficacy of vitamin C intra-articular injections in reducing inflammatory markers was further demonstrated in a 2017 study.⁴⁶ Chiu et al. outlined multiple inflammatory pathways upon which vitamin C conveys its effect in their two-part study. The first part involved in vitro analysis of rat chondrocytes derived from a chondrosarcoma cell line (SW1353), that were treated with monosodium iodoacetate (MIA) to replicate the conditions seen in OA. The MIA treatment led to increased production of pro-inflammatory markers (MMP, TNF-alpha, IL-6) ultimately leading to a myriad of pathological problems such as inhibition of cell growth, an increase in oxidative stress, limitations in the production of proteoglycans, and prolific apoptosis within articular cartilage. However, the addition of 100 μM of vitamin C led to a significant decrease in inflammatory cytokines and MMPs, as well as a substantial reduction in chondrocyte apoptosis. The second part of the study was used to see how the efficacy of vitamin C injections translated to in vivo analysis within MIA-induced OA rats. As expected, the treatment served as an effective antioxidant, slowing the progression of OA by decreasing chondrocyte apoptosis and reducing the production of pro-inflammatory markers.⁴⁶ Although the final results were promising, one unexpected finding was that of an optimal level of vitamin C dosage. The maximal efficiency was seen in rats receiving the lowest dose (100 mg/kg), with the antioxidant effect diminishing as the dose increases to 200 and 300 mg/kg. Researchers concluded that articular injections of vitamin C show a clear benefit in slowing OA progression by attenuating oxidative damage within the articular cartilage; however, too much of the substances can eventually lead to deleterious effects. Thus, further research is needed to find the optimal dosage required to maximize the beneficial properties of vitamin C in the setting of OA therapy.⁴⁶

Human clinical studies

Vitamin C supplementation in osteoarthritic patients

Although no double-blind placebo-controlled human clinical trials have been performed to date, there have been many prospective and cross-sectional studies looking at how vitamin C intake might affect the incidence and progression of OA (Table 2). In one of the largest longitudinal studies published to date, the relationship between vitamin C supplementation and its effects on human knee OA development and progression was investigated. The 2011 study included over 1023 patients aged 40 years or older, and with the use of an MRI, the OA status of each individual was determined.⁴⁰ Ten years later, each participant was subject to a second MRI to determine the progression of OA, as well as a detailed questionnaire aimed at determining daily vitamin C intake. Results showed that participants who engaged in supplementation of the vitamin were 11% less likely to develop OA when compared to those who did not supplement. However, results also demonstrated no significant difference in OA progression between the two groups. Thus, Peregoy and Wilder⁴⁰ concluded that vitamin C acted in a chondroprotective manner leading to the prevention of OA, but had no effect on delaying the progression of the disease once established. The same mixed results pertaining to the antioxidant therapy were reproduced in Joseph et al.’s 2019 cross-sectional and longitudinal study along with several other recently published manuscripts.^50–52 For instance, in the 2007 cross-sectional study, 293 healthy individuals were analyzed for their daily vitamin C intake over 10 years. After the time period, an MRI was performed in which cartilage volume, bone area, cartilage defects, and bone marrow lesions were assessed. Vitamin C intake was shown to have a beneficial effect by reducing the bone size and bone marrow lesions, both of which are important in knee OA’s pathogenesis.⁵⁰ Further beneficial evidence was exhibited in the 2019 study where diets of 314 subjects (⩾65 years old) diagnosed with dyslipidemia (a risk factor for OA) were followed for several years. After adjusting for the amount of vitamin C intake, sex, and several other variables, it was discovered that subjects within the lowest quartile of vitamin C intake had a 3.29 times higher risk of developing OA in their lifetime than did subjects in the high quartile.⁵¹

Table 2.

Complete list of human studies involving vitamin C and osteoarthritis used for analysis and commentary.

Human studies
Title of study	Study type	Patient population	Significant findings	Citation
Effect of antioxidants on knee cartilage and bone in healthy, middle-aged subjects: a cross-sectional study	Prospective cohort	297 Australians, 99% of which were aged 40–69 years	Tibial bone plateau area was smaller, fewer bone marrow lesions when supplementing AA	Wang et al.⁵⁰
The effects of vitamin C supplementation on incident and progressive knee osteoarthritis: a longitudinal study	Longitudinal study	1023 males and females aged 40 + years	11% less likely to develop OA when taking vitamin C supplement compared to control-No effect on pre-existing OA progression	Peregoy and Wilder⁴⁰
High plasma levels of vitamin C and E are associated with incident radiographic knee OA	Nested case-control	3026 males and females aged 50–79 years or at high risk of knee OA	Taking higher amounts than the RDA of both vitamin C and E may be associated with more OA changes	Chaganti et al.⁵³
Do antioxidant micronutrients protect against the development and progression of knee OA	Retrospective cohort	640 males and females	High dietary intake of AA was associated with reduced structural progression of OA. No effect on incidence	McAlindon et al.⁵⁴
Associations between dietary antioxidants intake and radiographic knee OA	Cross sectional study	4685 subjects over 40 years & undergoing weight bearing bilateral AP radiography of knee	More radiological evidence of knee OA in those supplementing with vitamin C	Li et al.⁵⁵
Synergistic chondroprotective effect of alpha-tocopherol, ascorbic acid, andSelenium . . .	In vitro analysis	Human chondrosarcoma cell lines (SW1353) induced into an inflammatory state	Adding additional antioxidant augments vitamin C’s ability to slow progression of OA in an vitro analysis.	Graeser et al.⁵⁶
Ascorbic acid provides protection forhuman chondrocytes against oxidative stress.	In vitro analysis	Human C28/I2 chondrocyte cell line treated with H2O2	AA reduced activity of pro-inflammatory markers, decreased apoptosis, and stimulated production of collagen and proteoglycan	Chang et al.⁵⁷
Comparative effects of vitamin C on the effects of local anesthetics ropivacaine, bupivacaine, and lidocaine on human chondrocytes.	In vitro analysis	Human chondrocytes isolated and exposed to local anesthetics	Adding vitamin C to intra-articular injections of local anesthetic reduces the chondrotoxicity seen with using the anesthetic injection alone	Tian and Li⁵⁸
Relationship of sociodemographic and anthropometric characteristics and nutrient and food intakes with osteoarthritis prevalence in elderly subjects with controlled dyslipidemia: a cross-sectional study	Cross-sectional study	314 subjects aged ⩾ 65 years old who were diagnosed with dyslipidemia	Average vitamin C intake was positively correlated with risk of developing osteoarthritis	Jeong et al.⁵¹
Ascorbic acid attenuates Senescence of Human osteoarthritic osteoblasts	Control trial	Bone chips from sclerotic and non-sclerotic regions of subchondral bone of human OA joints	Bone fragments grown in AA showed a negative correlation with senescent cells and a decreased expression of ROS. Supplementation with AA was found to help expand subchondral bone osteoblast in-vitro	Burger et al.⁵⁹
Dietary antioxidants, non-enzymatic antioxidant capacity and the risk of osteoarthritis in the Swedish National march Cohort	Prospective cohort study	29,406 males and females ⩾ 40 years old were included	No association between vitamin C intake and risk of developing OA was noted	Veen et al.⁶⁰
Associations Between Vitamins C and D Intake and Cartilage Composition and Knee Joint Morphology Over 4 Years: Data From the Osteoarthritis Initiative	Longitudinal Study	1785 male and females ⩾ 45 years old with Kellgren/Lawrence knee grades 0–3	The cross-sectional analysis found a beneficial effect of vitamin C on joint degeneration (having inverse associations with cartilage T2 values and WORMS scores), while the longitudinal results showed no significant associations.	Joseph et al.⁵²

AA, Ascorbic Acid; AP, Anteroposterior; OA, osteoarthritis; RDA, Recommended Dietary Allowance; ROS, reactive oxygen species; WORMS, Whole-organ magnetic resonance imaging score.

While the multiple studies mentioned above have provided data illustrating vitamin C’s chondroprotective ability, several other studies published in the literature have reached the opposite conclusion.^53,55,60 No association between vitamin C intake and risk of developing OA was noted in the large prospective cohort study conducted by Veen et al. in 2020.⁶⁰ Furthermore, Chaganti et al. performed a nested case-control study that examined the correlation between knee OA with circulating serum vitamin C and E levels. Participants were divided into tertiles based upon serum vitamin C levels through blood assays. Thereafter, patients underwent radiographic imaging for establishment of baseline. Repeat serum levels and imaging were performed at a 30-month follow-up. The results demonstrated that individuals within the highest tertile of initial serum vitamin C did not witness chondroprotection and may even be more prone to knee OA.⁵³ More recently, Li et al.⁵⁵ found the same results in their cross-sectional study that ultimately found a positive correlation between vitamin C intake and increased prevalence of knee OA. Overall human clinical studies demonstrated mixed results and thus remain controversial. An urgent need of double-blinded large multi-center clinical trial is needed to understand the beneficial effect of vitamin C in OA.

In vitro studies involving vitamin C for cartilage repair

To gain further insight into the mechanism by which vitamin C works, several in vitro studies utilizing human chondrocytes were performed. One particular study treated chondrocytes with hydrogen peroxide to induce ROS production. It is well known that elevated levels of ROS within joint spaces is detrimental to chondrocyte function, regeneration and proliferation.^61,62 To test the ability of vitamin C to attenuate the damage caused by ROS in human chondrocytes, cells were subjected to hydrogen peroxide with the subsequent treatment of various doses of vitamin C (100 or 200 μM). The vitamin C treatment reduces pro-inflammatory marker activity, decreases apoptosis, and stimulated the production of collagen and proteoglycan.⁵⁷ The beneficial effects of vitamin C reducing inflammation and osteoblast function were also documented by Burger et al. in vitro analysis. In this 2017 study, bone chips harvested from sclerotic and non-sclerotic regions of subchondral bone in human OA joints were grown in cultures. The cells cultured with the addition of 0.1 mM ascorbic acid showed enhanced proliferative capacity along with reductions in both senescent cells and ROS.⁵⁹ Another study looked at the effects of combining other known antioxidant species, selenium, and alpha-tocopherol, with vitamin C. The chondrocytes were exposed to a particular ROS to induce an inflammatory state. The combined administration of antioxidants reduced the cytotoxic effects more so than any of the antioxidant species administered alone.⁵⁶ Therefore, Graeser et al. concluded that it might be beneficial to combine multiple antioxidants with vitamin C to more effectively slow the progression of OA.

Discussion and suggestions for future research

Vitamin C remains at the top of the list in terms of future treatments options for OA due to its well-tolerated biophysical profile, cheap cost, and easy administration; whether that be via the sole supplementation of the substance or in conjunction with other pharmacologic compounds seen in several studies mentioned above. Two important points can be noted from our literature search, with the first being that the most recent data pertaining to the therapeutic potential of vitamin C in attenuating progression and prevention of OA are mixed and thus remain controversial. While many studies in animal models and humans generally point to vitamin C supplementation as an efficacious treatment in the prevention of OA, other studies have concluded that excess vitamin C intake may lead to detrimental effects within the body, including increased inflammation and even increased progression of OA.^{40,41,43,44,46,50,51,53–55,60} The second is that there does seem to be a general consensus around an optimal dosage for the substances to have a maximal effect.^44,46

Based on our and other published studies, we hypothesize that several important factors have not fully been considered in data collection and analysis, possibly resulting in the discrepancies seen in several of the data sets. These factors include (a) not taking the complexities of the SVCT1/2 transporter system expression into account in human clinical studies and (b) not properly accounting for the vitamin C biosynthesis mechanism in animal models (e.g. mice/rats). Therefore, the outcomes of such animal models do not translate effectively to the human condition. Moreover, we speculate that the data obtained from several of the human studies listed in Table 2 may be inconclusive due to not fully considering the altered regulation of the SVCT transporter during diseased conditions. Recent reports in various cells and tissue types, including cartilage, have shown that vitamin C transporter is dysregulated during pathophysiological conditions such as OA.^36,63,64 In such a condition, vitamin C uptake during supplementation or injection will not be able to act intracellularly as an antioxidant, but rather stay extracellularly where the vitamin can aid in ROS generation ultimately leading to further damage of surrounding tissues.^65,66

Conclusion

In conclusion, critical barriers in the development of an effective treatment option remain due to a poorly translatable humanized animal model for testing, dysregulation of vitamin C transporter in the osteoarthritic tissue, and an incomplete understanding of human OA pathophysiology. Given this fact, performing studies in the murine model do not translate well to human application. Thus, future human studies are essential, especially double-blind randomized control trials, to properly quantify the effectiveness of vitamin C treatment and identify the ideal amount of antioxidant supplementation needed to achieve the greatest response within an individual.

Footnotes

Acknowledgements

We would like to thank the Department of Orthopedic Surgery, Department of Medicine, and Division of endocrine for their support. Burton Dunlap and G. Taylor Patterson are equal contribution.

Funding

The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This work is funded by the Department of Orthopedic Surgery, Department of Medicine, and Division of endocrine, Augusta University.

Conflict of interest statement

The authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Consent statement and ethical approval

This study is based on published data (PubMed search). A consent statement and ethical approval are not required for the current study.

ORCID iD

Sadanand Fulzele

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Vitamin C supplementation for the treatment of osteoarthritis: perspectives on the past,present,and future

Abstract

Keywords

Introduction

Vitamin C

Vitamin C and its transporter

Vitamin C supplementation for OA

Animal studies

Vitamin C supplementation on prevention and progression of OA

Vitamin C injections on the reduction of oxidative stress parameters

Human clinical studies

Vitamin C supplementation in osteoarthritic patients

In vitro studies involving vitamin C for cartilage repair

Discussion and suggestions for future research

Conclusion

Footnotes

Acknowledgements

Funding

Conflict of interest statement

Consent statement and ethical approval

ORCID iD

References