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ORIGINAL RESEARCH article

Front. Nutr., 17 April 2023
Sec. Nutritional Epidemiology
This article is part of the Research Topic Nutrition and Quality of Life in the Elderly View all 16 articles

Relationship between high dose intake of vitamin B12 and glaucoma: Evidence from NHANES 2005–2008 among United States adults

Zhongwei Liu,,&#x;Zhongwei Liu1,2,3Yi Hu,,&#x;Yi Hu1,2,3Yuhan Wang,,Yuhan Wang1,2,3Baiwei Xu,,Baiwei Xu1,2,3Jiangyue Zhao,,
Jiangyue Zhao1,2,3*Ziyan Yu,,
Ziyan Yu1,2,3*
  • 1Department of Ophthalmology, Fourth Affiliated Hospital of China Medical University, Shenyang, China
  • 2Eye Hospital of China Medical University, Shenyang, China
  • 3Key Lens Research Laboratory of Liaoning Province, Shenyang, China

Objective: Glaucoma has currently become the second leading cause of blindness in the world. Serum vitamin B12 level has been found to be involved in the development and progression of glaucoma. We performed the present study to confirm this association.

Methods: This cross-sectional study included 594 participants aged 40 years and older in the National Health and Nutrition Examination Survey (NHANES) from 2005 to 2008. Retinal imaging was performed using the Ophthalmic Digital Imaging system (Retinography) to assess the retina for the presence of features of glaucomatous lesions. Logistic regression models were used to assess the association between dietary vitamin intake and glaucoma.

Results: After screening, 594 subjects were finally included. Among all vitamin intakes, we observed significant differences between the two groups for vitamin B12 intake (5.93 vs. 4.77 mg, p = 0.033). According to the logistic regression results, the intake of vitamin B12 was significantly positively associated with glaucoma (model 1: OR = 1.078, 95% CI = 1.019–1.141; model 2: OR = 1.092, 95% CI = 1.031–1.158; model 3: OR = 1.092, 95% CI = 1.029–1.158). After performing a quantile regression, we observed a significant positive association between vitamin B12 intake and incident glaucoma in the fourth quartile (model 1: OR = 1.133, 95% CI = 1.060–1.210; model 2: OR = 1.141, 95% CI = 1.072–1.215; model 3: OR = 1.146, 95% CI = 1.071–1.226).

Conclusions: Therefore, the above results, high-dose intake of vitamin B12 may promote the development of glaucoma.

1. Introduction

Glaucoma, a neurodegenerative disease, is the second leading cause of irreversible blindness, with a worldwide prevalence of 3.5% among people aged 40 to 80 years (1). With an increasing proportion of the elderly population, 111.8 million people are expected to have glaucoma by 2040 (2). The common types of glaucoma include primary open-angle glaucoma (POAG), primary closed-angle glaucoma (PCAG) and normal tension glaucoma (NTG). Commonalities between all types of glaucoma result in damage to the optic nerve, apoptosis of retinal optic ganglion cells and visual field.

defects (3–7). Retinal ganglion cell apoptosis may be the result of impaired blood supply to the head of the optic ganglion or direct toxic effects of multiple cytotoxic substances (8–10). Glaucoma is a multi-factorial disorder, and a strong association has been found between increasing age and sex and disease progression, while other factors including hypertension, genetic variation, and other environmental risk factors may also affect it (11–13). Vascular theory and mechanical theory are the two main mechanisms of glaucoma pathogenesis. For mechanical reasons, high intraocular pressure can damage ganglion cell axons (14). The vascular theory suggests that increased intraocular pressure and other risk factors contribute to insufficient blood flow to the eyes, which can cause damage to the optic nerve (15). The precise mechanism of glaucoma remains to be determined.

Vitamin B12 (cobalamin) therapy can reduce oxidative stress damage and inflammation levels of the nervous system, and it can promote the regulation of the antiviral activity and immune system, especially when combined with folic acid (16–22). Vitamin B12 (cobalamin) deficiency is the only vitamin deficiency definitively associated with optic neuropathy characterized by slow-progressing optic atrophy (23). Recent study indicates that vitamin B12 can alleviate COVID-19 symptoms, through its analgesic function and role in neuromuscular disorders (24). A cross-sectional study showed, that vitamin B12 intake was positively correlated with plasma concentration (25). Previous prospective studies have evaluated the correlation of B vitamin intake with risk of exfoliation glaucoma or exfoliation glaucoma suspect (EG/EGS) risk. Until now, there has still been conflicting results in different studies. Several authors found that vitamin B12 intake was not correlated with EG/EGS risk in different types of glaucoma (26–29). Some studies demonstrated that serum vitamin B12 levels are decreased in glaucoma patients (6, 12), but others found them to be elevated in NTG, POAG and EXG (7, 8, 11). A meta analysis demonstrated that high-dose intake of vitamins A and B, but not vitamins C, D, or E, was associated with a low prevalence of glaucoma (30, 31).

Overall, the sample size of the glaucoma group in the above studies was small (ranging from approximately 15 to 290), and the proper dose of vitamin B12 intake for glaucoma remains inconclusive. Therefore, we conducted the present study on the basis of data from national health and nutrition examination survey (NHANES) 2005–2008 aiming to further identify the evidence provided for the appropriate dose of vitamin B12 nutritional therapy for glaucoma.

2. Materials and methods

2.1. Data source and subject selection

This study is based on data from NHANES 2005–2008. NHANES is a large nationwide cross-sectional study performed by the national center for health statistics (NCHS). NHANES subjects were all U.S. masses randomly selected on the basis of a sampling design, who underwent universal examination and signed an informed con-sent form. The NCHS research ethics review board approved the survey protocol for NHANES (32).

2.2. Defining criteria for glaucoma

Participants aged 40 years or older underwent binocular non-mydriatic fundus photography in the Mobile Examination Center (MEC) using the Canon Non-Mydriatic Retinal Camera CR6-45NM. Digital images were graded at the University of Wisconsin. The optic disc images were classified into 4 severity levels, no, possible, probable, definite (33). To better assess the potential risk of vitamin intake on the occurrence of glaucoma, in this study, “possible, probable and definite” were all considered to have glaucoma or a greater likelihood of developing glaucoma, and thus these subjects were all defined as having glaucoma.

2.3. Determination of vitamin intake and daily energy intake

Dietary data were collected in the in-person interview using the automated multiple pass method (AMPM). The AMPM is a USDA’ dietary data collection instrument and a fully computerized recall method. The NHANES (MEC) provided a set of measuring guides that facilitated participants’ ability to describe the amount of foods they had ingested (34, 35). NHANES performed dietary data statistics for two consecutive days, and we considered the mean of two daily dietary data for each subject as the final dietary intake data in an effort to obtain an outcome that more closely approximated the true level of life. Our study included all vitamin data that appeared in NHANES 2005–2008.

2.4. Assessment of covariates

Sociodemographic variables including age, race/ethnicity, sex and educational level were obtained by computer-assisted in-person interview (36). Daily intake of calories and diabetes mellitus were defined by subject’s self-report (34, 35, 37).

2.5. Statistical analysis

All statistical analyses were performed using SAS 9.4 and R software 4.1.3. NHANES uses a stratified, multistage sampling method, so we incorporated sampling weights and strata, and sampling units in our statistical analysis to account for the complex sampling design. Continuous variables were presented with mean and standard error (SE), and categorical variables were presented with percentage and SE; the chi-square test or T-test was used to compare patients’ demographic characteristics. Logistic regression models were used to determine the association of vitamin intake with the presence of glaucoma. Model 1 was adjusted by age, race, sex, and educational level. Model 2 = model 1 and adjusted by daily energy intake. Model 3 = model 2 and adjusted by diabetes mellitus. Since a significant association between vitamin B12 and glaucoma was observed, we further performed quantile regression between vitamin B12 and glaucoma. In response to the above logistic regression results, we have created additional forest plots to show them more clearly.

3. Results

3.1. Description of baseline information of the study sample

On the basis of the study design of NHANES, we selected a total of 14,440 subjects for inclusion in this study. After screening, 594 subjects were finally included, and 13,846 subjects were excluded because of missing dietary data or ophthalmological examination data. The detailed flow is shown in Figure 1. Table 1 shows the demographic data as well as other characteristic data of the participants with and without glaucoma. Among the tested population, the number of subjects with or suspected glaucoma accounted for 41.9% after weighting. Of all covariates, only age differed significantly between the two groups (55.66 vs. 63.29 years, p < 0.001). Among all vitamin intakes, we observed significant differences between the two groups for three vitamins, retinol (474.49 vs. 401.42 mg, p = 0.014), vitamin A (704.61 vs. 605.62 mg, p = 0.0040), and vitamin B12 (5.93 vs. 4.77 mg, p = 0.033).

FIGURE 1
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Figure 1. Screening process of the included studies.

TABLE 1
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Table 1. Baseline information for the study sample.

3.2. Association between the intake of retinol, vitamin a, and vitamin B12 and the presence of glaucoma

Table 2 and Figure 2 show the associations that existed between the intake of retinol, vitamin A and, vitamin B12 and glaucoma as addressed by multivariate logistic regression models. A significant positive association between vitamin B12 intake and incident glaucoma was shown in all models (model 1: OR = 1.078, 95% CI = 1.019–1.141; model 2: OR = 1.092, 95%CI = 1.031–1.158; model 3: OR = 1.092, 95% CI = 1.029–1.158). No significant association with glaucoma was observed for the intakes of retinol and vitamin A.

TABLE 2
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Table 2. Association between intake of retinol, vitamin A, vitamin B12 and glaucoma.

FIGURE 2
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Figure 2. Forest plot of logistic regression results.

3.3. Relationship of different quartiles of vitamin B12 with the presence of glaucoma

Table 3 and Figure 3 demonstrate the analysis of the association of different grades of vitamin B12 intake with glaucoma after dividing vitamin B12 intake into quartiles. Significant positive correlations between the fourth quartiles (Q4, high dose of vitamin B12 intake) and the prevalence of glaucoma were seen in all models (model 1: OR = 1.133, 95%CI = 1.060–1.210; model 2: OR = 1.141, 95% CI = 1.072–1.215; model 3: OR = 1.146, 95% CI = 1.071–1.226). No significant association with glaucoma was observed for the intakes of vitamin B12 in the first quartiles (Q1, low dose of vitamin B12 intake), the second quartiles (Q2, normal dose of vitamin B12 intake) and the third quartiles (Q3, normal dose of vitamin B12 intake).

TABLE 3
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Table 3. Association between vitamin B12 intake levels and glaucoma in different quartiles.

FIGURE 3
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Figure 3. Forest plot of quantile regression results.

4. Discussion

In this study, the potential correlation between vitamin B12 intake and glaucoma was investigated by analyzing the NHANES database. Our results suggest that there is no significant correlation between normal or low doses of vitamin B12 intake and glaucoma, but that there is significant correlation between high dose intake of vitamin B12 and glaucoma.

According to past experience, the clinical consequences of multiple doses of oral vitamin B12 as a nutritional therapy for glaucoma have not been definitively studied (38). Studies have found that the main reason for high levels of serum cobalamin is the presence of potentially life-threatening diseases, and early diagnosis is often a decisive predictor (39, 40). Cobalt is a nerve agent that can cause optical neuropathy and retinopathy. Apostoli et al. injected cobalt alone intravenously, and observed optic nerve damage and loss of cochlear hair cells (41). This study, along with one by Carelli et al. exploited similarities between mitochondrial disease and cobalt-induced optic neuropathy (41, 42). Other studies have shown similar toxic effects of cobalt on the eye, such as optic nerve atrophy; however, as reported by Apostoli et al., the concentration required to produce this effect is 1/80 compared to the previous study (43). Our results showed that high-dose vitamin B12 intake may cause optic neuropathy and play a role in the development of glaucoma, consistent with these previous studies on cobalt induced visual impairment and neuropathy. There are three major pathological mechanisms underlying increased cobalamin in serum, and these mechanisms arise from any pathological factors, including: a direct increase of vitamin B12 in plasma via overuse or medical use; a direct increase in the level of vitamin B12 in the plasma due to release from the body via excessive secretion or excretion disorders; and lack of vitamin B12 levels or lack of affinity (44). Excess vitamin B12 intake when indoors is usually relatively undetected according to ANAMNEA data. In addition, long-term pastoral use of vitamin B12 may lead to the formation of an autoantibody to TK II, which leads to a decrease in its clearance (45, 46). A positive association has been observed between intake and plasma concentrations for vitamin B12 in physically active people (25). An increase in plasma vitamin B12 may indicate a functional deficit, with clinical results similar to vitamin B12 deficiency, which can lead to increased homocysteine levels, optic neuropathy, and more seriously, irreversible damage to the nervous system (47–54). This is presumed to be another mechanism of high doses of vitamin B12 as a risk factor for glaucoma development.

The strengths of this study included the focus on the relationship between vitamin B12 intake and glaucoma, and the relatively large sample size, but there were some limitations. First, the data of NHANES ophthalmology examination could not clearly indicate the type of glaucoma that the subject had and could not reveal the relationship between vitamin B12 and different types of glaucoma. Additionally, the diet data obtained from the self-reported recall of the subject could have had some errors.

There were also individual differences in the bioavailability of vitamin B12 in each participant, resulting in differences in serum vitamin concentrations (29). Therefore, further controlled trials or epidemiological peer studies are required to confirm the serious consequences of high doses of vitamin B12 in different types of glaucoma. Moreover, to further investigate the direct relationship between vitamin B12 and glaucoma, future research should be devoted to the analysis of serum vitamin levels. Despite the limitations, this study is valuable in light of the association between high-dose intake of vitamin B12 and glaucoma.

5. Conclusion

High-dose vitamin B12 intake may contribute to the development of glaucoma, which casts a new light on a warning about dietary intake doses and any drug administration.

Data availability statement

Publicly available datasets were analyzed in this study. This data can be found at: https://www.cdc.gov/nchs/nhanes/index.htm.

Author contributions

YH: conceptualization. BX and ZL: methodology, software, formal analysis, investigation, resources, and data curation. ZY and JZ: validation, supervision, project administration, and funding acquisition. ZY, JZ, YW, YH, and BX: writing—original draft preparation, and writing—review and editing. All authors contributed to the article and approved the submitted version.

Funding

The study was supported by the Natural Science Foundation of China (NSFC 82000877).

Acknowledgments

The authors would like to thank all reviewers for their valuable comments.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. Jonas, JB, Aung, T, Bourne, RR, Bron, AM, Ritch, R, and Panda-Jonas, S. Glaucoma. Lancet. (2017) 390:2183–93. doi: 10.1016/S0140-6736(17)31469-1

CrossRef Full Text | Google Scholar

2. Kang, JM, and Tanna, AP. Glaucoma. Med Clin North Am. (2021) 105:493–510. doi: 10.1016/j.mcna.2021.01.004

CrossRef Full Text | Google Scholar

3. Quigley, HA. Glaucoma. Lancet. (2011) 377:1367–77. doi: 10.1016/S0140-6736(10)61423-7

CrossRef Full Text | Google Scholar

4. Weinreb, RN, Aung, T, and Medeiros, FA. The pathophysiology and treatment of glaucoma: a review. JAMA. (2014) 311:1901–11. doi: 10.1001/jama.2014.3192

PubMed Abstract | CrossRef Full Text | Google Scholar

5. He, S, Stankowska, DL, Ellis, DZ, Krishnamoorthy, RR, and Yorio, T. Targets of neuroprotection in glaucoma. J Ocul Pharmacol Ther. (2018) 34:85–106. doi: 10.1089/jop.2017.0041

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Stein, JD, Khawaja, AP, and Weizer, JS. Glaucoma in adults-screening, diagnosis, and management: a review. JAMA. (2021) 325:164–74. doi: 10.1001/jama.2020.21899

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Mahabadi, N., Foris, L.A., and Tripathy, K.. (2022). Open Angle Glaucoma.

Google Scholar

8. Feldman, F, Sweeney, VP, and Drance, SM. Cerebro-vascular studies in chronic simple glaucoma. Can J Ophthalmol. (1969) 4:358–64.

PubMed Abstract | Google Scholar

9. Broadway, DC, and Drance, SM. Glaucoma and vasospasm. Br J Ophthalmol. (1998) 82:862–70. doi: 10.1136/bjo.82.8.862

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Young, C, Seibold, LK, and Kahook, MY. Cataract surgery and intraocular pressure in glaucoma. Curr Opin Ophthalmol. (2020) 31:15–22. doi: 10.1097/ICU.0000000000000623

CrossRef Full Text | Google Scholar

11. Chen, Y, Lin, Y, Vithana, EN, Jia, L, Zuo, X, Wong, TY, et al. Common variants near ABCA1 and in PMM2 are associated with primary open-angle glaucoma. Nat Genet. (2014) 46:1115–9. doi: 10.1038/ng.3078

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Kim, KE, Kim, MJ, Park, KH, Jeoung, JW, Kim, SH, Kim, CY, et al. Prevalence, awareness, and risk factors of primary open-angle glaucoma: Korea National Health and nutrition examination survey 2008-2011. Ophthalmology. (2016) 123:532–41. doi: 10.1016/j.ophtha.2015.11.004

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Zukerman, R, Harris, A, Oddone, F, Siesky, B, Verticchio Vercellin, A, and Ciulla, TA. Glaucoma heritability: molecular mechanisms of disease. Genes (Basel). (2021) 12. doi: 10.3390/genes12081135

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Weinreb, RN, Aung, T, and Medeiros, FA. The pathophysiology and treatment of glaucoma: areview. JAMA. (2014) 311:1901–11. doi: 10.1001/jama.2014.3192

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Flammer, J, Orgül, S, Costa, VP, Orzalesi, N, Krieglstein, GK, Serra, LM, et al. The impact of ocular blood flow in glaucoma. Prog Retin Eye Res. (2002) 21:359–93. doi: 10.1016/S1350-9462(02)00008-3

CrossRef Full Text | Google Scholar

16. Smith, AD, Warren, MJ, and Refsum, H. Vitamin B12. Adv Food Nutr Res. (2018) 83:215–79. doi: 10.1016/bs.afnr.2017.11.005

CrossRef Full Text | Google Scholar

17. Tamura, J, Kubota, K, Murakami, H, Sawamura, M, Matsushima, T, Tamura, T, et al. Immunomodulation by vitamin B12: augmentation of CD8+ T lymphocytes and natural killer (NK) cell activity in vitamin B12-deficient patients by methyl-B12 treatment. Clin Exp Immunol. (1999) 116:28–32. doi: 10.1046/j.1365-2249.1999.00870.x

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Yoshii, K, Hosomi, K, Sawane, K, and Kunisawa, J. Metabolism of dietary and microbial vitamin B family in the regulation of host immunity. Front Nutr. (2019) 6:48. doi: 10.3389/fnut.2019.00048

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Wolffenbuttel, B, et al. The many faces of cobalamin (vitamin B12) deficiency. Mayo Clin Proc Innov Qual Outcomes. (2019) 3:200–14. doi: 10.1016/j.mayocpiqo.2019.03.002

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Wee, A. COVID-19's toll on the elderly and those with diabetes mellitusis vitamin B12 deficiency an accomplice? Med Hypotheses. (2021) 146:110374. doi: 10.1016/j.mehy.2020.110374

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Romain, M, Sviri, S, Linton, DM, Stav, I, and van Heerden, PV. The role of vitamin B12 in the critically ill—a review. Anaesth Intensive Care. (2016) 44:447–52. doi: 10.1177/0310057X1604400410

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Naseri, M, Sarvari, GR, Esmaeeli, M, Azarfar, A, Rasouli, Z, Moeenolroayaa, G, et al. High doses of oral folate and sublingual vitamin B12 in dialysis patients with hyperhomocysteinemia. J Renal Inj Prev. (2016) 5:134–9. doi: 10.15171/jrip.2016.28

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Chan, W, Almasieh, M, Catrinescu, MM, and Levin, LA. Cobalamin-associated superoxide scavenging in neuronal cells is a potential mechanism for vitamin B(12)-deprivation optic neuropathy. Am J Pathol. (2018) 188:160–72. doi: 10.1016/j.ajpath.2017.08.032

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Batista, KS, Cintra, VM, Lucena, PAF, Manhães-de-Castro, R, Toscano, AE, Costa, LP, et al. The role of vitamin B12 in viral infections: a comprehensive review of its relationship with the muscle-gut-brain axis and implications for SARS-CoV-2 infection. Nutr Rev. (2022) 80:561–78. doi: 10.1093/nutrit/nuab092

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Baart, AM, Balvers, MGJ, Vries, JHM, Haaf, DSM, Hopman, MTE, and Klein Gunnewiek, JMT. Relationship between intake and plasma concentrations of vitamin B12 and folate in 873 adults with a physically active lifestyle: a cross-sectional study. J Hum Nutr Diet. (2021) 34:324–33. doi: 10.1111/jhn.12814

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Kang, JH, Loomis, SJ, Wiggs, JL, Willett, WC, and Pasquale, LR. A prospective study of folate, vitamin B(6), and vitamin B(1)(2) intake in relation to exfoliation glaucoma or suspected exfoliation glaucoma. JAMA Ophthalmol. (2014) 132:549–59. doi: 10.1001/jamaophthalmol.2014.100

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Li, W, Pan, J, Wei, M, Lv, Z, Chen, S, Qin, Y, et al. Nonocular influencing factors for primary glaucoma: an umbrella review of meta-analysis. Ophthalmic Res. (2021) 64:938–50. doi: 10.1159/000519247

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Li, J, Xu, F, Zeng, R, Gong, H, and Lan, Y. Plasma homocysteine, serum folic acid, serum vitamin B12, serum vitamin B6, MTHFR, and risk of Normal-tension glaucoma. J Glaucoma. (2016) 25:e94–8. doi: 10.1097/IJG.0000000000000269

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Li, S, Li, D, Shao, M, Cao, W, and Sun, X. Lack of association between serum vitamin B(6), vitamin B12, and vitamin D levels with different types of glaucoma: a systematic review and meta-analysis. Nutrients. (2017) 9. doi: 10.3390/nu9060636

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Ramdas, WD, Schouten, J, and Webers, C. The effect of vitamins on glaucoma: a systematic review and meta-analysis. Nutrients. (2018) 10. doi: 10.3390/nu10030359

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Han, FF, and Fu, XX. Vitamin intake and glaucoma risk: a systematic review and meta-analysis. J Fr Ophtalmol. (2022) 45:519–28. doi: 10.1016/j.jfo.2021.10.010

CrossRef Full Text | Google Scholar

32. Centers for Disease Control and Prevention About the National Health and Nutrition Examination Survey. Available at: http://www.cdc.gov/nchs/nhanes/about_nhanes.htm (Accessed October 18, 2022).

Google Scholar

33. National Health and Nutrition Examination Survey 2007–2008. Data documentation, codebook, and frequencies: Ophthalmologyretinal imaging (OPXRET_E). Available at: https://wwwn.cdc.gov/Nchs/Nhanes/2007-2008/OPXRET_E.htm (Accessed October 18, 2022).

Google Scholar

34. National Health and Nutrition Examination Survey 2007–2008. Data documentation, codebook, and frequencies: Dietary interview-Total nutrient intakes, first day (DR1TOT_E). Available at: https://wwwn.cdc.gov/Nchs/Nhanes/2007-2008/DR1TOT_E.htm (Accessed October 18, 2022).

Google Scholar

35. National Health and Nutrition Examination Survey 2007-2008. Data documentation, codebook, and frequencies: Dietary interview-individual foods, second day (DR2IFF_E). Available at: https://wwwn.cdc.gov/Nchs/Nhanes/2007-2008/DR2IFF_E.htm (Accessed October 18, 2022).

Google Scholar

36. National Health and Nutrition Examination Survey 2007–2008. Data documentation, codebook, and frequencies: Demographic Variables & Sample Weights (DEMO_E). Available at: https://wwwn.cdc.gov/Nchs/Nhanes/2007-2008/DEMO_E.htm (Accessed October 18, 2022).

Google Scholar

37. National Health and Nutrition Examination Survey 2007–2008. Data documentation, codebook, and frequencies: Diabetes (DIQ_E). Available at: https://wwwn.cdc.gov/Nchs/Nhanes/2007-2008/DIQ_E.htm (Accessed October 18, 2022).

Google Scholar

38. Morales-Gutierrez, J, Díaz-Cortés, S, Montoya-Giraldo, MA, and Zuluaga, AF. Toxicity induced by multiple high doses of vitamin B12 during pernicious anemia treatment: a case report. Clin Toxicol (Phila). (2020) 58:129–31. doi: 10.1080/15563650.2019.1606432

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Arendt, JF, and Nexo, E. Cobalamin related parameters and disease patterns in patients with increased serum cobalamin levels. PLoS One. (2012) 7:e45979. doi: 10.1371/journal.pone.0045979

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Jammal, M, Deneuville, T, Mario, N, Tiev, K, Tolédano, C, Josselin-Mahr, L, et al. High plasmatic concentration of vitamin B12: an indicator of hepatic diseases or tumors. Rev Med Interne. (2013) 34:337–41. doi: 10.1016/j.revmed.2012.10.006

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Apostoli, P, Catalani, S, Zaghini, A, Mariotti, A, Poliani, PL, Vielmi, V, et al. High doses of cobalt induce optic and auditory neuropathy. Exp Toxicol Pathol. (2013) 65:719–27. doi: 10.1016/j.etp.2012.09.006

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Carelli, V, Barboni, P, and Sadun, AA. Mitochondrial ophthalmology. Mitochondrial Med Oxf Inf Healthc. (2006):105–42. doi: 10.1201/b14623-7

CrossRef Full Text | Google Scholar

43. Monies, A, and Prost, M. Radiometric studies of eye tissues in experimental cobalt intoxication. Klin Ocz. (1994) 96:141–3.

PubMed Abstract | Google Scholar

44. Ermens, AA, Vlasveld, LT, and Lindemans, J. Significance of elevated cobalamin (vitamin B12) levels in blood. Clin Biochem. (2003) 36:585–90. doi: 10.1016/j.clinbiochem.2003.08.004

CrossRef Full Text | Google Scholar

45. Carmel, R, Tatsis, B, and Baril, L. Circulating antibody to transcobalamin II causing retention of vitamin B12 in the blood. Blood. (1977) 49:987–1000. doi: 10.1182/blood.V49.6.987.987

PubMed Abstract | CrossRef Full Text | Google Scholar

46. Bowen, RA, Drake, SK, Vanjani, R, Huey, ED, Grafman, J, and Horne, MDK III. Markedly increased vitamin B12 concentrations attributable to IgG-IgM-vitamin B12 immune complexes. Clin Chem. (2006) 52:2107–14. doi: 10.1373/clinchem.2006.073882

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Andres, E, et al. The pathophysiology of elevated vitamin B12 in clinical practice. QJM. (2013) 106:505–15. doi: 10.1093/qjmed/hct051

PubMed Abstract | CrossRef Full Text | Google Scholar

48. Herrmann, W, Schorr, H, Obeid, R, and Geisel, J. Vitamin B-12 status, particularly holotranscobalamin II and methylmalonic acid concentrations, and hyperhomocysteinemia in vegetarians. Am J Clin Nutr. (2003) 78:131–6. doi: 10.1093/ajcn/78.1.131

PubMed Abstract | CrossRef Full Text | Google Scholar

49. Devalia, V. More on failures of cobalamin assays in pernicious anemia. N Engl J Med. (2012) 367:1570–1571.

Google Scholar

50. Romano, MR, Biagioni, F, Carrizzo, A, Lorusso, M, Spadaro, A, Micelli Ferrari, T, et al. Effects of vitamin B12 on the corneal nerve regeneration in rats. Exp Eye Res. (2014) 120:109–17. doi: 10.1016/j.exer.2014.01.017

PubMed Abstract | CrossRef Full Text | Google Scholar

51. Chavala, SH, Kosmorsky, GS, Lee, MK, and Lee, MS. Optic neuropathy in vitamin B12 deficiency. Eur J Intern Med. (2005) 16:447–8. doi: 10.1016/j.ejim.2005.01.021

CrossRef Full Text | Google Scholar

52. Briani, C, Dalla Torre, C, Citton, V, Manara, R, Pompanin, S, Binotto, G, et al. Cobalamin deficiency: clinical picture and radiological findings. Nutrients. (2013) 5:4521–39. doi: 10.3390/nu5114521

PubMed Abstract | CrossRef Full Text | Google Scholar

53. Mikkelsen, K, Stojanovska, L, and Apostolopoulos, V. The effects of vitamin B in depression. Curr Med Chem. (2016) 23:4317–37. doi: 10.2174/0929867323666160920110810

CrossRef Full Text | Google Scholar

54. Berridge, MJ. Vitamin D and depression: cellular and regulatory mechanisms. Pharmacol Rev. (2017) 69:80–92. doi: 10.1124/pr.116.013227

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: vitamin B12, glaucoma, national health and nutrition examination survey, nutrition epidemiology, cross-sectional study

Citation: Liu Z, Hu Y, Wang Y, Xu B, Zhao J and Yu Z (2023) Relationship between high dose intake of vitamin B12 and glaucoma: Evidence from NHANES 2005–2008 among United States adults. Front. Nutr. 10:1130032. doi: 10.3389/fnut.2023.1130032

Received: 22 December 2022; Accepted: 31 March 2023;
Published: 17 April 2023.

Edited by:

Gabriela Salim de Castro, University of São Paulo, Brazil

Reviewed by:

Ivan Santolalla Arnedo, University of La Rioja, Spain
Kaamran Raahemifar, The Pennsylvania State University (PSU), United States

Copyright © 2023 Liu, Hu, Wang, Xu, Zhao and Yu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Ziyan Yu, eXV6aXlhbkBob3RtYWlsLmNvbQ==; Jiangyue Zhao, anl6aGFvQGNtdS5lZHUuY24=

†These authors have contributed equally to this work and share first authorship

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.