Journal List > J Korean Ophthalmol Soc > v.61(1) > 1141383

Kim, Rah, Kim, and Kim: Nationwide Cross-sectional Study of Association between Pterygium and Alkaline Phosphatase in a Population from Korea

Abstract

Purpose

We determined whether elevated serum alkaline phosphatase (ALP) was related to prevalence, location, type, length, and recurrence of pterygium in a population from the Republic of Korea.

Methods

A nationwide cross-sectional dataset, the Korean National Health and Nutrition Examination Survey (2008–2011), was used in this study. All participants were > 30 years of age and underwent the ALP test and ophthalmic evaluation (n = 22,359). One-way analysis of variance, the chi-square test, and Fisher's exact test were used to compare characteristics and outcomes among participants. Multivariable logistic regression was used to examine the possible associations between serum ALP levels and various types of pterygium. Data were adjusted for known risk factors for development of pterygium and ALP elevation (age, sex, residence, sunlight exposure, drinking, smoking, hypertension, diabetes, BMI, AST, ALT, vitamin D, and HDL).

Results

The overall prevalence of pterygium was 8.1%, and participants with pterygium had higher levels of serum ALP (p < 0.001). Participants with higher serum ALP had a significantly higher prevalence of all types of pterygium than those in the lower serum ALP quartiles. After adjusting for potential confounding factors, multivariate logistic regression analysis revealed that ALP was associated with the prevalence of pterygium (odds ratio [OR], 1.001; p = 0.038). Trend analysis between the OR and ALP quartiles revealed a linear trend in overall prevalence and in the intermediate type of pterygium. Subgroup analysis revealed a stronger correlation in participants > 50 years of age. One-way analysis of variance revealed an association between the size of pterygium and serum ALP quartile levels. Serum ALP was not associated with recurrence of pterygium.

Conclusions

Increased serum ALP was associated with the prevalence and size of pterygium.

Figures and Tables

Figure 1

Association between alkaline phosphatase and size of pterygium. Linear trends in pterygium size.

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Table 1

Demographic and clinical characteristics of the study participants

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Data are expressed as weighted means or weighted frequency (%) with standard errors.

HBV = hepatitis B virus; HCV = hepatitis C virus; BMI = body mass index; AST = aspartate aminotransferase; ALT = alanine aminotransferase; HDL = high-density lipoprotein cholesterol; TG = triglyceride; ALP = alkaline phosphatase.

*p < 0.05, chi-squared test.

Table 2

The relation of ALP quartile to prevalence, type, location and recurrence of pterygium

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Values are presented as number (%). ‘ALP 1’ is <177 IU/L; ‘ALP 2’ is >177 IU/L, < 217 IU/L; ‘ALP 3’ is >217 IU/L, < 264 IU/L; ‘ALP 4’ is >264 IU/L.

ALP = alkaline phosphatase.

*Fisher's exact test.

Table 3

Logistic regression analysis pterygium and associated demographic or clinical factors

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‘Model 1’ is adjusted for age, sex, residence, sunlight exposure, drinking, smoking, hypertension and diabetes. ‘Model 2’ is adjusted for all factors in Model 1 and BMI, AST, ALT, Vitamin D and HDL.

OR = odd ratio; HBV = hepatitis B virus; HCV = hepatitis C virus; BMI = body mass index; AST = aspartate aminotransferase; ALT = alanine aminotransferase; HDL = high-density lipoprotein cholesterol; TG = triglyceride; ALP = alkaline phosphatase.

*Logistic regression analysis.

Table 4

Odds ratios for association of pterygium and quantile of alkaline phosphatase

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‘Model 1’ is Adjusted for age, sex, residence, sunlight exposure, drinking, smoking, hypertension and diabetes. ‘Model 2’ is Adjusted for all factors in Model 1 and BMI, AST, ALT, Vitamin D and HDL.

OR = odd ratio; BMI = body mass index; AST = aspartate aminotransferase; ALT = alanine aminotransferase; HDL = high-density lipoprotein cholesterol.

*p < 0.05, multivariate logistic regression.

Notes

Conflicts of Interest The authors have no conflicts to disclose.

References

1. Liu L, Wu J, Geng J, et al. Geographical prevalence and risk factors for pterygium: a systematic review and meta-analysis. BMJ Open. 2013; 3:e003787.
crossref
2. Saw SM, Tan D. Pterygium: prevalence, demography and risk factors. Ophthalmic Epidemiol. 1999; 6:219–228.
crossref pmid
3. Cajucom-Uy H, Tong L, Wong TY, et al. The prevalence of and risk factors for pterygium in an urban Malay population: the Singapore Malay Eye Study (SiMES). Br J Ophthalmol. 2010; 94:977–981.
crossref pmid
4. Wong TY, Foster PJ, Johnson GJ, et al. The prevalence and risk factors for pterygium in an adult Chinese population in Singapore: the Tanjong Pagar survey. Am J Ophthalmol. 2001; 131:176–183.
crossref pmid
5. Hilgers JH. Pterygium: its incidence, heredity and etiology. Am J Ophthalmol. 1960; 50:635–644.
crossref pmid
6. Bahar I, Loya N, Weinberger D, Avisar R. Effect of pterygium surgery on corneal topography: a prospective study. Cornea. 2004; 23:113–117.
pmid
7. Ishioka M, Shimmura S, Yagi Y, Tsubota K. Pterygium and dry eye. Ophthalmologica. 2001; 215:209–211.
pmid
8. Fernandes M, Sangwan VS, Bansal AK, et al. Outcome of pterygium surgery: analysis over 14 years. Eye (Lond). 2005; 19:1182–1190.
crossref pmid
9. Moran DJ, Hollows FC. Pterygium and ultraviolet radiation: a positive correlation. Br J Ophthalmol. 1984; 68:343–346.
crossref pmid pmc
10. Jee D, Kim EC, Cho E, Arroyo JG. Positive association between blood 25-hydroxyvitamin d levels and pterygium after control for sunlight exposure. PLoS one. 2016; 11:e0157501.
crossref
11. Webber M, Krishnan A, Thomas NG, Cheung BM. Association between serum alkaline phosphatase and C-reactive protein in the United States National Health and Nutrition Examination Survey 2005-2006. Clin Chem Lab Med. 2010; 48:167–173.
crossref pmid
12. Schoppet M, Shanahan CM. Role for alkaline phosphatase as an inducer of vascular calcification in renal failure? Kidney Int. 2008; 73:989–991.
crossref pmid
13. Liuzzo G, Biasucci LM, Gallimore JR, et al. The prognostic value of C-reactive protein and serum amyloid a protein in severe unstable angina. N Engl J Med. 1994; 331:417–424.
crossref pmid
14. Kabat EA, Furth J. A histochemical study of the distribution of alkaline phosphatase in various normal and neoplastic tissues. Am J Pathol. 1941; 17:303–318.
pmid pmc
15. Tonelli M, Curhan G, Pfeffer M, et al. Relation between alkaline phosphatase, serum phosphate, and all-cause or cardiovascular mortality. Circulation. 2009; 120:1784–1792.
crossref pmid
16. Cheung BM, Ong KL, Cheung RV, et al. Association between plasma alkaline phosphatase and C-reactive protein in Hong Kong Chinese. Clin Chem Lab Med. 2008; 46:523–527.
crossref pmid
17. Ryu WS, Lee SH, Kim CK, et al. Increased serum alkaline phosphatase as a predictor of long-term mortality after stroke. Neurology. 2010; 75:1995–2002.
crossref pmid
18. Wannamethee SG, Sattar N, Papcosta O, et al. Alkaline phosphatase, serum phosphate, and incident cardiovascular disease and total mortality in older men. Arterioscler Thromb Vasc Biol. 2013; 33:1070–1076.
crossref pmid
19. Bandyopadhyay SK, Mukhopadhyay S, Chatterjee A. Study of alkaline phosphatase activity and DNA content of pterygium tissue showing its degenerative character. J Indian Med Assoc. 2011; 109:899–902.
pmid
20. Keating FR Jr, Jones JD, Elveback LR, Randall RV. The relation of age and sex to distribution of values in healthy adults of serum calcium, inorganic phosphorus, magnesium, alkaline phosphatase, total proteins, albumin, and blood urea. J Lab Clin Med. 1969; 73:825–834.
pmid
21. Chan-Yeung M, Ferreira P, Frohlich J, et al. The effects of age, smoking, and alcohol on routine laboratory tests. Am J Clin Pathol. 1981; 75:320–326.
crossref pmid
22. Gundberg CM, Looker AC, Nieman SD, Calvo MS. Patterns of osteocalcin and bone specific alkaline phosphatase by age, gender, and race or ethnicity. Bone. 2002; 31:703–708.
crossref pmid
23. Lomashvili KA, Garg P, Narisawa S, et al. Upregulation of alkaline phosphatase and pyrophosphate hydrolysis: potential mechanism for uremic vascular calcification. Kidney Int. 2008; 73:1024–1030.
crossref pmid pmc
24. Ketteler M, Giachelli C. Novel insights into vascular calcification. Kidney Int Suppl. 2006; 70:S5–S9.
crossref
25. Golub EE, Boesze-Battaglia K. The role of alkaline phosphatase in mineralization. Curr Opin Orthop. 2007; 18:444–448.
crossref
26. Maldonado O, Demasi R, Maldonado Y, et al. Extremely high levels of alkaline phosphatase in hospitalized patients. J Clin Gastroenterol. 1998; 27:342–345.
crossref pmid
27. Chui J, Di Girolamo N, Wakefield D, Coroneo MT. The pathogenesis of pterygium: current concepts and their therapeutic implications. Ocul Surf. 2008; 6:24–43.
crossref pmid
28. Doležalová V. Is the occurrence of a temporal pterygium really so rare? Ophthalmologica. 1977; 174:88–91.
crossref pmid
29. Ramasamy B, Quah SA, Wishart MS, Hiscott P. Temporal pterygium: benign or not? Br J Ophthalmol. 2005; 8:1533–1534.
crossref
30. Awan KJ. The clinical significance of a single unilateral temporal pterygium. Can J Ophthalmol. 1975; 10:222–226.
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