快樂小藥師
本部落格為介紹醫藥相關知識部落格,並沒有販賣藥品。此外文章部分內容可能會引起您的不安或是心理不適,在按下繼續閱讀前,請先自我評估,謝謝(原創文章如需轉載請先告知 左右水平廣告輪播-語法
  • // 如果你希望圖片繼續多一點,那就自己再複製增加

glaucoma.jpg  

JAMA Ophthalmol. 2013;():1-3. doi:10.1001/jamaophthalmol.2013.227.

 

The Centers for Disease Control and Prevention report that osteoarthritis affects 27 million adults in the United States. Glucosamine sulfate is a naturally occurring substance found in human cartilage and a precursor for glycosaminoglycans (GAGs). A combination of supplements, glucosamine and chondroitin sulfate, was shown in the Glucosamine/Chondroitin Arthritis Intervention Trial to aid moderate to severe osteoarthritic knee pain.1

 

Open-angle glaucoma affects more than 2 million individuals in the United States, and this number continues to increase owing to the rapid aging of the US population.2 Normal aqueous outflow of the eye is regulated by the content of GAGs.3 Researchers postulate that excessive deposits of GAG in the trabecular meshwork restrict outflow. Another theory suggests that increased release of GAG into the aqueous causes an osmotic effect, drawing more water into the anterior chamber, thus causing swelling, a decrease in pore size, and eventual increased resistance to outflow.3 Either of these proposed mechanisms could lead to an increased thickness of the pore lining and/or decreased outflow, resulting in increased intraocular pressure (IOP). Excessive glucosamine molecules may similarly elevate IOP.

 

In a small retrospective clinical study, we examine the relationship between glucosamine supplementation and increased IOP in patients with glaucoma who supplement with glucosamine.

METHODS

 

This retrospective study was reviewed by the University of New England College of Osteopathic Medicine Review Board Chair. Patients had been serially selected by their history of glucosamine supplementation and ocular hypertension (IOP >21 mm Hg) or established diagnosis of open-angle glaucoma, willingness to electively stop using glucosamine, IOP measurements at least 3 times within 2 years, and no concomitant changes in glaucoma medications or eye surgery.

 

For analysis, patients were divided into 2 groups: cohort A with between 1 and 3 previously measured baseline IOPs who then began glucosamine supplementation; and cohort B without preexisting IOP measurements prior to beginning glucosamine. Cohort A had IOP measured before glucosamine, while supplementing with glucosamine, and after discontinuing glucosamine. Cohort B had IOP measured only while supplementing with glucosamine and after discontinuing glucosamine. Statistical analysis used 2-way repeated-measures analysis of variance with 2-tailed t test.

RESULTS

A total of 21 patients were identified, and 17 met inclusion criteria (6 men, 11 women; mean age, 76 years; age range, 62-90 years) (Table). In cohort A (n = 11), IOP increased significantly from before glucosamine supplementation to during glucosamine supplementation (P = .001) and decreased significantly from during glucosamine supplementation to discontinuation of glucosamine (P = .002) (Figure, A). In cohort B (n = 6), IOP significantly decreased in the discontinuation group (P = .008) (Figure, B). In cohorts A and B combined, patients discontinuing glucosamine supplementation had significantly decreased IOP, with a mean (SD) change from 19.5 (3.4) to 16.7 (3.0) mm Hg OD (mean change, −2.8 mm Hg; range, −1.0 to −5.3 mm Hg) and from 20.3 (2.9) to 17.3 (2.4) mm Hg OS (mean change, 3.0 mm Hg; range, +0.5 to −9.5 mm Hg) (P < .001) (Figure, C). There was no significant difference between the left and right eyes in each patient for any of the categories or comparisons.

DISCUSSION

 

The connection between glucosamine supplementation and increased IOP observed herein deserves further exploration. Of note, variables for which we did not account include glucosamine dosage, duration of treatment, brand variability (some are sold in combination with chondroitin sulfate), patients' lack of recalling deviation from recommended doses, and compliance variability. While the pathological process of chronic ocular hypertension is not completely understood, morphological changes in collagen may precede increases in IOP. Some postulate that normal aqueous outflow is regulated by the content of GAGs and formation of a viscous, elastic, gel-like substance that acts as a filtration system.4 A critical level of hyaluronic acid may also be essential for maintaining a well-hydrated, semipermeable meshwork.4 In vitro research on human eyes has found a decrease in GAG synthesis, particularly hyaluronic acid, in glaucomatous eyes compared with healthy eyes.5 As mentioned, theories exist regarding an osmotic effect of GAGs leading to swelling and outflow resistance.3 We hypothesize that discontinuation of glucosamine supplementation reduces IOP by mechanisms similar to those of discontinuation of corticosteroid treatment, which shows a similar effect.6

 

Many questions are raised by glucosamine supplementation–associated IOP changes. This study shows a reversible effect of these changes, which is reassuring. However, the possibility that permanent damage can result from prolonged use of glucosamine supplementation is not eliminated. Monitoring IOP in patients choosing to supplement with glucosamine may be indicated.

figure1

table 1  

 

 

創作者介紹
創作者 快樂小藥師 的頭像
快樂小藥師

快樂小藥師 Im pharmacist nichts glücklich

快樂小藥師 發表在 痞客邦 留言(0) 人氣()


留言列表

發表留言

您尚未登入,將以訪客身份留言。亦可以上方服務帳號登入留言

請輸入暱稱 ( 最多顯示 6 個中文字元 )

請輸入標題 ( 最多顯示 9 個中文字元 )

請輸入內容 ( 最多 140 個中文字元 )

請輸入左方認證碼:

看不懂,換張圖

請輸入驗證碼