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Caffeine Metabolite May Slow Progression of Short-Sight In Children

Summary: 7-MX, a caffeine metabolite, may help to slow the progression of myopia or short-sightedness in children.

Source: BMJ

A metabolite of caffeine, known as 7-MX, may slow the progression of short-sightedness, also known as myopia, in children, suggests observational research published online in the British Journal of Ophthalmology.

If proved safe and effective in large clinical trials, 7-MX could become a valuable treatment for a condition for which current options are somewhat limited, say the researchers.

Myopia occurs when the eye grows too long, stretching and thinning it, and often starts at the age of 6–7, progressing until the age of 16–20.

It is associated with a heightened risk of various conditions that affect vision and eye health, including macular degeneration, cataracts, glaucoma and retinal detachment.

Preliminary research suggests that the caffeine metabolite 7-methylxanthine, or 7-MX for short, inhibits excessive lengthening of the eye (axial elongation).

7-MX has been used to treat childhood myopia in Denmark since 2009. But until now it has not been fully evaluated in long term studies, and the researchers wanted to find out how quickly myopia progresses in children taking 7-MX.

The researchers reviewed the medical records of 711 children (356 girls and 355 boys) treated for myopia at one eye clinic in Denmark between June 2000 and January 2021.

Comprehensive eye tests, including measurement of axial length, were carried out on the children. And 624 of the children took 7-MX tablets up to 1200 mg daily (average 470 mg) while 87 didn’t, for various reasons.

Their average age was 11 (range 7-15) when they started treatment, and their eye length and degree of myopia were tracked for an average of 3½ years (range 11 months–9 years).

Dioptres (D) are the units of measurement used to assess the extent of eye function: the average degree of refractive error (short-sight) to begin with was −2.43 D, which increased by an average of 1.34 D during the monitoring period. -3.00 D is regarded as moderately severe myopia; -6 D or more is regarded as severe myopia.

Average axial length was 24.4mm, to start with, increasing by an average of 0.21 mm/year.

Treatment with 7-MX was associated with a slower rate of worsening myopia and axial elongation, with higher doses seemingly more effective.

Based on these data, the researchers estimated that for a typical 7 year old with a refractive error of −2.53 D to start with, that child’s myopia would increase by −3.49 D over the next 6 years without treatment.

But with a daily dose of 1000 mg of 7-MX, that same child’s myopia would increase by −2.65 D over the next 6 years.

It is associated with a heightened risk of various conditions that affect vision and eye health, including macular degeneration, cataracts, glaucoma and retinal detachment. Image is in the public domain

Similarly, without treatment, axial length would increase by 1.80 mm over 6 the next years, whereas it would increase by 1.63 mm on a daily dose of 1000 mg.

The researchers calculated that, on average, for an 11 year-old taking 1000 mg 7-MX daily that child’s myopia would increase by −1.43 D over the next 6 years, compared with −2.27 D without treatment. And axial length would increase by 0.84 mm compared with 1.01 mm without treatment.

None of the children taking 7-MX reported any side effects during the monitoring period.

The findings echo those of experimental studies, say the researchers. But they acknowledge that their study is observational, nor were they able to account for potentially influential factors, such as genetic factors, time spent outdoors, ethnicity, and time spent on near work. Their findings cannot, therefore, establish causality.

“The question of causality and the size of a possible treatment effect can only be determined through a randomized trial,” they write.

But they conclude: “Existing myopia control intervention methods are not fully effective in preventing children from progressing to high myopia, and 7-MX may become a valuable supplement if causality and efficacy can be confirmed in future randomized controlled trials.”

About this visual neuroscience research news

Author: Press Office
Source: BMJ
Contact: Press Office – BMJ
Image: The image is in the public domain

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Original Research: Open access.
“Oral administration of caffeine metabolite 7-methylxanthine is associated with slowed myopia progression in Danish children” by Klaus Trier et al. British Journal of Opthalmology

Abstract

Oral administration of caffeine metabolite 7-methylxanthine is associated with slowed myopia progression in Danish children

Purpose 

Myopia is associated with an increased risk of permanent vision loss. The caffeine metabolite 7-methylxanthine (7-MX), licensed in Denmark since 2009 as a treatment to reduce the rate of childhood myopia progression, is the only orally administered therapy available. The purpose of the current study was to assess the rate of myopia progression in children taking 7-MX.

Methods 

Longitudinal cycloplegic refraction and axial length data for 711 myopic children from Denmark treated with varying doses of oral 7-MX (0–1200 mg per day) were analysed using linear mixed models.

Results 

The median age at baseline was 11.1 years (range 7.0 –15.0 years). Children were followed for an average of 3.6 years (range 0.9–9.1 years) and the average myopia progression was 1.34 dioptres (D) (range −6.50 to +0.75 D). Treatment with 7-MX was associated with a reduced rate of myopia progression (p<0.001) and axial elongation (p<0.002). Modelling suggested that, on average, an 11-year-old child taking 1000 mg 7-MX daily would develop −1.43 D of myopia over the next 6 years, compared with −2.27 D if untreated. Axial length in this child would increase by 0.84 mm over 6 years when taking a daily dose of 1000 mg of 7-MX, compared with 1.01 mm if untreated. No adverse effects of 7-MX therapy were reported.

Conclusions 

Oral intake of 7-MX was associated with reduced myopia progression and reduced axial elongation in this sample of myopic children from Denmark. Randomised controlled trials are needed to determine whether the association is causal.

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