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Vitamin D for the management of asthma

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Background Low blood levels of vitamin D risk of asthma attacks in children and adults Results from several studies about the benefit of vitamin D in asthma have not been evaluated a

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Vitamin D for the management of asthma

Dr Nguyen General Pediatric Department

Vitamin D for the management of asthma

Dr Nguyen Thuy Doan Trang General Pediatric Department

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Asthma is a chronic inflammatory condition

the airways, characterised by recurrent attacks of breathlessness, wheezing, cough, and chest

tightness, commonly termed 'exacerbations

Vitamin D is a fat-soluble micronutrient

cholecalciferol (vitamin D3) and

(vitamin D2)

Background

chronic inflammatory condition of

by recurrent attacks of breathlessness, wheezing, cough, and chest

'exacerbations'.

micronutrient:

) and ergocalciferol

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 Cholecalciferol (D3) is synthesised

by sunlight;or supplied by diet

Ergocalciferol (D2) is ingested in the diet

Ergocalciferol (D2) is ingested in the diet

Inadequate vitamin D status has been reported

to be common among people with asthma

Background

synthesised in human skin

diet

ingested in the diet

status has been reported

people with asthma.

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Vitamin D to prevent asthma

attacks

Review question

Does vitamin D prevent asthma attacks

control of asthma symptoms or both?

Background

Low blood levels of vitamin D

risk of asthma attacks in children and adults

Results from several studies about the benefit of vitamin

D in asthma have not been evaluated as a

Cochrane decided to synthetize all the studies and gave the conclusions

Vitamin D to prevent asthma

attacks

prevent asthma attacks or improve

or both?

D linked to an increased

in children and adults several studies about the benefit of vitamin

evaluated as a group

Cochrane decided to synthetize all the studies and gave

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Why it is important to do this

review

 Potential of administration of vitamin D to

exacerbation risk and improve

control.

 Several published trials of vitamin D in children with asthma have reported the

exacerbation rates among children

Why it is important to do this

review

of administration of vitamin D to reduce

and improve asthma symptom

Several published trials of vitamin D in children

the reductions in

children randomised

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Why it is important to do this

review

 Meta-analysis of these trials has the potential to increase statistical power to detect effects of

administering vitamin D on exacerbation risk

 We conducted a meta-analysis that was

restricted to double-blind, placebo

trials of at least 12 weeks' duration to determine

the effect of vitamin D on the primary outcome of exacerbation

Why it is important to do this

analysis of these trials has the potential to increase statistical power to detect effects of

administering vitamin D on exacerbation risk

analysis that was

blind, placebo-controlled

of at least 12 weeks' duration to determine the effect of vitamin D on the primary outcome of

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Search methods

We searched the Cochrane Airways Group Trial

Register and reference lists of articles

Date of last search: January 2016

Selection criteria

Double-blind, randomised, placebo

of vitamin D in children and adults with

Data collection and analysis

Two review authors independently applied study

inclusion criteria, extracted the data, and assessed risk of bias

Search methods

We searched the Cochrane Airways Group Trial

Register and reference lists of articles

of last search: January 2016

, placebo-controlled trials

of vitamin D in children and adults with asthma

Two review authors independently applied study

inclusion criteria, extracted the data, and assessed

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 7RCT involved 435 children

 2 RCT involved 658 adults

 Participants were ethnically diverse

 Participants were ethnically diverse

 The majority of participants had mild/moderate asthma, and a minority had severe asthma

 Median baseline serum 25(OH)D concentration ranged from 48 nmol/L to 89nmol/L

Participants

diverse majority of participants had mild/moderate asthma, and a minority had severe asthma

baseline serum 25(OH)D concentration

to 89nmol/L

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 All studies administered oral vitamin D

 4 studies used daily dosing ranging from

1200IU/day

1 used weekly dosing (Majak 2009

1 used weekly dosing (Majak 2009

1 used monthly dosing (Yadav 2014

1 used two-monthly dosing (Martineau 2015

2 gave a bolus dose, followed by

2014; Jensen 2016 )

Intervention

All studies administered oral vitamin D3 (cholecalciferol)

ranging from 500 IU/day to

2009)

2009)

2014 )

Martineau 2015)

followed by daily dosing (Castro

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Asthma exacerbation treated with

systemic corticosteroids

Reduction in the rate of asthma exacerbations treated with systemic corticosteroids

confidence interval (CI) 0.45 to 0.88; 680 participants; 3

studies; high-quality evidence;).

Benefit of vitamin D for the outcomes of time to first exacerbation (HR 0.69, 95% CI 0.48 to 1.00; 658

participants; 2 studies; moderate-quality evidence)

Outcomes

Asthma exacerbation treated with

in the rate of asthma exacerbations treated with systemic corticosteroids (RR 0.63, 95%

treated with systemic corticosteroids (RR 0.63, 95% confidence interval (CI) 0.45 to 0.88; 680 participants; 3

Benefit of vitamin D for the outcomes of time to

(HR 0.69, 95% CI 0.48 to 1.00; 658

quality evidence)

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Benefit of vitamin D for proportion of participants

experiencing one or more exacerbation

0.49 to 1.10; 933 participants; 7 studies; moderate

Asthma exacerbation precipitating emergency

Asthma exacerbation precipitating emergency

department or requiring hospitalisation

 Reduction in the proportion of participants experiencing

an asthma exacerbation precipitating an emergency

department visit or hospital admission or both

95% CI 0.19 to 0.78; NNTB 27, 95% CI 20 to 76; 963 participants; 7

studies; high-quality evidence)

Outcomes

Benefit of vitamin D for proportion of participants

experiencing one or more exacerbation (OR 0.74, 95% CI

0.49 to 1.10; 933 participants; 7 studies; moderate-quality evidence)

Asthma exacerbation precipitating emergency

hospitalisation

Reduction in the proportion of participants experiencing

an asthma exacerbation precipitating an emergency

department visit or hospital admission or both (OR 0.39, 95% CI 0.19 to 0.78; NNTB 27, 95% CI 20 to 76; 963 participants; 7

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Adverse reaction to vitamin D

Two participants in one trial experienced

hypercalciuria (Jensen 2016)

hypercalciuria (Jensen 2016)

 No other study reported episodes of

hypercalciuria or any other adverse events potentially attributable to administration of vitamin D

Outcomes

Adverse reaction to vitamin D

Two participants in one trial experienced

)

No other study reported episodes of

or any other adverse events potentially attributable to administration of

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Costs from healthcare providers

 No effect on total costs associated with

asthma/upper respiratory infection over 12 months

(adjusted mean difference GBP 66.78, 95% CI GBP

397.03).

Use of inhaled beta2-agonists

One trial investigated the effects of vitamin D on the number of uses of inhaled relief medication per 24 hours (Martineau 2015)

Allocation to vitamin D did not influence this

outcome at 12 months (adjusted ratio of geometric means 1.00, 95% CI 0.77 to 1.28).

Outcomes

providers

effect on total costs associated with asthma/upper respiratory infection over 12 months

(adjusted mean difference GBP 66.78, 95% CI GBP -263.47 to GBP

agonists

investigated the effects of vitamin D on the number of uses of inhaled relief medication per 24

to vitamin D did not influence this

(adjusted ratio of geometric means

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Reduction in the rate of asthma exacerbations

requiring treatment with systemic

Reduction in the risk of asthma exacerbations

Reduction in the risk of asthma exacerbations

resulting in emergency department

hospitalisation

 No effect of vitamin D on ACT score

Conclusion

in the rate of asthma exacerbations

treatment with systemic corticosteroids

in the risk of asthma exacerbations

emergency department attendance or

effect of vitamin D on ACT score

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Vitamin D did not influence the risk of any serious

adverse event

No fatal asthma exacerbations

No fatal asthma exacerbations

any trial included in this meta-analysis

evidence to clinical practice

Conclusion

influence the risk of any serious

No fatal asthma exacerbations were reported in

analysis

hat caution is warranted in applying this

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