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Is asthma prevention possible with dietary manipulation?

Craig M Mellis
Med J Aust 2002; 177 (6): S78. || doi: 10.5694/j.1326-5377.2002.tb04827.x
Published online: 16 September 2002

Abstract

What we know

What we need to know

Although most published reports on asthma prevention deal with tertiary prevention (ie, reducing morbidity in established asthma with the use of preventive agents such as inhaled corticosteroids), there is increasing interest in primary prevention (ie, the prevention of asthma in those genetically "at risk").

Logically, primary prevention should be possible given that asthma results from a complex interaction between genetic susceptibility and environmental risk factors, rates of childhood asthma are increasing,1,2 and therefore the recent increase must be due to environmental factors rather than a change in genetic susceptibility. If we can identify the modifiable environmental risk factors that have led to increasing rates of asthma, then primary prevention should be possible. Peat and Li3 have developed a useful classification of these risk factors (see Box 1).

A number of randomised controlled trials (RCTs) have been conducted to test the hypothesis that primary asthma prevention is possible. However, a major problem with these studies has been the difficulty of accurately defining asthma in children under five years of age.4 Further, most of the RCTs are recent and have had limited follow-up. Therefore, the focus has been on measuring outcomes that are assumed to be on the causal pathway to asthma rather than assessing rates of actual asthma. These outcomes have included the development of atopy (as defined by positive allergen skin-prick testing or detection of specific IgE) or the development of clinical atopic disease, particularly atopic dermatitis/eczema.

What is known?
Primary prevention

Most reported RCTs of primary asthma prevention use a "high-risk" selection strategy rather than a population-based strategy5 (ie, the subjects recruited have been identified as being at high risk of asthma, usually on the basis of a positive family history of asthma and/or atopy). Moreover, since the development of clinical atopy occurs in early life, studies have either recruited the subjects in utero (during the last trimester) or during the neonatal period.

A meta-analysis of maternal dietary allergen avoidance during pregnancy to prevent atopic disease in infants at high risk concluded that such avoidance is "unlikely to substantially reduce the risk of atopy in the child. Moreover, such a diet may have an adverse effect on maternal and/or fetal nutrition".6 This meta-analysis was based on three RCTs involving a total of 504 women. Although several trials suggested a lower incidence of positive allergen skin-prick testing initially, by the age of 18 months there was no benefit. Given the potential harm to the fetus (lower mean gestational weight gain), elimination diets during pregnancy are not recommended.

Another meta-analysis of three RCTs, involving a total of 209 women, assessed the efficacy of a maternal allergen-avoidance diet during lactation for preventing atopic disease in infants of women at high risk.7 Combined data from these trials suggest a strong protective effect on atopic eczema during the child's first 12–18 months of life. However, the author of the review noted substantial methodological weaknesses in all three trials.

The role of protein hydrolysed formulas on the development of atopy and asthma remains uncertain, and further studies are warranted. In a relatively small RCT (involving 177 subjects), early feeding of a protein hydrolysate (casein hydrolysate, "Pregestimil") formula to infants at risk of allergies had a long-term preventive effect on the prevalence of eczema, but not of asthma.8

The role of exclusive breastfeeding in protecting against asthma is controversial. Although most studies have shown a protective effect, several have found an increased rate of asthma in breastfed infants. A systematic review of prospective studies9 identified 12 relevant studies of adequate methodological quality. The summary odds ratio for the protective effect of at least three months' exclusive breastfeeding was 0.70 (95% CI, 0.60–0.81), indicating a 30% reduction in the development of childhood asthma. This protective effect was even greater in children with a family history of atopy (50% reduction). These results indicate a valid and important protective effect of breastfeeding on subsequent development of asthma.

Dietary supplementation with probiotics has shown encouraging results. In a double-blind, randomised, placebo-controlled trial, Lactobacillus (given prenatally to mothers and then postnatally for six months to their infants) resulted in a 50% reduction in the rate of atopic eczema at the age of two years (23% v 46%).10 As no definitive information concerning asthma can be derived at this early stage, the long-term results of this trial will be awaited with great interest. A key factor with probiotic intervention is that it does not cause any harm. Indeed, probiotics almost certainly result in a more "friendly" gut flora, which may have other beneficial effects on health apart from reducing rates of atopic disease.

Two RCTs have examined combined dietary manipulation and airborne allergen avoidance.11,12 The Isle of Wight study11 involved 120 "at risk" infants randomly allocated during pregnancy to an intervention group or a control group. The intervention group were either breastfed (with mothers excluding foods regarded as highly allergenic from their diet) or given a soy-based protein hydrolysate. In addition, exposure to house-dust mites was reduced by encasing the child's mattress and treating the home with an acaricide four times during the first nine months of life. The combined intervention resulted in a significant reduction in the rate of eczema and atopy (sensitisation to both dietary and aeroallergens) at four years of age. The rate of doctor-diagnosed asthma was also lower (24% v 35%), although this was not statistically significant. Clearly, this is an encouraging result and should be repeated in other countries, using larger numbers, and with prolonged follow-up of the subjects.

The second combined intervention RCT was conducted in Vancouver, Canada.12 This examined the effectiveness of a multifaceted intervention. A total of 545 "high-risk" infants were prenatally randomly assigned to either a multiple intervention group or a control group. The intervention involved avoidance of house-dust mite, pet allergens and environmental tobacco smoke; encouragement of breastfeeding; and supplementing the diet with a partially hydrolysed formula. The result of the intervention was a modest but statistically significant (P = 0.04) reduction in the risk of possible or probable asthma and rhinitis at the age of 12 months. The incidence of positive allergen skin-prick tests to one or more aeroallergens was similar in both groups (4.4% in the intervention group v 4.6% in the control group). Clearly, more prolonged follow-up of these infants will be essential to determine whether these differences in possible or probable asthma persist.

In the western suburbs of Sydney, a large placebo-controlled RCT (involving about 600 "high-risk" newborns recruited in pregnancy) is now in progress.13 The design is factorial, allowing two interventions to be evaluated in the one trial: a dietary supplement (omega-3 fatty acid) and comprehensive house-dust mite avoidance measures. Although this trial is only in its early stages, initial results show an impressive reduction in Der p 1 (dust mite) exposure levels in the intervention groups, plus good compliance with taking the omega-3 fatty acid supplement. When the children are old enough (ie, 5–6 years) for reliable medical outcome measures of asthma rates, this trial will supply definitive data on the effectiveness of omega-3 fatty acid supplementation alone and in combination with house-dust mite avoidance measures in the Australian environment.

In summary, RCTs have shown a consistent protective effect of a variety of dietary manipulations on subsequent asthma and/or atopy (see Box 2). Studies combining dietary manipulation with reduction in airborne allergen exposure suggest added protection. However, longer follow-up of the children in all these studies is essential to determine the long-term benefits of these preventive measures on rates of childhood asthma.

1: Risk factors for childhood asthma (modified from Peat and Li3)

Factors that identify "high-risk" children

Family history/genetic markers

Ethnicity, affluence, socioeconomic status

Male sex

Factors that provide insight into mechanisms

Early infections ("hygiene hypothesis")

Vaccination status and antibiotic use

Exposure to other children (eg, number of siblings, shared bedroom, daycare attendance)

Perinatal factors

Preterm birth

Head circumference (HC), birthweight (BW) and HC: BW ratio

Maternal age (very young or very old)

Factors that have potential for primary prevention

Indoor allergens:

Beds, pillows, floor coverings, pets

Dampness or mould

Heating, ventilation, house construction

Parental smoking:

Prenatal and postnatal exposures

Lack of breastfeeding:

Time of breast-feeding cessation

Timing of introduction of cow's milk and cereals

Dietary fatty acids:

Omega-3 fatty acids (eg, from fish and polyunsaturated foods)

2: Recommendations for dietary measures to reduce asthma and/or atopy (with levels of evidence14)

  • Cease strict elimination diets during pregnancy (Level I)

  • Ideally, exclusively breastfeed for 3–4 months (Level III)

  • Consider Lactobacillus probiotic supplements (before and after delivery)* (Level II)

If breastfeeding is not possible:

  • Consider supplementing infant with omega-3 fatty acids (Level III)

  • Consider Lactobacillus probiotic supplements* (Level II)

  • Consider protein hydrolysed formula (for 6–12 months)* (Level II)

*Data relate to atopy only, not asthma.

  • Craig M Mellis

  • Department of Clinical Epidemiology, The Children's Hospital at Westmead, Westmead, NSW.


Correspondence: craigm@chw.edu.au

  • 1. Burr ML, Butland BK, King S, et al. Changes in asthma prevalence: two surveys 15 years apart. Arch Dis Child 1989; 64: 1452-1456.
  • 2. Peat JK, van den Berg RH, Green WF, et al. Changing prevalence of asthma in Australian children. BMJ 1994; 308: 1591-1596.
  • 3. Peat JK, Li J. Reversing the trend: reducing the prevalence of asthma. J Allergy Clin Immunol 1999; 103: 1-10.
  • 4. Martinez FD, Helms PJ. Types of asthma and wheezing. Eur Respir J Suppl 1998; 27: 3s-8s.
  • 5. Rose G. The strategy of preventive medicine. Oxford: Oxford University Press, 1992.
  • 6. Kramer MS. Maternal antigen avoidance during pregnancy for preventing atopic disease in infants of women at high risk (Cochrane Review). In: The Cochrane Library, 2001; Issue 1. Oxford: Update Software (CD000133).
  • 7. Kramer MS. Maternal antigen avoidance during lactation for preventing atopic disease in infants of women at high risk (Cochrane review). In: The Cochrane Library, 2001; Issue 1. Oxford: Update Software (CD000132).
  • 8. Mallet E, Henocq A. Long-term prevention of allergic diseases by using protein hydrolysate formula in at-risk infants. J Pediatr 1992; 121: s95-s100.
  • 9. Gdalevich M, Mimouni D, Mimouni M. Breast feeding and the risk of bronchial asthma in childhood: a systematic review with meta-analysis of prospective studies. J Pediatr 2001; 139: 261-266.
  • 10. Kalliomaki M, Salminen S, Arvilommi H, et al. Probiotics in primary prevention of atopic disease: a randomised placebo-controlled trial. Lancet 2001; 357: 1076-1079.
  • 11. Hide DW, Matthews S, Tariq S, et al. Allergen avoidance in infancy and allergy at 4 years of age. Allergy 1996; 51: 89-93.
  • 12. Chan-Yeung M, Manfreda J, Dimich-Ward H, et al. A randomised controlled study on the effectiveness of a multifaceted intervention program in the primary prevention of asthma in high-risk infants. Arch Pediatr Adolesc Med 2000; 154: 657-663.
  • 13. Mihrshahi S, Peat JK, Webb K, et al. The childhood asthma prevention study (CAPS): design and research protocol of a randomized trial for the primary prevention of asthma. Control Clin Trials 2001; 22: 333-354.
  • 14. National Health and Medical Research Council. How to use evidence: assessment and application of scientific evidence. Table 1.3, page 8. February 2000. Available at: <http://www.nhmrc.health.gov.au/publications/pdf/cp69.pdf>. Accessed 30 July 2002, no longer available - see http://www.nhmrc.gov.au/publications/_files/135sess.pdf.

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