Food intolerance and allergy are both examples of ‘food hypersensitivity’ but the mechanisms by which they occur are very different.1
Lactose intolerance is where there is reduced capacity to digest lactose, a sugar naturally found in all mammalian milk due to an absence or deficiency of the enzyme lactase in the small intestine.1
Malabsorption, therefore, occurs when lactose passes through the intestines without being absorbed, acting as a bacterial substrate in the colon which fuels gastrointestinal symptoms such as:
The degree of gastrointestinal symptoms is dependent on the amount of lactose ingested and levels of lactase present in the small intestine.2-4
CMA, also known as Cow’s Milk Protein Allergy (CMPA), is an immunologic hypersensitivity to one or more of the proteins found in milk. This allergy is particularly prominent in infants and young children.1,5 Typically, it presents in early infancy soon after initial exposure to cow’s milk protein in formula or weaning solids but also in a lower incidence of exclusively breastfed infants.6,7 The prognosis is good with approximately 50% outgrowing their allergy by 5 years of age and 75% of patients outgrowing their milk allergy by adolescence8.
CMA can present as a broad range of symptoms involving many organ systems depending on the type of immune reaction causing the allergic response. Discriminating between the type of reaction is important as it can determine the risk of developing other food allergies and atopic disease9.
There are two main types of CMA1:
It can sometimes be difficult to differentiate between CMA and lactose intolerance, as some digestive symptoms overlap such as nausea, abdominal pain, and diarrhoea. However, there are some distinct differences to be aware of that can help inform diagnosis and, therefore, ensure correct management.1
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Luyt D et al. BSACI guideline for the diagnosis and management of cow's milk allergy. Clin Exp Allergy 2014;44(5): 642–72.
Lomer MC, et al. Review article: lactose intolerance in clinical practice--myths and realities. Aliment Pharmacol Ther. 2008; 15;27(2):93-103.
Büller HA, et al. Clinical aspects of lactose intolerance in children and adults. Scand J Gastroenterol Suppl. 1991; 188:73-80.
Storhaug CL, et al. Country, regional, and global estimates for lactose malabsorption in adults: a systematic review and meta-analysis. Lancet Gastroenterol Hepatol. 2017, 2(10):738-746.
Gupta RS, et al. The prevalence, severity, and distribution of childhood food allergy in the United States. Pediatrics. 2011; 128(1):e9-17.
Venter C, et al. Prevalence and cumulative incidence of food hyper-sensitivity in the first 10 years of life. Pediatr Allergy Immunol. 2016;27(5):452-8.
Host A, et al A prospective study of cow’s milk allergy in exclusively breast-fed infants. Incidence, pathogenetic role of early inadvertent exposure to cow’s milk formula, and characterization of bovine milk protein in human milk. Acta Paediatr Scand. 1988;77(5):663-70.
Flom JD, et al. Epidemiology of Cow's Milk Allergy. Nutrients. 2019 May 10;11(5):1051.
Saarinen KM, et al. Clinical course and prognosis of cow's milk allergy are dependent on milk-specific IgE status, Journal of Allergy and Clinical Immunology. 2005; 116 (4) 869-875.
Walsh J, et al. Differentiating milk allergy (IgE and non-IgE mediated) from lactose intolerance: understanding the underlying mechanisms and presentations. Br J Gen Pract. 2016 Aug;66(649):e609-11.
Labrosse R, et al. Non-IgE-Mediated Gastrointestinal Food Allergies in Children: An Update. Nutrients. 2020 Jul 14;12(7):2086.
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