Specialised Infant Formulas: Overused, Overpriced and Obesogenic

IF 6.3 2区 医学 Q1 ALLERGY Clinical and Experimental Allergy Pub Date : 2024-07-23 DOI:10.1111/cea.14532
Victoria L. Sibson, Susan Westland
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FSMP include low-allergy formulas such as soya formula, extensively hydrolysed formula and amino-acid formula, used for formula-fed infants with cows' milk allergy.</p><p>Legal definitions and regulatory requirements for FSMP are that they should be used under medical supervision and there should be scientific evidence that they are safe and meet the nutritional requirements of the intended target population. In Europe, there is also guidance on how to assess products against these requirements [<span>2</span>]. However, there is a lack of regulatory oversight for FSMP, and they are frequently used without medical supervision. Commercial milk formula companies are often able to choose whether to market a product as FSMP or as a standard infant formula. Thus, in the United Kingdom, antireflux and comfort milks are marketed as FSMP, despite the lack of evidence that comfort milks alleviate colic or constipation, whereas soya formula and lactose-free formula are not marketed as FSMP despite falling under the international definition of FSMP set by Codex. All four product types can be purchased over the counter in pharmacies, and in shops and supermarkets. In the United States, a comprehensive national survey found that almost 60% of formula purchased in stores had reduced or absent lactose [<span>3</span>]. Low-allergy formulas are also lactose-free or lactose-reduced, posing health risks above standard infant formulas because nonlactose carbohydrate sources such as maltodextrin and glucose syrup are associated with dental caries and early childhood obesity [<span>4</span>].</p><p>Other health risks associated with infant FSMP include increased risk of bacterial contamination due to the addition of probiotics, making proper sterilisation impossible, and potential adverse effects from components such as phyto-oestrogens in soya formula and thickeners in antireflux formula. In general, the health risks associated with FSMP are not clearly communicated to consumers through product labelling.</p><p>Infant FSMP not only carry health risks but also are more expensive than their brand-equivalent first infant formulas (Table 1). The record high prices of first infant formula in the current cost of living crisis are a concern for parents and carers, and high prices may lead to unsafe feeding practices [<span>5</span>]. This concern is exacerbated if FSMP are used unnecessarily or without appropriate medical supervision and support by the public health system. For prescribed, low-allergy formulas such as amino-acid formula, the cost sometimes falls on public health systems. For example, the UK National Health Service spends about £100 ($127, EU119) for each baby born in the country on low-allergy formula prescribing, ~90% of which is prescribed to infants with no milk allergy [<span>6</span>].</p><p>To summarise, current FSMP regulation is failing to contain increasing, often unnecessary and usually unsupervised use of these products. This occurs because of industry-led misclassification of products, and ineffective controls on their sale to the public, including cross-promotion and inadequate health warnings [<span>7</span>]. The situation is compounded by weak legal restrictions on marketing of commercial milk formulas to healthcare professionals, who are misled about the nature and effectiveness of products, using information that is not scientific or factual [<span>8</span>]. Ultimately, this is leading to widespread exposure of the world's infants to unhealthy, unnecessary and expensive nutrition products.</p><p>With such a major public health focus on preventing obesity, and so few proven solutions, improving regulation and consumer information regarding risks associated with alternative carbohydrates in FSMP seems like a relatively simple step for governments to make. Considering the recent UK General Election, we recommend that the new Government takes a two-step approach to closer enforcement and improved regulation of the marketing practices of the commercial milk formula industry, as outlined in Table 2. Acting on these recommendations would better protect all infants however they are fed.</p><p>The high cost of infant FSMP relative to brand-equivalent infant formula also needs to be addressed by the new Government, especially considering the current cost of living crisis and profiteering by the commercial milk formula industry on its infant formula sales [<span>5</span>]. 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Abstract

In Europe, North America and China, most infants are wholly or partially fed with a commercial milk formula during their first year despite consistent public health recommendations promoting breastfeeding. For some nonbreastfed babies, a standard first infant formula may not meet their nutritional needs, because of cows' milk allergy, an inherited metabolic condition, illness or prematurity. These infants may need ‘specialised’ infant formulas, which are classified by the World Health Organization and Food and Agriculture Organization Codex Alimentarius as Foods for Special Medical Purposes (FSMP) [1]. FSMP include low-allergy formulas such as soya formula, extensively hydrolysed formula and amino-acid formula, used for formula-fed infants with cows' milk allergy.

Legal definitions and regulatory requirements for FSMP are that they should be used under medical supervision and there should be scientific evidence that they are safe and meet the nutritional requirements of the intended target population. In Europe, there is also guidance on how to assess products against these requirements [2]. However, there is a lack of regulatory oversight for FSMP, and they are frequently used without medical supervision. Commercial milk formula companies are often able to choose whether to market a product as FSMP or as a standard infant formula. Thus, in the United Kingdom, antireflux and comfort milks are marketed as FSMP, despite the lack of evidence that comfort milks alleviate colic or constipation, whereas soya formula and lactose-free formula are not marketed as FSMP despite falling under the international definition of FSMP set by Codex. All four product types can be purchased over the counter in pharmacies, and in shops and supermarkets. In the United States, a comprehensive national survey found that almost 60% of formula purchased in stores had reduced or absent lactose [3]. Low-allergy formulas are also lactose-free or lactose-reduced, posing health risks above standard infant formulas because nonlactose carbohydrate sources such as maltodextrin and glucose syrup are associated with dental caries and early childhood obesity [4].

Other health risks associated with infant FSMP include increased risk of bacterial contamination due to the addition of probiotics, making proper sterilisation impossible, and potential adverse effects from components such as phyto-oestrogens in soya formula and thickeners in antireflux formula. In general, the health risks associated with FSMP are not clearly communicated to consumers through product labelling.

Infant FSMP not only carry health risks but also are more expensive than their brand-equivalent first infant formulas (Table 1). The record high prices of first infant formula in the current cost of living crisis are a concern for parents and carers, and high prices may lead to unsafe feeding practices [5]. This concern is exacerbated if FSMP are used unnecessarily or without appropriate medical supervision and support by the public health system. For prescribed, low-allergy formulas such as amino-acid formula, the cost sometimes falls on public health systems. For example, the UK National Health Service spends about £100 ($127, EU119) for each baby born in the country on low-allergy formula prescribing, ~90% of which is prescribed to infants with no milk allergy [6].

To summarise, current FSMP regulation is failing to contain increasing, often unnecessary and usually unsupervised use of these products. This occurs because of industry-led misclassification of products, and ineffective controls on their sale to the public, including cross-promotion and inadequate health warnings [7]. The situation is compounded by weak legal restrictions on marketing of commercial milk formulas to healthcare professionals, who are misled about the nature and effectiveness of products, using information that is not scientific or factual [8]. Ultimately, this is leading to widespread exposure of the world's infants to unhealthy, unnecessary and expensive nutrition products.

With such a major public health focus on preventing obesity, and so few proven solutions, improving regulation and consumer information regarding risks associated with alternative carbohydrates in FSMP seems like a relatively simple step for governments to make. Considering the recent UK General Election, we recommend that the new Government takes a two-step approach to closer enforcement and improved regulation of the marketing practices of the commercial milk formula industry, as outlined in Table 2. Acting on these recommendations would better protect all infants however they are fed.

The high cost of infant FSMP relative to brand-equivalent infant formula also needs to be addressed by the new Government, especially considering the current cost of living crisis and profiteering by the commercial milk formula industry on its infant formula sales [5]. We are hopeful that the market survey currently underway by the UK Government watchdog, the Competition and Markets Authority, will include recommendations which the new Government can act on to better control infant formula costs while protecting infant health.

This editorial builds on this 2022 policy report by the Baby Feeding Law Group UK: Infant milks marketed as foods for special medical purposes (FSMP): The case for regulatory reform to protect infant health [9].

Victoria L. Sibson conceptualised and drafted the editorial. Susan Westland undertook the analysis of formula costs and reviewed the final editorial.

The authors declare no conflicts of interest.

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专业婴儿配方奶粉:过度使用、定价过高和导致肥胖。
在欧洲、北美和中国,尽管公共卫生机构一直建议提倡母乳喂养,但大多数婴儿在出生后的第一年都全部或部分使用商业配方奶喂养。对于一些非母乳喂养的婴儿来说,由于牛奶过敏、遗传代谢疾病、疾病或早产等原因,标准的婴儿配方奶粉可能无法满足他们的营养需求。这些婴儿可能需要 "专用 "婴儿配方奶粉,世界卫生组织和联合国粮食及农业组织食品法典将其归类为 "特殊医学用途食品"(FSMP)[1]。FSMP 包括低过敏配方奶粉,如大豆配方奶粉、广泛水解配方奶粉和氨基酸配方奶粉,用于对牛奶过敏的配方奶粉喂养婴儿。FSMP 的法律定义和监管要求是,这些配方奶粉应在医疗监督下使用,并有科学证据证明它们是安全的,符合目标人群的营养要求。欧洲也有关于如何根据这些要求评估产品的指南[2]。然而,FSMP 缺乏监管监督,经常在没有医疗监督的情况下使用。商业配方奶粉公司通常可以选择将产品作为FSMP或标准婴儿配方奶粉销售。因此,在英国,抗反流奶和舒适奶被作为FSMP销售,尽管没有证据表明舒适奶能缓解肠绞痛或便秘,而豆奶粉和无乳糖奶粉尽管符合食品法典委员会对FSMP的国际定义,却不作为FSMP销售。这四种产品都可以在药店、商店和超市的柜台购买。在美国,一项全面的全国性调查发现,在商店里购买的配方奶粉中,近 60% 都含有或不含乳糖[3]。低敏配方奶粉也不含乳糖或降低乳糖含量,其健康风险高于标准婴儿配方奶粉,因为麦芽糊精和葡萄糖浆等非乳糖碳水化合物来源与龋齿和儿童早期肥胖有关[4]。与婴儿配方奶粉有关的其他健康风险包括:由于添加了益生菌,细菌污染的风险增加,导致无法进行适当消毒;大豆配方奶粉中的植物雌激素和抗反流配方奶粉中的增稠剂等成分可能产生不良影响。一般来说,FSMP 的健康风险并没有通过产品标签清楚地告知消费者。婴儿 FSMP 不仅有健康风险,而且价格也比同等品牌的婴儿配方奶粉高(表 1)。在当前的生活费用危机中,婴儿配方奶粉的价格屡创新高,这引起了父母和照护者的担忧,高价格可能会导致不安全的喂养方式[5]。如果不必要地使用或在没有适当的医疗监督和公共卫生系统支持的情况下使用 FSMP,则会加剧这种担忧。对于处方低敏配方奶粉,如氨基酸配方奶粉,费用有时由公共卫生系统承担。例如,英国国家卫生服务部门为国内每个出生的婴儿花费约 100 英镑(127 美元,119 欧元)用于开具低过敏配方奶粉处方,其中约 90% 开给了对牛奶不过敏的婴儿[6]。出现这种情况的原因是行业主导的产品分类不当,以及对向公众销售这些产品的控制不力,包括交叉促销和健康警告不足[7]。向医疗保健专业人员推销商业配方奶粉的法律限制薄弱,使情况更加复杂,医疗保健专业人员在产品的性质和有效性方面受到误导,使用的信息既不科学也不符合事实[8]。预防肥胖是公共卫生的重点,而行之有效的解决方案却寥寥无几,因此,对于政府而言,改善监管并向消费者提供更多有关配方奶粉中替代碳水化合物相关风险的信息似乎是一个相对简单的步骤。考虑到最近的英国大选,我们建议新政府采取表 2 所列的两步措施,对商业配方奶粉行业的营销行为进行更严格的执法和改进监管。新政府还需要解决婴儿配方奶粉相对于同等品牌婴儿配方奶粉的高成本问题,特别是考虑到当前的生活成本危机和商业配方奶粉行业在婴儿配方奶粉销售中的暴利[5]。 我们希望,英国政府的监督机构--竞争与市场管理局目前正在进行的市场调查将包括新政府可以采取行动的建议,以便更好地控制婴儿配方奶粉成本,同时保护婴儿健康。本社论以英国婴儿喂养法律小组 2022 年的政策报告为基础:本社论基于英国婴儿喂养法律小组的 2022 年政策报告:《作为特殊医学用途食品(FSMP)销售的婴儿奶粉:保护婴儿健康的监管改革案例》[9]。苏珊-韦斯特兰(Susan Westland)对配方奶成本进行了分析,并审阅了社论定稿。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
10.40
自引率
9.80%
发文量
189
审稿时长
3-8 weeks
期刊介绍: Clinical & Experimental Allergy strikes an excellent balance between clinical and scientific articles and carries regular reviews and editorials written by leading authorities in their field. In response to the increasing number of quality submissions, since 1996 the journals size has increased by over 30%. Clinical & Experimental Allergy is essential reading for allergy practitioners and research scientists with an interest in allergic diseases and mechanisms. Truly international in appeal, Clinical & Experimental Allergy publishes clinical and experimental observations in disease in all fields of medicine in which allergic hypersensitivity plays a part.
期刊最新文献
Linking Macronutrient Composition of Common Allergenic Foods to European and North American Food Allergy Prevalence. Defining Optimal Basophil Passive Sensitisation Parameters. Shaping Allergy Training in the UK Foundation Programme: A National Survey. Patch Testing Results From the Icahn School of Medicine at Mount Sinai Department of Dermatology 2017-2021. Comparison of Conventional IgE Assay and Measurement of Specific IgE to Haemocyanin for the Diagnosis of Adult Crab Allergy.
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