Lloyd B, Halter R J, Kuchan M J, Baggs G E, Ryan A S, Masor M L
Department of Pediatric Nutrition Research and Development Ross Products Division Abbott Laboratories, Columbus, OH 43215-1724, USA.
Pediatrics. 1999 Jan;103(1):E7. doi: 10.1542/peds.103.1.e7.
Perceived intolerance to infant formula is a frequently reported reason for formula switching. Formula intolerance may be related to perceived symptoms of constipation, fussiness, abdominal cramps, and excessive spit-up or vomit. Commercially available formulas differ from each other in processing and in sources and levels of protein, lipids, and micronutrients. These differences may affect tolerance. The objective of this article was to compare the tolerance of two commercially available powder infant formulas that differ in composition. Measures of tolerance in exclusively breastfed infants weaned to an infant formula and exclusively formula-fed infants were evaluated.
Two clinical studies were conducted. In study 1, 82 healthy, full-term infants who were exclusively breastfed at the time of enrollment were randomized at weaning to formula A (commercially available Similac With Iron Powder) or formula B (previously available Enfamil With Iron Powder). Parents completed daily records of tolerance during exclusive breast milk feeding, during the weaning period, and for a 2-week exclusive formula-feeding period. In study 2, 87 healthy, full-term infants who were exclusively formula-fed at the time of study enrollment (by 2 weeks of age) were fed a standard cow milk-based formula (previously commercially available Similac With Iron Powder) and then randomized to receive formula A or B for a 2-week period. Parents completed daily records of tolerance throughout the study. Formula A was a cow milk-based formula with a whey:casein ratio of 48:52 and a fat blend of 42% high-oleic safflower, 30% coconut, and 28% soy oils. Formula B was a cow milk-based formula with a whey:casein ratio of 60:40 and a fat blend of 45% palm olein, 20% soy, 20% coconut, and 15% high-oleic sunflower oils. Both formulas had lactose as the source of carbohydrate and contained 12 mg of iron per liter. Only formula A contained nucleotides at the time of the study. Measures of tolerance included volume of each formula feeding, occurrences of spit-up and/or vomit, and the color (yellow, green, brown, or black) and consistency (water, loose/mushy, soft, formed, or hard) of each stool.
In both studies, volume of formula intake, weight gain, and incidence of spit-up or vomit did not differ between feeding groups. In study 1, stool frequency decreased significantly from the exclusive breast milk period to weaning. Stools also became firmer as infants moved from breast milk to weaning and to exclusive formula feeding. When formula was introduced into the diet, stools became less yellow and more green. Infants weaned to formula B had less frequent stools, fewer brown stools, and more yellow stools than did infants fed formula A. In both studies, infants fed formula B experienced significantly firmer stools than did those fed formula A.
The present clinical studies indicate that the composition and/or processing of milk-based powder iron-fortified infant formulas affect stool characteristics experienced by infants. The inclusion of palm olein oil in formula B may be the reason for the observed differences in stool characteristics. Palm olein is used in infant formulas to provide palmitic acid at a level similar to that found in breast milk. However, palmitic acid from palm olein is arranged differently from that in breast milk triglyceride and is poorly absorbed. Unabsorbed palmitic acid tends to react with calcium to form insoluble soaps, and the level of these soaps is correlated with stool hardness. The pattern of softer stools and greater frequency of stooling associated with formula A is similar to the stool pattern in the exclusively breastfed infant. Thus, the use of formula A may ease the transition from breast milk to formula feeding and ameliorate parents' perception that constipation is associated with iron-fortified formula.
认为对婴儿配方奶粉不耐受是经常被提及的更换配方奶粉的原因。配方奶粉不耐受可能与便秘、烦躁、腹部绞痛以及过度吐奶或呕吐等症状有关。市售配方奶粉在加工过程以及蛋白质、脂质和微量营养素的来源与含量方面存在差异。这些差异可能会影响耐受性。本文的目的是比较两种成分不同的市售婴儿配方奶粉的耐受性。评估了完全母乳喂养婴儿断奶后改用婴儿配方奶粉以及完全配方奶粉喂养婴儿的耐受性指标。
进行了两项临床研究。在研究1中,82名健康足月婴儿在入组时为纯母乳喂养,断奶时随机分为A组(市售含铁奶粉Similac)或B组(曾有的含铁奶粉Enfamil)。家长记录婴儿在纯母乳喂养期间、断奶期以及两周纯配方奶粉喂养期的每日耐受性情况。在研究2中,87名健康足月婴儿在入组时(2周龄)为纯配方奶粉喂养,先喂食标准的以牛奶为基础的配方奶粉(曾有的含铁奶粉Similac),然后随机分为A组或B组,进行为期两周的喂养。家长在整个研究过程中记录每日耐受性情况。A组配方奶粉是以牛奶为基础,乳清与酪蛋白比例为48:52,脂肪混合比例为42%高油酸红花油、30%椰子油和28%大豆油。B组配方奶粉是以牛奶为基础,乳清与酪蛋白比例为60:40,脂肪混合比例为45%棕榈油精、20%大豆油、20%椰子油和15%高油酸葵花籽油。两种配方奶粉均以乳糖为碳水化合物来源,每升含铁12毫克。在研究期间,只有A组配方奶粉含有核苷酸。耐受性指标包括每次配方奶粉喂养量、吐奶和/或呕吐次数,以及每次粪便的颜色(黄色、绿色、棕色或黑色)和质地(水样、稀软/糊状、软便、成形便或硬便)。
在两项研究中,各喂养组的配方奶粉摄入量、体重增加以及吐奶或呕吐发生率均无差异。在研究1中,从纯母乳喂养期到断奶期,排便频率显著下降。随着婴儿从母乳喂养过渡到断奶再到纯配方奶粉喂养,粪便也变得更硬。当引入配方奶粉后,粪便颜色变黄减少,变绿增多。与喂食A组配方奶粉的婴儿相比,断奶改用B组配方奶粉的婴儿排便次数更少,棕色粪便更少,黄色粪便更多。在两项研究中,喂食B组配方奶粉的婴儿粪便明显比喂食A组配方奶粉的婴儿更硬。
目前的临床研究表明,以牛奶为基础的强化铁婴儿配方奶粉的成分和/或加工过程会影响婴儿的粪便特征。B组配方奶粉中含有棕榈油精可能是观察到粪便特征差异的原因。棕榈油精用于婴儿配方奶粉中,以提供与母乳中相似水平的棕榈酸。然而,棕榈油精中的棕榈酸排列方式与母乳甘油三酯中的不同,且吸收较差。未吸收的棕榈酸往往会与钙反应形成不溶性肥皂,这些肥皂的含量与粪便硬度相关。与A组配方奶粉相关的较软粪便和更高排便频率模式与纯母乳喂养婴儿的粪便模式相似。因此,使用A组配方奶粉可能会缓解从母乳喂养到配方奶粉喂养的过渡,并改善家长认为便秘与强化铁配方奶粉有关的看法。