1990
DOI: 10.1016/0016-5085(90)91165-3
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α1-antitrypsin excretion in stool in normal subjects and in patients with gastrointestinal disorders

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Cited by 107 publications
(45 citation statements)
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“…17 Another report on 70 healthy 3-month-old babies also revealed no difference in fecal calprotectin levels between exclusively BF and FF babies (P=0.09). 18 In addition, another study on 160 healthy babies who were either exclusively BF or received prebiotic/probiotic supplemented formula revealed no significant difference in fecal calprotectin level between the first sampling (< 6 weeks of age) and at second (3 months later) (P=0.393). 12 our study could not be compared to previous studies due to differences in age intervals of the subjects, thus the result consistently showed a higher level of fecal calprotectin in FF babies.…”
Section: Discussionmentioning
confidence: 96%
See 1 more Smart Citation
“…17 Another report on 70 healthy 3-month-old babies also revealed no difference in fecal calprotectin levels between exclusively BF and FF babies (P=0.09). 18 In addition, another study on 160 healthy babies who were either exclusively BF or received prebiotic/probiotic supplemented formula revealed no significant difference in fecal calprotectin level between the first sampling (< 6 weeks of age) and at second (3 months later) (P=0.393). 12 our study could not be compared to previous studies due to differences in age intervals of the subjects, thus the result consistently showed a higher level of fecal calprotectin in FF babies.…”
Section: Discussionmentioning
confidence: 96%
“…Higher fecal AAT level shows greater gut wall permeability which cause greater protein enteric loss. 12,18 However, using AAT measurements to assess gut wall integrity in infants has had varied results. We found a significantly higher mean AAT level in the BF group compared to the FF group (P=0.02).…”
Section: Discussionmentioning
confidence: 99%
“…17,20,23 Factors other than enteric protein loss may play an important role in determining serumal albumin concentration in humans affected with gastrointestinal disease. 32 These factors include the rate of synthesis of albumin, which is determined by nutritional status, the rate of extraintestinal catabolism, and contraction of plasma volume.…”
Section: Clinical and Clinicopathologic Features Of Horses With Gementioning
confidence: 99%
“…В настоящее время для верификации потерь белка через желудочно-кишечный тракт использу-ется определение содержания в кале α 1 -антитрип-сина -эндогенного белка, молекулярная масса которого близка к массе альбумина [25]. В норме α 1 -антитрипсин не секретируется клетками желу-дочно-кишечного тракта, не всасывается и не пере-варивается, устойчив в кале при температуре 37°C и не экскретируется с мочой.…”
Section: экссудативная энтеропатия вследствие повреждения слизистых жunclassified