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Functional characteristics of duodenal ulcer patients and their first-degree relatives.

Functional characteristics of duodenal ulcer patients and their first-degree relatives. Research Abstract Details 

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  • Functional characteristics of duodenal ulcer patients and their first-degree relatives. Abstract Text:

    m vuoristoM Vuoristo,p pikkarainenP Pikkarainen,i m samloffI M Samloff,p sipponenP Sipponen,m kekkiM Kekki,m siuralaM Siurala,

    The behaviour of acid secretion, serum pepsinogen I and II (PG I and PG II) and morphology of the gastric mucosa were analyzed in 59 duodenal ulcer probands (DU probands), their 199 first-degree relatives and 228 control subjects. DU probands had as a rule antral gastritis with normal or slightly altered corpus mucosa, and higher mean peak acid output (PAO), PG I and II levels than their relatives and controls. Sibs of DU probands differed from their controls mainly with regard to morphology which showed features characteristic of DU probands, i.e. antral gastritis with normal or slightly altered corpus mucosa. Moreover, high PAO levels were found highly significantly more often in sibs of DU probands (13%) than in controls (6%). Likewise, the prevalence of endoscopic signs of active or past duodenal ulcer were present in sibs highly significantly more often than in controls and they accumulated in the subgroup of sibs with high PAO or PG I levels. It seems probable that the occurrence of high PAO and PG I levels in sibs of DU probands can be considered as signs of increased liability to duodenal ulcer. PAO and PG I were as expected significantly higher in male than in female probands, relatives and controls. Exclusion of cases of corpus gastritis decreased the levels but the sex difference persisted. PAO, PG I and II revealed a significant increase of the levels in middle age followed in older age in case of PAO and PG I by a significant decrease. The decrease was abolished when the cases of corpus gastritis were excluded suggesting an effect of gastritis. However, the earlier increase of the levels remained virtually unaffected although there was a uniform decrease of the mean values. This suggests the participation of factors unrelated to gastritis. The nature of the factors remains unknown, but literature data and data derived from our recent study suggest involvement of anatomical factors such as an increase in the size of acid and PG I secreting area.

    Functional characteristics of duodenal ulcer patients and their first-degree relatives. Publishing Authors By Initials

    m vuoristoM Vuoristo,p pikkarainenP Pikkarainen,im samloffIM Samloff,p sipponenP Sipponen,m kekkiM Kekki,m siuralaM Siurala,

    For similar enzymes and coenzymes: enzyme precursors: pepsinogens research abstracts see: enzymes and coenzymes: enzyme precursors: pepsinogens research

    PUBMED ID PMID:

    MEDLINE DATE:

    Functional characteristics of duodenal ulcer patients and their first-degree relatives. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Scandinavian journal of gastroenterology. Suppleme

    VOLUME: 186

    Page Numbers: 52-61

    Journal Abbreviation: Scand. J. Gastroenterol. Suppl

    ISSN: 0085-5928

    DAY: 13

    MONTH: 02

    YEAR: 1991

    Functional characteristics of duodenal ulcer patients and their first-degree relatives. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 437034

    Functional characteristics of duodenal ulcer patients and their first-degree relatives. Keywords Mesh Terms:

    KEYWORDS: Pepsinogens

    MESH TERMS: blood

    Chemical & Substance for Abstract: Functional characteristics of duodenal ulcer patients and their first-degree relatives. Information

    Substance Name: Pepsinogens

    Registry Number: 0

    Grant and Affiliation Information for Functional characteristics of duodenal ulcer patients and their first-degree relatives.

    AFFILIATION: Second Dept. of Medicine, University of Helsinki, Finland.

    Country: NORWAY

    NORWAY Research PublicationNORWAY Research Publication

    AGENCY:

    GRANT:

    ACRONYM:

    MEDLINETA: Scand J Gastroenterol Suppl

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