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1.
Clin Transl Gastroenterol ; 11(8): e00192, 2020 08.
Artigo em Inglês | MEDLINE | ID: mdl-32955198

RESUMO

INTRODUCTION: Patients with functional gastrointestinal disorders (FGIDs) are classified based on their gastrointestinal (GI) symptoms, without considering their frequent extra-GI symptoms. This study defined subgroups of patients using both GI and extra-GI symptoms and examined underlying mechanisms with fructose and lactose breath tests. METHODS: Latent class analysis defined distinct clusters of patients with FGID based on their long-term GI and extra-GI symptoms. Sensory and breath gas responses after fructose and lactose ingestion were compared across symptom clusters to investigate differences in sensory function and fermentation by intestinal microbiota. RESULTS: Six symptom clusters were identified in 2,083 patients with FGID. Clusters were characterized mainly by GI fermentation-type (cluster 1), allergy-like (cluster 2), intense pain-accentuated GI symptoms (cluster 3), central nervous system (cluster 4), musculoskeletal (cluster 5), and generalized extra-GI (cluster 6) symptoms. In the 68% of patients with complete breath tests, the areas under the curve of GI and central nervous system symptoms after fructose and lactose ingestion differed across the clusters (P < 0.001). The clusters with extensive long-term extra-GI symptoms had greater symptoms after the sugars and were predominantly women, with family or childhood allergy histories. Importantly, the areas under the curves of hydrogen and methane breath concentrations were similar (P > 0.05) across all symptom clusters. Rome III criteria did not distinguish between the symptom clusters. DISCUSSION: Patients with FGID fall into clusters defined extensively by extra-GI symptoms. Greater extra-GI symptoms are associated with evidence of generalized sensory hypersensitivity to sugar ingestion, unrelated to intestinal gas production. Possible underlying mechanisms include metabolites originating from the intestinal microbiota and somatization.


Assuntos
Intolerância à Frutose/diagnóstico , Microbioma Gastrointestinal/fisiologia , Intolerância à Lactose/diagnóstico , Transtornos Somatoformes/diagnóstico , Adulto , Testes Respiratórios/métodos , Diagnóstico Diferencial , Feminino , Fermentação , Frutose/administração & dosagem , Frutose/análise , Frutose/metabolismo , Intolerância à Frutose/psicologia , Humanos , Lactose/administração & dosagem , Lactose/análise , Lactose/metabolismo , Intolerância à Lactose/psicologia , Masculino , Pessoa de Meia-Idade , Transtornos Somatoformes/psicologia , Adulto Jovem
2.
J Adolesc Health ; 64(1): 137-138, 2019 01.
Artigo em Inglês | MEDLINE | ID: mdl-30327278

RESUMO

Hereditary fructose intolerance is an autosomal recessive disorder of fructose metabolism caused by catalytic deficiency of aldolase B enzyme [1]. The disease is typically expressed when fructose- and sucrose-containing foods are first introduced in the diet; acute manifestations include nausea, vomiting, abdominal distress, and symptomatic hypoglycemia [1,2]. Chronic fructose ingestion eventually leads to poor feeding, growth retardation and gradual liver and/or renal failure [3,4]. Some patients may remain undiagnosed until adulthood because of a self-protective avoidance of sweet tasting food that prevents the development of acute toxicity from fructose containing food; however, these subjects may suffer intermittent symptoms throughout life, leading to potentially serious misdiagnosis [4]. We report the case of a patient with unrecognized hereditary fructose intolerance in which chronic gastrointestinal complaints, low body weight, and unexplained food avoidance were addressed as manifestations of an eating disorder during adolescence.


Assuntos
Preferências Alimentares , Intolerância à Frutose/diagnóstico , Adulto , Erros de Diagnóstico , Transtornos da Alimentação e da Ingestão de Alimentos/diagnóstico , Feminino , Preferências Alimentares/psicologia , Intolerância à Frutose/genética , Intolerância à Frutose/psicologia , Gastroenteropatias/etiologia , Humanos
3.
Psychiatry Res ; 262: 595-599, 2018 04.
Artigo em Inglês | MEDLINE | ID: mdl-28965810

RESUMO

This prospective cross-sectional study aimed to investigate the potential association between primary-adult lactose malabsorption, fructose malabsorption, tryptophan (TRP) metabolism and the presence of depressive signs. Overall 251 patients, who were referred for lactase gene C/T-13910 polymorphism genotyping and fructose hydrogen/methane breath testing, were included. All participants filled out the Beck Depression Inventory (BDI II). Serum concentrations of tryptophan (TRP), kynurenine (KYN), kynuric acid (KYNA), and TRP competing amino acids (leucine, isoleucine, valine, phenylalanine, tyrosine) were measured by high-pressure liquid-chromatography. Logistic regression analysis was performed with lactose malabsorption, fructose malabsorption and all potential biomarkers of TRP metabolism to assess the effect on signs of depression, defined as a BDI II score > 13. Primary-adult lactose malabsorption and fructose malabsorption was detected in 65 (25.90%) and 65 (25.90%) patients, respectively. Fructose malabsorption was significantly associated with BDI II score, whereas no such relationship was found for lactose malabsorption. Serum levels of TRP and TRP metabolites were no predictors of depression. The authors suggest to conduct further prospective longitudinal studies in order to get further insight of associations between carbohydrate malabsorption, biomarkers and mood disorders.


Assuntos
Depressão/etiologia , Intolerância à Frutose/psicologia , Lactase/deficiência , Intolerância à Lactose/psicologia , Triptofano/sangue , Adulto , Biomarcadores/sangue , Testes Respiratórios , Estudos Transversais , Depressão/sangue , Feminino , Frutose/sangue , Intolerância à Frutose/sangue , Humanos , Cinurenina/sangue , Lactase/sangue , Intolerância à Lactose/sangue , Modelos Logísticos , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Escalas de Graduação Psiquiátrica
4.
Scand J Gastroenterol ; 35(10): 1048-52, 2000 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-11099057

RESUMO

BACKGROUND: Fructose malabsorption is characterized by the inability to absorb fructose efficiently. As a consequence fructose reaches the colon where it is broken down by bacteria to short fatty acids, CO2 and H2. Bloating, cramps, osmotic diarrhea and other symptoms of irritable bowel syndrome are the consequences and can be seen in about 50% of fructose malabsorbers. We have previously shown that fructose malabsorption is associated with early signs of mental depression and low serum tryptophan concentrations. It was therefore of interest whether a fructose-reduced diet could not only improve gastrointestinal complaints but also depressive signs seen in fructose malabsorbers. METHODS: Fifty-three adults (12 males, 41 females), who were identified as fructose malabsorbers according to their breath-H2 concentrations, filled out a Beck's depression inventory-questionnaire, and a questionnaire with arbitrary scales for measurement of meteorism, stool frequency and quality of life for a 4-week period before dietary intervention and 4 weeks after dietary change as for fructose- and sorbitol-reduced diet. RESULTS: Depression scores were reduced by 65.2% after 4 weeks of diet (P < 0.0001), and there was a significant reduction of meteorism (P < 0.0001) and stool frequency (P < 0.01). Improvement of signs of depression and of meteorism was more pronounced in females than in males. CONCLUSION: Fructose- and sorbitol-reduced diet in subjects with fructose malabsorption does not only reduce gastrointestinal symptoms but also improves mood and early signs of depression.


Assuntos
Afeto , Sistema Digestório/fisiopatologia , Intolerância à Frutose/dietoterapia , Frutose , Sorbitol , Adolescente , Adulto , Idoso , Testes Respiratórios , Doenças Funcionais do Colo/etiologia , Depressão/etiologia , Feminino , Intolerância à Frutose/fisiopatologia , Intolerância à Frutose/psicologia , Humanos , Hidrogênio/análise , Masculino , Pessoa de Meia-Idade , Qualidade de Vida , Triptofano/sangue
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