B5-072 CBCL: Malabsorption Flashcards
associated with enterotoxin traveler’s diarrhea
secretory diarrhea
not affected by prolonged fasting
secretory diarrhea
ceases during prolonged fast
osmotic diarrhea
what kind of diarrhea does lactase deficiency cause?
osmotic
primary functions of bile acids
- promote bile flow
- breakdown cholesterol/phospholipids in gallbladder via mixed micelles
- enhance dietary lipid digestion and absorption in proximal intestine via mixed micelles
decreased bile acid synthesis due to decreased hepatic functions
cirrhosis
decreased biliary secretion due to defective canalicular excretion of organic anions
primary billiary cirrhosis
failure of maintenance of conjugated bile acids due to bacterial overgrowth
jejunal diverticulosis
decrease in the reabsorption of bile acids due to decreased delivery to the large intestine
Crohn’s or surgical resection
results in fatty acid diarrhea
bile acid diarrhea is due to […] ileal disease
limited
fatty acid diarhhea is due to […] ileal disease
extensive
in fatty acid diarrhea, the fecal-bile acid loss is not compensated by hepatic synthesis causing in impaired micelle formation and resulting in
steatorrhea
does bile acid diarrhea respond to cholestyramine?
yes
does fatty acid diarrhea respond to cholestyramine?
no
can make it worse
does bile acid diarrhea respond to a low fat diet?
no
does fatty acid diarrhea respond to a low fat diet?
yes
dietary fat is composed exclusively of
long chain triglycerides
assimilation of dietary lipids requires 3 phases:
- intraluminal (digestive)
- mucosal (absorptive)
- delivery (post absorptive)
abnormality of any of these may cause steatorrhea
an issue in the digestive phase with lipolysis due to decreased pancreatic lipase
2
can be due to gastrinoma or increased bicarb
chronic pancreatitis
cystic fibrosis
an issue in the absorptive phase with mucosal uptake and re-esterfication due to impaired movement of mixed micelles
can be due to bacterial overgrowth
celiac
issue in the post-absorptive phase with chylomicron formation due to impaired synthesis of B-lipoproteins
Abetalipoproteinemia
issue in the post absorptive phase with lipid delivery from the intestine due to abnormal intestinal lymphatics
intestinal lymphangiectasia
- present in coconut oil
- often used as nutritional supplement
medium chain fatty acids
is micelle formation necessary for the digestion of MCTs?
no
absorbed directly into cell
- synthesized by colon bacterial enzyme from non-absorbed carbohydrates
- rapidly absorbed and stimulat colon NaCl and fluid absorption
short chain fatty acids
most antibiotic diarrhea (except C. diff) is caused by a suppression of colonic bacteria resulting in a decrease of
SCFAs
lactose requires digestion by
brush border lactase
only clinical important disorder of carbohydrate absorption
lactose malabsorption
genetically determined decrease or absence of lactase while all other aspects of intestinal absorption and brush border enzymes are normal
primary lactase deficiency
caused by diseases that destroy the lining fo the small intestine along with the enzymes
secondary lactase deficiency
secondary lactase deficiency is often see in what conditions?
4
- celiac
- crohn’s
- UC
- chemo/long antibiotics
persistence of symptoms in an individual who exhibits lactose intolerance after adhering to a strict lactose free diet indicates
IBS
most individuals with primary lactase deficiency do not have
symptoms
due to a congenital absence of brush border SGLT1
glucose and galactose malabsorption
due to absence of the enzyme that converts trypsin to trypsinogen
enterokinase deficiency
associated with diarrhea, growth retardation, and hypoproteinemia
enterokinase deficiency
- due to a defect in nonpolar amino acids
- pellagra-like rash, neuropsych symptoms
hartnup’s syndrome
- due to a defect in dibasic amino acid transport
- renal calculi and chronic pancreatitis
cystinuria
symptoms of malabsorption in a patient who has recently undergone bowel resection
short gut syndrome
steatorrhea in a patient with longstanding alcohol abuse and chronic pancreatitis
assess pancreatic exocrine function
gold standard in establishing a diagnosis for steatorrhea
timed quantitative stool-fat determination
qualitative test for steatorrhea
Sudan III staining
rapid and inexpensive but not as precise
what laboratory studies should be ordered in a patient with suspected malabsorption disorder?
CBC
PTT
serum protein
alkaline phosphatase
fat soluble vitamins
ADEK
evidence of metabolic bone disease with elevated alkaline phosphatase and/or reduced calcium
vitamin D malabsorption
elevated PTT in an individual without liver disease that is not taking anti-coags might indicate
vitamin K deficiency
macrocytic anemia might indicate
cobalmin or folic acid malabsoprtion
iron deficiency anemia in the absence of occult bleeding might indicate
2
iron malabsorption
celiac
- test performed to determine the cause of cobalamin malabsorption
- establishes pernicious anemia
Schilling
- test to assess proximal small-intestinal mucosal function
- reflects duodenal/jejunal mucosal disease
urinary d-Xylose test
- autoimmune disorder
- reaction to gluten
- causes malabsorption
celiac
- anemia
- osteopenia
- infertility
- neurologic symptoms
may indicate…
atypical celiac disease
- abnormal small-intestinal biopsy with proximal-to-distal severity
- responds to elimination of gluten from diet
celiac
absence of HLA-DQ2/8 excludes the diagnosis of
celiac
association with gliadin
celiac
a 4 week course of […] can induce remission in celiacs
prednisolone
failure to responds to all treatments of celiac may indicate
intestinal T cell lymphoma
autoimmune enteropathy