Iron deficiency enhances cholesterol gallstone formation. 1997

S M Johnston, and K P Murray, and S A Martin, and K Fox-Talbot, and P A Lipsett, and K D Lillemoe, and H A Pitt
Department of Surgery, Johns Hopkins Medical Institutions, Baltimore, Md., USA.

BACKGROUND Cholesterol gallstones occur most commonly in multiparous women, but the causes for this phenomenon remain unclear. This same patient population is prone to chronic iron deficiency anemia. In addition, iron is known to play an important role in hepatic enzyme metabolism. Therefore, we tested the hypotheses that iron deficiency would alter hepatic cholesterol metabolism and enhance gallstone formation. METHODS Forty adult prairie dogs were fed either a control iron-supplemented (200 ppm), an iron-deficient (8 ppm), a 0.4% cholesterol iron-supplemented (200 ppm), or a 0.4% cholesterol iron-deficient (8 ppm) diet. After 8 weeks gallbladder bile, serum, and liver were harvested. Gallbladder bile was examined for cholesterol crystals and gallstones. Bile lipids and hepatic enzymes were measured, and a cholesterol saturation index (CSI) was calculated. RESULTS Animals receiving the iron-deficient diet were more likely to have cholesterol crystals in their bile than were animals on the control diet (80% vs. 20%; p < 0.05). Animals on the 0.4% cholesterol iron-deficient diet had more cholesterol crystals per high-powered field (79 +/- 10 vs. 49 +/- 9; p = 0.07), a higher molar % cholesterol (6.0 +/- 0.3 vs 4.4 +/- 0.5; p < 0.05), and a higher CSI (1.27 +/- 0.10 vs. 0.91 +/- 0.07; p < 0.05) compared to animals receiving the 0.4% cholesterol iron supplemented diet. The 7 alpha-hydroxylase levels were lower in the animals on the iron-deficient diet compared to those receiving the control diet (0.42 +/- 0.08 vs 1.17 +/- 0.40 pmol/mg per minute; p = 0.07). CONCLUSIONS These data suggest that an iron-deficient diet (1) alters hepatic enzyme metabolism, which, in turn, (2) increases gallbladder bile cholesterol and promotes cholesterol crystal formation. We conclude that iron deficiency plays a previously unrecognized role in the pathogenesis of cholesterol gallstone formation in women.

UI MeSH Term Description Entries
D007501 Iron A metallic element with atomic symbol Fe, atomic number 26, and atomic weight 55.85. It is an essential constituent of HEMOGLOBINS; CYTOCHROMES; and IRON-BINDING PROTEINS. It plays a role in cellular redox reactions and in the transport of OXYGEN. Iron-56,Iron 56
D008099 Liver A large lobed glandular organ in the abdomen of vertebrates that is responsible for detoxification, metabolism, synthesis and storage of various substances. Livers
D008297 Male Males
D008862 Microsomes, Liver Closed vesicles of fragmented endoplasmic reticulum created when liver cells or tissue are disrupted by homogenization. They may be smooth or rough. Liver Microsomes,Liver Microsome,Microsome, Liver
D002769 Cholelithiasis Presence or formation of GALLSTONES in the BILIARY TRACT, usually in the gallbladder (CHOLECYSTOLITHIASIS) or the common bile duct (CHOLEDOCHOLITHIASIS). Gallstone Disease,Cholelithiases,Gallstone Diseases
D002784 Cholesterol The principal sterol of all higher animals, distributed in body tissues, especially the brain and spinal cord, and in animal fats and oils. Epicholesterol
D002790 Cholesterol 7-alpha-Hydroxylase A membrane-bound cytochrome P450 enzyme that catalyzes the 7-alpha-hydroxylation of CHOLESTEROL in the presence of molecular oxygen and NADPH-FERRIHEMOPROTEIN REDUCTASE. This enzyme, encoded by CYP7, converts cholesterol to 7-alpha-hydroxycholesterol which is the first and rate-limiting step in the synthesis of BILE ACIDS. CYP7,CYP7A,Cytochrome P-450 CYP7,CYP 7,CYP 7A,Cholesterol 7-alpha-Monooxygenase,Cholesterol 7alpha-Hydroxylase,Cholesterol-7-Hydroxylase,Cytochrome P450 7,Cholesterol 7 Hydroxylase,Cholesterol 7 alpha Hydroxylase,Cholesterol 7 alpha Monooxygenase,Cholesterol 7alpha Hydroxylase,Cytochrome P 450 CYP7
D002791 Cholesterol, Dietary Cholesterol present in food, especially in animal products. Dietary Cholesterol
D003460 Crystallization The formation of crystalline substances from solutions or melts. (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed) Crystalline Polymorphs,Polymorphism, Crystallization,Crystal Growth,Polymorphic Crystals,Crystal, Polymorphic,Crystalline Polymorph,Crystallization Polymorphism,Crystallization Polymorphisms,Crystals, Polymorphic,Growth, Crystal,Polymorph, Crystalline,Polymorphic Crystal,Polymorphisms, Crystallization,Polymorphs, Crystalline
D005260 Female Females

Related Publications

S M Johnston, and K P Murray, and S A Martin, and K Fox-Talbot, and P A Lipsett, and K D Lillemoe, and H A Pitt
April 1995, Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology,
S M Johnston, and K P Murray, and S A Martin, and K Fox-Talbot, and P A Lipsett, and K D Lillemoe, and H A Pitt
December 1987, The Medical journal of Malaysia,
S M Johnston, and K P Murray, and S A Martin, and K Fox-Talbot, and P A Lipsett, and K D Lillemoe, and H A Pitt
August 1989, Surgery,
S M Johnston, and K P Murray, and S A Martin, and K Fox-Talbot, and P A Lipsett, and K D Lillemoe, and H A Pitt
January 1977, Clinics in gastroenterology,
S M Johnston, and K P Murray, and S A Martin, and K Fox-Talbot, and P A Lipsett, and K D Lillemoe, and H A Pitt
September 2009, Archives of pharmacal research,
S M Johnston, and K P Murray, and S A Martin, and K Fox-Talbot, and P A Lipsett, and K D Lillemoe, and H A Pitt
June 1988, Journal of hepatology,
S M Johnston, and K P Murray, and S A Martin, and K Fox-Talbot, and P A Lipsett, and K D Lillemoe, and H A Pitt
September 1990, Hepatology (Baltimore, Md.),
S M Johnston, and K P Murray, and S A Martin, and K Fox-Talbot, and P A Lipsett, and K D Lillemoe, and H A Pitt
July 2003, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver,
S M Johnston, and K P Murray, and S A Martin, and K Fox-Talbot, and P A Lipsett, and K D Lillemoe, and H A Pitt
May 1991, The Journal of surgical research,
S M Johnston, and K P Murray, and S A Martin, and K Fox-Talbot, and P A Lipsett, and K D Lillemoe, and H A Pitt
January 1968, Nihon geka hokan. Archiv fur japanische Chirurgie,
Copied contents to your clipboard!