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Digestive disorder in infants may be genetic, findings indicate

Date:
June 16, 2010
Source:
JAMA and Archives Journals
Summary:
In a study that includes nearly 2 million children born in Denmark, researchers have found that there is a higher rate of occurrence of the digestive tract disorder pyloric stenosis among twins and siblings, suggesting that this is a genetic and inherited disorder.

In a study that includes nearly 2 million children born in Denmark, researchers have found that there is a higher rate of occurrence of the digestive tract disorder pyloric stenosis among twins and siblings, suggesting that this is a genetic and inherited disorder, according to the report in the June 16 issue of JAMA.

Pyloric stenosis is a severe and potentially fatal condition in which apparently healthy in­fants, typically 2 to 8 weeks old, develop an inability to pass food from the stomach into the duodenum (part of the small intestine). "Today pyloric stenosis is the most common condition requir­ing surgery in the first months of life. Among white individuals, pyloric ste­nosis is relatively common, with an incidence of 1.5 to 3 per 1000 live births," the authors write. "Case reports have suggested familial aggregation [the occurrence of more cases of a given disorder in close relatives of a person with the disorder than in control families], but to what extent this is caused by common environment or inheritance is unknown."

Camilla Krogh, M.D., of the Statens Serum Insti­tut, Copenhagen, Denmark, and colleagues exam­ined the familial aggregation of py­loric stenosis from monozygotic twins (derived from a single fertilized egg) to fourth-generation relatives in the population of Denmark. The population-based cohort study included 1,999,738 chil­dren born in Denmark between 1977 and 2008 and followed up for the first year of life, during which 3,362 children had surgery for pyloric stenosis.

Among the findings of the researchers, 46 percent of children with an affected monozygotic twin were diagnosed as having pyloric stenosis. In dizygotic twins (derived from two separately fertilized eggs), 7.7 percent with an affected twin had py­loric stenosis.

"This nationwide study documented strong familial aggregation of pyloric stenosis, with a nearly 200-fold in­crease among monozygotic twins and 20-fold increase among siblings. Fa­milial aggregation of pyloric stenosis was pronounced even in more distant relatives," the authors write.

"Our findings argue for a hereditary component of pyloric stenosis: (1) pre­dominance in boys; (2) familial aggre­gation in first-, second-, and third-degree relatives; (3) high concordance rate in monozygotic twins; (4) similar degree of aggregation in dizygotic twins and siblings; (5) difference in risk for siblings vs. maternal half-siblings (as well as cousins vs. half-cousins); and (6) heritability of 87 percent."

"… with a heritability esti­mate of 87 percent, it seems that familial ag­gregation is primarily explained by shared genes that may affect re­sponses to postnatal factors. The high rates for twins and siblings should be considered in counseling families with affected children," the researchers conclude.


Story Source:

The above story is based on materials provided by JAMA and Archives Journals. Note: Materials may be edited for content and length.


Journal Reference:

  1. Camilla Krogh; Thea K. Fischer; Line Skotte; Robert J. Biggar; Nina Oyen; Axel Skytthe; Sanne Goertz; Kaare Christensen; Jan Wohlfahrt; Mads Melbye. Familial Aggregation and Heritability of Pyloric Stenosis. JAMA, 2010; 303 (23): 2393-2399

Cite This Page:

JAMA and Archives Journals. "Digestive disorder in infants may be genetic, findings indicate." ScienceDaily. ScienceDaily, 16 June 2010. <www.sciencedaily.com/releases/2010/06/100615163123.htm>.
JAMA and Archives Journals. (2010, June 16). Digestive disorder in infants may be genetic, findings indicate. ScienceDaily. Retrieved April 18, 2014 from www.sciencedaily.com/releases/2010/06/100615163123.htm
JAMA and Archives Journals. "Digestive disorder in infants may be genetic, findings indicate." ScienceDaily. www.sciencedaily.com/releases/2010/06/100615163123.htm (accessed April 18, 2014).

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