Aagenaes syndrome
| Aagenaes syndrome | |
|---|---|
| Other names | Aagenæs syndrome, Cholestasis-lymphedema syndrome |
 | |
| Aagenaes syndrome is inherited in an autosomal recessive manner | |
Aagenaes syndrome is a syndrome characterised by congenital hypoplasia of lymph vessels, which causes lymphedema of the legs and recurrent cholestasis in infancy, and slow progress to hepatic cirrhosis and giant cell hepatitis with fibrosis of the portal tracts.[1][2]
The genetic cause is unknown, but it is autosomal recessively inherited and the gene is located to chromosome 15q1,2. A common feature of the condition is a generalised lymphatic anomaly, which may be indicative of the defect being lymphangiogenetic in origin1. Approximately one hundred people with this disease are known.[3] The condition is particularly frequent in southern Norway, where more than half the cases are reported from, but is found in patients in other parts of Europe and the United States.[4] It is named after Øystein Aagenæs, a Norwegian paediatrician.[5] It is also called cholestasis-lymphedema syndrome (CLS).[6]
The first case of cholestasis usually improves spontaneously during preschool and early school age, respectively, and returns at various intervals of two to six months.[3] The severity of the disease varies in these patients, with some even experiencing complete liver failure. In these cases, liver transplantation is necessary.[3][7] Untreated cholestasis is accompanied by jaundice, itching, malabsorption of fat and fat-soluble vitamins. This can lead to skeletal abnormalities and a higher susceptibility to bleeding.[3] In early childhood and adolescence, lymphedema most often develops in the lower limbs in all patients, but the upper limbs or chest are no exception.[3][7] Untreated lymphedema can cause chronic tissue damage.[3]
Biochemical analysis
In patients over 10 years of age suffering from Aagenaes syndrome, a biochemical analysis revealed an increased amount of bile acids. Bilirubin levels were only slightly increased. The amount of serum enzymes (alanine aminotransferase, aspartate aminotransferase, gamma-glutamyl transferase) was ambiguous and mostly normal.[8]
Patients without observed liver cirrhosis compared to the control group had elevated levels of ALP (alkaline phosphatase) and GGT (gamma-glutamyl transferase). The differences in serum bile acid concentrations between patients and controls were slight. However, test patients had lower values for total protein, CRP, albumin and creatinine. On the other hand, the value for fibrinogen was higher in patients with Aagenaes syndrome.[8]
In terms of erythrocyte, leukocyte and platelet counts, there was only a slight increase in mean cell hemoglobin (MCH). Serum albumin concentrations decreased with age, but not in the control group.[8]
Treatment
Although no cure for this disease has been found, improvements in the course of the disease have been significantly seen after administration of nutritional and vitamin supplements, especially in children. It is stated that if there is no remission by about 12-18. months of childhood, liver transplantation is necessary at a later age.[3][8]
Neonatal cholestasis lasted no more than one year in some patients, or lasted until the age of 6/7 years in some cases. In recent decades, cholestatic episodes have lasted shorter time than before 1970. There has also been a decline in rickets, growth retardation, and neuropathy over time. The reasons for this are improved nutritional habits, vitamin and cholestyramine supplementation. Nevertheless, it is not yet possible to prevent serious liver disease.[8]
History
First reported cases of Aagenaes syndrome were described in a study in 1968 from the southwest of Norway.[9][10] Four out of five children born before 1939 died of bleeding in the first weeks of life. Vitamin K was introduced this year, after the birth of another four children after 1939, when these children received one dose of this vitamin, three of them died at the age of 5–9 months. The confirmed cause of death in one or two children in this group was bleeding. The remaining seven children, born in 1935 and in 1942–1966, who were part of a study published in 1968, were alive at the time.[9]
See also
References
- ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1.
- ^ Bull LN, Roche E, Song EJ, Pedersen J, Knisely AS, van Der Hagen CB, Eiklid K, Aagenaes O, Freimer NB (Oct 2000). "Mapping of the locus for cholestasis-lymphedema syndrome (Aagenaes syndrome) to a 6.6-cM interval on chromosome 15q". Am J Hum Genet. 67 (4): 994–9. doi:10.1086/303080. PMC 1287903. PMID 10968776.
- ^ a b c d e f g Iversen, Kristin; Drivdal, Lill Monica; Billaud Feragen, Kristin J.; Geirdal, Amy Østertun (2018-07-25). "Quality of life in adults with lymphedema cholestasis syndrome 1". Health and Quality of Life Outcomes. 16 (1): 146. doi:10.1186/s12955-018-0972-1. ISSN 1477-7525. PMC 6060525. PMID 30045736.
{{cite journal}}: CS1 maint: unflagged free DOI (link) - ^ Heiberg A (May 2001). "Aagenaes syndrome: lymphedema and intrahepatic cholestasis". Tidsskr Nor Laegeforen. 121 (14): 1718–9. PMID 11446017.
- ^ "Øystein Aagenæs".
- ^ Frühwirth, M.; et al. (Apr 2003). "Evidence for genetic heterogeneity in lymphedema-cholestasis syndrome". Journal of Pediatrics. 142 (4): 441–447. doi:10.1067/mpd.2003.148. PMID 12712065.
- ^ a b Atneosen-Åsegg, Monica; Melheim, Maria; Almaas, Runar (2020-09-15). "MicroRNA in dried blood spots from patients with Aagenaes syndrome and evaluation of pre-analytical and analytical factors". Pediatric Research. doi:10.1038/s41390-020-01153-3. ISSN 0031-3998.
- ^ a b c d e Drivdal, Monica; Trydal, Torleif; Hagve, Tor-Arne; Bergstad, Ingunn; Aagenæs, Øystein (January 2006). "Prognosis, with evaluation of general biochemistry, of liver disease in lymphoedema cholestasis syndrome 1 (LCS1/Aagenaes syndrome)". Scandinavian Journal of Gastroenterology. 41 (4): 465–471. doi:10.1080/00365520500335183. hdl:10852/41874. ISSN 0036-5521.
- ^ a b Aagenaes, O.; van der Hagen, C. B.; Refsum, S. (1968-12-01). "Hereditary recurrent intrahepatic cholestasis from birth". Archives of Disease in Childhood. 43 (232): 646–657. doi:10.1136/adc.43.232.646. ISSN 0003-9888.
- ^ AAGENAES, ØYSTEIN (January 1998). "Hereditary Cholestasis with Lymphoedema (Aagenaes Syndrome, Cholestasis-Lymphoedema Syndrome): New Cases and Follow-up from Infancy to Adult Age". Scandinavian Journal of Gastroenterology. 33 (4): 335–345. doi:10.1080/00365529850170955. ISSN 0036-5521.