Genealogical characteristics of children and adolescents with cholelithiasis and their families
DOI:
https://doi.org/10.14739/2310-1210.2018.5.141716Keywords:
children, cholelithiasis, pedigree, family, heredityAbstract
One of the common pathologies of the hepatobiliary tract is cholelithiasis. The prevalence of this disease among children and adolescents is of particular concern.
The purpose of the study is to identify the family aggregation of the hepatobiliary pathology and other multifactorial diseases in the pedigrees of children and adolescents with cholelithiasis.
Materials and methods. Genealogical analysis was performed in 105 families with sick children aged from 2 to 17 years who were examined and treated for hepatobiliary tract disorders in gastroenterological and somatic departments. The comparison group comprised 75 family pedigrees of peers, inhabitants of the Kharkiv region, who were not diagnosed with cholelithiasis and other serious non-communicable diseases.
Results. Gastroduodenal pathology ranked first among the families of sick children in the morbidity prevalence patterns in terms of gastrointestinal tract pathology (14.29 % vs. 6.19 % in relatives of healthy children, P < 0.001), followed by cholelithiasis (13.19 % vs. 0.44 % in relatives of healthy children, P < 0.001), and other diseases of the hepatobiliary system ranked third – (7,21 % vs. 5,59 % in relatives of healthy children, P > 0.05). In our studies, the calculation of cholelithiasis formation depending on the gender identity of sick children relatives also confirmed that in the female subjects the risk of cholelithiasis was 6.7 times increased compared with the male population (OR = 6.69; CI = 3.71–12.06; p < 0.05). Diseases such as cholelithiasis and other diseases of the hepatobiliary system, gastroduodenal pathology and cardiovascular disorders prevailed among the first-degree relatives of children suffering from cholelithiasis in comparison with these diseases diagnosis in relatives of healthy children.
Conclusions. Based on the family pedigree analysis of patients and healthy children, an inherited predisposition to cholelithiasis was determined in 63.81 % of sick children families, and it was 15.9 times higher than the incidence of this disease in healthy children families, thus made it possible to consider this indicator as a prognostic sign for cholelithiasis development. Familial aggregation of cholelithiasis, other diseases of the hepatobiliary system and gastroduodenal pathology in the first-degree relatives; cholelithiasis and gastroduodenal pathology in the second-degree relatives; cholelithiasis in the third-degree relatives was revealed compared with the frequency of these diseases in healthy children families. The maternal inheritance of cholelithiasis was found more frequently than paternal and both maternal and paternal. The odds ratio (OR) value in the presence of cholelithiasis in the sick children families was 24.7 times increased; 2,6 times – in the presence of gastroduodenal pathology; 1.5 times – in the presence of other diseases of the hepatobiliary system compared with the frequency of these diseases in healthy children families; and 6.7 times for females.
References
Atramentova, L. A., & Utevskaya, O. M (2008). Statisticheskie metody v biologii [Statistical methods are in biology]. Gorlovka. [in Russian].
Hoida, S. M. (2011). Tendentsii poshyrenosti zhovchnokamianoi khvoroby sered naselennia [Tendencies of prevalence of cholelithiasis illness are among the population of Ukraine]. Ukrainskyi medychnyi chasopys, 4, 112–113. [in Ukrainian].
Evseeva, I. V. (1994). Ustanovlenie v usloviyakh polikliniki riska razvitiya kholecistita [Establishment in the conditions of policlinic of risk of development of cholecystitis]. Terapevticheskij arkhiv, 66(1), 67–70. [in Russian].
Zoryk, M. M., & Nikonets, A. W. (2014). Zastosuvannia likuvalnoi fizychnoi kultury v kompleksnii reabilitatsii khvorykh na zhovchnokamianu khvorobu [The use of therapeutic physical culture in complex rehabilitation of people with gallbladder disease.]. Slobozanskyi naukovo-sportyvnyi visnyk, 2(40), 80–84. [in Ukrainian].
Skvorcova, T. E'., Sitkin, S. I., Radchenko, V. G., Seliverstov, P. V., & Tkachenko, E. I. (2013). Zhelchnokamennaya bolezn'. Sovremennye podkhody k diagnostike, lecheniyu i profilaktike: posobie dlya vrachej [Cholelithiasis. Modern going near diagnostics, treatment and prophylaxis: guidance for doctors]. Moscow: Forte print. [in Russian].
Shkenyova, L. N., Lavrova, A. E., Sazanova, N. E., Shirokova, N. Yu., & Borisova, E. Yu. (2011). Rol' nasledstvennykh faktorov riska v formirovanii nizkoj amiloliticheskoj aktivnosti slyuny u detej s khronicheskimi vospalitel'nymi zabolevaniyami zheludka i dvenadcatiperstnoj kishki [The role of hereditary risk factors in forming low amylolytic activity of saliva in children with chronic inflammatory gastric and duodenal diseases]. Sovremennye tekhnologii v medicine, 1, 141–143. [in Russian].
Sokolnyk, S. O. (2015). Znachennia henealohichnoho anamnezu v rozvytku shlunkovo-kyshkovykh krovotech u ditei, khvorykh na vyrazkovu khvorobu [The value of the genealogical history in the development of gastrointestinal bleeding in children with peptic ulcer]. Perinatolohiia i pediatriia, 2(62), 71–73. doi: 10.15574/PP.2015.62.71. [in Ukrainian].
(2013) Nakaz Ministerstva okhorony zdorovia Ukrainy «Unifikovani klinichni protokoly medychnoi dopomohy ditiam iz zakhvoriuvanniamy orhaniv travlennia» vid 29 sichnia 2013 roku №59 [Compatible clinical protocols of medicare to the children with the diseases of organs of digestion from January 29, 2013, №59]. Sovremennaya pediatriya, 4, 20–31. [in Ukrainian].
Tsukanov, V. V., Vasyutin, A. V., & Tonkikh, J. L. (2015). Sovremennye aspekty patogeneza i lecheniya kholelitiaza [Modern aspects of pathogenesis and treatment of cholelithias]. Sibirskij medicinskij zhurnal, 132(1), 10–14. [in Russian].
Shadrin, O. G., & Shutova, E. V. (2015). Ocenka pokazatelej apolipoproteinov APO-A1, APO-V, APO-E i ih vzaimosvjaz' s fenotipom APO-E u detej s zhelchnokamennoj bolezn'ju [Evaluation of indicators of АPO-АI, АPO-В, АPO-Е apolipoproteins and their correlation with phenotype АPO-Е in children with cholelithiasis]. East European Scientific Journal, 4(1), 149–153. [in Russian].
Shutova, O. V., & Bahatska, N. V. (2017). Otsinka endohennykh ta ekzohennykh faktoriv ryzyku formuvannia zhovchnokamianoi khvoroby v dytiachomu ta pidlitkovomu vitsi [Evaluation of endogenous and exogenous risk factors for the development of cholelithiasis in children and adolescents]. Visnyk problem biolohii i medytsyny, 4, 3(141), 245–249. [in Ukrainian].
Shcherbynina, M. B., & Babets, M. I. (2008). Epidemiolohichnyi analiz poshyrenosti ta zakhvoriuvanosti na zhovchnokamianu khvorobu v Ukraini [An epidemiology analysis of prevalence and morbidity is on cholelithiasis illness in Ukraine]. Okhorona zdorovia Ukrainy, 1(29), 67–71. [in Ukrainian].
Espinosa-Saavedra, D., Flores-Calderón, J., González-Ortiz, B., & Rodríguez-González, P. (2014). Characteristics of pediatric patients with biliary lithiasis. Immediate post-operative evolution. Rev Med Instituto Mexicano del Seguro Social, 52(2), S74–77.
European Association for the Study of the Liver (EASL) (2016) EASL Clinical Practice Guidelines on the prevention, diagnosis and treatment of gallstones. Journal of Hepatology, 65(1), 146–181. doi: 10.1016/j.jhep.2016.03.005.
Svensson, J., & Makin, E. (2012). Gallstone disease in children. Seminars in Pediatric Surgery, 21(3), 255–265. doi: 10.1053/j.sempedsurg.2012.05.008.
Marschall, H., Katsika, D., Rudling, M., & Einarsson, C. (2010). The genetic background of gallstone formation: An update. Biochemical And Biophysical Research Communications, 396(1), 58–62. doi: 10.1016/j.bbrc.2010.02.143.
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