CLINICAL PORTRAIT OF A PUBERTY GIRL WITH NON-ALCOHOLIC FAT LIVER DISEASE AND METABOLIC UNHEALTHY OBESITY

Authors

  • E. F. Chaikivska Danylo Halytsky Lviv National Medical University

DOI:

https://doi.org/10.11603/1811-2471.2020.v.i4.11768

Keywords:

obesity, non-alcoholic fatty liver disease, body composition, metabolic syndrome, liver enzymes, lipid metabolism

Abstract

SUMMARY. In Ukraine, 10 % of the child population is overweight. One of the current topical issues of puberty in obese girls is diffuse liver disease, of which non-alcoholic fatty liver disease (NAFLD) is becoming one of the most common health problems.

The aim – to study the characteristics of clinical and metabolic parameters and sexual development in adolescent girls with NAFLD and metabolically unhealthy obesity.

Material and methods. The study included 120 girls aged 12–17 years with NAFLD and metabolically unhealthy obesity, as well as 180 conditionally healthy girls with normal sexual development and normal body weight. Anthropometric indicators, parameters of enzyme, lipid, carbohydrate, purine metabolism, secretion of adipocytokines, 25 (OH) D were studied, sexual development was assessed.

Results. For girls of puberty with NAFLD and obesity, the following were most characteristic: an increase in body mass index by 2.80 times (p<0.01), mainly due to an increase in adipose tissue index by 3.07 times (p<0.01), the ratio waist/hip circumference 1.26 times (p<0.01). The level of leptin significantly exceeded that in the control by 14.58 times, ALT – 2.17, glucose – 1.25, C-peptide – 1.77, HOMA index – 1.90, uric acid – 2.27, and the level of 25 (OH) D was reduced by 1.34 times (p<0.01). Girls with NAFLD were characterized by an earlier onset of menarche – (11.45±0.03) versus (12.43±0.04) years in the control, a higher score for sexual development according to L. G. Tumilovich – (10.89±0.16) versus (10.27±0.18) points, menstrual dysfunction with the presence of oligomenorrhea in 62.50 % of cases, amenorrhea – in 27.50 %, heavy menstruation – in 10.00 %, dysmenorrhea – in 14.17 %.

Conclusions. The clinical portrait of a pubertal girl with NAFLD and metabolically unhealthy obesity is characterized by impaired lipid, carbohydrate, purine metabolism, secretion of adicytopokinids, vitamin D deficiency or deficiency and earlier puberty, accelerated adrenarche, inverted puberty, and impaired menstrual function.

References

Abaturov, O.Ye., & Nikulina, A.O. (2020). Fenotypy ozhyrinnia u ditei, klinichni proiavy y henetychni asotsiatsii [Phenotypes of obesity in children, clinical manifestations and genetic associations]. Zdorovia dytyny – Child’s Health, 15 (4), 238–251. DOI: 10.22141/2224-0551.15.4.2020.208476 [in Ukrainian].

Borshuliak, A.A., Bodnariuk, O.I., & Andriiets, O.A. (2017). Aspekty rozvytku porushen menstrualnoi funktsii v divchat yiz nadmirnoiu masoiu tila [Aspects of the development of menstrual disorders in overweight girls]. Akusherstvo. Hynekolohyia. Henetyka – Obstetrics. Gynecology. Genetics, 3 (3), 47-52 [in Ukrainian].

Berezenko, V.S., Mykhailiuk, Kh.Z., Dyba, M.B., & Tkalyk, O.M. (2014). Prychyny rozvytku, diahnostyka ta pidkhody do likuvannia steatozu pechinky ta nealkoholnoho steatohepatytu u ditei [Causes, diagnosis and approaches to the treatment of hepatic steatosis and non-alcoholic steatohepatitis in children]. Sovremennaya pediatriya – Modern Pediatrics, 4 (60),119–125 [in Ukrainian].

Asrih, M., & Jornayvaz, F.R. (2015). Metabolic syndrome and nonalcoholic fatty liver disease: is insulin resistance the link? Mol. Cell. Endocrinol., 418 (Pt 1), 55-65. DOI: 10.1016/j.mce.2015.02.018.

Caserta, C.A., Pendino, G.M., Amante, A., Vacalebre, C., Fiorillo, M.T., Surace, P., ..., & Marcucci, F. (2010). Cardiovascular risk factors, nonalcoholic fatty liver disease, and carotid artery intima-media thickness in an adolescent population in southern Italy. Am. J. Epidemiol., 171, 1195-1202. DOI: 10.1093/aje/kwq073.

D’Adamo, E., Santoro, N., & Caprio, S. (2013). Metabolic syndrome in pediatrics: old concepts revised, new concepts discussed. Curr. Probl. Pediatr. Adolesc. Health Care., 43, 114-123. DOI: 10.1016/j.cppeds.2013.02.004.

Mencin, A.A., & Lavine, J.E. (2011). Nonalcoholic fatty liver disease in children. Curr. Opin. Clin. Nutr. Metab. Care., 14, 151-157. DOI: 10.1097/MCO.0b013e328342baec.

Mikolasevic, I., Milic, S., Turk Wensveen, T., Grgic, I., Jakopcic, I., Stimac, D., ..., & Orlic, L. (2016). Nonalcoholic fatty liver disease - a multisystem disease? World J. Gastroenterol., 22, 9488-9505. DOI: 10.3748/wjg.v22.i43.9488.

Mann, J.P., Valenti, L., Scorletti, E., Byrne, C.D., & Nobili, V. (2018). Nonalcoholic fatty liver disease in children. Semin Liver Dis., 38, 1-13. DOI: 10.1055/s-0038-1627456.

Selvakumar, P.K.C., Kabbany, M.N., Nobili, V., & Alkhouri, N. (2017). Nonalcoholic fatty liver disease in children: hepatic and extrahepatic complications. Pediatr. Clin. North. Am., 64, 659-675. DOI: 10.1016/j.pcl.2017.01.008.

Lawlor, D.A., Callaway, M., Macdonald-Wallis, C., Anderson, E., Fraser, A., Howe, L.D., ..., & Sattar, N. (2014). Nonalcoholic fatty liver disease, liver fibrosis, and cardiometabolic risk factors in adolescence: a cross-sectional study of 1874 general population adolescents. J. Clin. Endocrinol. Metab., 99 (3), E410-417. DOI: 10.1210/jc.2013-3612.

Lonardo, A., Ballestri, S., Marchesini, G., Angulo, P., & Loria, P. (2015). Nonalcoholic fatty liver disease: a precursor of the metabolic syndrome. Dig. Liver Dis., 47, 181-190. DOI: 10.1016/j.dld.2014.09.020.

Bussler, S., Penke, M., Flemming, G., Elhassan, Y.S., Kratzsch, J., Sergeyev, E., ..., & Kiess, W. (2017). Novel insights in the metabolic syndrome in childhood and adolescence. Horm. Res. Paediatr., 88, 181-193. DOI: 10.1159/ 000479510.

Mann, J.P., De Vito, R., Mosca, A., Alisi, A., Armstrong, M.J., Raponi, M., ..., & Nobili, V. (2016). Portal inflammation is independently associated with fibrosis and metabolic syndrome in pediatric nonalcoholic fatty liver disease. Hepatology, 63 (3), 745-753. DOI: 10.1002/hep.28374.

Schwimmer, J.B., Deutsch, R., Kahen, T., Lavine, J.E., Stanley, C., & Behling, C. (2006). Prevalence of fatty liver in children and adolescents. Pediatrics, 118, 1388-1393. DOI: 10.1542/peds.2006-1212.

Yu, E.L., Golshan, S., Harlow, K.E., Angeles, J.E., Durelle, J., Goyal, N.P., ..., & Schwimmer, J.B. (2019). Prevalence of nonalcoholic fatty liver disease in children with obesity. J. Pediatr., 207, 64-70. DOI: 10.1016/j.jpeds.2018.11.021.

Yu, E.L., Golshan, S., Harlow, K.E., Angeles, J.E., Durelle, J., Goyal, N.P., …, & Schwimmer, J.B. (2018). Prevalence of nonalcoholic fatty liver disease in children with obesity. J. Pediatr., 207, 64-70. DOI: 10.1016/j.jpeds.2018.11.021.

Reaven, G.M. (1988). Banting Lecture Role of insulin resistance in human disease. Diabetes, 37, 1595-1607.

Anderson, E.L., Howe, L.D., Jones, H.E., Higgins, J.P., Lawlor, D.A., & Fraser, A. (2015). The prevalence of non-alcoholic fatty liver disease in children and adolescents: a systematic review and meta-analysis. PLoS ONE, 10 (10), e0140908. DOI: 10:e0140908.10.1371/journal.pone.0140908.

Published

2021-02-12

How to Cite

Chaikivska, E. F. (2021). CLINICAL PORTRAIT OF A PUBERTY GIRL WITH NON-ALCOHOLIC FAT LIVER DISEASE AND METABOLIC UNHEALTHY OBESITY. Achievements of Clinical and Experimental Medicine, (4), 158–165. https://doi.org/10.11603/1811-2471.2020.v.i4.11768

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Section

Оригінальні дослідження