The Role of Genetic Variants in the Long Non-Coding RNA Genes MALAT1 and H19 in the Pathogenesis of Childhood Obesity
by
,
Tatiana Pavlovna Shkurat
1, 
Manar Ammar
1,*
,
Olga Bocharova
2,
Elena Teplyakova
2,
Anzhela Aleksandrova
1,
Ruba Ali
1 and
Leonard Lipovich
3 
1
Academy of Biology and Biotechnology named after D I Ivanovsky, Southern Federal University, Rostov on Don 344090, Russia
2
Department of Children’s Diseases No. 3, Rostov State Medical University, Rostov on Don 344022, Russia
3
College of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai 505055, United Arab Emirates
*
Author to whom correspondence should be addressed.
Non-Coding RNA 2023, 9(2), 22; https://doi.org/10.3390/ncrna9020022
Submission received: 14 January 2023
/
Revised: 24 March 2023
/
Accepted: 28 March 2023
/
Published: 30 March 2023
(This article belongs to the Special Issue Selected Papers from IEEE BIBM 2021 Workshop on Long Non-coding RNAs: Mechanism, Function, and Computational Analysis (BIBM-LncRNA))
Abstract
:Long non-coding RNAs (lncRNAs) play important roles in the maintenance of metabolic homeostasis. Recently, many studies have suggested that lncRNAs, such as Metastasis Associated Lung Adenocarcinoma Transcript 1 (MALAT1) and Imprinted Maternally Expressed Transcript (H19), might participate in the pathogenesis of metabolic disorders such as obesity. We conducted a case-control study with 150 Russian children and adolescents aged between 5 and 17 years old in order to assess the statistical association between the single nucleotide polymorphisms (SNPs) rs3200401 in MALAT1 and rs217727 in H19, and the risk of developing obesity in this population. We further explored the possible association of rs3200401 and rs217727 with BMI Z-score and insulin resistance. The MALAT1 rs3200401 and H19 rs217727 SNPs were genotyped using Taqman SNP genotyping assay. The MALAT1 rs3200401 SNP was identified as a risk factor for childhood obesity (p < 0.05) under the dominant and allelic models, and the CT heterozygous genotype was associated with the risk of increased BMI and with insulin resistance. The H19 rs217727 SNP had no significant association with obesity risk (all p > 0.05). Our findings thus suggest that MALAT1 SNP rs3200401 is a potential indicator of obesity susceptibility and pathogenesis in children and adolescents.
1. Introduction
Obesity is a chronic metabolic disorder in which an individual’s caloric intake exceeds their energy expenditure for a long period of time and consequently, the excessive energy is stored as fat. At present, obesity is a worldwide public health burden, affecting the quality of life of both adults and children [1]. Pediatric obesity has a high prevalence and persistence, which makes targeting it a key objective in most nations’ healthcare agendas [2,3]. Robust evidence demonstrates that obesity in children and adolescents acts as a risk factor for being overweight and obese in adulthood, with comorbidities that include high blood pressure, type 2 diabetes (T2D), insulin resistance, and cardiovascular diseases, in addition to the psychosocial complications reported in obese children and adolescents [4]. The etiology of obesity in children, as in adults, is caused by different environmental, genetic, and epigenetic factors [3,5].
The long non-coding RNA (lncRNA) class of human genes is the most prevalent type of non-coding RNA transcriptional unit in humans. By now, it is widely accepted that the majority of human genes do not encode proteins, and that most non-coding genes are transcribed as lncRNAs [6]. LncRNAs are commonly defined as transcripts that are longer than 200 nucleotides and have the function of RNAs without being further translated into proteins [7,8]. Recent studies have pointed towards exploring the possible regulatory roles of lncRNAs in obesity development and progression, and their effect on metabolic homeostasis, adipogenesis, and insulin function [9,10]. One of the best-characterized lncRNA, isolated early in the history of the field and since studied using a variety of methods, is the metastasis-associated lung adenocarcinoma transcript 1 (MALAT1), also referred to as NEAT2. The MALAT1 gene is located on human chromosome 11q13, and is 8.7 kb in length. It is a highly evolutionarily conserved lncRNA, and it was initially identified in the early stage of non-small cell lung cancer, from which the name is derived [11]. The lncRNA MALAT1 functions mostly in the nucleus, and regulates gene transcription [12]. MALAT1 is involved in tumorigenesis and metastasis [11]. Recent research has reported that MALAT1 promotes lipid accumulation in the liver [13] and hyperglycemia-induced inflammation [14]. It also attenuates the function of pancreatic β cells and suppresses insulin secretion [15]. Another well-studied lncRNA gene, H19, is imprinted maternally expressed. H19 is a 3.0 kb gene that is located on the human chromosome 11p15.5. H19 was the first lncRNA to be discovered in the human genome [16]. H19 has been widely investigated due to its involvement in cell growth regulation, and has maximum expression in various tissues during embryogenesis [17]. LncRNA H19 also plays an important role in metastasis and osteoblast differentiation, through transcriptional, post-transcriptional, mRNA quality control and other epigenetic regulatory mechanisms [18,19]. Moreover, H19 participates in lipogenesis regulation, adipose tissue metabolism, and insulin sensitivity, and consequently plays a role in obesity pathogenesis [20].
The advent of genome-wide association studies (GWAS) has been essential to uncovering the contribution of non-coding genomes, including lncRNA genes, to common diseases with a genetic component, such as obesity [6,21]. Many rare and common single-nucleotide polymorphisms (SNPs) in lncRNAs have been shown to contribute to obesity susceptibility. Genetic polymorphisms in lncRNAs may influence their expression and function, and thus increase or decrease an individual’s susceptibility to the disease, to the extent that the lncRNAs are the direct causative contributors rather than mere genetic markers; this feature would help to assess disease risk and clinical prognosis [21,22]. The SNPs rs3200401 in MALAT1 and rs217727 in H19 are associated with increased risk of T2D [23,24] and different types of cancers [25,26]. Several studies have suggested that there is association between the SNPs rs3200401 and rs217727, and the etiological mechanisms of obesity, such as insulin dysregulation, and abnormal lipid and glucose metabolism [13,20,24]. For example, the SNP rs3200401 in MALAT1 is associated with a high concentration of triglycerides [14]. Nonetheless, there have been no reports on the association between rs3200401 and rs217727 and the susceptibility to childhood obesity. To remedy this gap in knowledge, here we have conducted a case-control study with the approval of the bioethics committee of the Academy of Biology and Biotechnology named after D I Ivanovsky of the Southern Federal University (protocol No. 2 of 17 January 2018). We aimed to evaluate the possible associations between the SNPs rs3200401 in MALAT1 and rs217727 in H19, and an individual’s risk of obesity. A further subgroup analysis was performed in order to explore the potential association between rs3200401 and rs217727 and BMI and/or insulin resistance. SNPs were genotyped in DNA samples from 150 children and adolescents from the Russian Federation. This study was motivated by the high prevalence of obesity among children in Russia [27]. Therefore, it is of great value to identify potential diagnostic markers and, in particular, potential new therapeutic targets in order to manage the epidemic of obesity.
2. Results
In this study, we analyzed the genotype distributions of the SNPs rs3200401 in MALAT1 and rs217727 in H19 in 150 children and adolescents aged between 5 and 17 years old. According to their BMI Z-score, participants were divided into two groups: the first was the insulin-sensitive control group that included 50 children and adolescents of a normal weight, and the second was the main comparison group, which included 100 obese children and adolescents. The obese group was further subdivided into two groups (50 insulin-sensitive participants, INS-S, and 50 insulin-resistant participants, INS-R) according to the HOMA-IR values.
2.1. Characteristics of Studied Population
The clinical features of the participants are summarized in Table 1. By conducting the Shapiro–Wilk normality test, we determined the parametric and non-parametric data based on the p-value of the test. When p > 0.05, the data were considered as parametric and have been presented as mean ± standard deviation. Otherwise, when p < 0.05, the data were non-parametric and expressed as a median. Accordingly, total cholesterol and LDL were compared using an ANOVA test. The TG, HDL, VLDL, AC, glucose, insulin and HOMA-IR were analyzed with the Kruskal–Wallis test. The mean ages of the participants were (10.46 ± 3.23), (10.89 ± 3.73), and (13.56 ± 2.43) in the control, INS-S, and INS-R groups, respectively. Our analysis showed no significant difference in the total cholesterol levels among the studied groups, although the levels of HDL (p = 0.0018), LDL (p = 0.0316), VLDL (p < 0.0001), and TG (p < 0.0001) significantly differed among groups. Moreover, there was a significant difference in the levels of insulin (p < 0.0001) and atherogenic coefficient (AC) (p = 0.0138), but not those of glucose (p = 0.3045). HOMA-IR values (p < 0.0001) showed significant variation among the participants, as shown in Table 1.
2.2. Genotype of the SNP rs3200401 in the MALAT1 Gene Has a Positive Association with the Obesity Risk
The genotype distributions of the SNP rs3200401 in the control group conformed to Hardy–Weinberg equilibrium (p = 0.7385). The proportions of homozygous of the major allele CC, heterozygous CT, and homozygous of the minor allele TT were 80, 18 and 2% in the control group, and 48, 46 and 6% in the obese group, respectively. Compared to the CC genotype, there was a significant difference in the frequency of CT (p = 0.0005) between the case and control groups. Our results confirmed the association between SNP rs3200401 in MALAT1 and the risk of obesity (p = 0.0009). We evaluated the association between rs3200401 and the risk of obesity using three genetic models; dominant (CT + TT vs. CC), recessive (TT vs. CC + CT), and allelic (T vs. C). The results revealed that the SNP rs3200401 is associated with obesity in the dominant (OR (95% CI) = 4.333 (1.934–9.319), p = 0.0002) and allelic models (OR (95% CI) = 3.305 (1.64–6.622), p = 0.0004), but not in the recessive model (OR (95% CI) = 3.128 (0.4844–36.57), p = 0.4251); the results are shown in Table 2.
To specifically determine whether the association of SNP rs3200401 with the risk of obesity occurs because of BMI and/or insulin resistance (IR), we analyzed the three genetic models in the subgroups of (control vs. INS-S for BMI) and (INS-S vs. INS-R for IR). Results showed that the SNP rs3200401 is significantly associated with BMI Z-score (p = 0.0002) in the dominant and allelic models. SNP rs3200401 is also associated with insulin resistance (p = 0.0283). The heterozygous genotype CT showed a significant difference in BMI and IR among the studied groups. The recessive model did not show any association in either of the comparison groups. The results of subgroup analysis are clarified in Table 3.
2.3. Genotype of the SNP rs217727 in the H19 Gene Has a Negative Association with the Obesity Risk
No significant deviations from the Hardy–Weinberg equilibrium for SNP rs217727 in H19 were detected in the control group (p = 0.9876). The proportions of homozygous of the major allele GG, heterozygous AG, and homozygous of the minor allele AA were 58.33, 35.42 and 6.25% in the control group, and 56, 38 and 6% in the obese group. Compared to the GG genotype, there was no significant difference in the frequency of the AG nor AA genotypes between the cases and controls (all p > 0.05). None of the three genetic models showed a significant association in the main comparison group nor in the subgroup analysis. SNP rs217727 is therefore not associated with BMI nor with insulin resistance. Results are shown in Table 4.
We also carried out an epistasis analysis of the SNPs rs3200401 in MALAT1 and rs217727 in H19, but did not find a significant association, which is explicable by the lack of any known direct interaction between these two RNAs in the same complex or network.
3. Materials and methods
3.1. Ethics Statement
This study was approved by the bioethics committee of the Academy of Biology and Biotechnology named after D I Ivanovsky of the Southern Federal University (protocol No. 2 of 17 January 2018). The applied methods were carried out in compliance with the World Medical Association Declaration of Helsinki: “ethical principles for medical research involving human subjects” [28], and the articles 20, 22, 23 of the Federal Law N 323-FZ of 21 November 2011. It was also carried out “on the basics of public health protection in the Russian Federation” (as amended on 26 May 2021). According to the norms of bioethics, all parents of the children and adolescents participating in this study were previously informed in detail about the objective and content of the research, and signed a written informed consent form before donating any biological samples.
3.2. Study Participants and Sample Collection
This case-control study comprised 150 children and adolescents aged between 5 and 17 years old. Participants were recruited between 10 January 2018 and 31 December 2019 in the Children’s Municipal Polyclinic No. 4 in Rostov-on-Don, Russian Federation, under the guidance of the head of the department and the chief physician of the polyclinic of Rostov State Medical University. Whole blood samples were collected from participants after an overnight fasting (10–12 h).
3.3. Biochemical Analysis and Obesity Assessment
Biochemical analysis was carried out in the clinical and diagnostic laboratory of the medical center “Nauka” (Rostov-on-Don, Russian Federation) to measure the following: total cholesterol (TChol), triglycerides (TG), high-density lipoprotein cholesterol (HDLc), low-density lipoprotein cholesterol (LDLc), and very low-density lipoprotein cholesterol (vLDLc) concentrations. Circulating levels of glucose and insulin were also determined. Other detailed clinical information about the study population, including age and gender, are shown in Table 1.
Children and adolescents were classified into a normal weight insulin-sensitive control (n = 50) group and a total obese (n = 100) group, according to the BMI Z-score (the standard deviation from the normal body mass index of the same-age same-sex child exemplar) and as clarified by the WHO standards (underweight children < −2 SD, normal weight is between −1 and +1, overweight is between +1 and +2 and obese children are over > +2) [29,30]. This was the main group comparison of the research. Furthermore, the obese group was divided into two insulin-sensitive (INS-S) and insulin-resistant (INS-R) subgroups based on their insulin sensitivity and resistance status, which had been evaluated by calculating the homeostasis model assessment of insulin resistance (HOMA-IR). The HOMA-IR was determined by using the following formula: [fasting insulin (µLU/mL) * fasting glucose (mmol/L)/22.5].
3.4. SNP Selection
Using the dbSNP database (https://www.ncbi.nlm.nih.gov/snp/ (accessed on 21 September 2022)), we selected all the SNPs within the lncRNA genes MALAT1 and H19 with a minor allele frequency >5%. After screening the database for evidence of SNPs in MALAT1 and H19 genes that have an association with obesity and metabolic dysregulation, two candidate SNPs were selected: rs3200401 in MALAT1 and rs217727 in H19. The rs3200401 and rs217727 had been, in other studies and populations, reported to be associated with abnormal lipid profile and metabolic disorders such as T2D [14,23,24].
3.5. DNA Extraction and Genotyping
DNA was extracted and SNPs were genotyped in the laboratory of the Genetic Institute of the Academy of Biology and Biotechnology named after D I Ivanovsky of the Southern Federal University. Genomic DNA was isolated from peripheral blood leukocytes using the thermocoagulation method and using the “DNA express blood” kit applied by Lytech Company (Moscow, Russian Federation, https://lytech.ru/ (accessed on 15 May 2018)). The single nucleotide polymorphisms rs3200401 in MALAT1 and rs217727 in H19 were genotyped using the TaqMan SNP Genotyping Assay in the Applied Biosystems™ QuantStudio™ 5 Real-Time PCR System (Applied Biosystems, Waltham, MA, USA) The RT-PCR reagents with specific primer/probe sets were synthesized and applied by Syntol Company (Moscow, Russia, http://www.syntol.ru/about/ (accessed on May 2022)). Primer and probe sequences are available upon request. No template sample was used as a negative control in the assays. In total, 10% of samples were chosen randomly to repeat the genotyping, and the results were 100% consistent. The reaction mixture (25 μL) contained 10 μL of 2.5 TaqMan® Genotyping Master Mix (Syntol, Moscow, Russian Federation), 0.25 μL of MgCl2, 0.5 μL of each primer, 0.25 μL of each probe, 8.25 μL of ddH2O and 5 μL of genomic DNA for each SNP. For MALAT1 rs3200401 SNP, the PCR program was set at 95 °C for 10 min; this was followed by 40 cycles at 95 °C for 15 s and 60 °C for 90 s. For H19 rs217727, there was one cycle at 95 °C for 5 min, then 40 cycles at 95 °C for 15 s and 60 °C for 40 s.
3.6. Statistical Analysis
The obtained data from the biochemical analysis and genotyping were computed and analyzed by GraphPad Prism, version 8.0.1 (https://www.graphpad.com (accessed on 5 December 2018)) software. Continuous data were tested for normality by the Shapiro–Wilk test. The parametric data were presented as means ± standard deviation (SD), and then analyzed using a one-way ANOVA test. The non-parametric data were presented as a median and were compared using the Kruskal–Wallis test. The Hardy–Weinberg equilibrium (HWE) was assessed by comparing the expected frequencies with the observed genotype frequencies among the control group using a chi-squared (χ2) test. The differences in the distribution of the categorical variables (genotypes) in the studied groups were evaluated by Fisher’s test. The association between the genotypes and obesity risk were assessed using the odds ratio (OR) with 95% confidence interval (CI). A p-value < 0.05 was considered statistically significant. For the epistasis analysis of the studied polymorphisms, a Multifactor Dimensionality Reduction v.1.1.0 (MDR) software was used (www.epistasis.org/mdr.html (accessed on 24 December 2014)) [31]. MDR is used to study intergenic interactions in polygenic diseases for case-control studies. The model with the lowest prediction error and the highest reproducibility was chosen among all the obtained models. To minimize type one statistical errors in the MDR analysis, we used Bonferroni correction. The differences were considered significant if the respective p values were less than (pbonf = 0.006).
4. Discussion
As we enter the third decade of the post-genomic era, the role of the non-coding parts of the human genome in diseases is becoming progressively better elucidated. An increasing number of lncRNAs have been recently linked to multiple pathogenesis mechanisms, including those underlying cancers, and developmental and metabolic disorders, as reported in lncRNA and the Disease Database (http://www.rnanut.net/lncRNAdisease/ (accessed on 15 May 2018)) [8,22,32]. Currently, LncRNAs that participate in the regulation of the metabolic pathways that lead to obesity are being investigated. In fact, both functional and population genomics approaches have been employed to highlight numerous lncRNAs as putative contributors to obesity [9,10,33]. This includes the widely studied MALAT1 and H19 lncRNAs, previously discovered in other contexts and more recently assigned to obesity-relevant roles. Most of the studies on these two lncRNAs focus on their role in cancer [11,17]. However, there is a recent tendency towards identifying their involvement in the pathogenic mechanisms of obesity, such as fat accumulation, insulin dysfunction and impaired lipid and glucose metabolism. In mice, MALAT1 suppresses insulin secretion by inhibiting PDX-1 expression in β cells, and MALAT1 depletion improves insulin secretion and signaling in response to glucose [34]. Another study found that MALAT1 regulates liver steatosis by promoting the accumulation of lipids in the hepatocytes [13]. H19 is an imprinted oncofetal gene, and encodes a lncRNA transcript involved in the inhibition of adipocyte differentiation in bone marrow mesenchymal stem cells [18]. It has been recently reported that H19 regulates lipogenesis by regulating the expression level of acetyl-CoA carboxylase, fatty acid synthesis and PPAR-Ƴ genes [20]. Furthermore, H19 induces hepatic glucose production [35] and gluconeogenesis [36] in the liver, which promotes hyperglycemia and insulin resistance. Many human disease risk loci map to MALAT1 and H19, which is consistent with the ubiquitous and high expression of these two lncRNAs in diverse tissues. In our study, we selected two candidate SNPs based on the published evidence showing that these SNPs are associated with an abnormal metabolic profile and disorders; however, the specific underlying mechanism remains to be elucidated. By searching the lncRNA SNP database (http://bioinfo.life.hust.edu.cn/lncRNASNP/ (accessed on 4 January 2018)), we found that rs3200401 in MALAT1 and rs217727 in H19 cause changes in the secondary structure of the lncRNA transcripts, which may lead to the loss or gain of the interactional function with other molecules. Our findings were supported by a study by Miao et al. [37], which suggested that the C > T status of rs3200401 could alter the sponging function of MALAT1 by changing its structure, which will lead to the loss of the hsa-miR–1324 miRNA binding site along this lncRNA. McCown et al. [38] demonstrated, based on RNAfold software, that rs3200401 decreases the stability of the hairpin domain of MALAT1, which means that the miR-217-5p cannot access its binding site as easily. Another study showed that H19 rs217727 may alter a local folding structure of lncRNA H19, thus affecting the functional interactions of H19 [39]. The SNPs rs3200401 in MALAT1 and rs217727 in H19 are associated with an increased risk of T2D and an irregular lipid profile [23,24]. However, no research has previously been conducted to evaluate their association with an individual’s susceptibility to childhood obesity, at least among Russian children. Accordingly, we performed this case-control study with 150 children and adolescents as a pilot investigation into the association between MALAT1 rs3200401 and H19 rs217727, and obesity in children and adolescents aged between 5 and 17 years old. The results showed that MALAT1 rs3200401 has a positive association with an individual’s susceptibility to obesity (p = 0.0009). The heterozygous CT genotype increased the risk of obesity, compared to the CC wild genotype (p = 0.0005). Moreover, the dominant (p = 0.0002) and allelic (p = 0.0004) genetic models revealed a significant association. To determine whether this association is more a function of increased BMI or of insulin resistance, we further divided the obese group according to their HOMA-IR values, into insulin-sensitive and insulin-resistant groups, and tested all the genetic models of rs3200401. The findings demonstrated that rs3200401 was significantly associated with BMI (p = 0.0002) and with insulin resistance (p = 0.0283). The heterozygous genotype CT of rs3200401 showed a significant difference when compared to the CC homozygous genotype of the major allele; thus, it can be considered as a risk factor for both an increased BMI and insulin resistance in children and adolescents from Russia. The CT genotype may be implicated in lipogenesis, fat accumulation, glucose metabolism, insulin secretion or signaling processes, but the molecular mechanism remains to be clarified. No effect of H19 rs217727 on obesity susceptibility (all p > 0.05) was revealed. Our study admittedly has several limitations. First, the participants were enrolled from only one polyclinic and hence represented merely a single location within one city. Secondly, the sample size was very low compared to typical obesity GWAS studies, such as those of the CHARGE Consortium and its related efforts, which include thousands of samples. Thirdly, the age range of children and adolescents was not used as an independent variable or as a criterion. However, the genotype distributions of the control group respected the HWE. Fourth, obesity has a polygenic nature, with complex gene–environment interactions; therefore, environmental factors should also be considered in any integrated future risk assessment. Indeed, they might help to unravel significant patterns that are obscured in our current analysis and to functionally pinpoint links between these lncRNAs’ interactions with environmental signals and the development of obesity. Additional studies that encompass a larger sample size of mixed ethnic groups from diverse geographical regions should be performed in order to determine whether these SNPs’ minor alleles confer population-specific risks; this is a possible finding given their significance in other populations in published studies. Understanding the role of different SNPs in the pathogenesis of obesity would serve to provide new markers for diagnosis, and thus pinpoint these, and other, lncRNAs as new potential targets for use in treatment and management strategies amidst the growing interest in drug-targeting the non-coding transcriptomes.
5. Conclusions
In conclusion, we found that the MALAT1 rs3200401 SNP is associated with the risk of obesity in Russian children and adolescents. The heterozygous genotype CT can be considered as a risk factor for increased BMI and insulin resistance in children. However, the rs217727 SNP in H19 has no association with BMI nor with IR in our studied group. The specific underlying molecular mechanism remains to be investigated. Future studies are required to validate our findings in a larger sample of different populations and ethnic groups.
Author Contributions
T.P.S. was responsible for conceptualization, methodology, funding acquisition, project administration, supervision and the review and editing of the manuscript. M.A. was responsible for data curation, formal analysis, software, and writing the original draft with the visualization. O.B., E.T. and A.A. were responsible for data curation, formal analysis, methodology and resources. R.A. was responsible for software and visualization. L.L. was responsible for supervision and validation. All authors have read and agreed to the published version of the manuscript.
Funding
This research was funded by the Ministry of Science and Higher Education of the Russian Federation, grant number FENW-2023-0018.
Institutional Review Board Statement
The study was conducted in accordance with the World Medical Association Declaration of Helsinki, and the articles 20, 22, 23 of the Federal Law N 323-FZ of 21 November 2011. And approved by the bioethics committee of the Academy of Biology and Biotechnology named after D I Ivanovsky of the Southern Federal University (protocol No. 2 of 17 January 2018).
Informed Consent Statement
Written informed consent was obtained from parents of all children and adolescents involved in the study before obtaining any biological sample for scientific and publication purposes.
Data Availability Statement
The data supporting the findings of this study are available within the article.
Acknowledgments
The researchers thank the Children’s Municipal Polyclinic No. 4 and the clinical and diagnostic laboratory of the medical center Nauka for recruiting the study population and providing the biological materials.
Conflicts of Interest
The authors declare there are no conflict of interest of any nature.
Abbreviations
| AC | Atherogenic coefficient |
| BMI | Body mass index |
| CI | Confidence interval |
| GWAS | Genome-wide association studies |
| HDLc | High-density lipoprotein cholesterol |
| HOMAIR | Homeostatic Model Assessment for Insulin Resistance |
| IR | Insulin resistance |
| LDLc | Low-density lipoprotein cholesterol |
| LncRNA | Long non-coding RNA |
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Table 1.
Characteristics of the studied groups.
| Control | INS-S | INS-R | p-Value | |
|---|---|---|---|---|
| n = 50 | n = 50 | n = 50 | ||
| Age | 10.46 ± 3.23 | 10.89 ± 3.73 | 13.56 ± 2.43 | |
| Gender | ||||
| Male | 32 | 28 | 32 | |
| Female | 18 | 22 | 18 | |
| Total cholesterol | 3.93 ± 0.7 | 3.80 ± 0.8 | 3.84 ± 0.7 | 0.6551 |
| HDL | 1.41 ± 0.35 | 1.45 ± 0.39 | 1.15 | 0.0018 |
| LDL | 2.24 ± 0.54 | 1.97 ± 0.63 | 1.97 ± 0.61 | 0.0316 |
| VLDL | 0.29 | 0.38 | 0.65 ± 0.32 | <0.0001 |
| TG | 0.59 | 0.77 | 1.32 ± 0.66 | <0.0001 |
| AC | 1.71 | 1.75 | 2.37 ± 0.99 | 0.0138 |
| Glucose | 4.84 | 4.83 ± 0.5 | 4.97 ± 0.81 | 0.3045 |
| Insulin | 11.68 ± 3.87 | 16.59 ± 4.8 | 37.14 | <0.0001 |
| HOMA-IR | 2.51 ± 0.9 | 3.32 | 7.82 | <0.0001 |
Table 2.
Genotype distributions and allele frequencies of SNP rs3200401 in MALAT1 gene in control vs. total obese group.
Table 2.
Genotype distributions and allele frequencies of SNP rs3200401 in MALAT1 gene in control vs. total obese group.
| Obese n (%) | Controls n (%) | p | OR (95% CI) | ||
|---|---|---|---|---|---|
| Control vs. Total obese | Genotype | 100 | 50 | 0.0009 | |
| CC | 48 (48%) | 40 (80%) | R 1 | ||
| CT | 46 (46%) | 9 (18%) | 0.0005 | 4.259 (1.93–10.18) | |
| TT | 6 (6%) | 1 (2%) | 0.4251 | 3.128 (0.4844–36.57) | |
| CT + TT | 52 | 10 | 0.0002 | 4.333 (1.934–9.319) | |
| Alleles | |||||
| C | 142 (71%) | 89 (89%) | R | ||
| T | 58 (29%) | 11 (11%) | 0.0004 | 3.305 (1.64–6.622) |
1 Reference genotype/allele.
Table 3.
Genotype distributions and allele frequencies of SNP rs3200401 in MALAT1 gene in control vs. INS-S and INS-S vs. INS-R groups.
Table 3.
Genotype distributions and allele frequencies of SNP rs3200401 in MALAT1 gene in control vs. INS-S and INS-S vs. INS-R groups.
| INS-S n | Control n | ||||
|---|---|---|---|---|---|
| Control vs. INS-S | Genotype | 50 | 50 | 0.0002 | |
| CC | 20 (40%) | 40 (80%) | R | ||
| CT | 29 (58%) | 9 (18%) | <0.0001 | 6.444 (2.61–15.21) | |
| TT | 1 (2%) | 1 (2%) | >0.9999 | 1 (0.05168–19.35) | |
| CT + TT | 30 | 10 | <0.0001 | 6 (2.529–14.43) | |
| Alleles | |||||
| C | 69 (69%) | 89 (89%) | R | ||
| T | 31 (31%) | 11 (11%) | 0.0008 | 3.635 (1.731–8.025) | |
| INS-R n | INS-S n | ||||
| INS-S vs. INS-R | Genotype | 50 | 50 | 0.0283 | |
| CC | 28 (56%) | 20 (40%) | R | ||
| CT | 17 (34%) | 29 (58%) | 0.0422 | 0.4187 (0.1803–0.9964) | |
| TT | 5 (10%) | 1 (2%) | 0.2044 | 5.444 (0.6843–65.28) | |
| CT + TT | 22 | 30 | 0.1609 | 0.5238 (0.2449–1.173) | |
| Alleles | |||||
| C | 73 (73%) | 69 (69%) | R | ||
| T | 27 (27%) | 31 (31%) | 0.6404 | 0.8232 (0.4536–1.551) |
Table 4.
Genotype distributions and allele frequencies of SNP rs217727 in H19 gene in control vs. obese, control vs. INS-S, and INS-S vs. INS-R groups.
Table 4.
Genotype distributions and allele frequencies of SNP rs217727 in H19 gene in control vs. obese, control vs. INS-S, and INS-S vs. INS-R groups.
| Obese n | Controls n | p | OR (95% CI) | ||
|---|---|---|---|---|---|
| Control vs. Total obese | Genotype | 100 | 48 | 0.9547 | |
| GG | 56 (56%) | 28 (58.33%) | R | ||
| GA | 38 (38%) | 17 (35.42%) | 0.8536 | 1.118 (0.5305–2.317) | |
| AA | 6 (6%) | 3 (6.25%) | >0.9999 | 0.9574 (0.255–3.622) | |
| GA + AA | 44 | 20 | 0.8601 | 1.1 (0.5542–2.264) | |
| Alleles | |||||
| G | 150 (75%) | 73 (76.04%) | R | ||
| A | 50 (25%) | 23 (23.96%) | 0.8863 | 1.058 (0.604–1.905) | |
| INS-S n | Controls n | ||||
| Control vs. INS-S | Genotype | 50 | 48 | 0.7967 | |
| GG | 26 (52%) | 28 (58.33%) | R | ||
| GA | 21 (42%) | 17 (35.42%) | 0.5318 | 1.33 (0.594–3.059) | |
| AA | 3 (6%) | 3 (6.25%) | >0.9999 | 0.9574 (0.2148–4.27) | |
| GA + AA | 24 | 20 | 0.5492 | 1.292 (0.5659–2.755) | |
| Alleles | |||||
| G | 73 (73%) | 73 (76.04%) | R | ||
| A | 27 (27%) | 23 (23.96%) | 0.7433 | 1.174 (0.6147–2.289) | |
| INS-R n | INS-S n | ||||
| INS-S vs. INS-R | Genotype | 50 | 50 | 0.7023 | |
| GG | 30 (60%) | 26 (52%) | R | ||
| GA | 17 (34%) | 21 (42%) | 0.5286 | 0.7016 (0.3081–1.553) | |
| AA | 3 (6%) | 3 (6%) | >0.9999 | 1 (0.2244–4.455) | |
| GA + AA | 20 | 24 | 0.5459 | 0.7222 (0.341–1.627) | |
| Alleles | |||||
| G | 77 (77%) | 73 (73%) | R | ||
| A | 23 (23%) | 27 (27%) | 0.6245 | 0.8076 (0.4159–1.54) |
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Shkurat, T.P.; Ammar, M.; Bocharova, O.; Teplyakova, E.; Aleksandrova, A.; Ali, R.; Lipovich, L. The Role of Genetic Variants in the Long Non-Coding RNA Genes MALAT1 and H19 in the Pathogenesis of Childhood Obesity. Non-Coding RNA 2023, 9, 22. https://doi.org/10.3390/ncrna9020022
AMA Style
Shkurat TP, Ammar M, Bocharova O, Teplyakova E, Aleksandrova A, Ali R, Lipovich L. The Role of Genetic Variants in the Long Non-Coding RNA Genes MALAT1 and H19 in the Pathogenesis of Childhood Obesity. Non-Coding RNA. 2023; 9(2):22. https://doi.org/10.3390/ncrna9020022
Chicago/Turabian StyleShkurat, Tatiana Pavlovna, Manar Ammar, Olga Bocharova, Elena Teplyakova, Anzhela Aleksandrova, Ruba Ali, and Leonard Lipovich. 2023. "The Role of Genetic Variants in the Long Non-Coding RNA Genes MALAT1 and H19 in the Pathogenesis of Childhood Obesity" Non-Coding RNA 9, no. 2: 22. https://doi.org/10.3390/ncrna9020022
APA StyleShkurat, T. P., Ammar, M., Bocharova, O., Teplyakova, E., Aleksandrova, A., Ali, R., & Lipovich, L. (2023). The Role of Genetic Variants in the Long Non-Coding RNA Genes MALAT1 and H19 in the Pathogenesis of Childhood Obesity. Non-Coding RNA, 9(2), 22. https://doi.org/10.3390/ncrna9020022
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