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Apolipoprotein B gene mutation related to familial hypercholesterolemia in an Iranian population: With or without hypothyroidism
Golnaz Vaseghi1, Zahra Malakoutikhah1, Zahra Shafiee1, Mojgan Gharipour2, Laleh Shariati2, Ladan Sadeghian2, Elham Khosravi2, Shaghayegh Haghjooy Javanmard1, Ali Pourmoghaddas2, Ismail Laher3, Sonia Zarfeshani2, Nizal Sarrafzadegan4
1 Applied Physiology Research Center, Cardiovascular Research Institute, Isfahan University of Medical Sciences, Isfahan, Iran
2 Isfahan Cardiovascular Research Center, Cardiovascular Research Institute, Isfahan University of Medical Sciences, Isfahan, Iran
3 Applied Physiology Research Center, Cardiovascular Research Institute, Isfahan University of Medical Sciences, Isfahan, Iran; Department of Anesthesiology, Pharmacology and Therapeutics, University of British Columbia, Vancouver, Canada
4 Isfahan Cardiovascular Research Center, Cardiovascular Research Institute, Isfahan University of Medical Sciences, Isfahan, Iran; School of Population and Public Health, University of British Columbia, Vancouver, BC, Canada
| Date of Submission | 21-Jan-2020 |
| Date of Decision | 07-Feb-2021 |
| Date of Acceptance | 24-May-2021 |
| Date of Web Publication | 18-Oct-2021 |
Correspondence Address:
Nizal Sarrafzadegan
Isfahan Cardiovascular Research Center, Cardiovascular Research Institute, Isfahan University of Medical Sciences, P.O. Bo × 81465-1148, Isfahan
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/jrms.JRMS_970_19
Background: Familial hypercholesterolemia (FH) leads to elevated low-density lipoprotein cholesterol (LDL-C) levels in plasma. Mutations of its related gene; apolipoprotein B (APOB) is seen in about two percent of the patient with FH. Thyroid disease is usually part of the exclusion criteria for the detection of FH which alters the lipid profile. We evaluated mutations in the APOB gene in patients with high LDL-C levels. Materials and Methods: Patients aged between 2 and 80 years with at least one LDL-C level of more than 190 mg/dl were selected (120 patients) from Isfahan Laboratories. Blood samples were obtained from all patients. Genomic DNA was extracted. Primer sequences were designed by Oligo 7.60 to amplify the desired 844 bp region of exon 26 of the APOB gene containing R3500Q and R3500W variants associated with FH. Results: Overall, two patients showed a heterozygous form of a common pathogenic variant in exon 26 named c. 10579 C > T (R3500W, cDNA.10707), and one patient was hypothyroidism. We also recognized another nonpathognomonic variant c. 10913G > A (rs1801701, cDNA.11041) in 13 patients, two of them were hypothyroidism. Conclusion: This study for the first time shows the coexistence of APOB mutation in hypothyroidism, which emphasis screening of patients with hypothyroid for FH detection.
Keywords: Apolipoprotein B, hypercholesterolemia, hypothyroidism, Iranian
How to cite this article:
Vaseghi G, Malakoutikhah Z, Shafiee Z, Gharipour M, Shariati L, Sadeghian L, Khosravi E, Javanmard SH, Pourmoghaddas A, Laher I, Zarfeshani S, Sarrafzadegan N. Apolipoprotein B gene mutation related to familial hypercholesterolemia in an Iranian population: With or without hypothyroidism. J Res Med Sci 2021;26:94 |
How to cite this URL:
Vaseghi G, Malakoutikhah Z, Shafiee Z, Gharipour M, Shariati L, Sadeghian L, Khosravi E, Javanmard SH, Pourmoghaddas A, Laher I, Zarfeshani S, Sarrafzadegan N. Apolipoprotein B gene mutation related to familial hypercholesterolemia in an Iranian population: With or without hypothyroidism. J Res Med Sci [serial online] 2021 [cited 2023 Apr 2];26:94. Available from: https://www.jmsjournal.net/text.asp?2021/26/1/94/328510 |
| Introduction | |  |
Familial hypercholesterolemia (FH) is a predominant but common inherited autosomal disorder that is associated with a severe or moderate increase in plasma low-density lipoprotein cholesterol (LDL-C) levels.[1] Heterozygous FH (HeFH) is a common form of the disease and patients usually develop early premature coronary heart disease.[2] Early diagnosis and treatment decrease risk of premature death in such patients.[3]
It has been proposed that mutations and/or polymorphisms of some genes can increase LDL-C levels.[4] Common genetic mutations in FH are often seen and reported in the following genes: LDL-C receptor (LDLR), apolipoprotein B (APOB) genes, or proportion converts subtilisin/kexin type-9 (PCSK9).[5] Reductions in receptor activities in patients with LDL R mutations increase LDL-C plasma levels in FH patients.[6] PCSK9 reduces the number of hepatic LDLR and therefore increases LDL-C levels.[7]
Mutations of the APOB gene, which encodes lipoprotein particles,[5] occur in 2.2% of patients with FH.[8] Three APOB mutations have been described to date: APOB R3500Q, APO B R3531C, and APOB R3500W.[9] Replacement of glutamine with arginine at nucleotide 10708 in exon 26 leads to mutation in Apo B R3500Q and decreases the apo B affinity for the LDL receptor.[10] On the other hand, R3500W and R3531C have been identified in R3500W alleles and are found to be associated with diverse haplotypes of chromosomes.[11],[12] However, previous studies in Iranian populations failed to report on mutations of the APOB gene.[13],[14],[15]
The goal of this study was to identify other potential diseases which could occur concurrently with hypercholesterolemia. Hypothyroidism is the most common thyroid disease and is characterized by elevated levels of thyroid-stimulating hormone (TSH) and reduced thyroid hormone levels. Thyroid hormones regulate metabolic rate, lipogenesis, glucose metabolism, food intake, and heat production. Modulation of all these multiple cellular processes affects body mass index, body weight, and percentage of the adipose tissue.[16] Patients with hypothyroidism showed elevated triglyceride (TG), total cholesterol (TC), and LDL-C levels.[17]
Thyroid disease is usually part of the exclusion criteria for the detection of FH because hypothyroidism is a common health condition which can alter the lipid profile. In the present study, mutations in the APOB gene in euthyroid patients and hypothyroidism patients with high levels of LDL have been investigated.
| Materials and Methods | | |
In this study, 120 patients, males or females aged between 2 and 80 years with minimum LDL-C level >190 mg/dl (LDL-C >150 mg/dl with pharmacological treatments) were selected from Isfahan laboratories and contacted by phone for further evaluation (National Clinical Trial No. 2865694).[18]
We excluded secondary causes of hypercholesterolemia but did not exclude patients who had a history of hypothyroidism. Hypothyroidism was defined as TSH level >4.2 μIU/mL + normal or low FT4.[19] All patients were treated, and their TSH levels were normal at the time of evaluation.
Blood sampling and DNA isolation
Blood samples (3 mL) were obtained from all patients followed by genomic DNA extraction from peripheral blood samples using a High Pure Polymerase Chain Reaction (PCR) Template Preparation Kit (version 20) and the standard salting-out method.[20]
Polymerase chain reaction
Primer sequences were designed specifically using Oligo 7.60 software to amplify the 844 bp segment of exon 26 of the APOB gene containing R3500Q and R3500W variants associated with FH. Specificity and affinity of the primers were checked by NCBI primer BLAST.
- Forward primer: ATGGAAGTGTCAGTGGCAAC
- Reverse primer: TGCTGTCTCCTACCAATGCT.
Primers and annealing temperatures
To perform PCR, an Eppendorf gradient type master cycler (Eppendorf, Germany) was used. A volume of 15 μl 2X Master Mix (Biofact®, Korea), 0.8 μl each primer (10 mM), and 1.4 μl genomic DNA were mixed gently, and by adding H2O, it reached the final volume of 20 μl. The reaction conditions set as follow: Initial denaturation step was carried out at 95°C for 5 min, annealing primers for 30 s at 60.8°C, continued by denaturation 32 cycles each cycle at 95°C for 45 s, and final extension at 72°C for 45 s.
Genotyping
Genotyping was performed using an automated Genetic Analyzer ABI 3130XL (Microsynth, Balgach, Switzerland). Chromatograms were compared with genomic reference sequence, NG_011793.1 using SeqMan software version 5.00© (DNASTAR, Madison, WI, USA).
| Results | | |
Genomic DNA was purified, and all the samples showed satisfactory results on agarose gel after PCR step. Demographic and clinical characteristics of the samples are listed in [Table 1]. | Table 1: Demographic feature of patients with low-density lipoprotein>190 mg/kg included in this study
Click here to view |
Sequencing results for APOB gene
A total of 120 of the 121 samples presented suitable results in molecular studies for inclusion in the analysis. The demographic features and genetic studies of patients are shown in [Table 1]. Two of the 120 samples showed a heterozygous form of a common pathogenic variant in exon 26 named c. 10579 C > T (R3500W, cDNA.10707) [Figure 1]a and [Figure 1]b, providing a prevalence of 1.7% for this variant one of them was hypothyroidism. We also recognized another known variant c. 10913G > A (rs1801701, cDNA.11041) in 13 patients [Figure 1]c and [Figure 1]d. This variant was shown to be benign in in-silico analysis. Predictions of pathogenicity of identified variants were verified using online software tools [Table 2]. There were no hypothyroid patients in sample without mutations. All the patients with hypothyroidism were on treatment but had at least one previous LDL-C above 190 mg/dl. | Figure 1: Chromatograms of variants identified in exon 26 of apolipoprotein B gene in patients with familial hypercholestrolemia. (a) Position 10579 of coding DNA (p. R3500W), (b) Position 10579 of coding DNA (p. R3500W), (c) Position 10913 of coding DNA (p. R3638Q) and (d) Position 10913 of coding DNA (p. R3638Q)
Click here to view |
 | Table 2: List of variants and their pathogenicity investigation using software prediction tools
Click here to view |
| Discussion | | |
We report the presence of c. 10579 C > T (R3500W), a common pathogenic FH variant in exon 26 in Iran. Another benign variant, c. 10913G > A (rs1801701), was also identified in 13 patients with FH. Previous studies failed to show mutations in Apo B in FH patients.[21] In studies of 130 patients with hypercholesterolemia by Fard-Esfahani et al., thirty patients had the criteria for FH; however, the R3500Q was not detected in them.[15] Another study in which 16 children with the FH phenotype from five different regions of Iran were screened to detect any possible mutations that may occur in APOB, LDLR, and PCSK9 genes. Of them, 14 had a clinical diagnosis of homozygous FH and 2 were heterozygous FH. They reported no mutations in APOB, but seven different LDLR mutations were identified.[14] The APOB gene, which is located in the 2p24.1 region, is used for the molecular diagnosis of FH. The mutation of the APOB mutation was discovered in phenotypic FH patients with FH who did not have mutations in LDLR.[22]
We identified mutations in two Iranian patients, of which one had a history of hypothyroidism. The patient was receiving treatment with levothyroxine and atorvastatin and her plasma LDL-C was 130 mg/dl. Her fT3 and fT4 levels were normal, indicating that her hypercholesterolemia was not due to hypothyroidism. This finding emphasizes the screening of FH in patients with thyroid diseases. Thyroid hormones modulate the metabolism of glucose and lipid. Hypothyroidism may be due to the decreased 3-hydroxy-3-methyl-glutaryl-coenzyme A reductase activity. Thyroid hormones increase LDL receptors in liver and other tissues, as well as absorption of cholesterol, thereby altering the process of excretion of cholesterol from the intestine by bile acids.
The coexistence of heterozygous FH and hypothyroidism has been reported in previous studies.[23],[24] The coexistence of hypothyroidism and heterozygous FH in adolescent girls was estimated to be about 1 in 500,000, which is similar to the prevalence of homozygous FH in patients with LDL-R mutations.[25],[26]
Another novel finding of our study is of APOB gene mutations and polymorphisms in patients with hypothyroidism [Table 1]. Patients with hypothyroidism and high LDL-C levels had greater reductions in LDL-C after treatment, likely because LDLR-independent mechanisms may be involved in reducing serum cholesterol levels, possibly by induction of Cyp7a1 and increased bile acid synthesis.[27]
Limitations
Our study has a small sample size, and we did not perform LDL-R and PCSK9 sequencing. We did not have access to patient's families, we could not screen for the whole APO B gene.
| Conclusion | | |
The present study reported a mutation in the APO B gene in patients with high cholesterol level and possible phenotype of FH for the first time. Results showed the importance of including patients with thyroid disease in the FH registry, as these patients may be missed if their LDL-C levels are reduced below 150 mg/kg following thyroid hormone replacement.
Acknowledgments
We gratefully acknowledge from Mahdieh Medical Lab in Isfahan city, for their constant cooperation in referring patients with FH. This project would not have succeeded without the sincere efforts of FH staff, so we would also like to thank the colleagues who were involved in this research project.
Financial support and sponsorship
This work was partly supported by the National Institute for Medical Research Development research grant (No 963548). In addition, this work was partly supported by Behestan Darou Co. and Spadan Heart Health Foundation. The funding agencies have no role in the design of the study. Moreover, they played no role in collection, analysis, and interpretation of the data.
Conflicts of interest
There are no conflicts of interest.
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[Figure 1]
[Table 1], [Table 2]
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