The CYP7A1 gene rs3808607 variant is associated with susceptibility of tuberculosis in Moroccan population
Mounia Qrafli, Youssef Amar, Jamaleddine Bourkadi, Jouda Ben Amor, Ghali Iraki, Youssef Bakri, Saad Amzazi, Ouafae Lahlou, Fouad Seghrouchni, Rajae El Aouad, Khalid Sadki
The Pan African Medical Journal. 2014;18:1. doi:10.11604/pamj.2014.18.1.3397

Innovations in Measles Elimination Innovations in Measles Elimination
"Better health through knowledge sharing and information dissemination "


The CYP7A1 gene rs3808607 variant is associated with susceptibility of tuberculosis in Moroccan population

Cite this: The Pan African Medical Journal. 2014;18:1. doi:10.11604/pamj.2014.18.1.3397

Received: 19/09/2013 - Accepted: 22/04/2014 - Published: 01/05/2014

Key words: Tuberculosis, cholesterol 7-alpha-hydroxylase, polymorphisms, SNPs, cholesterol

© Mounia Qrafli et al. The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Available online at:

Corresponding author: Khalid Sadki, Laboratory of Biochemistry and Immunology, Faculty of Sciences, University Mohammed V-Agdal, Rabat, Morocco. 4, Avenue, Ibn battouta BP1014. (

The CYP7A1 gene rs3808607 variant is associated with susceptibility of tuberculosis in Moroccan population


Mounia Qrafli1,2, Youssef Amar2, Jamaleddine Bourkadi3, Jouda Ben Amor3, Ghali Iraki3, Youssef Bakri2, Saad Amzazi2, Ouafae Lahlou1, Fouad Seghrouchni1, Rajae El Aouad1, Khalid Sadki2,&


1Laboratory of Human Genomic, National Institute of Hygiene, Rabat, Morocco, 2Laboratory of Biochemistry and Immunology, Faculty of Sciences, University Mohammed V, Rabat, Morocco, 3Department of Pneumophtisiology, Moulay Youssef Hospital, Rabat, Morocco.



&Corresponding author
Khalid Sadki, Laboratory of Biochemistry and Immunology, Faculty of Sciences, University Mohammed V-Agdal, Rabat, Morocco. 4, Avenue, Ibn battouta BP1014.




Introduction: Despite the medical progress in treatment. Tuberculosis (TB) continues to be a serious global health problem. A genome-wide linkage study identified a major susceptibility locus on chromosomal region 8q12-q13 in Moroccan TB patients. The CYP7A1 gene is located in this region and codes for cholesterol 7a-hydroxylase, an enzyme involved in cholesterol catabolism.


Methods: We selected three SNPs (rs3808607, rs8192875 and rs8192879) and studied their genotype and allele frequencies distribution in patients with pulmonary (PTB) or pleural TB (pTB), and compared them to Healthy Controls (HC). Genotyping of rs8192875 and rs8192879 SNPs was carried out using the Taq Man SNP genotyping Assay while rs3808607 was investigated by PCR-RFLP.


Results: We reported here for the first time a statistically significant increase in the AA homozygote genotype frequency of rs3808607 in PTB patients compared to HC (p = 0.02, OR = 1.93, 95% CI: 1.93 (1.07;3.49). The increased risk of developing TB was maintained when we combined the groups of patients (PTB-pTB) (p = 0.01, OR= 1.91, 95% CI = (1.07 - 3.42). In contrast, no genetic association was observed between the rs8192875 or rs8192879 polymorphisms and TB.


Conclusion: Our investigations suggest that rs3808607 may play a role in susceptibility to TB in a Moroccan population.




Tuberculosis (TB) is one of the oldest diseases to still affect the human race and is the cause of high mortality and morbidity worldwide. According to the seventeenth global report on TB published by the World Health Organization (WHO) the numbers of TB patients will increase in coming decades [1]. It has been estimated that one-third of the worlds population is infected by Mycobacterium tuberculosis (Mtb). However, approximately only 10 % develop the disease, which suggests that TB is due to an as yet unde@257;ned risk factor.

Host cholesterol levels have been implicated in the outcome of mycobacterial infections. It has been found that TB patients have a low serum level of cholesterol so hypocholesterolemia was proposed as a risk factor for TB [2]. Cholesterol has been considered for treatment of pulmonary TB since a cholesterol-rich diet signi?cantly accelerated the bacteriological sterilization of sputum of pulmonary tuberculosis patients [3]. Furthermore, it has been observed that the total serum cholesterol, HDL-C and LDL-C correlated with the evaluated radiological extent of the disease and the degree of smear positivity in pulmonary TB patients [4]. Likewise, molecular and biochemical analyses suggested that the development of the human TB granuloma to caseation correlated with pathogen-mediated dysregulation of host lipid metabolism [5]. Several studies have demonstrated the important role played by cholesterol in the function of the immune system [6,7]. Cholesterol is required for the adequate development of the cytotoxic function of human lymphocytes [6]; it participates in cytotoxic lymphocyte differentiation and proliferation [7]. Furthermore, lipid rafts (LR), plasma membrane microdomain enriched in cholesterol and sphingolipid, are involved in diverse signaling pathways of the immune system. It has been shown that δγ T cells stimulation by Mtb antigens induces LR aggregation suggesting contribution of LR to δγ T cells activation [8]. Importantly, in view of the toxicity associated with the accumulation in Mtb of some cholesterol metabolites such cholest-4-en-3-one [9], it has been suggested that the cholesterol degradation pathway could be an interesting avenue for the development of new anti-tuberculosis agents [10]. It has been reported that host cholesterol is also involved in Mtb infection and persistence [11,12]. Moreover, several studies have reported the important role played by LR in the pathogenesis of Mtb infections [13]. So the implication of cholesterol in determining the fate of TB is still not completely understood. Nevertheless, there is a yet undefined link between TB and cholesterol. The homeostasis of cholesterol is regulated principally by the cholesterol 7-alpha-hydroxylase pathway. The CYP7A1 gene codes for cholesterol 7-alpha-hydroxylase (CYP7A1), a cytochrome P450 that plays an essential role in maintaining a balance in cholesterol and bile acid since its catalytic reaction is the rate-limiting step and the major step in regulating homeostasis of cholesterol and bile acids [14]. The CYP7A1 gene spans about 10 kb and contains 6 exons, 5 introns, one 5-UTR, and one 3-UTR and is localized on chromosome 8q12.1.

Genetic variations in the CYP7A1 gene have been associated with metabolic disorders of cholesterol and bile acids, in addition to a risk of developing several diseases. In this context, it has been reported that a polymorphism in the promoter region of CYP7A1 named -278 A>C (rs3808607), from the translation initiation codon, or -204 A>C from the transcriptional start site were found to be associated with hypercholesterolemia-hyperlipidemia [15-17], a risk of atherosclerosis [18], colorectal cancer [19] and hypertension [20]. In addition, a CYP7A1 enzyme deficiency caused by a homozygous 13021303 delTT deletion mutation in CYP7A1 exon 6, leading to a frameshift (L413fsX414), has been linked to a hypercholesterolemic phenotype [16]. Importantly, CYP7A1 gene is located within an interesting chromosomal region, the 8q12-q13 that is associated with pulmonary TB in a Moroccan population [21]. In the present study, we examined the polymorphism of three SNPs located in the CYP7A1 gene and evaluated their impact on susceptibility to TB of a Moroccan population by using a case-control approach.




Study designs

Three hundred and twenty-four informed and unrelated adult volunteers were recruited for this immunogenetic study during two years, as of 2010. TB patients were represented by 136 PTB patients with sputum positive for acid-fast staining and mycobacterial culture and 50 pTB patients biopsy positive for granulomatous lesions and mycobacterial culture. All patients were tuberculin skin test positive. Patients were recruited from 19 public health centres, including the Centers of TB Treatment and Respiratory Disease (CTRD) and the university hospitals. Healthy controls (HC) included 138 subjects matched for sex and age and were recruited from the Regional Centers of Blood Transfusion (RCBT). All moroccan ethnic groups (Arabs, Sahraoui and Berbers) are equally represented between Patients and healthy subjects.

All HC were tuberculin skin test negative and retained this immunological status during the two years after recruitment to a posterior telephonic check-contact. Ten ml of peripheral blood was collected in ethylenediaminetetraacetic acid tubes from all participants. Structured questionnaires were used to collect all information about demographic parameters and data on the medical history. The observed sex ratio (males /females) for TB patients was almost similar to that of HC (106/30 vs 105/33, respectively). The mean age standard deviation (SD) was 33.43 13.24 years, ranging from 18 to 67 years, and 32.41 11.10 years, ranging from 18 to 61 years, for patients and HC, respectively. All subjects were negatives for HIV-1/2 infection (tested by Axsym Assays, Abbott Laboratories, Chicago, IL, USA). This study was approved by the local ethics committee (Faculty of Medicine and Pharmacy from the Mohammed V-Souissi University) and informed written consent was obtained from all subjects.

CYP7A1 genotyping

DNA extraction: Total genomic DNA was extracted from peripheral blood of all TB patients and HC using QIAampDNA Blood Maxi kit (QIAamp DNA Blood Mini Kit, Qiagen GmbH, Hilden, Germany). DNA samples were stored at -20C until use. CYP7A1 selected SNPs: Three functional SNPs of the CYP7A1 gene were selected for genotyping. When considering their position on the gene and the quality of the mutations we supposed that they could have a potential effect on the expression of the CYP7A1 enzyme: the first SNP rs8192875 C>T is located in the fourth exon and it represents a nonsense mutation. The second SNP rs8192879 C>T is in the 3UTR region, in a linkage disequilibrium block (YRI-B1) [22]. The third SNP rs3808607 A>C is located in the promoter region

Real time PCR genotyping: Two of the three selected SNPs were genotyped by Real time PCR technology for 136 PTB and 138 HC. In fact, rs8192875 and rs8192879 SNP genotyping was performed with a TaqMan Drug Metabolism Genotyping Assays (Applied Biosystems, Foster City, CA). Reactions were performed as recommended by the manufacturer (Applied Biosystems), in a total volume of 25 l containing 1.25 l of Drug metabolism genotyping assay 20 X, 12.5 l of TaqMan 2 X Universal PCR Master Mix (Applied Biosystems) and 11.25 l of DNA sample diluted in DNase-free water. Ampli?cation was carried out for 50 cycles at 92C for 15sec as a denaturation step, followed by an annealing/extension period at 60C for 90 sec, with an initial denaturation period of 10 min at 95C. PCR allelic discrimination was performed on a 7500 Fast Real-Time PCR System (Applied Biosystems, Foster City, CA, USA), which measured the specific allele fluorescence of each sample.

PCR-RFLP Genotyping: The A204C of the CYP7A1 gene was genotyped in 100 PTB, 50 pTB and 100 HC. Genotyping was done by the PCR-BsaI restriction fragment length polymorphism method, using primers 5'-AATGTTTTTCCCAGTTCTCTTTC-3' (sense) and 5'-AATTAGCCATTTGTTCATTCTATTAG-3' (antisense), as described previously (Wang et al., 1998). PCR primers were designed to amplify a product of 393 bp. Briefly, the PCR was performed in a reaction mixture of 10 L containing 0.5 IU of Taq DNA polymerase and 1 L of template DNA with a concentration of approximately 50150 ng/L. Preceded by the initial denaturation at 94C for 4 min, the amplification was carried out for 30 cycles for 30 sec at 94C, 30 sec at 53C and 30 sec at 72C, with a ?nal extension at 72C for 7 min. The PCR product of 393 bp was digested in a total volume of 20 L with 10 IU of BsaI for 3 hr at 50C. After enzymatic digestion two fragments of 93 bp and 300 bp for the A allele, and three fragments of 39 bp, 93 bp and 261 bp for the C allele were obtained. The digested products were visualized and photographed in 3% agarose gels stained with ethidium bromide. To validate the results obtained by PCR-RFLP, the genotyping of some randomly selected samples of each genotype profile were confirmed by DNA sequencing using an automated sequencing system (ABI Prism 3730 Genetic Analyzer), following the manufacturers protocols.

Statistical analysis

The genotype frequencies and allele distribution between patients and HC were estimated by direct counting. The Hardy-Weinberg equilibrium was tested in the first step of statistical analysis. Statistical analysis was carried using EPI INFOTM software, version (Centers for Disease Control and Prevention, Atlanta, GA; 08 September 2012). All results corresponding to p-values below 0.05 were considered statistically significant. Moreover, the odds ratio (OR) with a 95% confidence interval (CI) was calculated to evaluate the risk of association between genotypes or alleles and TB disease.




All genotype frequencies of patients and HC were consistent with respect to the Hardy-Weinberg equilibrium. In fact, each Khi2 value calculated for each SNPs for both patient and HC groups are inferior to 3.84.

CYP7A1 promoter polymorphism and risk of TB

The genotype and allele frequency distribution of the CYP7A1 -204 A>C polymorphism (rs3808607) between PTB and pTB patients and the HC groups are given in Table 1. A significant statistical difference in both the AA genotype and A allele frequencies have been observed between PTB patients and HC (43% vs 28 %, p = 0.026, OR = 1.94, 95% CI = 1.03-3.65 and 65% vs 54%, p = 0.025, OR = 1.58, 95% CI =1.042.4, respectively). The same tendency in the AA genotype and allele frequencies distribution was found between pTB and HC, differences were not statitical reached (42% vs 28%, p>0,05 and 64% vs 54%, p> 0,05, respectively). Furthermore, We observed a significant increase of homozyote AA genotype and A allele frequencies in combined patient groups (PTB - pTB) compared with HC (43% vs 28 %, p =0.018, OR = 1.91, 95% CI= 1.07-3.42 and 65 % vs 54 %, p = 0.016, OR = 1,56 (1.06-2.28), respectively).

rs8192879 CYP7A1 SNP genotyping

Statictical analysis of the rs8192879 polymorphism showed no significant difference in the genotype or allele frequency distribution for HC compared to PTB patients (p> 0,05) (Table 2). At allelic level, we observed a high frequency of C allele than T allele in both PTB patients and HC groups (75.72 % vs 24.28 % and 72.79% vs 27.21%, respectively).

rs8192875 CYP7A1 SNP genotyping

The results regarding the CYP7A1 rs8192875 C>T SNP are shown in Table 3. No homozygous TT or heterozygous CT individuals were observed among neither the PTB patients nor the HC. There was no significant difference in the genotype and allele frequencies distribution between these two groups 100% vs 100% for AA genotype, p > 0,05).

However, there was no significant difference in the genotype and allele frequencies distributions for each SNP between Moroccan ethnic groups (p-value > 0.05) (data not shown).




On the basis of numerous observations, evidence supports the hypothesis of contribution of host genetic factors in determining of susceptibility/resistance to TB [23, 24]. In this context, a previous reported studied genetic association in a Moroccan population with TB and suggested the potential involvement of some genes in the susceptibility or resistance to TB [25-27].

Here, using a candidate gene approach we investigated the association of three genetic variants in the CYP7A1 gene with susceptibility to TB disease. To our knowledge the work presented here reported for the first time the relationship between CYP7A1 gene polymorphism and susceptibility to TB. In fact, to reach this principal objective, we also report for the first time the genotype and allele frequencies distribution in a Moroccan population, which represents a North-African population. Comparison of the allele frequencies of all the SNPs investigated with those reported in HapMap database and in the literature revealed an interesting result: the mutant allele frequency seems to be different for each SNP between Caucasians, Chinese, Nigeria and Japanese populations. Hence, in our population the T allele of rs8192875 C>T could be considered as a rare allele as determined by its allele frequency. This result seems to be similar to that observed in Caucasians and Chinese populations (0 % and 1%, respectively) and little different to that reported in Nigerian and Japanese populations (2% and 6%, respectively). In addition, the T allele frequency of rs8192879 C>T SNP reported here (24.28%) was similar to that observed in Nigerian, Japanese and Chinese populations (22%, 26%, 27 %, respectively). In contrast, this allele frequency is lower than that reported in a Caucasian population (37%).The lack of association between the rs8192875 and rs8192879 polymorphisms and TB disease may indicate that these variations had no effect on conferring predisposition to TB in our population.

Interestingly, the C allele frequency of rs3808607 SNP found in our study is comparable to that reported in Chinese population (45.2 %) [20], and it appears to be relatively higher than that reported in Caucasian (39 %) [17] and North Indian populations (39.8%) [28].This allele may play a protective role since it is negatively associated with TB. Statistical analysis of our data report a significant positive association between the A allele and the AA homozygote genotype of the rs3808607 SNP and TB disease. It seems that AA genotype-carriers had almost a double risk of developing TB disease in our population. Furthermore, in the pTB patient group, the AA homozygote genotype was also found at a higher frequency compared to the HC (42% vs 28%), though this difference failed to reach statistical significance, suggesting a potential contribution of this specificity on susceptibility to pTB disease. The lack of association observed in this case could be attributed to the small size of the pTB patient group.

While we put together all the TB patients into the same group: PTB-pTB, the increase risk of developing TB was still sustained. These finding should be confirmed in a larger population. The genetic association revealed that the promoter region could play an important role in the control of the disease. Earlier studies reported that deletion of the -213 to 91 segment from the CYP7A1 promoter caused a 40 % reduction in the promoter activity suggesting the location of an important regulatory element [29]. The location of this polymorphism in the promoter region could influence the interaction of transcription factors with theirs receptors on this region and consequently could modulate the transcriptional activity of this gene.

Based on the substantial and relevant data concerning on the one hand the function of cholesterol 7 alpha-hydroxylase in regulation of the balance in cholesterol and the crucial role played by cholesterol on the immune system [6, 7] and on the other hand the impact of genetic variations occurring at position -204 at the promoter region of the CYP7A1 gene [16, 19], we can hypothesize on the development of TB disease in patients carrying an AA genotype of the rs3808607SNP. First of all, the AA genotype of CYP7A1 was associated with an elevated low-density lipoprotein (LDL) cholesterol concentration in an Inuit Canadian population but not in Hutterites and Oji-Cree Canadian populations [30]. In addition, a significant increase in serum triglycerides in a healthy normolipidaemic male population and with significantly higher concentrations of total cholesterol in hypertriglyceridemic patients AA genotype carriers it was observed in a Netherlands population [17]. In contrast, others studies reported the opposite results, since the LDL-cholesterol concentrations were higher in CC than AA homozygotes both men and women [15]. Differences in the genetic background of the populations may be among the reasons for these discrepancies. Furthermore, the AA genotype was associated with other diseases such as hypertension in obese male patients [20]. De Castros-Or?s and colleagues suggested that compared with the A-allele, the C-allele variation was associated with enhanced gene expression [31]. According to this observation we could suppose that the AA genotype is associated with decreased gene expression. The -204A allele may participate in the repression of gene expression by increasing the affinity to negative regulators or in an opposite manner by decreasing the affinity to one or more positive regulators acting on the promoter region of the CYP7A1 gene,which is linked the cholesterol metabolism to immune system. This hypothesis is supported by Lu and his colleagues from studies into liver X receptors (LXRs) [32]. LXRs are nuclear receptors that play a central role in the transcriptional control of cholesterol homeostasis. They comprise two members LXRa and LXR?. LXRs are also important for the proper control of genes involved in the innate immune response to bacterial pathogens and mice lacking LXRs were more susceptible to Mtb infection [33].

Interestingly, in a murine model, it has been reported that LXRa stimulates the expression of CYP7A1 via binding to a potent LXR response element (LXRE) present in the CYP7A1 promoter [34]. Additionally, it has been shown that LXRa with LHR-1 can act as a positive gene expression regulator of CYP7A1 in mice [32]. So, we can hypothesize that any genetic variation occurring in this region of the CYP7A1 promoter (LXRE) could theoretically influence CYP7A1 gene expression. The CYP7A1 will be repressed and consequently the cholesterol will be more available to pathogens. As cholesterol is required by Mtb for infection and persistence, it acts as a virulence factor [11, 12]. So, it seems that the AA homozygous subjects were more susceptible to develop TB disease.

Finally, we cannot exclude the possibility that the -204 A allele is in linkage disequilibrium with a yet unidentified functional polymorphism at the CYP7A1 gene itself or other closely located genes directly or indirectly related to immune system pathways implicated in defense against TB. More recently, Grant and colleagues have identified a statistically significant association between two genetic variants (rs2726600 and rs1568952), located within the TOX gene and PTB disease in a Moroccan population [35]. The CYP7A1 gene is located close to the TOX gene and it would be interesting to do a statistical haplotype analysis to evaluate the risk of each variant on the susceptibility in the Moroccan population.




In summary, we identified for the first time a significant association of the A-204C polymorphism of the CYP7A1 gene and development of TB in a Moroccan population. This finding should be confirmed on a larger sample size. In addition, further studies should give a better understanding of the involvement of CYP7A1 in terms of the susceptibility to TB.



Competing interests

The authors declare that they have no competing interest.



Authors contributions

All authors contributed to the conduct of the research and writing of this manuscript. Authors reviewed and approved the final version of the manuscript.




The current study was supported by research grants from the Hassan II Academy of Science and Technology, kingdom of Morocco. We would like to thank all patients and HC for their participation. We are sincerely grateful to the clinicians and nurses of the different prefectures (Marrakech, Rabat, Temara, Fes, Oujda, Tanger and Casablanca) for their contribution to the clinical examinations. All authors declare no conflict of interest concerning the submission of this manuscript.




Table 1: Genotypes and alleles frequencies for the rs3808607CYP7A1 polymorphism in TB (TBP, pTB) patients vs HC

Table 2: Genotypes and alleles frequencies for the rs8192879 CYP7A1 polymorphism in PTB patients and HC

Table 3: Genotypes and alleles frequencies for the rs8192875 CYP7A1 polymorphism in PTB patients and HC




  1. World Health Organization. Global tuberculosis report. 2012. Accessed 30 April 2014.

  2. Prez-Guzmn C, Vargas MH. Hypocholesterolemia: a major risk factor for developing pulmonary TB. Med Hypotheses. 2006; 66(6):12271230. PubMed | Google Scholar

  3. Prez-Guzmn C, Vargas MH, Qui?onez F, Bazavilvazo N, Aguilar A. A cholesterol-rich diet accelerates bacteriologic sterilization in pulmonary TB. Chest. 2005; 127(2):643651. PubMed | Google Scholar

  4. Deniz O, Gumus S, Yaman H, Ciftci F, Ors F, Cakir E, Tozkoparan E, Bilgic H, Ekiz K. Serum total cholesterol, HDL-C and LDL-C concentrations significantly correlate with the radiological extent of disease and the degree of smear positivity in patients with pulmonary TB. Clin Biochem. 2007; 40(3-4):162166. PubMed | Google Scholar

  5. Kim MJ, Wainwright HC, Locketz M, Bekker LG, Walther G, et al. Caseation of Human TB Granulomas Correlates with Elevated Host Lipid Metabolism. EMBO Mol Med. 2010; 2(7):258274. PubMed | Google Scholar

  6. Drabowsky MP, Peel WE, Thomson AER. Plasma membrane cholesterol regulates human lymphocyte cytotoxic function. Eur J Immunol. 1980; 10(11):821827. PubMed | Google Scholar

  7. Heiniger HJ, Marshall JD. Cholesterol synthesis in polyclonally activated cytotoxic lymphocytes and its requirements for differentiation and proliferation. Proc Natl Acad Sci. 1982; 79(12):38233827. PubMed | Google Scholar

  8. L HZ, Zhu AY, Chen Y, Tang J, Li BQ. Formation and aggregation of lipid rafts in δγ Tcells following stimulation with Mycobacterium tuberculosis antigens. J Exp Med. 2011; 233(3):193-198. PubMed | Google Scholar

  9. Ouellet H, Guan S, Johnston JB, Chow ED, Kells PM, et al. Mycobacterium tuberculosis CYP125A1, a steroid C27 monooxygenase that detoxifies intracellularly generated cholest-4-en-3-one. Mol Microbiol. 2010; 77(3):730-742. PubMed | Google Scholar

  10. Ouellet H, Johnston JB, Ortiz de Montellano PR. Cholesterol catabolism as a therapeutic target in Mycobacterium Tuberculosis. Trends Microbiol. 2011; 19(11):530-539. PubMed | Google Scholar

  11. Pandey AK, Sassetti CM. Mycobacterial persistence requires the utilization of host cholesterol. Proc Natl Acad Sci. 2008; 105(11) 43764380. PubMed | Google Scholar

  12. Miner MD, Chang JC, Pandey AK, Sassetti CM, Sherman DR. Role of cholesterol in Mycobacterium TB infection. Indian J Exp Biol. 2009; 47(6):407411. PubMed | Google Scholar

  13. Muoz S, Rivas-Santiago B, Enciso JA. Mycobacterium tuberculosis entry into mast cells through cholesterol-rich membrane microdomains. Scand J Immunol. 2009; 70(3):256263. PubMed | Google Scholar

  14. Schwarz M, Lund EG, Russell DW. Two 7α-hydroxylase enzymes in bile acid biosynthesis. Curr Opin Lipidol. 1998; 9(2):113118. PubMed | Google Scholar

  15. Wang J, Freeman DJ, Grundy SM, Levine DM, Guerra R, Cohen JC. Linkage between cholesterol 7a-hydroxylase and high plasma low-density lipoprotein cholesterol concentrations. J Clin Invest. 1998; 101(6):12831291. PubMed | Google Scholar

  16. Pullinger CR, Eng C, Salen G, Shefer S, Batta AK, Erickson SK, et al. Human cholesterol 7α-hydroxylase (CYP7A1) deficiency has a hypercholesterolemic phenotype. J Clin Invest. 2002; 110(1):109117. PubMed | Google Scholar

  17. Hofman MK, Groenendijk M, Verkuijlen PJJH, Jonkers IJ, et al. Modulating effect of the A?278C promoter polymorphism in the cholesterol 7α-hydroxylase gene on serum lipid levels in normolipidaemic and hypertriglyceridaemic individuals. Eur J Hum Genet. 2004; 12(11):935941. PubMed | Google Scholar

  18. Lambrinoudaki IV, Kaparos GI, Vlachou SA, Stamatelopoulos KS, Georgiopoulos GA, Sergentanis TN, Panoulis CP, Christodoulakos GE, Alexandrou AP, Kouskouni EE, Creatsa MG, Papamichael CM. CYP A-204C polymorphism is associated with subclinical atherosclerosis in postmenopausal women. Menopause. 2008; 15(6):1163-1168. PubMed | Google Scholar

  19. Hagiwara T, Kono S, Yin G, Toyomura K, Nagano J, et al. Genetic Polymorphism in Cytochrome P450 7A1 and Risk of Colorectal Cancer: The Fukuoka Colorectal Cancer Study. Cancer Res. 2005; 65(7):2979-2982. PubMed | Google Scholar

  20. Fu L, Zhao Y, Wu X, Liu H, Shi J, Lu J, Zhou B. CYP7A1 genotypes and haplotypes associated with hypertension in an obese Han Chinese population. Hypertens Res. 2011; 34 (6): 722727. PubMed | Google Scholar

  21. El Baghdadi J, Orlova M, Alter A, Ranque B, Chentoui M, et al. An autosomal dominant major gene confers predisposition to pulmonary TB in adults. J Exp Med. 2006; 203(7):16791684. PubMed | Google Scholar

  22. Nakamoto K, Wang S, Jenison RD, Guo GL, Klaassen CD, YvonneWan YJ, Zhong X. Linkage disequilibrium blocks, haplotype structure, and htSNPs of human CYP7A1 gene. BMC Genet. 2006; 7:29. PubMed | Google Scholar

  23. Kallmann FJ, Reisner D. Twin studies on the significance of genetic factors in tuberculosis. Am Rev Tuberc. 1943; 47:549-574. PubMed | Google Scholar

  24. Yim JJ, Selvaraj P. Genetic susceptibility in tuberculosis. Respirology. 2010; 15(2):241-256. PubMed | Google Scholar

  25. Lamsyah H, Rueda B, Baassi L, Elaouad R, Bottini N, Sadki K, Martin J. Association of PTPN22 gene functional variants with development of pulmonary tuberculosis in Moroccan population. Tissue Antigens. 2009; 74(3):228232. PubMed | Google Scholar

  26. Sadki K, Lamsyah H, Rueda B, Akil E, Sadak A, Martin J, El Aouad R. Analysis of MIF, FCGR2A and FCGR3A gene polymorphisms with susceptibility to pulmonary tuberculosis in Moroccan population. J Genet Genomics. 2010; 37(4):257?264. PubMed | Google Scholar

  27. Arji N, Busson M, Iraqi G, Bourkadi JE, Benjouad A, Boukouaci W, et al. The MCP-1 (CCL2) -2518 GG genotype is associated with protection against pulmonary tuberculosis in Moroccan patients. J Infect Dev Ctries. 2012; 6(1):73-78. PubMed | Google Scholar

  28. Srivastava A, Choudhuri G, Mittal B. CYP7A1 (-204 A>C; rs3808607 and -469 T>C; rs3824260) promoter polymorphisms and risk of gallbladder cancer in North Indian population. Metabolism. 2010; 59(6):767773. PubMed | Google Scholar

  29. Cooper AD, Chen J, Botelho-Yetkinler MJ, Cao Y, Taniguchi T, Levy-Wilson B. Characterization of hepatic-specific regulatory elements in the promoter region of the human cholesterol 7 α-hydroxylase gene. J Biol Chem. 1997; 272(6):34443452. PubMed | Google Scholar

  30. Hegele RA, Wang J, Harris SB, Brunt JH, Young TK, et al. Variable association between genetic variation in the CYP7 gene promoter and plasma lipoproteins in three Canadian populations. Atherosclerosis. 2001; 154(3):579587. PubMed | Google Scholar

  31. De Castros-Orós I, Pampin S, Cofn M, Mozas P, et al. Promoter variant - 204A > C of the cholesterol 7α-hydroxylase gene: Association with response to plant sterols in humans and increased transcriptional activity in transfected HepG2 cells. Clin Nutr. 2011; 30(2):239-246. PubMed | Google Scholar

  32. Lu TT, Makishima M, Repa JJ, Schoonjans K, Kerr TA, Auwerx J, Mangelsdorf DJ. Molecular basis for feedback regulation of bile acid synthesis by nuclear receptors. Mol Cell. 2000; 6(3):507-515. PubMed | Google Scholar

  33. Korf H, Beken SV, Romano M, Steffensen KR, Stijlemans B, et al. Liver X receptors contribute to the protective immune response against Mycobacterium tuberculosis in mice. J Clin Invest. 2009; 119(6):1626 1637. PubMed | Google Scholar

  34. Zhao C, Dahlman-Wright K. Liver X receptor in cholesterol metabolism. J Endocrinol. 2010; 204(3):233240. PubMed | Google Scholar

  35. Grant AV, El Baghdadi J, Sabri A, El Azbaoui S, Alaoui-Tahiri K, Rhorfi IA, et al. Age-Dependent Association between Pulmonary Tuberculosis and Common TOX Variants in the 8q1213 Linkage Region. American J of Hum Genet. 2013; 92(3):407414. PubMed | Google Scholar






















The Pan African Medical Journal articles are archived on Pubmed Central. Access PAMJ archives on PMC here

Volume 33 (May - August 2019)

Article tools

PDF (430 Kb)
Contact the corresponding author
Download to Citation Manager
Reference Manager


Cholesterol 7-alpha-hydroxylase

Rate this article


PAMJ is a member of the Committee on Publication Ethics
PAMJ Authors services
Next abstract

PAMJ is published in collaboration with the African Field Epidemiology Network (AFENET)
Currently tracked by: DOAJ, AIM, Google Scholar, AJOL, EBSCO, Scopus, Embase, IC, HINARI, Global Health, PubMed Central, PubMed/Medline, Ulrichsweb, More to come . Member of COPE.

ISSN: 1937-8688. © 2019 - Pan African Medical Journal. All rights reserved