- Research article
- Open Access
- Open Peer Review
KCNE1D85N polymorphism — a sex-specific modifier in type 1 long QT syndrome?
© Lahtinen et al; licensee BioMed Central Ltd. 2011
- Received: 11 November 2010
- Accepted: 18 January 2011
- Published: 18 January 2011
Long QT syndrome (LQTS) is an inherited ion channel disorder manifesting with prolongation of the cardiac repolarization phase and severe ventricular arrhythmias. The common KCNE1 D85N potassium channel variant prolongs QT interval by inhibiting IKs (KCNQ1) and IKr (KCNH2) currents and is therefore a suitable candidate for a modifier gene in LQTS.
We studied the effect of D85N on age-, sex-, and heart rate-adjusted QT-interval duration by linear regression in LQTS patients carrying the Finnish founder mutations KCNQ1 G589D (n = 492), KCNQ1 IVS7-2A>G (n = 66), KCNH2 L552S (n = 73), and KCNH2 R176W (n = 88). We also investigated the association between D85N and clinical variables reflecting the severity of the disease.
D85N was associated with a QT prolongation by 26 ms (SE 8.6, p = 0.003) in males with KCNQ1 G589D (n = 213), but not in females with G589D (n = 279). In linear regression, the interaction between D85N genotype and sex was significant (p = 0.028). Within the KCNQ1 G589D mutation group, KCNE1 D85N carriers were more often probands of the family (p = 0.042) and were more likely to use beta blocker medication (p = 0.010) than non-carriers. The number of D85N carriers in other founder mutation groups was too small to assess its effects.
We propose that KCNE1 D85N is a sex-specific QT-interval modifier in type 1 LQTS and may also associate with increased severity of disease. Our data warrant additional studies on the role of KCNE1 D85N in other genetically homogeneous groups of LQTS patients.
- Founder Mutation
- Cardiac Repolarization
- Multiplicative Interaction Term
- LQTS Patient
- Beta Blocker Medication
Long QT syndrome (LQTS) is an inherited arrhythmia disorder associated with risk of torsades de pointes, ventricular fibrillation, and sudden death. LQTS is caused by mutations of the ion channel genes controlling the repolarization phase of the cardiac action potential cycle [1, 2]. The potassium channel KCNE1, also known as minK, regulates both the voltage-gated slowly activating IKs potassium channel [3, 4], encoded by the KCNQ1 gene, and the rapidly activating IKr potassium channel , encoded by the KCNH2 gene. Mutations in KCNE1 underlie the LQT5 subtype of LQTS  and account for approximately 3% of known LQTS mutations . In homozygous form, KCNE1 mutations may cause sensorineural hearing loss in association with LQTS, or Jervell-Lange-Nielsen syndrome .
A common variant D85N of KCNE1 was originally detected by Tesson et al. . This variant has subsequently been shown to slow IKs potassium channel, when studied in Xenopus oocytes , and to exhibit significant loss-of-function effects on both the KCNQ1- and KCNH2-mediated potassium currents, as measured in Chinese hamster ovarian cells . In general population, KCNE1 D85N has a minor allele frequency of 0.8-1.4% [11–13] and is associated with a significant prolongation of the electrocardiographic QT interval [12–14]. Moreover, D85N has been detected in many LQTS patients as a second variant in addition to a more severe mutation [10, 11], as well as in some individuals with drug-induced LQTS .
These findings prompted us to study whether KCNE1 D85N would also modify the QT interval and/or the clinical picture in patients with genetically homogeneous forms of LQTS in which the variability caused by the disease-causing mutation itself can be controlled for. To this end, we took advantage of the unique situation in Finland where four different mutations account for approximately 70% of the known spectrum of LQTS genes  and where the prevalence of molecularly defined LQTS appears to be the highest in the world . Our results indicate a sex-specific QT-prolonging effect for D85N in KCNQ1 mutation carriers.
The study sample consisted of all available (n = 712) carriers of the Finnish LQTS founder mutations, including 492 carriers of KCNQ1 G589D (5 of them also carried KCNH2 R176W, 1 KCNH2 L552S, and 1 a non-founder nonsense mutation KCNQ1 Y171X), 66 carriers of KCNQ1 IVS7-2A>G (1 of them also carried KCNH2 R176W), 73 carriers of KCNH2 L552S (2 of them homozygous), and 88 carriers of KCNH2 R176W. These four founder mutations account for 70%, and KCNQ1 G589D alone 50%, of all Finnish LQTS patients with an established molecular diagnosis of LQTS . The collective prevalence of these four founder mutations in the general Finnish population is as high as 0.4% .
Subjects taking any known QT-prolonging medication at the moment of electrocardiogram (ECG) recording were excluded from the study. QT intervals were measured manually by a single cardiologist (H.S.) using the mean of two consecutive QT intervals in lead II in standard 12-lead ECG. Heart rate-corrected QT (QTc) was calculated using the Bazett's formula (QT/√RR). The study was performed in accordance with the Declaration of Helsinki and written informed consent was obtained from all participants. The Ethics Review Committee of the Department of Medicine, University of Helsinki, approved the study.
Molecular genetic analyses
KCNE1 253G>A (D85N, rs1805128) was genotyped in DNA from venous blood samples using polymerase chain reaction with primers 5'-GAGATTGGAGTGGTGGATGGA-3' and 5'-CACCCCTTACAACAGCCAAAA-3' followed by Lwe I digestion (Fermentas, Ontario, Canada) and agarose gel electrophoresis. Previously identified heterozygous and major and minor homozygous samples served as controls in the assay.
Normality of continuous distributions was reviewed visually. Non-normally distributed age was normalized by Blom's method. The effect of KCNE1 D85N on age-, sex-, and heart rate (RR interval) -adjusted QT interval was studied by linear regression analysis using 1-df additive model (genotype coded as D85D = 0, D85N = 1, N85N = 2). Because gender differences were detected, an additional model included also a multiplicative interaction term between KCNE1 D85N genotype and sex. In KCNQ1 G589D carriers, association of D85N with proband/family member status (information available for all 492 G589D carriers), appearance of syncope (information available, n = 488), use of beta blocker medication (information available, n = 347), and occurrence of pacemaker or implantable cardioverter-defibrillator (information available, n = 349) was studied by Fisher exact test. Statistical analyses were performed with SPSS 17.0 (Statistical Package for Social Sciences, SPSS Inc., Chicago, IL, USA). A p value < 0.05 was considered statistically significant.
Effect of KCNE1D85N on QT interval in LQTS founder mutation carriers
The clinical characteristics of the study sample
D85D major homozygotes
N85N minor homozygotes
29.7 ± 20.0
28.7 ± 20.2
7.0 ± 4.2
458 ± 36.8
472 ± 35.2
468 ± 34.6
Founder mutation status
459 ± 36.2
479 ± 31.0
468 ± 34.6
465 ± 30.0
464 ± 48.3
490 ± 7.1
445 ± 30.6
442 ± 46.5
Effect of KCNE1 D85N on age-, sex-, and heart rate-adjusted QT interval
n with D85N
All founder mutation carriers
KCNQ1 G589D carriers
When all founder mutation carriers were considered together, KCNE1 D85N was associated with a 13 ms (SE 6.0) prolongation of QT interval per each N85 minor allele (p = 0.028, Table 2). A similar gender-specific analysis revealed that this association was confined to males (Table 2).
Association of KCNE1D85N with selected clinical variables
The KCNE1 D85N variant has been shown to lead to a substantial QT-interval prolongation in the general population [12–14]. In fact, we are not aware of any other gene variant showing a population-based frequency of >1% and an equally large effect on QT interval. In order to test the effect of this variant on cardiac repolarization in patients with LQTS, we studied the association of KCNE1 D85N to QT interval in a homogeneous group of Finnish LQTS founder mutation carriers. We found that the minor N85 allele significantly prolongs age-, sex-, and heart rate-adjusted QT interval in type 1 LQTS patients with the mutation G589D. An interaction between D85N genotype and sex was detected (p = 0.028), and a sex-specific analysis revealed that the N85 allele prolongs QT interval by 26 ms in males but not in females (Table 2). Our material is too small to draw conclusions of the role of D85N in LQTS type 2 caused by KCNH2 mutations.
In this study, we detected a gender difference in the effect of KCNE1 D85N on QT interval in type 1 LQTS. We reported previously that the occurrence of the N85 minor allele was associated with a 10 ms prolongation of the QT interval in the general Finnish population . We carried out a retrospect analysis of our population sample  and found that the effect of D85N on QT interval was slightly larger in males (+11.3 ms) than in females (+10.0 ms). Gender is known to influence QT interval at the population level, with females in general showing longer QT intervals than males , and there are sex- and age-specific differences in risk of arrhythmias in the different subtypes of LQTS [19, 20]. It is of note that also KCNQ1 G589D presents a gender difference since the female carriers have >20 ms longer QTc compared to the male carriers , a finding replicated in the present study (Figure 1, D85D homozygotes). KCNE1 D85N appears to invert this sex difference. Interestingly, Friedlander et al.  found that G38S, another polymorphism of KCNE1, was associated with QT-interval variation in healthy males but not in females.
Sex differences in cardiac repolarization appear to result from both transcriptional and non-transcriptional regulatory mechanisms. In female mice hearts, KCNE1 mRNA is more abundant compared to males . Differences in KCNE1 protein levels may therefore influence the sex-specific sensitivity to KCNE1 variants. Sex hormones have also been reported to alter the gating kinetics of cardiac ion channels and to modulate the effects of channel blocking agents [24, 25]. For example, 17β-oestradiol inhibits IKs  and IKr  channels and enhances the effect of a KCNH2 blocker . It is therefore possible that KCNE1 D85N interferes with the binding of sex-specific IKs channel regulators, but the exact mechanisms underlying the sex difference reported in the present study remain to be explored.
In previous studies, KCNE1 D85N has been found to associate with congenital LQTS [10, 11]. Compound carriers of two or more LQTS mutations have a longer heart rate-corrected QT interval (QTc) and a more severe phenotype than carriers of only one mutation [10, 26]. KCNE1 D85N has also been proposed to cause LQTS in the absence of any documented mutation in known LQTS genes, but the age at onset may be higher and QTc shorter than in patients with a more severe LQTS mutation . In vitro experiments indicate that KCNE1 N85 significantly reduces both IKs and IKr currents, thus delaying repolarization in mammalian cells . This gene variant also contributes to loss of IKs function together with a KCNQ1 mutation in Xenopus oocytes . In another study of mammalian cells, however, D85N did not affect IKs current when co-expressed with KCNQ1 .
In the present study, we found that the QT-prolonging effect of KCNE1 D85N is substantially larger in males with the LQTS mutation KCNQ1 G589D (26 ms) than in the general population (10 ms). This result suggests that KCNQ1 and KCNE1 mutations and variants may interact with each other, at least in males, to produce an even more pronounced QT-prolonging effect than when occurring separately. This interaction could be caused by the coassembly of the two proteins to form a functional IKs channel. However, due to small number of subjects with the KCNE1 N85 allele and LQT1 mutations other than KCNQ1 G589D, we cannot draw conclusions on the general applicability of this effect in LQT1, nor provide sufficient data on a possible similar relation in LQT2. It should be emphasized that the association between D85N and QT interval in type 1 LQTS should be replicated in another material. However, we realize that this is not an easy task considering the population prevalence of D85N. Thus, any replication material should contain hundreds of genetically uniform patients with type 1 LQTS.
Our study also provides evidence that the KCNE1 D85N variant may be associated with a more severe phenotype of type 1 LQTS, as the proportions of probands and users of beta blocker medication were significantly higher in D85N heterozygotes than in non-carriers (Figure 2). Indirectly, these associations suggest that D85N carriers may seek medical help more often than non-carriers. A similar but non-significant trend was detected in the occurrence of syncope and use of pacemaker or implantable cardioverter-defibrillator. Paulussen et al.  identified 2 carriers of the N85 allele among 32 patients with drug-induced LQTS, while no such carriers were observed in the series of 34 patients with torsades de pointes studied by Mank-Seymour et al. . Sotoodehnia et al.  suggested that D85N could be associated with a higher death rate in males but not in females. Clearly, more extensive population-based studies are required in which the role KCNE1 D85N variation as determinant of life-threatening and fatal arrhythmias will be explored. Polymorphisms in another gene, NOS1AP, have also been associated with QT prolongation and cardiac events in LQTS patients .
Our study suggests that KCNE1 D85N variation has a gender-dependent QT-prolonging effect in KCNQ1 G589D mutation carriers and could thus complicate the symptoms of LQTS. Previously, this variant has not been studied in vivo in a large cohort of LQTS mutation carriers. As KCNE1 D85N is relatively frequent occurring in 2-3% of the general population, this interaction between KCNQ1 and KCNE1 could ultimately have direct implications in counseling of LQTS patients. However, future studies are required to assess the direct risks of arrhythmias and/or sudden death in LQTS patients carrying KCNE1 N85.
The authors acknowledge Susanna Saarinen, Hanna Nieminen, and Hanna Ranne for their expert technical assistance. Financial support was received from The Sigrid Jusélius Foundation, The Academy of Finland, The Finnish Foundation for Cardiovascular Research, The Finnish Cultural Foundation (to AML), and The Emil Aaltonen Foundation (to AM).
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