Abstract
Background. Familial hypercholesterolemia (FH) is a genetic disorder characterized by high levels of low-density lipoprotein cholesterol (LDL-C). Because of underdiagnosis, acute coronary syndrome (ACS) is often the first clinical manifestation of FH. In Japan, there are few reports on the prevalence and diagnostic ratios of FH and the proportion of ACS among FH patients in clinical settings. Methods. This retrospective, observational study used anonymized data from electronic healthcare databases between April 2001 and March 2015 of patients who had ≥2 LDL-C measurements recorded after April 2009. The index date was defined as the date of the first LDL-C measurement after April 2009. The primary endpoint was the prevalence of definite or suspected FH; secondary endpoints included the proportion of FH patients hospitalized for ACS, the proportion of patients using lipid-lowering drugs (LLDs), and LDL-C levels. Results. Of the 187,781 patients screened, 1547 had definite or suspected FH (0.8%) based on data from the entire period; 832 patients with definite (, 0.16%) or suspected FH (, 0.28%) before the index date were identified in the main analysis cohort. LLDs were used in 214 definite FH patients (71.6%) and 137 suspected FH patients (25.7%). Among definite or suspected FH patients with ACS () and without ACS (), 32.1% and 30.1% with definite FH and 3.2% and 2.4% with suspected FH had LDL-C (<100 mg/dL), respectively. Sixty patients (7.2%) were hospitalized due to ACS at the index date. Conclusions. The prevalence of FH in this Japanese cohort of patients with ≥2 LDL-C measurements at hospitals was 0.8%, which is higher than that currently reported in epidemiological studies (0.2–0.5%). Patients with suspected FH, with or without ACS, had poorly controlled LDL-C levels and were undertreated. The proportion of FH patients who were hospitalized due to ACS was 7.2%.
1. Introduction
Familial hypercholesterolemia (FH) is an autosomal dominant genetic disorder with heterozygous and homozygous forms [1]. The underlying cause of FH is a mutation in the gene for the low-density lipoprotein (LDL) receptor or its related genes, such as the genes encoding apolipoprotein B and proprotein convertase subtilisin/kexin-type 9 (PCSK9) [1]. The prevalence of FH varies from study to study. A systematic review and meta-analysis of 19 studies reporting the prevalence of FH found that 1 in 250 people in the general population has this condition [2]. The prevalence of FH in Japan was estimated at between 1 in 200 (0.5%) and 1 in 500 people (0.2%) [3–5].
The principal driver of coronary artery disease (CAD) in FH patients is elevated LDL cholesterol (LDL-C) [6], with a 13-fold increase in the risk of CAD in those not on lipid-lowering drugs (LLDs) [7]. Early diagnosis of FH is necessary for therapy to be effective in reducing the risk of premature CAD [1, 8]. According to the Japan Atherosclerosis Society (JAS) 2017 guidelines, in the absence of secondary hyperlipidemia, fulfilment of ≥2 of the following criteria in years old is diagnostic of FH: hyper-LDL-cholesterolemia (untreated LDL-C of ≥4.7 mmol/L [≥180 mg/dL]); tendon xanthomas on the back of the hands, elbows, or knees, or Achilles tendon hypertrophy or xanthoma tuberosum; or family history of FH or premature CAD (in second-degree relatives of the patient) [4]. The guidelines also mention that a diagnosis of FH should be strongly suspected in patients with LDL-C levels of ≥6.5 mmol/L (≥250 mg/dL) [4], as only 5% of these patients do not have FH [9]. Genetic testing is recommended to confirm the diagnosis of FH in this population [4].
Underdiagnosis of FH is a globally recognized issue [10]. For most undiagnosed FH patients, acute coronary syndrome (ACS) is the first clinical manifestation [11]. It is important to have an early and accurate diagnosis of FH in patients with ACS in order to decide whether aggressive lipid-lowering treatment is necessary. Therefore, we sought to assess the prevalence of FH in Japanese patients and to determine the proportion of FH patients who required hospitalization due to ACS. In addition, we studied the use of LLDs and their effectiveness in this population.
2. Methods
2.1. Data Source
This was a retrospective observational study using anonymized information on patient demographics, drug prescriptions, comorbidities, and laboratory parameters from cases reported between April 1, 2001, and March 31, 2015 (Supplementary Figure 1). The data were combined from two electronic health record (EHR) databases, the nationwide database developed by the Nomura Research Institute, Ltd. in 2001, which includes data from 70 state and private Japanese hospitals (12 facilities with 1–99 beds, 27 with 100–299 beds, 11 with 300–499 beds, 16 with 500–899 beds, and 4 with ≥900 beds), and the database of the Teikyo University Hospital (Tokyo, Japan). Patients were informed regarding the study and had the right to request that their data should not be used in this study (opt-out style of informed consent).
2.2. Patients
Patients with ≥2 LDL-C measurements between April 1, 2009, and March 31, 2015, were identified from the EHR databases. The index date was defined as the date of the first LDL-C measurement during this time period. Based on the index LDL-C measurement, patients were categorized into the following five groups: <1.8 mmol/L (<70 mg/dL), ≥1.8 to <2.6 mmol/L (≥70 to <100 mg/dL), ≥2.6 to <3.6 mmol/L (≥100 to <140 mg/dL), ≥3.6 to <4.7 mmol/L (≥140 to <180 mg/dL), or ≥4.7 mmol/L (≥180 mg/dL) group based primarily on the JAS guidelines [4].
The overall prevalence of FH was based on the number of patients with definite or suspected FH at any time during the entire period between April 1, 2001, and March 31, 2015. Patients with a confirmed diagnosis of FH by a physician, using diagnosis records from the EHR databases, were considered to have definite FH. The remaining patients with ≥1 measured LDL-C (≥250 mg/dL), as per the 2017 JAS guidelines [4], were considered to have suspected FH (FH prevalence cohort). The main study cohort included all patients with definite or suspected FH (per definitions above) prior to the index date (Figure 1).
From this main cohort, patients with comorbid ACS were defined as any patient who had experienced ≥1 ACS between April 1, 2001, and the index date plus 90 days or March 31, 2015, whichever is earlier (Supplementary Figure 1). Among those identified with comorbid ACS, the “hospitalization for ACS cohort” was the subset of patients hospitalized for ACS at the index date.
Comorbidity burden was assessed in the main study cohort between April 1, 2001, and the index date plus 90 days or March 31, 2015, (whichever is earlier) for the six diseases outlined in the Charlson Comorbidity Index (CCI), including CAD, hypertension, diabetes mellitus (DM), noncardiogenic stroke, peripheral artery disease (PAD), and diabetic microangiopathy [12]. The diagnosis of these conditions was based on physician’s discretion. LLD use was defined as prescription of an LLD within 90 days prior to the index date.
2.3. Endpoints
The primary endpoint of the study was to determine the prevalence of FH (both definite and suspected) in the overall patient population. Secondary endpoints included (1) the diagnostic ratio of definite FH to all FH (definite+suspected), (2) the proportion of patients with FH who were hospitalized for ACS, (3) the proportion of patients with FH using LLDs, (4) the LDL-C levels among patients with FH with and without ACS, and (5) the LDL-C levels of patients according to LLD use.
2.4. Statistical Analysis
Demographic and clinical characteristics of patients were summarized using descriptive statistics. Median and interquartile range were calculated for continuous variables, and absolute and relative frequencies were calculated for categorical variables.
The prevalence of FH was calculated as the sum of the number of patients with a definite diagnosis of FH and the number of patients with suspected FH, divided by the total number of patients. The proportion of FH patients with ACS was calculated as the number of patients with hospitalization due to ACS divided by the number of patients with FH, including definite and suspected, before the index date.
Data collection and creation of analysis datasets were performed using R version 3.2.3, and all statistical analyses were performed using SAS 9.4 (SAS Institute Inc., Cary, NC), and values < 0.05 were considered statistically significant.
3. Results
3.1. FH Prevalence
A total of 187,781 patients had ≥2 LDL-C measurements, and 1547 of these patients had definite or suspected FH between April 1, 2001, and March 31, 2015. The prevalence of FH, including both definite and suspected FH, was 0.8% ().
3.2. Patient Characteristics and the Proportion of Patients Hospitalized due to ACS
A total of 832 patients with definite (, 0.16% of all patients) or suspected FH (, 0.28% of all patients) prior to the index date were identified (Table 1). The diagnostic ratio of definite FH was 35.9% (). Of the 832 patients, 84 had comorbid ACS and 60 patients had been hospitalized for ACS at the index date. Among FH patients, the proportion of patients hospitalized due to ACS was 7.2% ().
Women comprised 34.5% of patients with comorbid ACS () and 55.7% of patients without comorbid ACS (). The median age of patients with or without comorbid ACS was 63.0 years and 60.0 years, respectively, and LLDs were being taken by 71.4% and 38.9% of patients, respectively. CAD, hypertension, and DM were the most common comorbidities both in patients with (95.2%, 76.2%, and 70.2%, respectively) and without (24.1%, 40.4%, and 46.4%, respectively) comorbid ACS.
3.3. LDL-C Levels
Among patients with a definite diagnosis of FH and comorbid ACS, 11.3% () had LDL-C (<70 mg/dL), as defined by the 2017 JAS guidelines [4], whereas among patients with suspected FH and comorbid ACS (), none had LDL-C (<70 mg/dL) (Figure 2(a)). A similar pattern was observed in patients with definite FH (, 8.1%) and suspected FH (, 0.8%) who did not have comorbid ACS (Figure 2(b)).
(a)
(b)
3.4. LDL-C Levels according to LLD Use
LLD use was recorded in 71.6% () of patients with definite FH and 25.7% () of patients with suspected FH. Among patients with comorbid ACS, 48.4% () of patients with suspected FH used LLD compared with 84.9% () of patients with definite FH (Table 1).
Among patients with suspected FH and ACS, those who were taking LLDs had better control of LDL-C levels compared with those who were not (Figure 3(a), Supplementary Table 1). In patients without ACS, control of LDL-C levels was poorer in patients with suspected FH than in those with definite FH (Figure 3(b), Supplementary Table 4). On the other hand, there was little difference in LDL-C levels between patients who were and were not taking LLDs among those with definite FH and no comorbid ACS.
(a)
(b)
Among overall FH patients with comorbid ACS, those who were taking LLD, regardless of sex or age (<65 or ≥ 65 years), had better control of LDL-C levels compared with those who were not (Figure 3(a), Supplementary Tables 1–3). Among overall FH patients without comorbid ACS, those who were taking LLD regardless of sex or age (<65 or ≥ 65 years) also showed better control of LDL-C levels (Figure 3(b), Supplementary Tables 4–6).
4. Discussion
To the best of our knowledge, this was the first study to assess the prevalence of definite or suspected FH, the proportion of FH patients hospitalized due to ACS, and associated management practices in a large sample of in- and outpatients treated in clinical settings in Japan. This study used anonymized data from 187,781 patients, and the data from the FH prevalence cohort were used to estimate the prevalence of FH more accurately. This is considered to have prevented the omission of diagnosed cases due to the lack of data such as LDL-C levels. The results show that the prevalence of FH between 2001 and 2015 was 0.8% (1 in 125 individuals). This value was higher than previous estimates in Japan, such as 1 in 200–500 [3, 5], but similar to the 0.73% (1 in 137) genetically determined prevalence reported in Denmark [7]. A systematic review and meta-analysis of 19 studies conducted in various countries reported that the prevalence of FH in the general population was 0.4% (1 in 250 individuals) [2]. One potential reason for higher prevalence in the present study could be differences between our study population and the general population. Participants of the present study were in- or outpatients with ≥2 LDL-C measurements who were likely to have cardiovascular risk factors or clinical disease severe enough to warrant specialist assessment. However, the results of this study may be more useful for physicians and other healthcare professionals than population-based studies, because they treat similar patients in routine clinical practice. Another potential reason for the higher prevalence of FH in the current study population could be the use of different diagnostic criteria. Previous studies mainly relied on DNA analysis to establish the diagnosis of FH and reported lower estimates for the prevalence of FH compared with studies that used LDL-C measurements (0.40% vs. 0.45%) [2]. Whereas, in the present study, the diagnosis of FH was based on JAS diagnostic criteria for FH [4, 9].
In the present study, 7.2% of patients who had FH at the index date were hospitalized for ACS. Even though this figure is a proportion value, not prevalence, it could be deemed to be a reference value for the prevalence of ACS in patients with FH. The prevalence of ACS in patients with FH also depends on risk factors for ACS, such as increased age, hyperlipidemia, hypertension, diabetes, smoking, obesity, and lack of exercise [13]. To our knowledge, no study has examined the prevalence of ACS in patients with FH, although the prevalence of FH in patients with ACS has been reported in several previous studies. For example, in a study of 4778 Swiss patients with ACS, 1.6% () had probable/definite FH (Dutch Lipid Clinic Network ) [11]. The prevalence of genetically confirmed FH was 8.7% () in a study that included 103 patients with ACS who were aged ≤65 years and had LDL-C (≥160 mg/dL) [14]. In a study of 296 Japanese patients with ACS, the prevalence of FH was 5.7% based on JAS criteria [15]. EXPLORE-J was another study conducted in 1944 Japanese patients with ACS to assess the prevalence of FH using JAS criteria. It reported that 2.7% () of patients in this population had FH [16]. Although the prevalence of FH in patients with ACS varied widely, it was much higher than that in the general population, highlighting the importance of lipid level control in the prevention of cardiovascular diseases. ACS is a serious condition with a high rate of mortality [17], and its prevalence has been increasing in Japan over recent decades. For example, according to the MIYAGI-AMI registry, the incidence of acute myocardial infarction in the Miyagi prefecture of Japan increased significantly from 7.4 to 27.0 per 100,000 person-years between 1979 and 2008 () [18]. The prevalence of dyslipidemia, as well as hypertension and diabetes, also increased significantly () [18]. Therefore, it is important to identify modifiable risk factors, such as FH, early and treat them effectively to reduce the risk of ACS and its associated sequelae.
Although it is important for patients with FH to achieve target LDL-C values to prevent or delay the development of ACS [19], 37% of the FH patients with comorbid ACS in the present study had suspected FH, but without a confirmed diagnosis despite having abnormally high LDL-C levels. In addition, LDL-C control in patients with suspected FH was poor regardless of the presence of ACS, and patients with definite FH had better LDL-C control with much higher rates of LLD use. This study analyzed LDL-C data between April 1, 2009, and March 31, 2015. At that time, the target LDL-C level was <2.6 mmol/L (<100 mg/dL), as recommended by earlier versions of the JAS guidelines, but the proportion of patients with suspected FH who achieved target LDL-C levels was still poor, even considering the previous target level (definite FH with ACS: 32.1% []; suspected FH with ACS: 3.2% [], respectively). Similar results have been reported in patients with suspected FH (LDL-C threshold: ≥4.9 mmol/L [≥190 mg/dL]) in another Japanese study [20]. The mean LDL-C was 3.4 mmol/L (131.3 mg/dL) in patients with suspected FH who were receiving statins and 4.1 mmol/L (157.9 mg/dL) in patients who were receiving non-statin LLDs. LDL-C levels were <3.4 mmol/L (<130 mg/dL) in 39.3% of patients with suspected FH [20]. Although these results cannot be compared directly with our findings because of the different criteria used to categorize LDL-C levels in the two studies, together they highlight a treatment gap in patients with suspected FH.
Among FH patients overall, those who were taking LLDs, regardless of sex or age (<65 or ≥65 years) or the presence or absence of comorbid ACS, had better control of LDL-C levels compared with those who were not taking LLDs. In the clinical setting, administration of LLDs may be more likely to be postponed in premenopausal women, which may affect their LDL-C levels. However, the proportion of women who were taking or not taking LLDs showed little difference in FH patients with comorbid ACS (33.3% and 37.5%, respectively) and in FH patients without comorbid ACS (58.8% and 53.8%, respectively). In addition, since the median age of all patients was around 60.0 years, the proportion of premenopausal women was not high. Therefore, we concluded that there was little influence of sex on LLD prescription bias. LLD administration may also be postponed in elderly patients due to the risk of polypharmacy and declining renal function. The median age of LLD users and non-LLD users was 62.0 and 68.5 years, respectively, among FH patients without comorbid ACS and 60.0 and 59.0 years, respectively, among FH patients with comorbid ACS. Therefore, some influence of age on LLD prescription bias may exist among FH patients without comorbid ACS.
In the present study, the proportion of patients who used LLDs was much lower in patients with suspected FH than in those with definite FH (25.7% vs. 71.6%). The fact that patients on LLDs have been shown to have better control of LDL-C levels, regardless of whether they have a history of ACS, and that patients with suspected FH have been found to have low proportions of LLD usage, emphasizes the importance of a timely FH diagnosis in controlling LDL-C levels. Taken together, these findings highlight the need for more proactive diagnosis and management of FH before patients develop clinical cardiovascular disease, as recommended in current JAS guidelines [4].
The results of this study regarding LDL-C control during treatment are comparable with those observed in previous studies. Treated LDL-C levels were notably higher than target levels (<2.6 mmol/L [<100 mg/dL]) in the SAFEHEART registry (3.0–4.2 mmol/L [116.0–162.1 mg/dL]) [21] and in the CASCADE-FH study (3.5 mmol/L [134 mg/dL]) [22].
Recent guidelines recommend more stringent targets and aggressive therapy for FH patients. The 2017 JAS guidelines introduced a new target LDL-C level of 2.6 mmol/L (100 mg/dL) for primary prevention and 1.8 mmol/L (70 mg/dL) for secondary prevention [4]. The guidelines recommend starting treatment with a statin at the maximum tolerated dose and/or combining a statin with ezetimibe, and if the response is not sufficient, a PCSK9 inhibitor and/or resin and/or probucol should be used [4]. On the other hand, the 2018 Japanese Circulation Society Guidelines on Diagnosis and Treatment of Acute Coronary Syndrome recommends administering strong statins at the maximum tolerated dose [23]. In patients with a diagnosis of FH, lipid-lowering treatment may be started according to the JAS guidelines [4], but in patients without diagnosis, there is a risk of lack or delay of appropriate intervention.
This study had several limitations, including a lack of data from community-based hospitals, inability to ascertain additional relevant data such as family history of FH, history of premature CAD, socioeconomic status, lifestyle-related risk factors, treatment adherence, and potential variations in LDL-C levels based on methodology and measurement errors. Furthermore, as this was a study of in- and outpatients treated in clinical settings at hospital, the prevalence of comorbid disease was expected to be higher than in the general population. The results of this study may be more useful for application to clinical practice than population-based studies. In addition, there was a lack of information on whether genetic analyses were implemented to diagnose FH, the definition of “definite FH” was based only on the physician’s diagnosis, and the of “suspected FH” was based on ≥1 LDL-C measurement of ≥6.5 mmol/L (≥250 mg/dL) as per the 2017 JAS guidelines [4]. As a result, it is possible that the number of patients in our FH cohort may have been overestimated and included some patients with similar clinical manifestations, including those with secondary hyperlipidemia. Comparing the results of the present study with those from others, especially non-Japanese, should be approached with caution due to inconsistencies in FH diagnostic criteria between the JAS guidelines [4], the Dutch Lipid Clinic Network criteria [24], the Simon Broome system criteria [25], the Make Early Diagnosis-Prevent Early Death criteria [26], and others.
5. Conclusion
The results of the present study show that the prevalence of FH in this Japanese cohort of patients with ≥2 LDL-C measurements at hospitals was 0.8%, which is higher than its currently reported prevalence in epidemiological studies (0.2–0.5%). In addition, the proportion of patients with FH who were hospitalized due to ACS was notably high (7.2%). Patients with suspected FH, with or without ACS, had poorly controlled LDL-C levels and were undertreated. Therefore, improving the diagnostic ratio of FH is important to channel patients to receive appropriate treatments and subsequently have controlled LDL-C levels. Early diagnosis of FH and more aggressive lipid-lowering treatment have the potential to address this issue.
Data Availability
The data used to support the findings of this study are available from the corresponding author upon reasonable request.
Additional Points
Authorship. All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this article, take responsibility for the integrity of the work as a whole, and have given their approval for this version to be published.
Conflicts of Interest
Tamio Teramoto received honoraria from Bayer Yakuhin, Ltd., Pfizer Japan Inc., Takeda Pharmaceutical Company Limited, Astellas Pharma Inc., Kowa Company, Ltd., Sanofi K.K., MSD K.K., Amgen Astellas BioPharma K.K., and AstraZeneca K.K.; received fees for promotional materials from Daiichi Sankyo Company Limited; received clinical research funding from Amgen Astellas BioPharma K.K.; received scholarship grants from Daiichi Sankyo Company Limited, Takeda Pharmaceutical Company Limited, Astellas Pharma Inc., Kissei K.K., and Shionogi & Co., Ltd.; and belongs to courses endowed by Kowa Company, Ltd., MSD K.K., and Bayer Yakuhin, Ltd. Tomohiro Sawa received clinical research funding from Amgen Astellas BioPharma K.K. Satoshi Iimuro received clinical research funding from Amgen Astellas BioPharma K.K., Public Health Research Foundation, Kanebo Cosmetics, Japan Medical Agency, Japan Heart Foundation, Toho University, and Asahi Kasei Pharma Corporation; and received other non–research-related compensation from EP - CRSU Co., Ltd., and Chugai Pharmaceutical Co., Ltd. Hyoe Inomata was an employee of Amgen Astellas BioPharma K.K. and a stockholder of Amgen Inc. at the time this study was conducted. Takashi Koshimizu and Katsutoshi Hiramatsu are employees of Amgen K.K. and were employees of Amgen Astellas BioPharma K.K. at the time this study was conducted and stockholders of Amgen Inc. Iori Sakakibara was a full-time employee of Amgen Astellas BioPharma K.K. at the time this study was conducted.
Authors’ Contributions
Tamio Teramoto, Hyoe Inomata, and Katsutoshi Hiramatsu contributed to data analysis and interpretation. Tomohiro Sawa and Satsohi Iimuro contributed to data interpretation. Takashi Koshimizu and Iori Sakakibara were the statisticians/statistical programmers for this study, performed statistical analyses described in this manuscript, and contributed to the interpretation of these data. All authors have read and approved the final version of the manuscript before submission.
Acknowledgments
Data collection and creation of analysis datasets were supported by Kinya Kokubo and Ayako Shoji of Nomura Research Institute, Ltd. Quality control of the data used for analysis was performed by Izumi Sato of Kyoto University. The authors thank Yoshiko Okamoto and Georgii Filatov of inScience Communications, Springer Healthcare, for writing the outline and the first draft of this manuscript, respectively, and Sarah Greig, PhD, of inScience Communications, Springer Healthcare, who edited the manuscript after submission. This medical writing assistance was funded by Amgen Astellas BioPharma K.K and Amgen K.K
Supplementary Materials
Table 1: LDL-C levels in patients with comorbid ACS. ACS = acute coronary syndrome; FH = familial hypercholesterolemia; LDL-C = low-density lipoprotein cholesterol; LLD = lipid-lowering drugs. Table 2: LDL-C Levels in patients with comorbid ACS separated by sex. ACS = acute coronary syndrome; FH = familial hypercholesterolemia; IQR = interquartile range; LDL-C = low-density lipoprotein cholesterol; LLD = lipid-lowering drugs. Table 3: LDL-C levels in patients with comorbid ACS separated by age (<65 or ≥65). ACS = acute coronary syndrome; FH = familial hypercholesterolemia; IQR = interquartile range; LDL-C = low-density lipoprotein cholesterol; LLD = lipid-lowering drugs. Table 4: LDL-C levels in patients without comorbid ACS. ACS = acute coronary syndrome; FH = familial hypercholesterolemia; LDL-C = low-density lipoprotein cholesterol; LLD = lipid-lowering drugs. Table 5: LDL-C levels in patients without comorbid ACS separated by sex. ACS = acute coronary syndrome; FH = familial hypercholesterolemia; IQR = interquartile range; LDL-C = low-density lipoprotein cholesterol; LLD = lipid-lowering drugs. Table 6: LDL-C levels in patients without comorbid ACS separated by age (<65 or ≥65). ACS = acute coronary syndrome; FH = familial hypercholesterolemia; IQR = interquartile range; LDL-C = low-density lipoprotein cholesterol; LLD = lipid-lowering drugs. Figure 1: comorbid ACS and hospitalization for ACS assessment periods. Comorbidities include acute coronary syndrome (ACS), coronary artery disease (CAD), hypertension, diabetes mellitus (DM), noncardiogenic stroke, peripheral artery disease (PAD), and diabetic microangiopathy. (Supplementary Materials)