Prevalence of the metabolic syndrome and cardiovascular disease risk in chemotherapy-treated testicular germ cell tumour survivors.

BACKGROUND: Testicular cancer patients have an increased risk for cardiovascular disease (CVD), which might be related to the increased prevalence of the metabolic syndrome (MetS) in this group of patients.
METHODS: We assessed the prevalence of MetS and calculated the 10-year CVD risk in a cohort of 255 testicular germ cell tumour survivors (median age, 38.7 years; interquartile range, 31-48) at a mean of 7.8 years after anti-cancer treatment, and compared these with data obtained from 360 healthy men.
RESULTS: Survivors had an age-adjusted increased risk for MetS of 1.9 compared with that of healthy controls. The risk for MetS was highest in survivors treated with combination chemotherapy (CT) 2.3 (Adult Treatment Panel of the National Cholesterol Education Program classification) and 2.2 (International Diabetes Federation classification). The risk of MetS was especially increased in survivors with testosterone levels in the lowest quartile (OR, 2.5). Ten-year cardiovascular risk as assessed by the Framingham Risk Score (3.0%) and Systemic Coronary Risk Evaluation (1.7%) algorithms was low, independent of treatment, and was comparable to controls.
CONCLUSION: Testicular germ cell tumour survivors have an increased prevalence of MetS, with hypogonadism and CT treatment being clear risk factors for the development of the syndrome. The increased prevalence of MetS was not associated with an increased 10-year cardiovascular risk.

Testicular cancer, the most common cancer in male patients between 25 and 35 years of age, holds an excellent prognosis since the introduction of cisplatin-based chemotherapy (CT) in the treatment regimen (Einhorn, 1997). However, testicular cancer patients treated with CT or radiotherapy are reported to have a 25-year risk of long-term cardiovascular complications of ∼16% (van den Belt-Dusebout ). An increased incidence of cardiovascular events was indeed recently reported in germ cell tumour (GCT) survivors (Haugnes ). Patients who had received CT were found to be more at risk than those patients treated with orchidectomy only (Huddart ). Over the last two decades, concerns have been raised about the increased risk of cardiovascular morbidity and the increased prevalence of the metabolic syndrome (MetS) with the use of certain treatment modalities in specific cancer types (de Forni and Armand, 1994; Yeh ; Carver ). Studies in GCT survivors report a wide variation in the prevalence of MetS ranging from 13% to 39% (Nuver ; Haugnes ; Wethal ) compared with a prevalence of 15% in non-diabetic adult Europeans (Hu ).

MetS is a cluster of metabolic and interrelated cardiovascular risk factors, which directly promotes atherosclerotic cardiovascular disease (CVD) (Ingelsson ). Various expert panels have developed classifications of MetS to facilitate screening for cardiovascular risk factors, including the Adult Treatment Panel of the National Cholesterol Education Program (NCEP-ATP III), which modified the definition based on similar characteristics used by the WHO (Table 1; Balkau and Charles, 1999; World Health Organization, 1999) and the MetS score developed by the International Diabetes Federation (IDF) (Alberti ). A meta-analysis of 21 prospective American and European cohort studies using the NCEP-ATPIII or WHO criteria indicated that patients with high MetS prevalence have an increased incidence and mortality for CVD (Galassi ). Another meta-analysis, including 37 studies and 172 573 individuals (Gami ), showed that MetS carried a relative risk (RR) of cardiovascular events and deaths of 1.78 (95% CI, 1.58–2.0).

Table 1

Metabolic syndrome criteria according to two different classification systems

	NCEP-ATPIII	IDF
Hypertension	BPsystolic⩾135 mm Hg and BPdiastolic⩾85 mm Hg	BPsystolic⩾135 mm Hg or BPdiastolic⩾85 mm Hg
Obesity	Waist circumference ⩾102 cm	Waist circumference⩾94 cm or BMI>30 kg m−2
Insulin resistance	fasting glucose⩾6.1 mmol l−1 (110 mg dl−1)	Fasting glucose⩾5.6 mmol l−1 (100 mg dl−1)
Dyslipidemia	HDL-cholesterol<1.03 mmol l−1 (40 mg dl−1) or statin usage	HDL-cholesterol<1.03 mmol l−1 (40 mg dl−1) or statin usage
Hypertriglyceridemia	Triglyceride⩾1.7 mmol l−1 (150 mg dl−1)	Triglyceride⩾1.7 mmol l−1 (150 mg dl−1)
Metabolic syndrome	⩾3 Criteria	Obesity and ⩾2 other criteria

Abbreviations: BMI=body mass index; IDF=International Diabetes Federation; HDL=high-density lipoprotein; NCEP-ATPIII=National Cholesterol Education Program Adult Treatment Panel III 2002.

In all classifications used for the MetS, main risk factors for CVD, such as smoking, age, and prothrombotic and proinflammatory state, are excluded to simplify outpatient screening. Of particular interest for GCT patients is that androgen deficiency has been found to be a risk factor for the development of the MetS, and cured survivors are often found to have some degree of CT-induced hypogonadism, which may persist for up to 10 years after treatment (Nord ). Hypogonadism can itself promote obesity and insulin resistance, and in turn visceral obesity promotes hypogonadism. Another possible explanation for the observed increased CVD risk in GCT survivors is the fact that patients' testicular germ cell cancer may be aetiologically linked to other male reproductive abnormalities as a part of the so-called ‘testicular dysgenesis syndrome' (TDS) (Skakkebaek ). This syndrome is present in a proportion of GCT patients before the diagnosis of the malignancy and in the survivors, and it is biologically plausible that the syndrome may predispose to development of MetS in later years (Ivell and Nand-Ivell, 2009).

Increasing numbers of patients in Europe and the United States have risk factors for CVD. This has led physicians to stratify patients according to risk algorithms of which the Framingham Risk Score (FRS) (Wilson ) and the Systemic Coronary Risk Evaluation (SCORE) are most commonly used (Conroy ). In contrast to the fasting blood samples used in the assessment of the MetS, the FRS can be calculated using non-fasting blood samples for cholesterol and HDL-cholesterol, and the major CVD risk factors, such as smoking and age, are also included in the FRS. The SCORE project, which collected and analysed data from 12 European cohort studies, was developed to estimate cardiovascular risk in European clinical practice.

The large differences in MetS and CVD prevalence reported in the literature in GCT patients has prompted us to use both the risk CVD prediction models to calculate 10-year cardiovascular risk in our cohort of long-term GCT survivors compared with healthy male subjects. We assessed MetS prevalence using both NCEP-ATPIII and IDF classifications to compare differences in outcome and to facilitate comparison with other studies.

Patients and methods

Patients

In a cross-sectional study design, all patients with a primary GCT originating in the testis, who attended the outpatient clinic of the Clinical Oncology Department of the Leiden University Medical Center between 2008 and 2010 for routine follow-up, were invited to take part in the study and 255 eligible patients were included (Figure 1). Seventy-nine patients had stage-I disease; 58 were treated with orchidectomy alone (‘surgery patients') and 21 seminoma patients also received one adjuvant dose of carboplatin (AUC7; ‘carboplatin patients'). Patients (n=176) with disseminated disease were treated with orchidectomy and combination CT, primarily bleomycin, etoposide, and cisplatin (‘combination-CT patients').

Figure 1

Flowchart inclusion of GCT patients. Major events (dates of diagnosis and mortality of CVD, defined as coronary heart disease, but not as stroke or peripheral artery disease, and date of most recent medical information, vital status during follow-up, and discharge), including annual verification of mortality and cause of death from hospital medical records, general practitioner, and municipal and national cancer data records were retrieved from the cancer registry and medical.

Data of 360 healthy men from the general population, living in the same geographical area, obtained from the general practitioners' health screening records were used as control. These data were obtained in 2009 as part of a programme in which apparently healthy subjects were screened for cardiovascular risk factors.

Methods

For all patients and controls, medical history (including smoking behaviour) was taken; body weight, height, body mass index (BMI, kg m−2), and waist circumference (WHO standards) were recorded, and blood pressure was measured in duplicate with the participants in a semi-recumbent position after at least 5 min rest. Blood samples were obtained after an overnight fast and measured for cholesterol, HDL-cholesterol, LDL-cholesterol, and triglycerides using routine assays. The patients' blood was also analysed for C-reactive protein (CRP) concentrations (standard assay), HbA1c and insulin (LEIA), and gonadal status. The latter was evaluated by measuring serum concentrations of luteinising hormone (LH), follicle-stimulating hormone (FSH) by using electrochemoluminescene immunoassays, total testosterone (TT) and estradiol (E2) by using standard radioimmunoassays, and sex hormone-binding globulin (SHBG) by using a luminescence enzyme immunoassay. Hypogonadism was defined as a fasting-morning serum TT concentration of <10.4 nmol l−1 (Lackner ). Four patients with disseminated disease received testosterone replacement therapy and were excluded for hormonal analysis.

Metabolic syndrome and 10-year cardiovascular risk evaluation

We used the NCEP-ATPIII criteria (National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III), 2002) and IDF risk score charts (Alberti ; Table 1) to establish the prevalence of MetS. The 10-year cardiovascular risk profile was calculated using FRS (Wilson ) and SCORE (Conroy ).

Statistical analysis

SPSS 19 for Windows software package (SPSS Inc., Chicago, IL, USA) was used for statistical analysis. The χ2-test for categorical variables and Student's t-test or Mann–Whitney test (two-sided) for non-normally distributed variables were used as appropriate. Results are expressed as interquartile range (IQR), mean±s.d., or as median (range). Odds ratios for MetS were calculated using logistic regression analysis and with adjustment for age and kidney function as continuous variables, and smoking and hypogonadism as binary variables. The incidence of MetS was also analysed according to serum testosterone quartiles using χ2-test for categorical variables. A P-value of <0.05 (two-tailed) was considered statistically significant. We also investigated whether there was an association between the time elapsed between treatment and the occurrence of MetS by linear regression.

Finally, we used the raw data provided in three reports (Nuver ; Haugnes ; Wethal ) in the literature on MetS in GCT patients to calculate the odds ratios.

Results

Patient characteristics

The median (range) cumulative carboplatin dose administered to survivors was 1015 (730–1700) mg (Table 2). Seven survivors who were eventually treated with combination CT were first treated with single-dose carboplatin for stage-1 seminoma, and one survivor was treated with three cycles of carboplatin before they developed distant metastasis. The median cumulative cisplatin dose administered to the survivors receiving combination CT was 604 (0–1750) mg; two patients received carboplatin instead of cisplatin as part of their combination CT.

Table 2

Characteristics of GCT survivors according to treatment group and of healthy subjects

		Treatment groups
Parameters	Healthy subjects N=360)	Surgery (N=58)	Carboplatin (N=21)	Combination CT (N=176)	All survivors (N=255)	P-valuea	P-valueb
Demographics mean±s.d., median (min–max)
Age at diagnosis (years)	NA	30.4±8.3 28.9 (20.0–61.9)	37.6±12.2 33.8 (24.8–50.6)	31.2±8.8 29.6 (14.2–54.2)	31.4±8.7 29.8 (14.2–61.9)	∼	∼
Age at blood analysis (years)	43.1±14.6 44.0 (18–70)	36.6±10.4 36.5 (20.1–69.5)	42.1±12.0 39.3 (26.8–57.4)	38.7±10.9 38.7 (18.2–63.4)	39.2±10.7 38.3 (18.2–69.5)	NS	NS
Interval between curative treatment and blood analysis (years)	NA	6.2±6.7 3.2 (0.1–2)	4.5±3.5 3.1 (0.7–13.2)	8.8±7.8 6.3 (0.6–30.2)	7.8±7.4 5.0 (0.1–30.2)	∼	∼
Clinical characteristics: median (min–max)
Body weight (kg)	85 (54–138)	82 (60–138)	83 (64–132)	85 (60–126)	84 (60–138)	0.005	0.01
Height (m)	1.80 (1.57–2.06)	1.85 (1.65–1.99)	1.83 (1.69–1.98)	1.83 (1.65–2.01)	1.83 (1.65–2.01)	0.006	<0.001
Body mass index (kg m−2)	25.8 (19.5–42.6)	24.2 (16.8–38.5)	25.0 (20.5–35.8)	25.6 (18.4–36.4)	25.5 (16.8–38.5)	NS	0.01
Waist circumference (cm)	94 (74–130)	92 (85–134)	96 (81–137)	96 (67–124)	96 (67–137)	<0.001	0.003
Systolic blood pressure (mm Hg)c	130 (110–200)	122 (95–185)	130 (90–155)	126 (90–200)	125 (90–200)	NS	0.006
Diastolic blood pressure (mm Hg)c	80 (62–110)	80 (54–110)	80 (65–90)	80 (53–114)	80 (53–114)	NS	NS
Creatinine clearance (Cockroft formula; ml min−1)		122 (84–205)	120 (70–165)	123 (56–217)	122 (56–217)	∼	∼

Abbreviations: CT=chemotherapy; GCT=germ cell tumour; NA=not applicable; NS=not significant.

P-value for comparison between values of combination-CT survivors and healthy subjects (independent-samples Student's t-test or independent-samples Mann–Whitney where appropriate).

P-value for comparison between values of all survivors and healthy subjects (independent-samples Student's t-test or independent-samples Mann–Whitney where appropriate).

Systolic and diastolic blood pressure measurements for survivors treated with anti-hypertensive medication are excluded.

The summary of the patient characteristics (Table 2) showed that at the time of the analysis there were no major differences in age between the different treatment groups of GCT survivors and the controls. Seminoma patients (42.4 years; IQR 35–50) were older than non-seminoma patients (38.0 years; IQR 29–45; P=0.003). The BMI and waist circumference were comparable between the groups.

Smoking behaviour was comparable in all groups of patients and the controls, and amounted to ∼40%. Moreover, there were no major differences in blood pressure and renal function, assessed as creatinine clearance using the Cockroft formula, between the groups.

Combination-CT patients had significantly higher fasting serum concentrations of cholesterol, LDL-cholesterol, and triglyceride than that in controls, and higher serum cholesterol and triglyceride concentrations compared with that in surgery patients (Table 3). Carboplatin patients had higher fasting serum cholesterol (P=0.04) and LDL-cholesterol (P=0.004) concentrations than that in healthy subjects. Survivors treated with surgery only had higher LDL-cholesterol concentrations than that in healthy subjects (P=0.04). Fasting serum HDL-cholesterol concentrations did not differ significantly between treatment groups. Fasting serum glucose concentrations did not differ between treatment groups and healthy subjects (Table 3), and only five patients developed diabetes in the follow-up period. The CRP concentrations were elevated in 10 survivors (3.8%), but did not differ between the groups. Patients with disseminated disease treated with combination CT had significantly lower testosterone and higher FSH levels than that in stage-I patients who only underwent orchidectomy (Table 3). Thirty-four (12.9%) GCT survivors had hypogonadism; three of whom (4.5%) had orchidectomy alone and 31 (17.6%) had combination CT in addition to orchidectomy (Table 3). There were no differences in gonadal hormone levels between patients treated with orchidectomy only or patients treated with adjuvant single-dose carboplatin.

Table 3

Serum concentration of lipids, glucose and gonadal hormones in GCT survivors according to treatment group and in healthy subjects

		Treatment groups
Parameters: median (min–max)	Healthy subjects (N=360)	Surgery (N=58)	Carboplatin (N=21)	Combination CT (N=176)	All survivors (N=255)	P-valuea	P-valueb	P-valuec	Normal reference range
Glucose and fat metabolism
S. glucosed	5.1 (3.4–7.1)	4.8 (3.6–6.5)	5.0 (4.1–6.2)	5.1 (3.0–9.7)	5.0 (3.0–9.7)	NS	NS	NS	3.1–6.4 mmol l−1
S. cholesterole	4.90 (2.50–8.10)	4.42 (2.88–7.11)	5.30 (3.75–7.40)	5.20 (2.42–9.25)	5.07 (2.42–9.25)	0.006	0.001	0.01	3.90–7.30 mmol l−1
S. HDL-cholesterole	1.34 (0.64–2.90)	1.33 (0.68–2.70)	1.43 (0.94–1.70)	1.36 (0.60–4.07)	1.35 (0.60–4.07)	NS	NS	NS	0.70–1.50 mmol l−1
S. LDL-cholesterole	2.88 (1.26–5.66)	3.17 (1.59–5.28)	3.63 (1.77–5.80)	3.46 (0.54–7.08)	3.40 (0.54–7.08)	NS	<0.001	<0.001	0.70–4.50 mmol l−1
S. triglyceridee	1.17 (0.40–4.25)	1.00 (0.40–4.31)	1.26 (0.67–3.42)	1.27 (0.27–7.40)	1.25 (0.27–7.40)	0.01	0.005	0.05	0.80–2.30 mmol l−1
Gonadal hormones
S. testosteronef		16.8 (7.6–33.9)	15.8 (11.1–25.8)	14.1 (6.4–32.1)	14.9 (6.4–38.2)	0.04			8–35 (nmol l−1)
S. estradiol		69 (28–151)	67 (29–106)	76 (10–226)	74 (10–226)	0.05			70–200 (pmol l−1)
S. LH		5.9 (0.1–36.4)	4.7 (2.6–25.9)	6.8 (0.4–48.1)	6.4 (0.1–48.1)	NS			2.0–10.0 (U l−1)
S. FSH		9.7 (3.6–46.7)	10.1 (3.9–42.8)	14.5 (0.2–98.1)	12.4 (0.2–98.1)	<0.002			2.0–10.0 (U l−1)
S. SHBG		28 (3–75)	28 (16–55)	29 (2–67)	28 (2–75)	NS			20–55 (nmol l−1)
Biochemical parameters
S. lactate dehydrogenase		319 (129–753)	176 (130–494)	319 (72–531)	316 (72–753)	NS			100–248 (U l−1)
S. C-reactive protein		<3 (<3–18)	<3 (<3–6)	<3 (<3–30)	<3 (<3–30)	NS			<10 (μmol l−1)

Abbreviations: CT=chemotherapy; FSH=follicle-stimulating hormone; GCT=germ cell tumour; HDL=high-density lipoprotein; LDL=low-density lipoprotein; LH=luteinising hormone; NS=not significant; S.=serum; SHBG=sex hormone-binding globulin.

P-value for comparison of gonadal hormones and biochemical parameters between surgery and combination-CT survivors (independent-samples Mann–Whitney used).

P-value for comparison of glucose and fat metabolism between healthy subjects and combination-CT survivors (independent-samples Mann–Whitney used).

P-value for comparison of glucose and fat metabolism between healthy subjects and all survivors (independent-samples Mann–Whitney used).

Serum glucose and insulin measurements for survivors treated with anti-diabetic medication are excluded.

Serum cholesterol measurements for survivors treated with cholesterol-lowering medication are excluded.

34 Survivors; 1 surgery and 31 combination-CT survivors had serum testosterone levels<10.4 μmol l−1.

Prevalence of MetS

Using the NCEP-ATPIII criteria, GCT survivors had a significantly higher prevalence of obesity, dyslipidemia, and hypertriglyceridemia compared with age-matched healthy subjects (Table 4, upper part). In particular, survivors treated with combination CT had the highest prevalence of all NCEP-ATPIII criteria compared with healthy subjects. The prevalence of MetS did not differ between survivors treated with orchidectomy only or survivors treated with an orchidectomy and carboplatin. The prevalence of MetS in all groups was almost twofold higher when classified according to the IDF criteria compared with the NCEP-ATPIII criteria. There was only a minimal influence (β-coefficient=0.02 cases per year) of the time elapsed between curative treatment and the prevalence of MetS.

Table 4

Prevalence of metabolic syndrome according to NCEP-ATPIII (upper part) and IDF criteria (lower part) in survivors and in healthy subjects

		Treatment groups
Parameters ℰ𝒩𝒯ℐ𝒯𝒴𝒮𝒯𝒜ℛ𝒯ℰ𝒩𝒯ℐ𝒯𝒴ℰ𝒩𝒟	Healthy subjects (N=360)	Surgery (N=57a	Carboplatin (N=20a	Combination CT (N=174a	Survivors (N=251a	Combination CT, OR (95% CI)b	Survivors OR (95% CI)c
According to NCEP-ATP III
Hypertension	81 (22.5)	8 (14.0)	4 (20.0)	53 (31.0)	66 (26.3)	1.6 (1.0–2.3)	1.2 (0.8–1.8)
Obesity	70 (19.4)	10 (17.5)	6 (30.0)	51 (29.3)	67 (26.7)	1.7 (1.1–2.6)	1.5 (1.0–2.2)
Insulin resistance	16 (4.4)	2 (3.5)	1 (5.0)	11 (6.3)	14 (5.6)	1.5 (0.7–3.2)	1.3 (0.6–2.7)
Dyslipidemiad	36 (10.0)	7 (12.3)	4 (20.0)	35 (20.1)	46 (18.3)	2.3 (1.4–3.8)	2.0 (1.3–3.2)
Hypertriglyceridemiad	84 (23.3)	13 (22.8)	6 (30.0)	61 (35.1)	80 (31.9)	1.8 (1.2–2.6)	1.5 (1.1–2.2)
Metabolic syndrome	29 (8.1)	5 (8.8)	2 (10.0)	29 (16.7)	36 (14.3)	2.3 (1.3–4.0)	1.9 (1.1–3.2)
According to IDF
Hypertension	170 (47.2)	21 (36.8)	8 (40.0)	83 (47.7)	112 (44.6)	1.0 (0.7–1.5)	0.9 (0.7–1.2)
Obesity	165 (45.8)	24 (42.1)	13 (65.0)	107 (61.5)	144 (57.4)	1.9 (1.3–2.7)	1.6 (1.1–2.2)
Insulin resistance	57 (15.8)	6 (10.5)	3 (15.0)	34 (19.5)	43 (17.1)	1.3 (0.8–2.1)	1.1 (0.7–1.7)
Dyslipidemiad	36 (10.0)	7 (12.3)	4 (20.0)	35 (20.1)	46 (18.3)	2.3 (1.4–3.8)	2.0 (1.3–3.2)
Hypertriglyceridemiad	84 (23.3)	13 (22.8)	6 (30.0)	61 (35.1)	80 (31.9)	1.8 (1.2–2.6)	1.5 (1.1–2.2)
Metabolic syndrome	59 (16.4)	9 (15.8)	5 (25.0)	52 (29.9)	66 (26.3)	2.2 (1.4–3.3)	1.8 (1.2–2.7)

Abbreviations: CT=chemotherapy; CI=confidence interval; GCT=germ cell tumour; IDF=International Diabetes Federation; OR=odds ratio; NCEP-ATPIII=National Cholesterol Education Program Adult Treatment Panel III 2001.

Four survivors diagnosed with diabetes mellitus before orchidectomy (N=1), single-dose carboplatin (N=1), or combination CT (N=2) are excluded in this table.

OR for risk stratification between healthy subjects and combination CTsurvivors.

OR for risk stratification between healthy subjects and all GCT survivors.

Prevalence of dyslipidemia and hypertriglyceridemia are similar according to NCEP-ATPIII and IDF criteria.

GCT survivors had an increased age-adjusted NCEP-ATPIII risk of 1.9 (95% CI, 1.1–3.2) and an IDF risk of 1.8 (95% CI, 1.2–2.7; Table 4). Compared with healthy subjects, combination-CT survivors had the highest age-adjusted risk to develop MetS, that is, 2.3 (95% CI, 1.3-4.0, NCEP-ATPIII classification) and 2.2 (95% CI, 1.4-3.3, IDF classification; Table 4). In surgery-alone survivors, age-adjusted risk to develop MetS was, respectively, 1.5 (95% CI, 0.6–3.9, NCEP-ATPIII) and 1.7 (95% CI, 0.8–3.6, IDF) compared with healthy subjects. Irrespective of the use of the IDF or NCEP-ATPIII criteria, survivors with the lowest quartile testosterone levels (<12.0 nmol l−1) had a MetS prevalence higher than the other three quartiles (OR, 2.5 and 95% CI, 1.3–4.7; and OR, 1.7 and 95% CI, 0.8–3.6, respectively). The prevalence of MetS was not associated with other gonadal hormone concentrations or with alcohol use (data not shown).

According to the NCEP-ATPIII criteria, GCT survivors who were smokers had a twofold increased risk (95% CI, 1.0–4.0) for MetS compared with non-smokers. In healthy subjects, smokers had a 1.6-fold increased risk (95% CI, 0.7–3.4) for MetS compared with non-smokers. Smoking-adjusted risk of MetS for all survivors and for combination-CT survivors alone compared with healthy subjects was, respectively, 1.8 (95% CI, 1.1–3.1) and 1.5 (95% CI, 1.1–2.0).

Ten-year cardiovascular risk profile

According to the FRS analysis, the calculated 10-year cardiovascular risk was 3.0% (IQR, 0.0–5.0) in the survivors and 3.6% (IQR, 0.0–6.0) in the controls. When using the SCORE algorithm, these values were 1.6% (IQR, 0.1–1.7) and 2.0% (IQR, 0.1–2.7), respectively. There was no treatment-related difference in age-adjusted 10-year cardiovascular risk in GTC survivors

Discussion

We observed that the prevalence of the MetS is 2.2- to 2.3-fold higher at a mean duration of 7.8 years after cure in testicular GCT survivors treated with combination CT compared with age-matched healthy subjects. In particular, abdominal obesity, hypertension, hypertriglyceridemia, and other dyslipidemias were more frequently observed in CT-treated cancer survivors. Notably, also fasting LDL-cholesterol, which is not included in any MetS classification was consistently higher in all GCT survivors. It is remarkable that in our cohort all GCT survivors, but in particular combination-CT survivors, had higher BMI and were significantly more overweight than controls. In the survivor population, low testosterone concentrations correlated with MetS and the patients treated with combination CT had an average 2.7 nmol l−1 lower testosterone than those treated with surgery alone. After adjusting for testosterone, there still was a significant difference in MetS prevalence between the two groups, also after adjusting for age and smoking. In GCT survivors, MetS may be related to a possible pre-existing underlying TDS (Skakkebaek ) as well as to partial hypogonadism induced by CT, or both. The 10-year cardiovascular risk estimated with either FRS or SCORE was low (3.0% and 1.6%, respectively) and did not differ between treatment groups or between treatment groups and controls.

Different definitions are used for MetS worldwide, and we show here that depending on the classification that is used, the prevalence of MetS may vary greatly. There was an almost twofold higher absolute MetS prevalence when using IDF (26.9%) compared with using NCEP-ATPIII (14.6%). However, the RR for MetS was shown to be independent of the scoring system and showed that GCT survivors had a 1.9- (NCEP-ATPIII) or 1.8-fold higher MetS prevalence compared with controls. The increased prevalence of MetS according to the IDF criteria compared with that of the NCEP-ATPIII has been repeatedly demonstrated in worldwide cohorts (Rathmann ). The use of different or adapted scoring systems may also explain why the prevalence of MetS in our cohort varied with those previously reported. Three other cross-sectional studies reported different MetS prevalences in GCT survivors, possibly because of the different methodologies used in the evaluation of the MetS (Table 5). In keeping with our data, Nuver observed a higher MetS prevalence and an increased RR for MetS in a smaller GCT survivor cohort with a similar incidence of MetS in their controls (Table 5). A large multicentre cross-sectional study conducted in five university hospitals in Norway (Haugnes ) reported an unusually high MetS prevalence of 52% in healthy subjects, and 45% and 33%, respectively, in GCT survivors treated with CT or orchidectomy alone. Discrepancies may be explained by non-adherence to the 2002 NCEP-ATPIII classification, the use of non-fasting blood samples, using (at least two) modified criteria to assess the MetS and of only serum total cholesterol. In another report from a single institution (Wethal ), which participated in the multicentre study (Haugnes ), the authors also did not adhere to above mentioned classification methodology, which may have led to an overestimation of MetS.

Table 5

Metabolic syndrome prevalence and odds ratio's in four cross-sectional studies

Parameters	Nuveret al (2005)	Haugneset al (2007)		Wethalet al (2007)	this study
Number of survivors	130	1135		589	251
Mean age (years) (range)	38.5 (20–65)	42.5 (23–60)		42 (23–60)	39.6 (18–70)
Mean follow-up time (years) (range)	7.5 (3–13)	11.2 (5–22)		11 (7.7–14.5)	7.8 (0.1–30.0)
Healthy subjects (N)	47	1150		8835	360
Metabolic syndrome definition	NCEP-ATP III	Modified NCEP-ATP III ⩾ 2 criteriaa	Modified NCEP-ATP III ⩾3 criteriaa	Modified criteria ⩾3 criteriaa	NCEP-ATP III	IDF
Metabolic syndrome prevalence (%)
All GCT survivors	38 (29.2)	447 (39.4)	92 (8.1)	82 (13.9)	36 (14.3)	66 (26.3)
Combination CT	22 (25.6)	191 (41.2)	40 (8.6)	38 (17.4)	29 (16.7)	52 (29.9)
Single-dose carboplatin	∼	∼	∼	∼	2 (10.0)	5 (25.0)
Radiotherapy	∼	184 (42.0)	37 (8.3)	35 (15.2)	∼	∼
Surgery only	16 (34.0)	72 (33.0)	15 (6.7)	9 (6.4)	5 (8.8)	9 (15.8)
Healthy subjects	4 (8.5)	584 (51.5)	170 (14.8)	Not mentioned	29 (8.1)	59 (16.4)
OR (95% CI) adjustmentsb
GCT survivors vs healthy subjects	4.4 (1.5–13.2)	0.6 (0.5–0.7)	0.5 (0.4–0.7)	∼	1.9 (1.1–3.2)	1.8 (1.2–2.7)
Combination CT vs healthy subjects	3.7 (1.2–11.5)	0.7 (0.5–0.8)	0.5 (0.4–0.8)	3.7 (1.5–9.1)	2.3 (1.3–4.0)	2.2 (1.4–3.3)
Combination chemotherapy vs surgery only	0.6 (0.3–1.3)	1.5 (1.1–2.1)	1.3 (0.7–2.4)	3.1 (1.4–6.6)	2.1 (0.8–5.7)	2.3 (1.0–5.0)

Abbreviations: CI=confidence interval; CT=chemotherapy; GCT=germ cell tumour; IDF=International Diabetes Federation; OR=Odds ratio; NCEP-ATPIII=National Cholesterol Education Program Adult Treatment Panel III 2001.

Non-fasting blood samples.

Calculated from the raw data presented in the individual reports.

As in other studies the high prevalence of MetS does not necessarily translate into increased cardiovascular risk. In keeping with the 2.2% cumulative incidence reported by Haugnes in their patients , our GCT survivors have a low 10-year cardiovascular risk of 3.0% as estimated by FRS. This risk estimate is similar to that observed in the general population by van den Belt-Dusebout and to the 3.0% cardiovascular risk reported for another Dutch cohort of 408 healthy males of the same age (de Visser ). Although FRS calculations for individuals under the age of 40 years are less specific, a main shortcoming of MetS prediction for cardiovascular events is that it does not take into account major risk factors for CVD, such as age, exercise, and smoking status. The association between the severity of risk factors and CVD risk is also not taken in consideration in the MetS criteria.

Our cross-sectional single-centre study has some limitations, including the relatively short follow-up time after cure, related to the past policy of discharging GCT patients 5 years after establishment of cure. Moreover, the subgroup of patients who received only one single administration of carboplatin is relatively small, as single-dose adjuvant carboplatin has only recently been introduced as an alternative treatment in patients with stage-I seminoma (Oliver ; Krege ). Although few patients received adjuvant carboplatin treatment, the data suggest that the cumulative dose of cisplatin added to that of cytotoxic drugs of the standard combination drug regimens is a decisive determinant to develop MetS. Although more of our GCT patients were smokers than controls, adjustment for smoking differences did not alter the significantly increased MetS prevalence in combination-CT patients. This was also the case when all survivors were compared with healthy subjects. Finally, it may be argued that there was a substantial variability in the time that had elapsed between the diagnosis and initial treatment and the time of assessment of the survivors. However, we investigated whether there was a time dependency between the time of assessment and the prevalence of MetS, and whether there was only a weak association between these variables. This suggests that the effects of combination CT are likely to be acute and maintained over time. Thirty to fifty per cent of GCT patients treated with CT are infertile and most of the GCT survivors have long-term partial or complete hypogonadism (Berger ). As a proportion of GCT patients already have TDS, it is unknown whether the infertility results from this condition, the CT, or from both (Williams ). Whatever the explanation is, low testosterone and SHBG levels are considered risk factors for MetS in otherwise healthy men (Muller ; Kupelian ; Miner and Sadovsky, 2007). We indeed found an association between low serum concentrations of testosterone and MetS in all patients and, in particular, CT patients, but there was no association between SHBG, LH, or FSH levels and MetS. We argue that because hypogonadism is associated with increased cardiovascular risk GCT survivors should be treated with testosterone supplementation. Although testosterone supplementation has not (yet) been shown to prevent CVD, clinical trials with testosterone supplementation have resulted in a significant reduction of cholesterol levels (Fernandez-Balsells ; Monroe and Dobs, 2013). Apart from these favourable effects on lipid metabolism, testosterone supplementation also results in increased BMD, muscle mass, and fat-free body mass (Snyder ; Aversa ). In particular, use of daily transdermal testosterone gel may be attractive, as this is reported to be without side effects. As the risk to develop prostate cancer after long-term use of transdermal androgens is currently unknown, it may be prudent to consider monitoring of PSA when initiating treatment (Lakshman and Basaria, 2009).

Our data confirm that according to the NCEP-ATPIII and IDF criteria, the subgroup of hypogonadal GCT survivors who received combination CT is the main group at increased risk for developing a MetS compared with the general population. We observed no clear increase in the calculated 10-year CVD risk in long-term GCT survivors, although the follow-up period was perhaps too short. Long-term CT-related cardiovascular toxicity may result from acute direct endothelial damage or from indirect long-term CT-induced hormonal and metabolic changes, including liver and gut damage, thereby affecting lipid uptake, transport, and metabolism over a period of many years.

In conclusion, our findings suggest an increased prevalence of MetS in GTC survivors who received CT. Of these CT patients, we further identify patients with low androgen levels as a subgroup that is particularly at risk of developing MetS. On the basis of this important clinical finding we advocate that guidelines to monitor blood pressure, lipid- and glucose metabolism, and assessment of gonadal hormone status should be introduced in international urology/oncology guidelines rather than monitoring potential complications of treatment. This is particularly important, as the current standard of follow-up is focused on the detection of tumour recurrence. In our opinion, this would allow for evidence-based counselling of GCT survivors to adhere to a lifestyle that favourably affects the modifiable risk factors for MetS and cardiovascular risk, such as regular exercise, low-carbohydrate diet, and smoking cessation. We would be in favour of correcting androgen deficiency more liberally in this group of relatively young male cancer survivors. Obviously, the beneficial effect of this intervention on prevention or reversal of the MetS remains to be established, but longer-lasting intervention studies should be able to establish whether this approach of lifetime monitoring, lifestyle intervention, and correction of hypogonadism by wider use of testosterone supplementation at some stage during the natural course of GCT may prevent or revert the development of MetS and associated risk of CVD in long-term survivors of GCT.