Adverse effects of anabolic androgenic steroids abuse on gonadal function, glucose homeostasis and cardiovascular function

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Adverse effects of anabolic androgenic steroids abuse on gonadal function, glucose homeostasis and cardiovascular function Associate Professor Caroline Kistorp, Ph.D Department of Internal Medicine, Herlev University Hospital University of Copenhagen Disclosures Received unrestricted research grants from: Antidoping Denmark Danish Heart Foundation Titel/beskrivelse (Sidehoved/fod) Navn (Sidehoved/fod) 2 1

Agenda Background Study Protocol Results Hormonal disturbances (Androgens and Fertility Markers) Insulin Sensitivity Blood Pressure and Arterial Stiffness The Heart Hypotheses Is AAS abuse associated with: Persistent symptoms of hypogonadism after AAS discontinuation? Decreased insulin sensitivity? Hypertension and arterial stiffness? Impaired cardiac function and myocardial fibrosis? 2

Cross-sectional study ( Pseudo-longitudinal design ) No AAS Current AAS abuse After AAS abuse Variables Control Participants N=30 Current AAS Abusers N=37 Former AAS Abusers N=33 P-value Age (years) 31.5 (1.2) 31.4 (1.4) 34.8 (1.2) 0.11 Accumulated duration on AAS (weeks) Duration since AAS cessation (years) - 142.3 (99.7-203.1) 111.8 (81.3-153.7) 0.32 - - 2.6 (1.7 3.7) Exclusion Criteria: known DM/CVD, congenital hypogonadism, medically prescribed testosterone therapy Physical exam Orchidometer Hormone analyses (morning) Total/free testosterone (+other androgens) Estrogens Gonadotropins Inhibin B og Anti-Müllerian Hormone Questionaires Erectile dysfunction (IIEF-5) Depressive symptoms (BDI-II) SF-36 3

Glucose tolerance (OGTT) and body composition 24-hour BP monitoring Pulse wave analysis (PWA) Advanced Echocardiography Cardiac MRI (with Late-Gadolineum Enhancement) Blood samples 4

Results Rasmussen et al PLOS ONE (2016) 5

Testicular size 25 20 * 15 * 10 5 0 Control Group Ongoing AAS Former AAS Rasmussen et al PLOS ONE (2016) 11 Fig 1. Association between accumulated duration of AAS abuse (log 2 scale) and testis size in current AAS (spline function) and former AAS. Rasmussen JJ, Selmer C, Østergren PB, Pedersen KB, Schou M, et al. (2016) Former Abusers of Anabolic Androgenic Steroids Exhibit Decreased Testosterone Levels and Hypogonadal Symptoms Years after Cessation: A Case-Control Study. PLoS ONE 11(8): e0161208. doi:10.1371/journal.pone.0161208 http://journals.plos.org/plosone/article?id=info:doi/10.1371/journal.pone.0161208 6

Rasmussen et al PLOS ONE (2016) Total Testosterone < 12.1 nmol/l Rasmussen et al PLOS ONE (2016) 7

S-Inhibin B (pg/ml) (Sertoli cells, spermatogenesis) 200,0 180,0 160,0 140,0 *P<0.05 120,0 100,0 80,0 * 60,0 40,0 20,0 0,0 Control Group Ongoing AAS Former AAS Rasmussen et al PLOS ONE (2016) Impaired spermatogenesis (Inhibin B<92) Rasmussen et al. PLOS ONE (2016) 8

Fig 4. Association between accumulated duration of AAS abuse (log 2 scale spline function) and serum inhibin B levels in current AAS. Rasmussen JJ, Selmer C, Østergren PB, Pedersen KB, Schou M, et al. (2016) Former Abusers of Anabolic Androgenic Steroids Exhibit Decreased Testosterone Levels and Hypogonadal Symptoms Years after Cessation: A Case-Control Study. PLoS ONE 11(8): e0161208. doi:10.1371/journal.pone.0161208 http://journals.plos.org/plosone/article?id=info:doi/10.1371/journal.pone.0161208 Fig 5. Association between accumulated duration of AAS abuse (log2 scale) and serum anti- Müllerian hormone levels (AMH, log2 scale) in current AAS. Rasmussen JJ, Selmer C, Østergren PB, Pedersen KB, Schou M, et al. (2016) Former Abusers of Anabolic Androgenic Steroids Exhibit Decreased Testosterone Levels and Hypogonadal Symptoms Years after Cessation: A Case-Control Study. PLoS ONE 11(8): e0161208. doi:10.1371/journal.pone.0161208 http://journals.plos.org/plosone/article?id=info:doi/10.1371/journal.pone.0161208 9

Fig 6. Symptoms of depression, erectile dysfunction and decreased libido in the three groups. Rasmussen JJ, Selmer C, Østergren PB, Pedersen KB, Schou M, et al. (2016) Former Abusers of Anabolic Androgenic Steroids Exhibit Decreased Testosterone Levels and Hypogonadal Symptoms Years after Cessation: A Case-Control Study. PLoS ONE 11(8): e0161208. doi:10.1371/journal.pone.0161208 http://journals.plos.org/plosone/article?id=info:doi/10.1371/journal.pone.0161208 AAS-induced hypogonadism Frequent condition among AAS Decreased testosterone levels seem to persist among many former AAS years after AAS discontinuation Spermatogenesis seem to recover within 6-12 months Withdrawal/hypogonadal symptoms persist years after AAS discontinuation 20 10

Perspectives: treatment with clomiphene? Rahnema et al. Fertility and Sterility (2014) Supraphysiologic levels of androgens Insulin resistance? 11

Oral glucose tolerance test (120 min) Rasmussen et al. Clinical Endocrcrinology (in press) Insulin sensitivity (Matsuda index) Rasmussen et al. Clinical Endocrcrinology (in press) 12

Impaired Glucose Tolerance 20,0% Trend test: P = 0.04 18,0% 16,0% 14,0% 12,0% 10,0% 8,0% 6,0% 4,0% 2,0% 0,0% Control group Current AAS Former AAS Rasmussen et al umpublished AAS adverse effect on adipose tissue? *P<0.05 Rasmussen et al. unpublished 13

Body Composition Body composition and fat mass distribution Controls Current AAS Former AAS BMI (kg/m 2 ) 27.2 (0.6) 30.8 (0.4) 28.5 (0.6) <0.01 Total lean mass (kg) 70.7 (1.5) 81.3 (1.4) 71.2 (1.6) <0.01 Total fat mass (kg) 15.3 (0.9) 13.4 (0.5) 17.5 (0.8) <0.01 Body fat (%) 17.5 (0.7) 14.1 (0.4) 19.4 (0.6) <0.01 Abdominal VAT volume (cm 3 ) 293.3 (11.7) 388.4 (17.1) 347.4 (17.3) <0.01 Android fat mass (g) 1300 (95) 1198 (54) 1603 (91) b <0.01 Total testosterone inversely associated with fat mass: Age-adjusted: -1.1 (-2.0 ; -0.1), P = 0.02) Rasmussen et al unpublished Cardiovascular risks Hypertension? Stroke? Dyslipidemia? Atherosclerosis? Sudden cardiac death? Heart Failure (myocardial fibrosis)? 14

24-hour Blood Pressure Monitoring *P<0.05 Current AAS exhibited higher 24-hour systolic BP compared with control participants (8.8 (2.9 ; 14.8) mmhg) Diastolic BP and MAP did not differ among the 3 groups Rasmussen et al. unpublished 24-hour systolic hypertension Rasmussen et al. unpublished 15

Cardiac natriuretic peptides and testosterone *P<0.05 Rasmussen et al. unpublished 31 Center of Endocrinology and Metabolism Lab Analyses Noradrenaline (pg/ml) Hematocrit (%) 52 50 48 46 44 42 40 0,35 0,30 0,25 0,20 0,15 0,10 0,05 0,00 Controls Controls * Current AAS * Current AAS Former AAS Former AAS MR-proANP (pmol/l) 60,0 50,0 40,0 30,0 20,0 10,0 0,0 Aldosterone (pmol/l) 400 350 300 250 200 150 100 50 0 Controls Controls * Current AAS * Current AAS Former AAS Former AAS Rasmussen et al, unpublished Adjustment for differences in lab analyses balanced differences in systolic BP (P = 0.94) 16

Center of Endocrinology and Metabolism Method Maximal areal Minimal areal 33 Center of Endocrinology and Metabolism Aortic Stiffness Aorta Distensibility Index: Rasmussen et al. unpublished 34 17

Albuminuria (Spot urine Albumin-creatinine-ratio) 35,0% 30,0% 25,0% 20,0% 15,0% 10,0% 5,0% 0,0% Controls Current AAS Former AAS Spearman s rank coeff among current AAS : 24-hour systolic BP and urine ACR: r = 0.39, P < 0.01 Rasmussen et al, unpublished Hazard ratios for cardiovascular events, positive doping tests Thiblin et al. Drug and Alcohol Dependence (2015) 18

Cardiac MRI: Myocardial Fibrosis? No focal signs of myocardial scars (LGE) No indications of diffuse fibrosis (similar post T1 mapping time (P = 0.68)) Rasmussen et al, unpublished Cardiac MRI: Function and Dimensions Variables Controls Current AAS Former AAS P-value LV EF (%) 67.1 (1.0) 60.1 (1.2)* 66.7 (1.2) P < 0.01 LV mass (g) 163 (6) 213 (7)* 152 (3) P < 0.01 LV mass/total lean mass 2.3 (0.1) 2.6 (0.1)* 2.2 (0.1) P < 0.01 (g/kg) RV EF (%) 54.2 (1.4) 48.1 (1.1)* 50.8 (1.8) P < 0.01 No differences in ventricular volumes (adjusted for lean mass) Measures of diastolic function and strain? Rasmussen et al, unpublished 19

Strain Titel/beskrivelse (Sidehoved/fod) Navn (Sidehoved/fod) 39 Summary AAS abuse leads to: Long-term subclinical hypogonadism Decreased insulin sensitivity Hypertension Increased central arterial stiffness Impaired cardiac function 20