Cardiovascular Disease After Spinal Cord Injury: Achieving Best Practice. Suzanne Groah, MD, MSPH Walter Reed Army Medical Center February 12, 2010

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Cardiovascular Disease After Spinal Cord Injury: Achieving Best Practice Suzanne Groah, MD, MSPH Walter Reed Army Medical Center February 12, 2010

CAVEAT LECTOR 2

CVD-related Mortality in Aging SCI GU complications accounted for 43% of SCI-related deaths in the 40s and 50s GU mortality was reduced to 10% in the 80s and 90s CVD-related diseases are now the most frequent cause of death long-term 46% of those surviving 30 years 35% of those older than 60 years 3

Cardiometabolic Risk Clustering Metabolic syndrome has been supplanted by cardiometabolic risk Better defines CVD and endocrine risks Clustering is the unique combinations of risk factors in populations that may impart a health hazard Risk clustering linked to CVD-related morbidity and mortality, which worsens nonlinearly with identification of additional risk 4 factors

5

EVALUATING RISK FACTORS SMOKING 6

Smoking in the U.S. Healthy People 2010 goal 12% Most recent CDC data 19.8% Down from 23% (1998) Non smoking states Utah, CA, CT Smoking states KY, WV, OK 7

Tobacco Use after SCI 19-22% in the community Veterans have a similar or slightly higher prevalence 8 Banerjea, 2009; Johnston, 2005; Weaver, 2007

EVALUATING RISK FACTORS BLOOD PRESSURE 9

Hypertension in the U.S. 1 in 3 adults Cause in 90-95% unknown Death due to hypertension Rate increased 25.2% Number of deaths increased by 56.4% At risk groups Non-Hispanic blacks Middle-aged or older Less educated Overweight or obese Physically inactive Comorbid diabetes

Hypertension after SCI Well-known decrease in BP after SCI More pronounced with higher and more complete injuries Hypertension clearly more prevalent in paraplegia compared with tetraplegia Hypertension more likely in those with incomplete injuries 11

Questions Related to Hypertension But is hypertension more common than in the U.S. population? Is hypotension protective for CVD? What is hypertension in tetraplegia? 12

Autonomic Dysregulation Autonomic dysreflexia 10% of people with chronic SCI have AD Much AD is silent 2.5% incomplete paraplegia 3% complete paraplegia 12% incomplete tetraplegia 22.5% complete tetraplegia 13

EVALUATING RISK FACTORS OVERWEIGHT/OBESITY 14

Obesity High body fat relative to lean body mass (>22% body fat) Waist circumference Men > 42 in Women > 35 in Waist to hip ratio (WHR) Waist Circ / Hip Circ Men < 0.9 safe; > 1 at risk Women < 0.8 safe; > 1 at risk

NHLBI Obesity Education Initiative Body mass index (kg/m 2 ) BMI >= 30 Obesity is a defining component of CMR Category BMI Underweight <18.5 Normal 18.5-24.9 Overweight 25.0-29.9 Obesity I 30.0-34.9 Obesity II 35.0-39.9 Obesity III 40.0 Clinical Guidelines on the Identification, Evaluation, and Treatment of Overweight and Obesity in Adults (1998)

UNITED STATES OBESITY TRENDS 17

Obesity Trends* Among U.S. Adults BRFSS, 1985 (*BMI 30, or ~ 30 lbs. overweight for 5 4 person) No Data <10% 10% 14%

Obesity Trends* Among U.S. Adults BRFSS, 1986 (*BMI 30, or ~ 30 lbs. overweight for 5 4 person) No Data <10% 10% 14%

Obesity Trends* Among U.S. Adults BRFSS, 1987 (*BMI 30, or ~ 30 lbs. overweight for 5 4 person) No Data <10% 10% 14%

Obesity Trends* Among U.S. Adults BRFSS, 1988 (*BMI 30, or ~ 30 lbs. overweight for 5 4 person) No Data <10% 10% 14%

Obesity Trends* Among U.S. Adults BRFSS, 1989 (*BMI 30, or ~ 30 lbs. overweight for 5 4 person) No Data <10% 10% 14%

Obesity Trends* Among U.S. Adults BRFSS, 1990 (*BMI 30, or ~ 30 lbs. overweight for 5 4 person) No Data <10% 10% 14%

Obesity Trends* Among U.S. Adults BRFSS, 1991 (*BMI 30, or ~ 30 lbs. overweight for 5 4 person) No Data <10% 10% 14% 15% 19%

Obesity Trends* Among U.S. Adults BRFSS, 1992 (*BMI 30, or ~ 30 lbs. overweight for 5 4 person) No Data <10% 10% 14% 15% 19%

Obesity Trends* Among U.S. Adults BRFSS, 1993 (*BMI 30, or ~ 30 lbs. overweight for 5 4 person) No Data <10% 10% 14% 15% 19%

Obesity Trends* Among U.S. Adults BRFSS, 1994 (*BMI 30, or ~ 30 lbs. overweight for 5 4 person) No Data <10% 10% 14% 15% 19%

Obesity Trends* Among U.S. Adults BRFSS, 1995 (*BMI 30, or ~ 30 lbs. overweight for 5 4 person) No Data <10% 10% 14% 15% 19%

Obesity Trends* Among U.S. Adults BRFSS, 1996 (*BMI 30, or ~ 30 lbs. overweight for 5 4 person) No Data <10% 10% 14% 15% 19%

Obesity Trends* Among U.S. Adults BRFSS, 1997 (*BMI 30, or ~ 30 lbs. overweight for 5 4 person) No Data <10% 10% 14% 15% 19% 20%

Obesity Trends* Among U.S. Adults BRFSS, 1998 (*BMI 30, or ~ 30 lbs. overweight for 5 4 person) No Data <10% 10% 14% 15% 19% 20%

Obesity Trends* Among U.S. Adults BRFSS, 1999 (*BMI 30, or ~ 30 lbs. overweight for 5 4 person) No Data <10% 10% 14% 15% 19% 20%

Obesity Trends* Among U.S. Adults BRFSS, 2000 (*BMI 30, or ~ 30 lbs. overweight for 5 4 person) No Data <10% 10% 14% 15% 19% 20%

Obesity Trends* Among U.S. Adults BRFSS, 2001 (*BMI 30, or ~ 30 lbs. overweight for 5 4 person) No Data <10% 10% 14% 15% 19% 20% 24% 25%

Obesity Trends* Among U.S. Adults BRFSS, 2002 (*BMI 30, or ~ 30 lbs. overweight for 5 4 person) No Data <10% 10% 14% 15% 19% 20% 24% 25%

Obesity Trends* Among U.S. Adults BRFSS, 2003 (*BMI 30, or ~ 30 lbs. overweight for 5 4 person) No Data <10% 10% 14% 15% 19% 20% 24% 25%

Obesity Trends* Among U.S. Adults BRFSS, 2004 (*BMI 30, or ~ 30 lbs. overweight for 5 4 person) No Data <10% 10% 14% 15% 19% 20% 24% 25%

Obesity Trends* Among U.S. Adults BRFSS, 2005 (*BMI 30, or ~ 30 lbs. overweight for 5 4 person) No Data <10% 10% 14% 15% 19% 20% 24% 25% 29% 30%

Obesity Trends* Among U.S. Adults BRFSS, 2006 (*BMI 30, or ~ 30 lbs. overweight for 5 4 person) No Data <10% 10% 14% 15% 19% 20% 24% 25% 29% 30%

Obesity Trends* Among U.S. Adults BRFSS, 1990, 1998, 2006 (*BMI 30, or about 30 lbs. overweight for 5 4 person) 1990 1998 2006 No Data <10% 10% 14% 15% 19% 20% 24% 25% 29% 30%

Body Composition Authors # SCI Gender Age BMI SCI %BF AB % BF Method Buchholz, 2003 Bulbanian, 1987 Clasey, 2006 George, 1988 28 Para M/F 29 23.5 30.8 22.8 H20 Dil 22 Para M 27.5 22.3 22.4 11.3 Hydro 13 Para M/F 37 24.3 27.7 NA 4-C 15 P/T M/F 31 22.3 25.5 20.2 Hydro Jones, 2003 20 P/T M 16-52 23.1 27.5 18.1 DXA Lussier, 1983 Maggioni, 2003 Spungen, 2000 Spungen, 2003 2 Para F 30.5 17.9 30.5 NA Hydro 13 Para M 34 25.7 31.1 20.8 DXA 8 Para M 40 22.3 33.5 26.3 DXA 66 Tetra M 40 25.4 36.3 24.2 DXA 41

Body Habitus After SCI Routine BMI Tables BMI ( Population Guidelines) U.S. Men 34 All SCI Men Males Tetra U.S. Women 34 Females All SCI Women Tetra Recommended < 25 Overweight 25.1 29.9 Obesity 30.0 39.9 Extreme Obesity > 40 29.2% 39.3% 37.5% 40.5% 38.2% 75.0% 81.8% 49.2% 50.0% 48.6% 16.7% 18.2% 31.1% 11.5% 12.5% 10.8% 33.2% 2.8% 0% 0% 0% 6.9% 8.3% 100% Overweight or Obese 70.8% 60.7% 62.5% 59.5% 61.8% 25% 100% 18.2% 42 Groah, 2009

Body Habitus After SCI Adjusting for SCI, 74% of the SCI population studied were overweight or obese Using standard BMI tables, 59.5% of males and 18.2% of females were overweight or obese 43 Groah, 2009

Obesity After SCI Obesity is at epidemic proportions Obesity is due to Obligatory sarcopenia Blunted anabolism Blunted sympathetic NS Positive energy balance Obesity is UNDERestimated by BMI in people with SCI 44

Obesity After SCI Obesity mediates Insulin resistance Hypertension Dyslipidemia Thromboembolism Coronary artery disease 45

Adipocytes: Fat is not Benign! Secretes inflammatory mediators Interleukin-6 Tumor necrosis factor Secretes fibrinolysis inhibitors Increase thrombus risk Mediates CRP and hscrp Reduce vasodilation and promote atherogenesis Hypertension Cause insulin resistance

EVALUATING RISK FACTORS PHYSICAL ACTIVITY 47

Motivators and Deterrents to Exercise 26 adults with SCI were polled from a survey of 596 with SCI All were active prior to injury and expressed an interest in being physically active 15 exercisers and 11 non-exercisers 48 Kehn & Kroll, 2008

Motivators and Deterrants to Exercise No differences between the groups in age, gender, marital status, education, income, employment, injury level, or completeness Duration of injury was associated with exercising Barriers to exercise Limited return on investment Time, motivation, lack of knowledge of equipment 49 Kehn & Kroll, 2008

EVALUATING RISK FACTORS: ATHEROGENIC DYSLIPIDEMIA 50

National Cholesterol Education Panel Guidelines HDL < 40 is abnormal LDL 130 159 is borderline high LDL > 160 is high LDL target is 100 Triglyceride 150-199 is borderline high Triglyceride < 150 is normal

HDL-C Roles HDL-C function includes protection against development of vascular disease HDL-C is directly related to insulin sensitivity 52

HDL-Cholesterol After SCI Nonveterans with SCI and matched sedentary controls HDL-C was lower in the SCI population 39 mg/dl vs. 45 mg/dl HDL-C and race Caucasians and Latinos with SCI have lower HDL-C than AB controls AA with or without SCI had higher HDL-C when matched on ethnicity and SCI AA with SCI do not have HDL-C levels significantly different from non-sci AA

Atherogenic Lipid Profile Normal total cholesterol Normal or elevated LDL Normal or elevated triglycerides Consistently low HDL Significantly elevated TC:HDL ratio Bauman, 1992; 1992; 1999; Bostom 1991; Zlotolow 1992

EVALUATING RISK FACTORS INSULIN RESISTANCE 55

Diagnostic Criteria for Disorders of Carbohydrate Metabolism Normal (NGT) Impaired (IGT) Diabetic (DM) FPG (mg/dl) <100 100*-125 126 OGTT 120 min (mg/dl) <140 140-199 200 Report of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus: Diabetes Care 20:1183-1197, 1997. *Updated from 110, Diabetes Care 2003

Glucose Intolerance in SCI Hyperinsulinemia 34% of SCI had IGT Impaired glucose tolerance 73% complete tetra 44% incomplete tetra 24% complete para 31% incomplete parad 57 Bauman, 1994; Bauman 1999

Relationship of Age with Glucose Tolerance in Veterans Bauman WA and Spungen AM. Metabolism. 43: 749-756, 1994

Insulin Resistance Peak Glucose correlated with: Highest level of lesion Older age at time of injury Increased TB %fat Peak Insulincorrelated with: Male gender Increased TB %fat Bauman WA, Adkins RH, Spungen AM, Waters RL. The effect of residual neurological deficit on oral glucose tolerance in persons with chronic spinal cord injury. Spinal Cord. 1999; 37: 765-771.

CHO Metabolism Summary Increased prevalence of IGT and DM The more severe the neuro impairment, the worse the CHO metabolism Peak Glucose is independently related to %fat, neuro, age at time of injury, and male gender Hyperinsulinemia: >50% Tetra and >30% Para OGTT to diagnose early disease (IGT, mild DM, and hyperinsulinemia)

ALL OF THESE FACTORS RELATE TO CARDIOMETABOLIC RISK 61

Cardiometabolic Risk Central obesity (WC) European men >94cm (37 ) Or US men > 102 cm (40 ) European women > 80 cm (31.5 ) Or US women > 88 cm (34.5 ) Plus any 2 of the following: TG >= 150 md/dl Low HDL-C High BP Fasting glucose >= 100 md/dl

Metabolic Syndrome after SCI N=487 vets with SCI Mean age 55.2 yrs; 48.7% tetra 63.4% HDL < 40 56.5% BMI > 25 kg/m2 56.5 % htn 44.8% IDF metabolic syndrome 37% dyslipidemia 63 Castillo, 2007 (JSCM)

EVALUATING RISK FACTORS INFLAMMATION 64

Evidence that CRP is a Strong Predictor of Future Cardiac Events CRP has strong prognostic value for detection of 1 st vascular events, even after adjustment for all traditional CVD risks 1 hs-crp levels are strongly correlated with future CHD mortality. 2 Baseline hs-crp levels are significantly higher among men who subsequently sustain MI. 3 Combined modeling with hs-crp and Total Cholesterol (TC) improved forecasting of future MI by TC alone. 3 Meta-analyses consistently find CRP a significant CVD risk marker. 1 Women s Health Study (WHS), 2 Multiple Risk Factor Intervention Trial (MRFIT), 3 Physicians Health Study (PHS)

Relative Risk Categories for hs-crp Levels: Two Stratification Methods Low Moderate High < 1 mg/dl 1-3 mg/dl > 3 mg/dl Quintile of TC:HDL-C ratio Disease Risk Stratification by Cutpoints of the American Heart Association Centers for Disease Control and Prevention Quintile of hs-crp (mg/l) 1 2 3 4 5 Male Female < 0.7 0.7-1.1 1.2-1.9 2.0-3.8 3.9-15 1 < 3.4 < 3.4 1 1.2 1.4 1.7 2.2 2 3.4-4.0 3.4-4.1 1.4 1.7 2.1 2.5 3.0 RR s 3 4.1-4.7 4.2-4.7 2.0 2.5 2.9 3.5 4.2 4 4.8-5.5 4.8-5.8 2.9 3.5 4.2 5.1 6.0 5 > 5.5 >5.8 4.2 5.0 6.0 7.2 8.7 Combined: Physicians Health Study and Women s Health Study RCTs

CVD Risk Based Upon Tertiles of hs-crp: 45.8% of Population at 2x or Greater Risk Number Number of of Subjects Subjects in in Each Each CRP CRP Range Range 20 20 18 18 16 16 14 14 12 12 10 10 8 8 6 6 4 4 2 2 19 19 6 6 Risk Risk hs-crp n (59) (59) % Low Low < 1 mg/dl 19 19 32.2 32.2 Moderate 1-31 1-3 3 mg/dl 13 13 22 22 High > 3 mg/dl 27 27 45.8 45.8 10 10 7 7 7 7 3 3 3 3 2 2 1 1 1 1 0 0 0.0-0.99 1.0-1.99 2.0-2.99 3.0-3.99 4.0-4.99 5.0-5.99 6.0-6.99 7.0-7.99 8.0-8.99 9.0-9.99 0.0-0.99 1.0-1.99 2.0-2.99 3.0-3.99 4.0-4.99 5.0-5.99 6.0-6.99 7.0-7.99 8.0-8.99 9.0-9.99

Homocysteine and C-Reactive Protein Summary 44% of SCI patients studied in a large sample had a homocysteine level associated with an increased mortality ratio 62% of SCI pts studied had moderate to high CRP levels When applying risk assessment methods (Physicians Health Study), 78%, 56%, and 46% had double, triple or quadruple the normal risk Ridker, 2000; Nash, 2006

CARDIOMETABOLIC RISK CLUSTERING 69

Framingham Risk Scores 121 (97 male, 24 female) Age 18-73 (mean 37 years) Duration of injury (mean 11 years) Paraplegia (N=73) and tetraplegia (N=48) 70 Groah, 2010

CMR Clustering 90%, 8.3% and 1.7% were in low, medium and high risk groups Most prevalent CMR Overweight/obesity (74%) Elevated LDL (64%) Low HDL (53%) Elevated sbp (33%) Elevated TC (30%) In addition, TG, FI, HgbH1c, HOMA-IR were all associated with Framingham Risk Groah, 2010

CMR Clustering Paraplegia vs. Tetraplegia Paras had higher sbp Tetras had higher 2-hour glucose Tetras had higher 2-hour insulin 72 Groah, 2010

73

SUMMARIZING THE EVIDENCE 74

AHRQ Evidence Report Carbohydrate and Lipid Disorders After SCI 75

AHRQ Evidence Report Results the quality of evidence regarding the prevalence, impact, and outcomes of carbohydrate and lipid disorders in adults with chronic SCI is weak. Evidence is limited by relatively few studies, small sample size, lack of appropriate control groups, failure to adjust for known confounding variables, and variation in reported outcomes. 76

AHRQ Evidence Report Results However, the existing evidence does not indicate that adults with SCI are at a markedly greater risk for carbohydrate and lipid disorders or subsequent cardiovascular morbidity and mortality than AB adults. Body mass index is not reliable for assessing body composition, especially percent body fat, in adults with SCI. There are no high quality studies evaluating the impact of exercise, diet, or pharmacologic therapies on these disorders. 77

AHRQ Evidence Report Conclusions Evidence does not support using different thresholds to define or treat abnormal lipid and carbohydrate measures or to incorporate other markers to assess risk (e.g. insulin resistance, impaired fasting glucose, or impaired glucose tolerance) for individuals with SCI compared with AB adults. Due to physiologic differences between adults with SCI and AB individuals, caution may be required when extrapolating data. 78

ACHIEVING BEST PRACTICE: WHAT DOES THE CLINICIAN DO WHEN A SYSTEMATIC REVIEW DEVIATES FROM PREVIOUSLY HELD BELIEFS OR EVIDENCE? 79

Systematic Review Appraisal Evidential Hierarchy(s) Levels of Evidence Category I: Evidence from at least one properly randomized controlled trial. Category II-1: Evidence from well-designed controlled trials without randomization. Category II-2: Evidence from well-designed cohort or case-control analytic studies Category II-3: Evidence from multiple times series with or without intervention and uncontrolled 80 Category III: Opinions of respected authorities, based on clinical experience, descriptive studies and case reports, or reports of expert committees.

Questions and Answers 81