Blood Disorder, Digestive System Disease, Liver Diseases
Conditions
Keywords
NAFLD, NASH
Brief summary
Nonalcoholic fatty liver disease (NAFLD) is the leading cause of chronic liver disease in the United States. The most advanced forms of NAFLD are associated with increased liver-related mortality and lower overall survival. The current standard of care for NAFLD is lifestyle changes through diet and exercise. The human genome and regulation of gene expression is influenced by physical activity. NAFLD is a prothrombotic state with derangements in all three phases of hemostasis leading to clinically important clotting events. Exercise can improve coagulation in healthy persons. In this proposal, we seek to begin a line of work to answer the question Can lifestyle changes effectively mitigate the increased risk of clotting in patients with NAFLD? focusing initially on the at-risk population genetically susceptible to advanced disease.
Detailed description
Often comorbid with obesity, nonalcoholic fatty liver disease (NAFLD) is the leading cause of chronic liver disease in the United States affecting 75-100 million adults, of which 15-20 million have the more severe variant nonalcoholic steatohepatitis (NASH). Conservative estimates project a doubling in NASH by 2025.The most advanced forms of NAFLD are associated with increased liver-related mortality and lower overall survival. The most effective treatment for NAFLD remains adopting healthy dietary and exercise patterns, however NAFLD patients are among the least physically active individuals. Predicting exercise behavior on an individual level is highly complex due to differing motivation, physiologic response to and subjective experience of exercise as well as emerging genetic evidence. The human genome and regulation of gene expression is influenced by physical activity. Patatin like phospholipase-3 (PNPLA3) rs738409 polymorphism (GG, GC and CC genotypes) plays a crucial role in the development of NAFLD. The GG genotype is both associated with advanced NAFLD, and predicts response to physical activity. Patients with NASH have extensive extrahepatic disease and are hypercoagulable. NASH is a prothrombotic state with fibrinolytic dysfunction through elevated plasminogen activator inhibitor (PAI-1), an independent risk factor for venous thromboembolism (VTE). Consequently, patients with NASH are predisposed to VTE; the risk of portal vein thrombosis (PVT) in NASH is 210% greater than in other liver disease. NASH patients are also at increased risk for pulmonary embolism (PE) and deep vein thrombosis (DVT).The most advanced forms of NASH have the greatest thrombotic risk. While studies observe that change in diet, weight and physical activity patterns improve NASH, it is not clear whether these lifestyle changes also reduce the elevated clot risk, however, moderate-intensity exercise leads to improved fibrinolysis in healthy persons.The NASHFit study is being done to find out if exercise is beneficial in decreasing the risk of clotting problems in patients with NASH. Exercise has been shown to decrease markers of clotting in healthy individuals as well as in those with cardiovascular disease.
Interventions
Subjects in the aerobic exercise group will be supervised to exercise 30 minutes, 5 times per week at a moderate intensity. Formal exercise instruction and supervision will be provided by ACSM certified fitness professionals at the Penn State University Fitness Center. Aerobic exercise can be completed on either the treadmill, exercise bike, rowing machine or the elliptical machine.
Sponsors
Study design
Intervention model description
Standard of care Aerobic exercise
Eligibility
Inclusion criteria
Adults age \>=18 or \<70 years Liver biopsy \<= 6months prior to enrollment Biopsy proven NASH(79) Lack of secondary causes of hepatic fat accumulation: Significant alcohol consumption (\<21 drinks/week for men and \<14 drinks/week for women) Chronic hepatitis C Wilson disease Lipodystrophy Parenteral nutrition Long-term use of steatogenic medications (mipomersen, lomitapide, amiodarone, methotrexate, tamoxifen, corticosteroids) Monogenic hereditary disorders
Exclusion criteria
\>90 minutes/week of at least moderate intensity exercise over the previous three months Pregnancy BMI \<18 or \>40 kg/m2(16) Uncontrolled diabetes (changes in medication dosing over the previous three months or hemoglobin A1c \>9%)(12) Active cardiac symptoms Severe medical comorbidities/psychiatric illness Decompensated cirrhosis (history of esophageal varices, ascites or hepatic encephalopathy) Abdominal hernia Cancer with life expectancy \<6 months MRI contraindications (severe claustrophobia, implanted ferrous metal) Other liver disease (positive hepatitis B surface antigen, antinuclear antibody titer \>1:160) Active weight-loss program participation or weight-loss supplement use Active substance abuse/smoking Inability to provide informed consent Institutionalized/prisoner Inability to walk \> 2 blocks or ¼ mile. Physical Activity Readiness Questionnaire (PAR-Q) score \>=1 at the discretion of the study PI
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| PAI-1 Level | 5 months | Change in fibrinolysis as indicated by PAI-1 level was calculated by taking the difference of measurements at baseline and 5 months. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in Protein S | 5 months | Change in protein S was calculated by taking the difference of measurements at baseline and 5 months. |
| Change in Factor VIII | 5 months | Change in factor VIII was calculated by taking the difference of measurements at baseline and 5 months. |
| Change in Fibrinogen | 5 months | Change in fibrinogen was calculated by taking the difference of measurements at baseline and 5 months. |
| Change in Antithrombin | 5 months | Change in antithrombin was calculated by taking the difference of measurements at baseline and 5 months. |
| Change in Protein C | 5 months | Change in protein C was calculated by taking the difference of measurements at baseline and 5 months. |
| Change in Von Williebrand Factor (vWF) | 5 months | Change in vWF was calculated by taking the difference of measurements at baseline and 5 months. |
| Patatin Like Phospholipase-3 (PNPLA3) rs738409 Polymorphism | 5 months | Patatin like phospholipase-3 (PNPLA3) rs738409 polymorphism genotyping subjects (GG, GC and CC genotypes) |
| Change in PAI-1 Stratified by Fibrosis Stage | 5 months | Change is the difference between measurements at baseline and 5 months |
| Change in % Hepatic Fat | 5 months | Change in % hepatic fat was calculated by taking the difference of measurements at baseline and 5 months. |
| Health Related Quality of Life (HRQOL) Change | 5 months (20 weeks) | Data was collected at baseline and at 5 months to assess changes in domains of health. PROMIS-29 Profile v2.1 (Physical function & pain interference) PROMIS Bank v2.0 - Instrumental Support (Social Support) Scores are reported as standardized T-score metrics derived from population means, with a mean of 50 and standard deviation of 10. The minimum is 0 and the maximum is 90. A higher score for fatigue, pain intensity, pain interference, sleep disturbance, anxiety and depression means a worse outcome. A higher score for physical function and social roles means a better outcome. |
| Change in Adiponectin | 5 months | Change in adipontin was calculated by taking the difference of measurements at baseline and 5 months. |
Countries
United States
Participant flow
Pre-assignment details
31 patients were screened for this study. Three were excluded after screening (two declined and one was excluded because they were actively smoking)
Participants by arm
| Arm | Count |
|---|---|
| Standard of Care Subjects in the control condition will be instructed to continue their medical care at the discretion of their treating medical professional. They will be informed to maintain their current physical activity level. Weekly phone calls will be performed by study personnel to ensure adherence to the protocol (no changes in activity). Subjects will report to Penn State on a monthly basis for anthropometric assessment to confirm their self-reports and study investigators will perform and interim history and physical examination at that time. | 10 |
| Aerobic Exercise Subjects in the aerobic exercise group will be supervised to exercise 30 minutes, 5 times per week at a moderate intensity. Formal exercise instruction and supervision will be provided by ACSM certified fitness professionals at the Penn State University Fitness Center. Aerobic exercise can be completed on either the treadmill, exercise bike, rowing machine or the elliptical machine.
Aerobic Exercise: Subjects in the aerobic exercise group will be supervised to exercise 30 minutes, 5 times per week at a moderate intensity. Formal exercise instruction and supervision will be provided by ACSM certified fitness professionals at the Penn State University Fitness Center. Aerobic exercise can be completed on either the treadmill, exercise bike, rowing machine or the elliptical machine. | 18 |
| Total | 28 |
Baseline characteristics
| Characteristic | Standard of Care | Aerobic Exercise | Total |
|---|---|---|---|
| Age, Categorical <=18 years | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical >=65 years | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical Between 18 and 65 years | 10 Participants | 18 Participants | 28 Participants |
| Ethnicity (NIH/OMB) Hispanic or Latino | 1 Participants | 1 Participants | 2 Participants |
| Ethnicity (NIH/OMB) Not Hispanic or Latino | 9 Participants | 17 Participants | 26 Participants |
| Ethnicity (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Asian | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Black or African American | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) More than one race | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 1 Participants | 0 Participants | 1 Participants |
| Race (NIH/OMB) White | 9 Participants | 18 Participants | 27 Participants |
| Region of Enrollment United States | 10 participants | 18 participants | 28 participants |
| Sex: Female, Male Female | 5 Participants | 6 Participants | 11 Participants |
| Sex: Female, Male Male | 5 Participants | 12 Participants | 17 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 0 / 10 | 0 / 18 |
| other Total, other adverse events | 1 / 10 | 6 / 18 |
| serious Total, serious adverse events | 1 / 10 | 0 / 18 |
Outcome results
PAI-1 Level
Change in fibrinolysis as indicated by PAI-1 level was calculated by taking the difference of measurements at baseline and 5 months.
Time frame: 5 months
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Standard of Care | PAI-1 Level | 151.4 ng/mL | Standard Deviation 51.5 |
| Aerobic Exercise | PAI-1 Level | 176.2 ng/mL | Standard Deviation 71.9 |
Change in Adiponectin
Change in adipontin was calculated by taking the difference of measurements at baseline and 5 months.
Time frame: 5 months
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Standard of Care | Change in Adiponectin | 3482.3 ng/mL | Standard Deviation 1728.8 |
| Aerobic Exercise | Change in Adiponectin | 1065.1 ng/mL | Standard Deviation 1220.7 |
Change in Antithrombin
Change in antithrombin was calculated by taking the difference of measurements at baseline and 5 months.
Time frame: 5 months
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Standard of Care | Change in Antithrombin | 95.6 percentage of protein | Standard Deviation 12.1 |
| Aerobic Exercise | Change in Antithrombin | 102.2 percentage of protein | Standard Deviation 15.6 |
Change in Factor VIII
Change in factor VIII was calculated by taking the difference of measurements at baseline and 5 months.
Time frame: 5 months
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Standard of Care | Change in Factor VIII | 210.0 International Units/Liter | Standard Deviation 75 |
| Aerobic Exercise | Change in Factor VIII | 188.6 International Units/Liter | Standard Deviation 66.4 |
Change in Fibrinogen
Change in fibrinogen was calculated by taking the difference of measurements at baseline and 5 months.
Time frame: 5 months
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Standard of Care | Change in Fibrinogen | 352.4 mg/dL | Standard Deviation 56.1 |
| Aerobic Exercise | Change in Fibrinogen | 377.2 mg/dL | Standard Deviation 83.5 |
Change in % Hepatic Fat
Change in % hepatic fat was calculated by taking the difference of measurements at baseline and 5 months.
Time frame: 5 months
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Standard of Care | Change in % Hepatic Fat | 22.5 percentage of liver | Standard Deviation 10.5 |
| Aerobic Exercise | Change in % Hepatic Fat | 20.4 percentage of liver | Standard Deviation 7.7 |
Change in PAI-1 Stratified by Fibrosis Stage
Change is the difference between measurements at baseline and 5 months
Time frame: 5 months
Population: The intended analysis was not performed for both groups, and instead this subset analyzed exercise group participants only.
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Standard of Care | Change in PAI-1 Stratified by Fibrosis Stage | Baseline | 176.7 ng/mL | Standard Deviation 120.9 |
| Standard of Care | Change in PAI-1 Stratified by Fibrosis Stage | Post exercise | 122.7 ng/mL | Standard Deviation 36.6 |
| Aerobic Exercise | Change in PAI-1 Stratified by Fibrosis Stage | Baseline | 241.4 ng/mL | Standard Deviation 4.8 |
| Aerobic Exercise | Change in PAI-1 Stratified by Fibrosis Stage | Post exercise | 196.1 ng/mL | Standard Deviation 46.5 |
| F3 Fibrosis | Change in PAI-1 Stratified by Fibrosis Stage | Post exercise | 127.8 ng/mL | Standard Deviation 36.7 |
| F3 Fibrosis | Change in PAI-1 Stratified by Fibrosis Stage | Baseline | 131.7 ng/mL | Standard Deviation 24.4 |
Change in Protein C
Change in protein C was calculated by taking the difference of measurements at baseline and 5 months.
Time frame: 5 months
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Standard of Care | Change in Protein C | 169.0 IU/dL | Standard Deviation 50.6 |
| Aerobic Exercise | Change in Protein C | 152.6 IU/dL | Standard Deviation 55.9 |
Change in Protein S
Change in protein S was calculated by taking the difference of measurements at baseline and 5 months.
Time frame: 5 months
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Standard of Care | Change in Protein S | 106.3 IU/dL | Standard Deviation 24.6 |
| Aerobic Exercise | Change in Protein S | 101.5 IU/dL | Standard Deviation 22.4 |
Change in Von Williebrand Factor (vWF)
Change in vWF was calculated by taking the difference of measurements at baseline and 5 months.
Time frame: 5 months
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Standard of Care | Change in Von Williebrand Factor (vWF) | 140.1 International Units/Liter | Standard Deviation 63.1 |
| Aerobic Exercise | Change in Von Williebrand Factor (vWF) | 128.4 International Units/Liter | Standard Deviation 39.8 |
Health Related Quality of Life (HRQOL) Change
Data was collected at baseline and at 5 months to assess changes in domains of health. PROMIS-29 Profile v2.1 (Physical function & pain interference) PROMIS Bank v2.0 - Instrumental Support (Social Support) Scores are reported as standardized T-score metrics derived from population means, with a mean of 50 and standard deviation of 10. The minimum is 0 and the maximum is 90. A higher score for fatigue, pain intensity, pain interference, sleep disturbance, anxiety and depression means a worse outcome. A higher score for physical function and social roles means a better outcome.
Time frame: 5 months (20 weeks)
Population: ITT
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Standard of Care | Health Related Quality of Life (HRQOL) Change | Physical function | -2.5 T-score | Standard Deviation 6.5 |
| Standard of Care | Health Related Quality of Life (HRQOL) Change | Pain interference | 4.3 T-score | Standard Deviation 9.6 |
| Standard of Care | Health Related Quality of Life (HRQOL) Change | Social support | -0.7 T-score | Standard Deviation 6.6 |
| Aerobic Exercise | Health Related Quality of Life (HRQOL) Change | Pain interference | -3.4 T-score | Standard Deviation 5.6 |
| Aerobic Exercise | Health Related Quality of Life (HRQOL) Change | Physical function | 1.5 T-score | Standard Deviation 5 |
| Aerobic Exercise | Health Related Quality of Life (HRQOL) Change | Social support | 5.0 T-score | Standard Deviation 7 |
Patatin Like Phospholipase-3 (PNPLA3) rs738409 Polymorphism
Patatin like phospholipase-3 (PNPLA3) rs738409 polymorphism genotyping subjects (GG, GC and CC genotypes)
Time frame: 5 months
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| Standard of Care | Patatin Like Phospholipase-3 (PNPLA3) rs738409 Polymorphism | CC | 3 Participants |
| Standard of Care | Patatin Like Phospholipase-3 (PNPLA3) rs738409 Polymorphism | GC | 5 Participants |
| Standard of Care | Patatin Like Phospholipase-3 (PNPLA3) rs738409 Polymorphism | GG | 2 Participants |
| Aerobic Exercise | Patatin Like Phospholipase-3 (PNPLA3) rs738409 Polymorphism | CC | 8 Participants |
| Aerobic Exercise | Patatin Like Phospholipase-3 (PNPLA3) rs738409 Polymorphism | GC | 5 Participants |
| Aerobic Exercise | Patatin Like Phospholipase-3 (PNPLA3) rs738409 Polymorphism | GG | 5 Participants |