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Acute Renal Injury During High Intensity Training

Hematological Risk Factors Related to Acute Renal Injury During High Intensity Training

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03678285
Acronym
HIFRT-KH
Enrollment
42
Registered
2018-09-19
Start date
2018-10-01
Completion date
2019-06-30
Last updated
2021-07-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Kidney Injury, Exercise

Keywords

High intensity exercise, Proenkephalin-A

Brief summary

The proposed work is designed to be the first in a series of studies investigating the health benefits and risks related to high intensity training (HIT) exercise. Our specific aims are to determine, 1) if participation in a single bout of HIT induces hematological markers consistent with acute kidney injury (AKI), and 2) if risk is predicted by the pre-exercise concentration of plasma proenkephalin-A. This investigation is an observational case control study. In year one, data collection procedures will be refined with \ 40 participants local to the University of Wyoming and training will occur for collaborators from Wyoming community and tribal colleges. In year two, data collection will expand to some of the 12 CrossFit® gyms in Wyoming with assistance from the community and tribal colleges. Blood and urine samples will be collected before and up to 48 h after a standardized bout of HIT exercise on \ 100 participants. Baseline blood samples will be analyzed for proenkephalin-A. All blood samples will be analyzed for markers of muscle damage (e.g., creatine kinase and myoglobin), and markers of kidney function (e.g., serum creatinine and blood urea nitrogen). Urine will be analyzed for markers of filtration function (e.g., albumin, creatinine, neutrophil gelatinase-associated lipocalin \[NGAL\], and kidney injury molecule 1 \[KIM-1\]). Lastly, the severity of kidney damage will be compared with the number of risk alleles and proenkephalin-A concentration. The investigators envision that the bout of HIT exercise will induce markers consistent with skeletal muscle damage in most participants and, based on literature from other styles of intense exercise, that acute kidney injury will be diagnosable in between 50-75% of participants. Secondarily, the investigators predict that the concentration of proenkephalin-A will be inversely related to the change in kidney function from before to after the HIT exercise bout.

Detailed description

The HIT-KH investigation is proposed to take place over the course of two calendar years. During year one collaborations with gyms specializing in High Intensity Resistance and Functional Training style workouts (referred to from this point forward as satellite data collection sites) as well as community and tribal colleges (referred to from this point forward as partner institutions) local to these facilities will be solidified. Also, during the summer of year one data collection will occur on a small subset of individuals (\ 40) at a data collection site local to the University of Wyoming (Figure 1.). It is our plan to use this first data collection in Laramie, WY as a training session for all students from partner institutions so that the students are prepared when the data collection is expanded to the satellite data collection sites in year 2. In order to properly power this investigation the investigators have estimated that about 100 participants will be needed. Given that the investigators can expect about 40 participants from the local Larmie data collection gym (CrossFit® 7220)this will require the investigators to partner with other high intensity resistance and functional training gyms around the state of Wyoming in year 2. The investigators have chosen to reach out to CrossFit® gyms specifically because it is common practice for most CrossFit® gyms to program the workout the investigators are interested in observing (Murph), at least once per year. Collection data on 60 additional participants will require partnership with 3 additional gyms (i.e., 20 participants / facility). At this point the investigators have been in contact with 3 gym owners all of whom have offered verbal agreement to assisting with data collection. Among these gyms is CrossFit® Leveler, located on the Wind River Reservation in Fort Washikie, Wyoming. This facility is a Native American owned business and it primarily caters to those Native American's living on the reservation. Because the state of Wyoming is \ 2% Native American in population, the inclusion of this facility in our investigation is very important for proper sampling (see attached letter of support from owner Mike Ute). Additional gyms that have been contacted and are in the process of providing written approval are CrossFit® Frontier (Cheyenne), and, Cloud Peak CrossFit® (Sheridan). Because our data collection will be occurring throughout the state the investigators also plan to partner with local community and tribal colleges local to many of the above satellite data collection sites. Briefly, the investigators plan to incorporate up to three students and one faculty mentor from each of the following educational institutions; Laramie County Community College, Wind River Tribal College, and Sheridan Community College. Regarding the inclusion of Wind River Tribal College and the Wind River Indian Reservation, Investigator Johnson is under the guidance of Dr. Christine Porter who is also in the University of Wyoming Division of Kinesiology and Health. Dr. Porter has successfully implemented several research studies on the Wind River Reservation and is well versed in the intricacies and requirements necessary for the completion of data collection in this partnership. Lastly, the partner institutions are beneficial to the project because the data collection takes place over the course of 5 consecutive days, training and working with local researchers will enable this project to reduce the cost because a large research team from Laramie, Wyoming will not be required for each data collection. As mentioned above 1-3 students from each of the above institutions will be requested to assist with data collection for HIT-KH. Part of our grant funding is devoted to payment of fees for these student's training. This includes travel fees to travel and stay in Laramie, Wyoming during year 1 for observation and basic level assistance with the initial data collection. During the end of year 1 and/or beginning of year 2 additional funds have been allocated to provide phlebotomy training to interested students. These students will then be utilized during year two data collections to assist with blood draws. Finally, funds have been allocated for travel to and attendance of the Rocky Mountain Regional American College of Sports Medicine conference. It is our goal that at least one student will be able to use the preliminary data from the year 1 data collection to compile a research abstract that will be submitted for presentation. All other students will be offered the ability to attend and participate in the conference during the spring of 2019. Blood samples will be collected one day before participants take part in the workout, and 24 and 48hrs after completion. Sampling will take place by single venipuncture to an antecubital vein by a trained investigator using sterile technique and universal precautions. Following any needle removal, firm pressure will be applied over the site of the blood draw with gauze to minimize the occurrence of a hematoma. Blood will be drawn into vacutainers specific for each of the analytes to be analyzed later. Tubes will be centrifuged as soon as possible, then the blood plasma, serum, or white blood cells will be removed and aliquoted into separate cryovials. These cryovials will be frozen in the -80C freezer as soon as possible. For satellite data collections, if -80C freezers are not available at the local partner institution, liquid nitrogen will be used to freeze and store samples until the samples can be transported back to the University of Wyoming for more permanent storage. Urine samples will be collected in 24 hr collection jugs for the period immediately prior to the workout and for two 24hr periods following. Each sample will be weighed for measurement of total volume, evaluated for urine color and urine specific gravity. Dipsticks will be used on fresh samples while three 2mL aliquots of each 24hr sample will be separated and stored at room temperature until the samples are returned to the University of Wyoming where the samples will be frozen at -80C for future analysis. Fresh 24hr urine samples will be analyzed using traditional dipsticks for the following variables: leukocytes, nitrite, urobilinogen, protein, pH, hemoglobin, ketone, bilirubin, and glucose. Additionally, fresh samples will be evaluated for urine color and specific gravity via handheld refractometer in order to establish hydration state. Further biochemical urinary analysis are reviewed below. Proenkephalin-A will be analyzed at the Clinical Research Center by the use of a chemiluminometric sandwich immunoassay. The laboratory group in Malmo has previously successfully measured this hormone (Schulz et al., 2017). All remaining blood and urine samples will be analyzed within the Human Integrated Physiology laboratory located at the University of Wyoming using colorimetric enzyme-linked immunosorbent assays (ELISA). These samples will be analyzed for the following variables; serum creatinine, blood urea nitrogen, urinary creatinine, neutrophil gelatinase-associated lipocalin \[NGAL\], and kidney injury molecule 1 \[KIM-1\]). All ELISA antibodies will be supplied by Abcam, (Cambridge, Massachusetts, USA) and microplates will be read according the manufacturer's instructions on spectrophotometer (Epoch 2, Biotek, Winooski, Vermont, USA).

Interventions

OTHERHIFRT Workout

A single high intensity functional resistance training (HIFRT) exercise bout.

Sponsors

Lund University
CollaboratorOTHER
University of Wyoming
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SCREENING
Masking
NONE

Masking description

No other parties besides the participants will be masked.

Intervention model description

All participants will take part in the same, single bout, exercise intervention

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

1\. Healthy individual who has completed this specific workout on at least one prior occasion

Exclusion criteria

1. Score of 0 on the Functional Movement Screening (FMS) test as evaluated by two investigators \* indicating pain during any of the seven functional movements 2. Self- reported Kidney (chronic kidney disease, polycystic kidney disease, glomerulonephritis, diabetic nephropathy, interstitial nephritis, Goodpasture syndrome) or other medical condition contraindicating participation in HIFRT (Hypertension, dyslipidemia, type II diabetes mellitus, BMI \>30) 3. Pregnancy, suspected pregnancy, or breastfeeding 4. Blood donations within the last eight weeks leading up to testing day 5. Any musculoskeletal injuries which have resulted in \> 1 week of absence from HIFRT within the last six months 6. Not passing the physical activity readiness questionnaire (PAR-Q) 7. Allergy to ibuprofen or non-steroidal anti-inflammatory medication 8. Surgical operation on digestive tract or kidneys, except appendectomy 9. Inability to participate in the entire study 10. Recurrent urinary tract infections or kidney stones 11. History of protein or blood in urine 12. Moving from a location of low altitude (\< 3,000') to Laramie within the past 3 months 13. Inability to understand and write English

Design outcomes

Primary

MeasureTime frameDescription
Change in Serum CreatinineBaseline, Immediately pre-exercise, immediately post-exercise, 24 hours post-exercise, 48 hours post-exercise.Marker of kidney function measured as a change in concentration between baseline to 4 time-points surrounding the workout
Change in 24 Hour Urinary Kidney Injury Molecule 1Baseline, Day 2, Day 3Marker of Kidney Injury measured as a change in concentration between baseline to 2 time points surrounding exercise
Change in 24 Hour Urinary Neutrophil Gelatinase-associated LipocalinBaseline, Day 2, Day 3Marker of kidney damage measured as a change in concentration between baseline and 2 time points surrounding the exercise
Change in Concentration of Proenkephalin-A From Baseline to 4 Time-points Surrounding the WorkoutBaseline, Immediately pre-exercise, immediately post-exercise, 24 hours post-exercise, 48 hours post-exercisean endogenous opioid polypeptide hormone which, via proteolytic cleavage, produces the enkephalin peptides \[Met\]enkephalin, and to a lesser extent, \[Leu\]enkephalin.
Change in Creatinine KinaseBaseline, Immediately pre-exercise, immediately post-exercise, 24 hours post-exercise, 48 hours post-exerciseMarker of skeletal muscle damage measured as a change in concentration between baseline and 4 time-points surrounding exercise

Secondary

MeasureTime frameDescription
Post Exercise HypotensionBaseline, immediately pre-exercise, immediately post-exercise, 24 hours post-exercise, 48 hours post-exerciseSystolic and Diastolic blood pressure measurements
Change in the Short-form McGill Pain QuestionnaireBaseline, immediately pre-exercise, immediately post-exercise, 24 hours post-exercise, 48 hours post-exerciseSubjective perception of muscle pain. The participant responds to 15 word prompts designed to describe types of pain (e.g., shooting), with none, mild, moderate, or severe. These are scored as 0, 1, 2, and 3 respectively. A participant's Pain Score is the cumulative score for all prompt responses added together. As a participant's total score increases this denotes greater subjective feeling of pain which may be associated with the above markers of skeletal muscle and/or kidney damage. The minimum score for this questionnaire is 0 and the maximum score is 45. Typically, the total score is only reported. However, if there are prompts (i.e., subscales) that are consistently rated high or low, we will report these as a way to further describe the type of pain that is being reported (e.g., throbbing versus sharp). This will only be done after the total score is reported.

Countries

United States

Participant flow

Recruitment details

Subjects recruited between October 2018 and May 2019

Participants by arm

ArmCount
HIFRT Workout
Consecutive completion of; 1 mile run, 100 pull ups, 200 push-ups, 300 bodyweight squats, 1 mile run. HIFRT Workout: A single high intensity functional resistance training (HIFRT) exercise bout.
42
Total42

Withdrawals & dropouts

PeriodReasonFG000
Overall StudyAdverse Event2
Overall StudyDehydrated prior to start of workout1
Overall StudyWithdrawal by subject prior to start of workout1

Baseline characteristics

CharacteristicHIFRT Workout
Age, Continuous28.1 years
STANDARD_DEVIATION 8.8
Creatine Kinase267.8 U/L
STANDARD_DEVIATION 185.3
Diastolic Blood Pressure74 mmHg
STANDARD_DEVIATION 7
Ethnicity (NIH/OMB)
Hispanic or Latino
2 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
35 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
5 Participants
Proenkephalin61.1 pmol/L
STANDARD_DEVIATION 16.9
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
Race (NIH/OMB)
Asian
0 Participants
Race (NIH/OMB)
Black or African American
0 Participants
Race (NIH/OMB)
More than one race
0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
Race (NIH/OMB)
Unknown or Not Reported
7 Participants
Race (NIH/OMB)
White
35 Participants
Region of Enrollment
United States
42 participants
Serum Creatinine1.05 mg/dL
STANDARD_DEVIATION 0.16
Sex: Female, Male
Female
12 Participants
Sex: Female, Male
Male
30 Participants
Systolic Blood Pressure119 mmHg
STANDARD_DEVIATION 11
urinary kidney injury molecule 1170.5 pg/mL
STANDARD_DEVIATION 180.8
urinary neutrophil gelatinase-associated Lipocalin9.2 (ng/ml)/(ml/min)
STANDARD_DEVIATION 25.7
Visual Analog Pain Perception3 units on a scale
STANDARD_DEVIATION 6

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
0 / 42
other
Total, other adverse events
2 / 42
serious
Total, serious adverse events
0 / 42

Outcome results

Primary

Change in 24 Hour Urinary Kidney Injury Molecule 1

Marker of Kidney Injury measured as a change in concentration between baseline to 2 time points surrounding exercise

Time frame: Baseline, Day 2, Day 3

Population: One subject declined to collect 24hr urine at any time during the study. One subject did not provide an adequate sample for the baseline measurement (therefore no change scores could be calculated from baseline at either of the follow up points). Two additional subjects did not return complete collections on the final day of measurement

ArmMeasureGroupValue (MEAN)Dispersion
HIFRT WorkoutChange in 24 Hour Urinary Kidney Injury Molecule 1Day 1 to Day 2 Change71.17 pg/mLStandard Deviation 132.63
HIFRT WorkoutChange in 24 Hour Urinary Kidney Injury Molecule 1Day 1 to Day 3 Change45.44 pg/mLStandard Deviation 226.49
Primary

Change in 24 Hour Urinary Neutrophil Gelatinase-associated Lipocalin

Marker of kidney damage measured as a change in concentration between baseline and 2 time points surrounding the exercise

Time frame: Baseline, Day 2, Day 3

Population: One subject declined to collect 24hr urine at any time during the study. One subject did not provide an adequate sample for the baseline measurement (therefore no change scores could be calculated from baseline at either of the follow up points). Two additional subjects did not return complete collections on the final day of measurement

ArmMeasureGroupValue (MEAN)Dispersion
HIFRT WorkoutChange in 24 Hour Urinary Neutrophil Gelatinase-associated LipocalinDay 1 to Day 2 Change5.52 (ng/ml)/(ml/min)Standard Deviation 20.94
HIFRT WorkoutChange in 24 Hour Urinary Neutrophil Gelatinase-associated LipocalinDay 1 to Day 3 Change2.50 (ng/ml)/(ml/min)Standard Deviation 15.06
Primary

Change in Concentration of Proenkephalin-A From Baseline to 4 Time-points Surrounding the Workout

an endogenous opioid polypeptide hormone which, via proteolytic cleavage, produces the enkephalin peptides \[Met\]enkephalin, and to a lesser extent, \[Leu\]enkephalin.

Time frame: Baseline, Immediately pre-exercise, immediately post-exercise, 24 hours post-exercise, 48 hours post-exercise

Population: Number analyzed for 48 hour post-exercise change is 1 less than total sample due to a blood sample that was not able to be analyzed at the final time point

ArmMeasureGroupValue (MEAN)Dispersion
HIFRT WorkoutChange in Concentration of Proenkephalin-A From Baseline to 4 Time-points Surrounding the WorkoutImmediately pre-exercise1.65 pmol/LStandard Deviation 13.18
HIFRT WorkoutChange in Concentration of Proenkephalin-A From Baseline to 4 Time-points Surrounding the WorkoutImmediately post-exercise3.69 pmol/LStandard Deviation 15.49
HIFRT WorkoutChange in Concentration of Proenkephalin-A From Baseline to 4 Time-points Surrounding the Workout24 hours post-exercise2.50 pmol/LStandard Deviation 12.58
HIFRT WorkoutChange in Concentration of Proenkephalin-A From Baseline to 4 Time-points Surrounding the Workout48 hours post-exercise2.13 pmol/LStandard Deviation 12.68
Primary

Change in Creatinine Kinase

Marker of skeletal muscle damage measured as a change in concentration between baseline and 4 time-points surrounding exercise

Time frame: Baseline, Immediately pre-exercise, immediately post-exercise, 24 hours post-exercise, 48 hours post-exercise

Population: There is a discrepancy in the number of participants analyzed because one participant's samples were unable to be analyzed at all time points. One additional participant had a sample that was missing at the final time point.

ArmMeasureGroupValue (MEAN)Dispersion
HIFRT WorkoutChange in Creatinine Kinase48 hours post-exercise1152 U/LStandard Deviation 2406
HIFRT WorkoutChange in Creatinine KinaseImmediately pre-exercise-48 U/LStandard Deviation 76
HIFRT WorkoutChange in Creatinine KinaseImmediately post-exercise98 U/LStandard Deviation 107
HIFRT WorkoutChange in Creatinine Kinase24 hours post-exercise781 U/LStandard Deviation 1631
Primary

Change in Serum Creatinine

Marker of kidney function measured as a change in concentration between baseline to 4 time-points surrounding the workout

Time frame: Baseline, Immediately pre-exercise, immediately post-exercise, 24 hours post-exercise, 48 hours post-exercise.

Population: One sample at the final time point was not able to be analyzed.

ArmMeasureGroupValue (MEAN)Dispersion
HIFRT WorkoutChange in Serum CreatinineImmediately pre-exercise0.001 mg/dLStandard Deviation 0.066
HIFRT WorkoutChange in Serum CreatinineImmediately post-exercise0.211 mg/dLStandard Deviation 0.119
HIFRT WorkoutChange in Serum Creatinine24 hours post-exercise0.008 mg/dLStandard Deviation 0.062
HIFRT WorkoutChange in Serum Creatinine48 hours post-exercise-0.014 mg/dLStandard Deviation 0.086
Secondary

Change in the Short-form McGill Pain Questionnaire

Subjective perception of muscle pain. The participant responds to 15 word prompts designed to describe types of pain (e.g., shooting), with none, mild, moderate, or severe. These are scored as 0, 1, 2, and 3 respectively. A participant's Pain Score is the cumulative score for all prompt responses added together. As a participant's total score increases this denotes greater subjective feeling of pain which may be associated with the above markers of skeletal muscle and/or kidney damage. The minimum score for this questionnaire is 0 and the maximum score is 45. Typically, the total score is only reported. However, if there are prompts (i.e., subscales) that are consistently rated high or low, we will report these as a way to further describe the type of pain that is being reported (e.g., throbbing versus sharp). This will only be done after the total score is reported.

Time frame: Baseline, immediately pre-exercise, immediately post-exercise, 24 hours post-exercise, 48 hours post-exercise

ArmMeasureGroupValue (MEAN)Dispersion
HIFRT WorkoutChange in the Short-form McGill Pain QuestionnaireChange to Immediately pre-exercise-1 score on a scale in millimetersStandard Deviation 5
HIFRT WorkoutChange in the Short-form McGill Pain QuestionnaireChange to immediately post-exercise23 score on a scale in millimetersStandard Deviation 23
HIFRT WorkoutChange in the Short-form McGill Pain QuestionnaireChange to 24 hours post-exercise18 score on a scale in millimetersStandard Deviation 16
HIFRT WorkoutChange in the Short-form McGill Pain QuestionnaireChange to 48 hours post-exercise18 score on a scale in millimetersStandard Deviation 17
Secondary

Post Exercise Hypotension

Systolic and Diastolic blood pressure measurements

Time frame: Baseline, immediately pre-exercise, immediately post-exercise, 24 hours post-exercise, 48 hours post-exercise

Population: No blood pressure measurement was recorded for a single subject at the immediately pre-exercise time point.

ArmMeasureGroupValue (MEAN)Dispersion
HIFRT WorkoutPost Exercise Hypotensionsystolic change to immediately pre-exercise3 mm/HgStandard Deviation 8
HIFRT WorkoutPost Exercise Hypotensionsystolic change to immediately post-exercise-8 mm/HgStandard Deviation 11
HIFRT WorkoutPost Exercise Hypotensionsystolic change to 24 hours post-exercise-3 mm/HgStandard Deviation 7
HIFRT WorkoutPost Exercise Hypotensionsystolic change to 48 hours post exercise-3 mm/HgStandard Deviation 8
HIFRT WorkoutPost Exercise Hypotensiondiastolic change to immediately pre-exercise2 mm/HgStandard Deviation 6
HIFRT WorkoutPost Exercise Hypotensiondiastolic change to immediately post-exercise-3 mm/HgStandard Deviation 6
HIFRT WorkoutPost Exercise Hypotensiondiastolic change to 24 hours post-exercise-3 mm/HgStandard Deviation 6
HIFRT WorkoutPost Exercise Hypotensiondiastolic change to 48 hours post-exercise-2 mm/HgStandard Deviation 5

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026