Changes in Body Composition and Cardiometabolic Health After Detraining in Older Men with Osteosarcopenia: 6-Month Follow-Up of the Randomized Controlled Franconian Osteopenia and Sarcopenia Trial (FrOST) Study
Received 31 December 2020
Accepted for publication 20 February 2021
Published 6 April 2021 Volume 2021:16 Pages 571—582
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Professor Nandu Goswami
Wolfgang Kemmler,1 Daniel Schoene,1 Matthias Kohl,2 Simon von Stengel1
1Institute of Medical Physics, Friedrich-Alexander University of Erlangen-Nürnberg, Erlangen, 91053, Germany; 2Faculty Medical and Life Sciences, University of Furtwangen, Villingen-Schwenningen, 78054, Germany
Correspondence: Wolfgang Kemmler
Institute of Medical Physics, Friedrich-Alexander University of Erlangen-Nürnberg, Henkestrasse 91, Erlangen, 91052, Germany
Tel +49 9131 8523999
Fax +49 9131 8522824
Email [email protected]
Purpose: Temporary cessation of exercise but maintenance of habitual physical activity might be a frequent situation in older people’s lives. Particularly the COVID-19 induced lockdown of exercise training facilities with individual outdoor activities still being allowed might be a blueprint for this potentially harmful scenario. Thus, the aim of the present study was to determine the effects of 6 months of detraining after 18 months of high-intensity resistance exercise (HIT-RT) on body composition and cardiometabolic outcomes in predominately obese older men with osteosarcopenia.
Materials and Methods: Community-dwelling predominately obese men 72– 91 years old with low muscle and bone mass (n=43) were randomly assigned to an 18-month HIT-RT (EG: n=21) or a non-training control group (CG, n=22). After the intervention, participants of the EG discontinued HIT-RT for 6 months, but increased their habitual physical activity. Study outcomes were group differences in detraining changes (“effects”) for lean body mass (LBM), total and abdominal body fat rate (determined by dual-energy x-ray absorptiometry) and the Metabolic Syndrome Z-Score (MetSZ). We applied an intention-to-treat analysis with multiple imputation to analyze the data.
Results: After the 18-month HIT-RT, we observed significant positive training effects for LBM, total and abdominal body fat rate and the MetSZ (all p< 0.001). Abrupt cessation of HIT-RT for 6 months resulted in significantly higher unfavorable changes in the HIT-RT compared with the CG for LBM (p=0.001), total body fat (p=0.003) and the MetSZ (p=0.003), apart from abdominal body fat (p=0.059). However, significant overall effects were still present after 24 months for LBM and body fat indices but not for the MetSZ.
Conclusion: The present study clearly indicates the unfavorable effects of 6 months of detraining after HIT-RT. Correspondingly, exercise protocols particularly for older people should focus on continuous exercise with short regeneration periods rather than on intermitted protocols with pronounced training breaks.
Keywords: resistance exercise, detraining, lean body mass, body fat, metabolic syndrome, older men
Temporary breaks of exercise routines e.g. due to the intermitted character of an exercise program, lack of time, or simple reluctance might be a frequent situation in older adults’ lives.1,2 Although exercise routines were not stopped that abruptly, the present COVID-19 induced lockdown in winter/spring 2020 in Bavaria might serve as a blueprint for the effects of a sudden cessation of supervised group exercise training with otherwise maintained or even enhanced physical (outdoor) activity. Reviewing the literature, the vast majority of studies that focus on detraining effects in older adults (e.g.3–16) reported severe negative effects a mere 8 weeks after cessation of the intervention.3 However, most of the studies focus on the detraining effect on musculoskeletal outcomes after short-term interventions (ie 12–16 weeks), while the effects on body composition and cardiometabolic parameters after resistance training (RT) periods that exceed 6 months were rarely evaluated. This refers particularly to older obese people with low muscle and bone mass,17,18 who can be considered as a high-risk group. In order to close this gap, the aim of this study was to determine the effect of 6 months of detraining after an 18-month HIT-RT intervention on body composition and cardiometabolic risk in older, predominately obese, osteosarcopenic men.
Our primary hypothesis was that changes in the HIT-RT vs control group during the detraining period (ie detraining effects) were significantly more pronounced in the HIT-RT group for (1.1) lean body mass (LBM, primary study outcome), (1.2) total body fat, (1.3) abdominal body fat and (1.4) metabolic syndrome Z-Score in older, community-dwelling (cdw) men with osteosarcopenia and increased body fat.
Our secondary hypothesis was that the significant training effects on (2.1) LBM, (2.2) total body fat (2.3.), abdominal body fat and (2.4) the Metabolic Syndrome Z-Score observed after 18 months of intervention will be reduced to non-significant levels after 6 months of detraining.
Materials and Methods
The aim of the randomized controlled FrOST (Franconian Osteopenia and Sarcopenia Trial), was to determine the effects of an 18-month HIT-RT on health- and fitness-related outcomes in cdw 73–91-year-old men with osteosarcopenia. The present detraining project (FrOST-FU) aimed to determine the effect of 6 months of detraining on outcomes addressed by FrOST. A recent publication thereby focus on detraining effects on musculoskeletal parameters,19 while the present work aimed to address cardiometabolic outcomes in the FrOST cohort. The project was initiated and conducted by the Institute of Medical Physics (IMP), University of Erlangen-Nürnberg (FAU), Germany. FroST and FrOST-FU were approved by the FAU ethics committee (4464b, 4464b amendment) and the federal bureau of radiation protection (BfS, number Z 5 - 2246212 - 2017-002). The project fully complies with the Helsinki Declaration.20 All the study participants gave their written informed consent after receiving detailed information. The studies were registered under ClinicalTrials.gov NCT03453463 (FrOST) and NCT04444661 (FrOST-FU). The exercise intervention of FrOST was conducted between June 2018 and December 2019; the observational period of FrOST-FU ranges from the end of December 2019 to mid-June 2020 (6-month follow-up).
The recruitment process of FrOST started in February 2018 and has been described in detail in previous articles.18,21,22 Briefly, cdw men, 72 years and older with (a) morphometric sarcopenia (skeletal muscle mass index lower than −2 SD T-Score23,24) and (b) osteopenia or osteoporosis (bone mineral density at LS or proximal femur lower than −1 SD T-Score25) were included in the study. Men (a) with diseases and/or (b) taking pharmaceutical agents (eg bisphosphonates, alfacalcidol, glucocorticoids) that either affected muscle/bone metabolism or hinder intense resistance exercise, (c) with experience in resistance-type exercise (≥60 min/week previous 2 years) and (d) with alcohol abuse (>60 g/d ethanol consumption) were excluded. Of importance, the final decision about eligibility was always taken by the study physician. After application of the criteria listed above and detailed study information, the finally 43 eligible men willing to participate in FrOST were randomly allocated to an HIT-RT (n=21) or control (CG, n=22) group. While the CG was asked to maintain their physical activity/exercise (CG) habits, the HIT-RT conducted the resistance exercise training described below for 18 months (Figure 1).
Figure 1 Adapted participant flow through the study.
In December 2019, the 18-month study intervention period ended. After 18-month FU-testing, we made an appointment with the participants to restart exercise after a short training break in February 2020. However, due to logistic and budget problems, we failed to start in February and the COVID-19 induced lock-down of all exercise facilities in March 2020 prevented all further group and/or indoor exercise programs for the next 14 weeks (up to June 2020). After the termination of the lock down, we invited participants to the 6-month detraining-follow-up (June 2020). Thirty-seven participants accepted our invitation and were assessed for 6-month detraining-FU (Figure 1).
Randomization Procedures and Blinding
The randomization and blinding procedures have been described in detail in previous publications.18,21,22 Briefly, participants allocated themselves to the HIT-RT or control group by drawing lots. Of importance, neither the participants nor the researcher knew the allocation beforehand (allocation concealment). Blinding only refers to test assistants and outcome assessors who were kept unaware of the participants’ group status (EG or CG).
During the intervention period, all participants were provided with protein,26 Cholecalciferol and Calcium27 as per recent recommendations. Apart from the exercise intervention of the HIT-RT, participants were asked to maintain their dietary habits and lifestyle including physical activity and exercise routines. Protein and calcium supplementation stopped at the end of the intervention, but all participants were provided with cholecalciferol up to the end of the detraining period.
As per recent recommendations26 we provided whey protein supplementation (WPS; Active PRO80, inkospor, Roth, Germany) to generate a daily protein intake of 1.5–1.6 in the EG and 1.2–1.3 g/kg/d in the CG during the intervention period. Based on the dietary calcium questionnaire (Rheumaliga, Switzerland), we intended a calcium intake of ≈1000 mg/d.27 Participants with dietary calcium intake below 950 mg/d were provided with calcium capsules (Sankt Bernhard, Bad Dietzenbach, Germany). Based on their 25 OH Vitamin-D 3 (25-OHD) levels (ECLIA; Roche Diagnostics, Penzberg, Germany) participants were provided with cholecalciferol (MYVITAMINS, Manchester, UK). Participants with 25 OHD levels <30 ng/mL were provided with 10,000 IE/week and participants with OHD-level of 30–40 ng/mL were supplemented with 5000 IE/week. We verified adherence to the prescribed supplementation of protein, Vit-D and calcium by (a) checking our distribution logs; (b) biweekly phone calls and (c) personal interviews conducted at FU assessments.
The HIT-RT intervention has been described in detail in previous publications18,22 thus only a brief overview will be provided here. In summary, we applied a progressive, periodized single set, dynamic resistance exercise protocol (HIT-RT) without any other type of exercise, be it in parallel or during warm-up or cool down. Our HIT-RT protocol focused on the application of frequent phases of high intensity (… up to 85% 1RM), high effort28,29 and/or high movement-velocity without any training breaks for 18 months. Two consistently supervised exercise sessions per week with 12–14 exercises/session from a pool of 18 exercises (calf raises, leg press, -extension, -curls, -adduction, -abduction, hip extension, latissimus front pulleys, pull-overs, seated rowing, back extension, inverse fly, bench press, military press, lateral raises, butterfly with extended arms, crunches, lateral crunches) exclusively on machines (MedX, Ocala, USA) were conducted in a well-equipped gym (Kieser Training, Erlangen, Germany). After 12 weeks of familiarization and conditioning, the exercise training was structured into 8–12 week phases that included two or three linearly periodized 4-week mesocycles with each 4th week as a regeneration week. Relative intensity during the mesocycles varied between 60% and 85% 1RM; after 4 months of exercise, in about 40–65% of the sets/session the number of repetition per set was conducted to repetition maximum.29 Supersets and drop-sets were used to further intensify the exercise protocol, however, after 13–14 months of exercise no further changes of the exercise protocol were intended.
During the FrOST 6-month detraining-FU, all but one previous outcomes of FrOST were evaluated. However, due to logistic problems and radiation protection specifications, we were unable to evaluate integrated BMD of the LS as assessed by quantitative computed tomography (QCT). In this contribution, we focus on body composition and cardiometabolic health.
Main outcome of the present study
- Lean body mass as determined by Dual-Energy x-ray Absorptiometry (DXA)
Secondary study outcomes
- Total body fat rate (%) as determined by DXA
- Abdominal body fat rate (%) as determined by DXA
- Metabolic Syndrome Z-Score based on the definition of the International Diabetes Federation (IDF).30
No changes of trial outcomes were made after trial commencement.
Assessments were conducted at baseline, after 6, 12, 18 months of intervention and after 6 months of detraining. We placed great emphasis on standardized assessments. This included all assessments and analyses being completed (a) by the same research assistant, (b) at the same time of the day (±2h), (c) at the identical location, (d) in the same order, (e) with the same calibrated devices and (f) with the same configuration of the device. Further, study participants were strictly asked to maintain their habitual diet and avoid intense physical activity during the two days prior to the assessments.
Body height was determined by a Holtain stadiometer (Crymych Dyfed, Great Britain). Body mass was evaluated by the scale function of a direct-segmental, multi-frequency Bio-Impedance-Analysis (DSM-BIA; InBody 770, Seoul, Korea). Lean body mass, total and abdominal body fat percentage were determined with a DXA-scanner (QDR 4500a, Discovery-upgrade, Hologic Inc., Bedford, USA) according to the manufacturer’s specifications. The “compare mode” was used to exactly reproduce baseline specifications during FU-assessments.
Representative for cardiometabolic risk, we calculated the metabolic syndrome Z-Score (MetSZ) based on the IDF-definition:30 [(40 – HDL-cholesterol)/SD HDL-C] + [(triglycerides - 150)/SD TriGly] + [(Glucose - 100)/SD Glucose] + [(waist circumference - 88)/SD WC] + [(Mean arterial blood pressure - 100)/SD MAP]. For details on assessments of MetS-components the reader is kindly referred to another publication.31
Standardized questionnaires asked for several baseline and follow-up parameters. Baseline questionnaires solicit (a) demographic parameters, (b) diseases, limitations, injuries, operations, (c) pharmacologic agents, dietary supplements, (d) lifestyle, with specific emphasis on physical activity and exercise habits,32,33 (e) falls and low trauma fractures during the previous year, and (f) independence status. The follow-up questionnaires focus on potential changes with impact on our study result. This includes in particular injuries, operations, changes of medication, complaints or diseases and physical activity. Very high emphasis was placed on the detection of changes of exercise and physical activity habits during the detraining period. In order to properly evaluate intensity and volume of physical activity and in particular exercise we used our physical activity and exercise questionnaire32,33 specifically developed to determine mechanical loading. In order to generate high consistency, completeness and accuracy, the primary investigator lastly checked the FU-questionnaire in close interaction with the participants.
In order to monitor dietary intake and to calculate individual whey protein doses, all participants completed dietary records (Freiburger Nutrition Record, nutri-science, Hausach, Germany) at baseline and FU 6, 12, 18 and 24 months. Participants were asked to record 3 weekdays and one weekend day representative for their dietary habits. Protocols were analyzed consistently by the same research assistant.
We conducted an Intention-to-treat (ITT) analysis that included all participants who were randomly assigned to the study arms at baseline. Missing data was imputed using R statistics software (R Development Core Team Vienna, Austria) in combination with Amelia II.34 Imputation was repeated 100 times using the full data set for the multiple imputation procedure. Imputation diagnostic plots indicate that imputation worked well. To compare the changes of the detraining period between the CG and the HIT-RT (ie time–group interactions = effects) we applied an ANCOVA that adjusted for 18-month data of the corresponding parameter using group as covariate. The changes from baseline and to the end of the detraining period were also analyzed by an ANCOVA that adjusted for baseline data of the corresponding parameter and again included group as covariate. The within-group changes over time were analyzed by paired t-tests. Within- and between-imputation variances were analyzed using the approach suggested by Rubin35 and Barnard and Rubin.36 We consistently applied 2-tailed tests and accepted significance at p <0.05.
Participant and Exercise Characteristics
Participants’ baseline and 18-month FU characteristics (ie baseline values of the detraining period) are displayed in Table 1. Applying a DXA-based cutoff point of 27% body fat rate to diagnose obesity37 the vast majority of our cohort (93%) can be considered as obese.
Table 1 Characteristics of the Participants of the High-Intensity Resistance Exercise Training (HIT-RT) and Control Group (CG) at Study Start and After 18 Months of Intervention
Baseline but not 18-month dietary protein intake varied significantly between the groups. Further, we observed a significant increase (p<0.001) in 25-OHD concentration in both groups during the interventional period, indicating that cholecalciferol supplementation was successful in most subjects.
Three participants quit the study during the intervention phase and were also lost for 6-month detraining-FU (Figure 1). The two participants of the CG who were unable to attend the 18-month FU assessment were evaluated at 6-month detraining-FU. Two HIT-RT participants and one participant of the CG refused to visit the detraining-FU, due to fear of being infected during the assessments.
Figure 2 shows intervention and detraining effects on LBM in the HIT-RT and CG. After 18 months of intervention LBM increased significantly in the HIT-RT (p<0.001) and decreased slightly in the CG (p=0.11). Intervention effect (ie group differences in 18-month changes) was significant (p<0.001; 1.73 kg, 95%-CI: 1.13–2.32 kg). During the detraining period, LBM gains of the HIT RT were nearly halved (p<0.001), but still remained significantly (p<0.001) above baseline (Figure 2). In parallel, LBM of the CG decreased further during the detraining period, resulting in a significant 24-month overall change from baseline (p=0.007). Briefly, LBM mass reduction during the detraining period was significantly more pronounced in the HIT-RT compared with the CG (p<0.001). However, even after 6 months of detraining the intervention effect remained significant (1.04 kg, 0.46–1.59 kg, p<0.001). In summary, we thus confirmed our hypothesis (1.1) that 6 months of detraining after 18 months of HIT-RT significantly decrease LBM compared to the non-training control group (Figure 2). However, even after this significant 6-month detraining effect, we observed a significant training effect at study end, thus we reject our hypothesis (2.1).
Figure 2 Mean values and 95%-CI for changes of lean body mass after training and detraining in the HIT-RT and CG.
Abbreviation: n.s., non-significant.
Figures 3 and 4 display changes of total and abdominal body fat rate (%) during training and detraining in the HIT-RT and CG. Both fat proportions increased in the CG during the 24-month study period (total body fat: p=0.048; abdominal body fat: p=0.053). In parallel, in the HIT-RT group total and abdominal fat decreased significantly (both p<0.001) during the intervention period and increased significantly for total (p=0.015) and abdominal (p=0.007) body fat rate during the detraining period. Detraining effects differ significantly between the groups for total (p=0.003) but not for abdominal (p=0.059) body fat. Effects that were significant after the end of the intervention (total body fat: 2.54%, 95%-CI: 1.90–3.21%; abdominal body fat: 2.66%, 1.70–3.60%; both p<0.001) remained significant after 6 months of detraining (total body fat: 1.99%, 1.25–2.77%; abdominal body fat: 1.94%, 0.91–2.99%, both p≤.001) (Figures 2 and 3). However, in summary we accepted hypothesis (1.2) and rejected hypothesis (1.3) of a significantly more pronounced detraining effect in the HIT-RT vs the control group on total body fat and abdominal body fat rate. We further reject our secondary hypotheses ((2.2) and (2.3)) that the significant HIT-RT effects on total and abdominal body fat are lost after 6 months of detraining.
Figure 3 Mean values and 95%-CI for changes of total body fat rate after training and detraining in the HIT-RT and CG.
Abbreviation: n.s., non-significant.
Figure 4 Mean values and 95%-CI for changes of abdominal body fat rate after training and detraining in the HIT-RT and CG.
Abbreviation: n.s., non-significant.
Changes of the MetSZ during training and detraining are displayed in Table 2. MetSZ of the CG deteriorated non-significantly (p=0.080) during the intervention and detraining period (Table 1). In contrast, MetSZ in the HIT-RT improved significantly (p<0.001) during the interventional and decreased significantly (p=0.002) during the detraining period. Detraining effects differ significantly between the groups (p=0.003). The significant effect observed after 18 months of exercise (p=0.001) was lost after 6 months of detraining (p=0.441). In summary, however, we confirmed hypothesis (1.4) of a significantly more pronounced detraining effect in the HIT-RT compared with the CG. Additionally, we confirmed our hypothesis (2.4).
Table 2 Mean Values and 95%-CI for Changes of the Metabolic Syndrome Z-Score After Training and Detraining in the CG and HIT-RT Group
In detail, all components of the MetSZ improved during the intervention, but only results on waist circumference, MAP and HDL-C showed significant training effects.31 Detraining changes of waist circumference, MAP and Triglycerides (all p>0.188) in the HIT-RT did not differ significantly from the CG. However, we observed a significant detraining effect for HDL-C (p=0.017) with significant HDL-C declines in the HIT-RT (p=0.029). In contrast, glucose levels remained stable in the HIT-RT, but declined considerably in the CG resulting in a significant detraining effect (p=0.040). At study end, only the effect for waist circumference remained statistically significant (p<0.001).
According to our physical activity questionnaire,33 habitual physical activity did not vary significantly in the EG and CG over the intervention period (Table 1). Habitual exercise volume was also stable during the intervention period. However, both groups increased the amount of individual aerobic outdoor activities, ie walking and/or biking (20±29%, p≥.103) during the detraining period. This can be largely attributed to the COVID-19 induced restrictions, with individual outdoor activities still being allowed. None of the participants attended supervised group exercise training or resistance-type exercise training during the six-month observational (detraining) period of the present study.
Dietary calcium and protein intake did not vary significantly over the two-year period. However, due to the different recommendations26 on total protein intake in CG and HIT-RT (1.2 vs 1.5–1.6 g/kg/d), total protein intake of the HIT-RT decreased after cessation of WPS by 0.35–0.45 g/kg/d, while on average no relevant changes in total protein intake were recorded for the CG. As reported, cholecalciferol supplementation was maintained during the detraining period, and hence 25-OHD levels did not change significantly during the detraining period (HIT-RT: 28.1±6.1 to 30.3±7.5 ng/mL; CG: 29.6±5.8 to 30.8±6.6 ng/mL). None of the participants reported injuries, operations, diseases, periods of physical inactivity >1 week, or changes of pharmacologic therapy with impact on muscle or bone metabolism during the detraining period.
The present 18-month RT exercise study clearly substantiates the deleterious effects of 6 months of detraining on LBM, total and abdominal body fat rate and the MetS-Z-Score in our predominately obese cohort of cdw men 72–91 years old with low muscle and bone mass. However, although 6 months of detraining reduced the training effect of an 18-month HIT-RT protocol, apart from the METS-Z-Score, the effects remained significant after the detraining period (ie after 24 months). We speculate that this sustainability can be attributed to the long intervention period, ie to the phenomenon that adaptation achieved over a longer period might be characterized by a lower susceptibility to failure (“adaptation stability”39). Of importance for the present detraining issue, the cessation of exercise refers exclusively to the dedicated HIT-RT, while the volume of outdoor physical activity and exercise training (ie brisk walking, Nordic walking, cycling) increased in both groups during the detraining period. One may argue that in addition to the cessation of (RT) exercise, the termination of whey protein supplementation (WPS) might have contributed to the significant deterioration not only of body composition but also in cardiometabolic risk factors. Indeed, some studies suggested evidence for a positive effect of isolated protein and amino acid supplementation on LBM (e.g.40–45), body fat (e.g.46,47) and cardio-metabolic risk factors (review in48) in older adults. We are unable to separate the exercise vs WPS effects on our outcomes during training18,31 and detraining; however, (1) based on the rather high dietary protein intake (Tables 1 and 2) considering that the 1.5 g/d/kg WPS of the HIT-RT was derived from recommendations of the PROT-AGE group26 for exercising older adults, we speculate that the cessation of WPS after the end of the intervention had only a minor additional impact on our result of detraining effects on body composition and cardiometabolic risk.
A meaningful comparison of our result on detraining effects on body composition and cardiometabolic health in older people with other studies is far from trivial. Considering that apart from age3,49 particularly the (1) length of the intervention period (e.g.39), (2) type, intensity and volume of the exercise applied (e.g.3,7,15,50,51), (3) length of the detraining period (e.g.3,52) and (4) activity during the detraining period contribute considerably to the detraining result of a given outcome (… that might be also more or less sensitive to detraining,8,50), inconsistency of detraining study results become comprehensible. Applying 5 cycles of 9 months of RT intermitted by 3 months of detraining each, although predominately non-significant, Douda et al4 consistently reported reversions of training effects on LBM and body fat during the detraining periods in their cohort of women 60 years and older. After 24 weeks of RT-training and detraining each, Hakkinen et al8 reported a significant detraining effect on cross-sectional area of the quadriceps femoris in younger and older men, that average below baseline. Applying a RT and detraining protocol for 24 weeks each in people 65–83 years old, Taaffe et al14 found significant detraining effects on LBM and body fat. The authors additionally reported a significant increase of fatty infiltration of thigh muscles during detraining. Applying an albeit shorter RT period of 16 weeks, Bickel et al.3 reported significant reductions in thigh lean mass that dropped below baseline values already after 8 weeks of detraining. On the other hand, the authors observe a complete reversal of the training-induced myofiber type IIx to IIa shift not before 32 weeks of detraining.
Detraining effects on cardiometabolic risk factors after RT are very rarely evaluated in older people.53,54 Further, no RT study with older people focused on detraining effects on the MetS-Z-Score. Additionally, most studies on RT (or at least with an RT-component) applied short intervention (≤16 weeks) and/or short detraining (<12 weeks) periods (e.g.5,53,55–59). However, a summary of (very) roughly comparable detraining studies provided inconsistent results on cardiometabolic risk factors. Applying 8 months of RT in coronary artery disease (CAD) patients 62±8 years old, Theodorou et al52 reported no significant detraining effects for HDL-C or Triglycerides after 1, 2 or 3 months of detraining. Leitao et al54 who prescribed multicomponent exercise with an RT component for 9 months listed significant detraining effects on systolic and diastolic blood pressure and Triglycerides after 3 months of detraining in women 60–75 years old. Takmakidis and Volaklis60 confirmed these unfavorable results on Triglycerides after 8 months of training and 3 months of detraining in men 57±10 years old with CAD.
Summing up the features and limitations of the present study on detraining, the main limitation might be the non-preplanned detraining approach. After the 18-month study intervention, we did not intend to tell our aged participants that they had to stop exercising (…. which would be a morally reprehensible approach), but aimed to continue the RT-exercise training in a sustainable setting. However, our inability to quickly reorganize the training and the subsequent COVID-19 related lockdown offered the opportunity for the present detraining study. Due to the initially non-intended detraining period, we supplemented all participants with a further 180 capsules each of 2500 IE cholecalciferol from our remaining stocks after the end of the intervention. Additionally, related to the lack of an a priori sample size analysis for the detraining approach, there is some evidence that our approach is underpowered to successfully address some of the study outcomes. Another biometrical issue was that following the recommendations of Li61 we do not adjust on secondary outcomes, thus the reader should be aware of potential multiplicity. This feature might be further aggravated since we addressed different endpoints of the detraining aspect. As the decisive outcome, we consider differences in detraining changes between HIT-RT and CG. However, we also listed changes during detraining in the HIT-RT, as well as baseline-adjusted overall effects after 24 months. In contrast, most other studies simply focus on detraining changes in the exercise group without considering adjuvant changes in the CG. Lastly, we selected LBM and not, as initially registered, skeletal muscle mass index as the primary study outcome, in order to increase the comparability with other trials.
Addressing the generalization of our results on detraining is a daunting task. Although our cohort of predominately obese, 72–91-year-old HIT-RT completers with osteosarcopenia might not be “fully representative” for older cdw cohorts, we nevertheless think the aspects listed below can be generalized. Hence, addressing the clinical relevance of our results, we conclude that (1) although training breaks must be long enough to allow full regeneration of the system(s) addressed, 6 months of detraining result in significant and clinically relevant negative effects on body composition and cardiometabolic outcomes and should therefore be avoided. (2) Detraining effects after abrupt cessation of (HIT-)RT cannot be compensated by maintaining or slightly increasing physical activity with an aerobic character (ie walking, cycling). (3) Nevertheless, there is some evidence that adaptation achieved over a longer period of time (ie 18 months) is characterized by higher stability and lower susceptibility to failure39 during detraining. Correspondingly, exercise training protocols particularly for older people should focus on continuous exercise protocols with short training breaks.
Data Sharing Statement
The data that support the findings of this study are available from the corresponding author (WK), upon reasonable request.
WK, DS, MK, SvS made a significant contribution to the work reported, whether that is in the conception, study design, execution, acquisition of data, analysis and interpretation, or in all these areas. WK, DS, MK, SvS have drafted or written, or substantially revised or critically reviewed the article and have agreed on the journal to which the article will be submitted. Further, all authors reviewed and agreed on all versions of the article before submission, during revision, the final version accepted for publication, and any significant changes introduced at the proofing stage. Finally, WK, DS, MK, SvS agree to take responsibility and be accountable for the contents of the article.
The authors are very grateful to the support of the Universitäts-Bund of the University of Erlangen-Nürnberg, Erlangen that provided resources for the 6-month follow-up assessment. The authors further acknowledge the support of Kieser Training (Erlangen, Germany) which provided the gym facilities and exercise supervision support. The authors also acknowledge the contribution of the Institute of Radiology, FAU, Erlangen, Germany.
The authors report no conflicts of interest in this work.
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