- Open Access
Weight gain, overweight and obesity in solid organ transplantation—a study protocol for a systematic literature review
Systematic Reviews volume 4, Article number: 2 (2015)
Overweight and obesity, which have a substantial impact on health in the general population, have similar prevalence in solid organ transplant recipients but carry even more serious ramifications. As this group’s use of immunosuppressive medication increases the risk for comorbidities, e.g. metabolic syndrome and cardiovascular disease, the prevention of additional risk factors is vital. This systematic review will be the first to summarize the issue of weight gain, overweight and obesity concurrently within and across solid organ transplantation. The three research questions relating to solid organ transplantation are the following: (1) What are the prevalence and evolution of overweight and obesity from pre- to post-transplant?; (2) Which pre- and post-transplant risk factors are associated with post-transplant weight gain, overweight or obesity? and (3) Which post-transplant patient outcomes and comorbidities are associated with pre- and post-transplant weight gain, overweight and obesity?
MEDLINE via PubMed, The Cochrane Library, Cumulative Index to Nursing and Allied Health (CINAHL), PsycINFO and Excerpta Medica DataBase (EMBASE) will be searched for original quantitative studies in adult liver, heart, lung or kidney transplant patients. Topics of interest will be the prevalence and evolution of overweight and obesity over time, risk factors associated with changes in weight or body mass index (BMI), overweight and obesity, and the relationship of weight or BMI with post-transplant outcomes and comorbidities. Screening of titles and abstracts, full-text reading and data extraction will be divided between three researchers. Researchers will cross-check one another’s screening decisions for random samples of studies to adhere as closely as possible to the recommendations of The Cochrane Collaboration. For quality assessment, a purpose-adapted 19-item instrument will be used. Effect sizes will be calculated for relationships investigated in a minimum of five studies. Random effects meta-analysis with moderator analyses will be conducted if applicable.
This systematic review will comprehensively synthesize the existing evidence concerning weight gain, overweight and obesity in solid organ transplantation in view of magnitude, influencing factors and associations with patient outcomes and comorbidities. The results can fuel the development of interventions to prevent weight gain in the solid organ transplant population.
Systematic review registration
In recent decades, overweight and obesity have become a global public health issue. Weight categories are often specified in terms of body mass index (BMI), i.e. the quotient of body mass in kilograms and the square of height in metres (kg/m2). The World Health Organization (WHO) proposed the most commonly used classification system, defining overweight as a BMI from 25 to 29.9 and obesity as a BMI ≥30 . In 2008, more than 1.4 billion adults were overweight, of whom roughly 500 million were obese, indicating that the worldwide prevalence of obesity doubled from 1980 to 2008 . This development is underpinned by the fact, between 1990 and 2010, in terms of worldwide ranking, “high BMI” climbed as a risk factor for disease burden from the tenth position to the sixth . In Europe, North and South America, Central Asia and parts of Africa, “high BMI” even ranked among the top four risk factors for disease burden, following only high blood pressure, smoking and alcohol use .
In addition to the BMI-based definition cited above, the WHO defines overweight and obesity functionally as abnormal or excessive fat accumulation that may impair health . Overweight and obesity are associated with increased risks for all-cause mortality, cancer, non-alcoholic fatty liver disease, hypertension, type 2 diabetes and metabolic syndrome [3, 5–9]. Metabolic syndrome is defined as a cluster of three or more of the following cardiovascular risk factors: (a) waist circumference >102 cm in men and >88 cm in women, or BMI ≥30; (b) triglycerides ≥150 mg/mL; (c) fasting glucose ≥100 mg/dL; (d) blood pressure ≥130/85 mm Hg and (e) high-density lipoprotein <40 mg/dL in men and <50 mg/dL in women . Associated with increased cardiovascular disease and all-cause mortality , but rarely occurring in persons with BMI values <25, metabolic syndrome is closely related to overweight and obesity .
Considering these relationships, the negative impact of overweight and obesity on health may also be exacerbated by existing comorbidities. However, a recent prospective cohort study of 71,527 persons showed that, independent of the presence of metabolic syndrome, overweight and obesity were associated with increased risks of myocardial infarction and ischemic heart disease . These results support the hypothesis that the studied outcomes are associated directly with higher body weight per se and are not necessarily related to metabolic syndrome.
The energy balance framework and prevention of weight gain as key concept
According to the energy balance equation, i.e. energy storage = energy intake − energy expenditure , weight gain is the result of a positive energy balance due to increased energy intake or decreased energy expenditure . Therefore, the most obvious causes of weight gain, overweight and obesity are a sedentary lifestyle and a high-calorie diet. Unfortunately, this statement oversimplifies the complex system behind the development of overweight and obesity. A growing body of evidence has revealed several environmental (e.g. automation and mechanization, cohabitation, easy access and low cost of food), behavioural (e.g. eating large portions or high-density food, physical inactivity, television-watching habits), psychological (e.g. conscious control over behaviour), biological (e.g. hormonal disturbances) and genetic factors (e.g. polygenetic defects, monogenetic mutations) influencing the balance of energy intake and expenditure [16, 17]. Interrelationships between these factors further complicate the underlying mechanisms . However, knowledge of the factors influencing weight gain is crucial to further intervention development. As stated in numerous national reports, research to develop interventions against weight gain is a high priority [16–19]. The argument to favour prevention of overweight and obesity over treatment is based on a physiological compensatory mechanism. The reduction of energy intake by food restriction leads to decreased body energy requirements. This is a dynamic assimilation process which helps maintain body functions and energy reserves during phases of shortage . Overfeeding stimulates no such compensatory changes, i.e. human biology protects us from weight reduction but not weight gain. Therefore, the prevention of weight gain should be easier than losing weight and maintaining weight loss .
Weight gain, overweight and obesity in the transplant population
The rising overall prevalence of obesity is mirrored in the transplant population. For example, Leonard et al. noted that between 1990 and 2003, the percentage of liver transplant candidates obese at the time of transplantation increased from 15% to 25% , and later, Kim et al. reported that, by 2011, 34.4% of liver transplant candidates were obese . Similar developments have been shown in kidney, heart and lung transplantation [24–26]. Additionally, excessive (up to 10 kg) weight gain in the first year post-transplant has been described, particularly in liver, kidney and heart transplantation [27–29]. In liver transplantation, for example, the prevalence of obesity 1 year post-transplant was double the pre-transplant figure [30–32]. This alarming development has been described in various settings (e.g. single-centre studies, database-related reports) and countries (e.g. the USA, Great Britain, Brazil). Immunosuppressive medication is often cited as a risk factor for weight gain. For example, prednisone is associated with craving sweets and increasing weight, especially when dosed >5 mg/day . Interestingly, conflicting evidence concerning this relationship has also been reported [34–36]. Moreover, risk factors for post-transplant weight gain, overweight and obesity have not been part of any systematic review and thus have not yet been outlined so far.
Weight gain, overweight and obesity are serious issues in the solid organ transplant population as they may be contributing factors to limited improvement in long-term outcomes in transplantation. Indeed, while the last 20 years have seen impressive first-year graft survival increases across all solid organ groups, long-term survival has not kept pace , and cardiovascular events have been reported as a leading cause of mortality after solid organ transplantation [38–40]. This can be linked to lifestyle-related factors as well as to the development of new comorbidities, related to the side effects of immunosuppressive regimens such as hypertension, dyslipidemia and diabetes mellitus, which are all cardiovascular risk factors that also contribute to increased risk of post-transplant metabolic syndrome [41–44]. A major therapeutic aim after solid organ transplantation is therefore to prevent and treat any risk factors, which might increase the occurrence of those new comorbidities. Based on the evidence from the general population, weight gain, overweight and obesity must be regarded as additional risk factors for the occurrence of those new comorbidities after transplantation. Two recent meta-analyses showed the impact of obesity on patient outcomes after kidney  and liver  transplantation. In kidney transplantation, pre-transplant obesity, defined as BMI ≥30, was associated with an increased risk for delayed graft function (relative risk, 1.41; 95% confidence interval, 1.26–1.57), but not with acute rejection. The impact of pre-transplant obesity on patient and graft survival in this analysis seemed to be depending on the era of transplantation, with significant associations only in studies published before 2003, compared to those published afterwards . In liver transplantation, neither BMI by itself nor BMI after correction for ascites had an impact on patient survival after transplantation . Whereas these meta-analyses provide important insights in view of pre-transplant BMI associated with post-transplant outcomes, the evidence base regarding its impact on post-transplant comorbidities as well as the impact of post-transplant weight gain, overweight or obesity on patient outcomes has not yet been summarized.
Our systematic literature review will consider all solid organ groups concurrently using the same methodological approach to identify organ-specific impacts of weight gain, overweight and obesity on patient outcomes and risk factors for weight gain. To summarize the evidence on risk factors, we propose a model based on the dynamic energy balance framework incorporating the environmental, behavioural, psychological, biological and genetic factors as well as their interrelationships and we will expand the model with specific treatment- and disease-related factors in transplantation.
The overall purpose of this systematic literature review is to summarize and synthesize the evidence about weight gain, overweight and obesity in the adult solid organ transplant (liver, heart, lung and kidney transplant) population, in view of its magnitude, influencing factors and associations with patient outcomes. The following research questions will guide the literature search:
What are the prevalence and evolution of overweight and obesity from pre- to post-transplant in adult solid organ transplant patients?
Which pre- and post-transplant risk factors are associated with post-transplant weight gain, overweight or obesity in adult solid organ transplant recipients?
Which post-transplant patient outcomes and comorbidities are associated with pre- and post-transplant weight gain, overweight and obesity in adult solid organ transplant recipients?
This review is registered with the International Prospective Register of Systematic Reviews (PROSPERO) under registration number CRD42014009151. The structure of this study protocol follows the recommendations of the Cochrane Handbook for Systematic Reviews of Interventions .
Criteria for considering studies for review
Type of studies
Original quantitative studies, including prospective or retrospective cohort studies, case-control studies and cross-sectional studies, will be considered for review. Although this systematic review will not specifically assess the effectiveness of interventions, randomized controlled trials (RCTs) with intervention and control groups will be included and data extracted according to our inclusion and exclusion criteria. Mixed methods studies will be included if the aim of the quantitative part is sufficiently described to meet our inclusion criteria.
Types of participants
Only first-time liver, heart, lung or kidney transplant candidates or recipients aged ≥18 years will be included. The following patients will be excluded: candidates without post-transplant data collection or patients awaiting or having received multi-organ transplantation or re-transplantation.
Topics of interest
Studies should examine at least one of the following topics:
Changes in weight or BMI over time, either pre- to post-transplant or post-transplant. Quantitative studies which provide only a point prevalence of weight and BMI as part of their sample characteristics but no examination of relationships between weight or BMI and associated risk factors, outcomes or comorbidities will be excluded.
Any pre- or post-transplant risk factors and correlates associated with post-transplant weight gain, overweight and obesity. Depending on the study design (e.g. longitudinal) and statistical tests (e.g. multivariate analysis), special attention will be paid as to whether a factor may be regarded as a true predictive risk factor for weight gain, overweight and obesity. As weight gain may be the result of multiple interrelated factors, we will predefine neither risk factors nor correlates of interest. For guidance, following factor categories for both, the time before and after transplantation will be applied in every organ group: treatment- and disease-related, biological, genetic, environmental, behavioural and psychological.
The relationship of weight to any post-transplant outcome or comorbidity. Again, specific outcomes of interest will not be predefined as we rather aim to compile all relevant information to describe and discuss the current state of evidence. Relevant outcomes will likely include patient and graft survival, acute and late rejection, length of stay in hospital and the intensive care unit, costs, any post-operative, cardiovascular or pulmonary complications, any comorbidities and quality of life. We will also check and report whether any other outcomes of interest have been assessed and include these in the analysis.
Search methods for identification of studies
The following electronic databases will be searched: MEDLINE via PubMed, The Cochrane Library, Cumulative Index to Nursing and Allied Health (CINAHL), PsycINFO and Excerpta Medica DataBase (EMBASE). The reference lists of included studies will be searched to identify additional studies. No limits will be applied to the search.
The set of search terms was developed according to the PICOD criteria (Participants, Interventions/Exposure, Comparisons, Outcomes/Topics, Design) and modified based on an earlier scoping review (by SB) of this topic. All terms within each PICOD concept were combined with the Boolean operator OR, and then the PICOD concepts were combined with the Boolean operator AND. In order to allow a broad variety of search results regarding risk factors, patient outcomes and comorbidities, the search strings will be restricted to two concepts: “participants” and “exposure”. The search string for MEDLINE was developed first and then translated for the remaining databases. The process was discussed with a librarian, who also checked the peculiarities of every database and consequences for the search strategy and the search strings. A detailed PubMed search string is provided as follows:
((“Body Mass Index” [Mesh] OR “obesity” [Mesh] OR “overweight” [MeSH Terms] OR “Weight Gain” [Mesh] OR “Body Weight Changes” [Mesh:noexp] OR “Body Weight” [Mesh:noexp]) OR (“BMI” [Text Word] OR “Body Mass Index” [Text Word] OR “obesity” [Text Word] OR “overweight” [Text Word] OR “weight gain” [text word] OR “body weight change*” [Text Word] OR “body weight” [Text Word] OR “weight” [Text Word] OR “Ideal Body Weight” [Mesh] OR “weight management” [Text Word] OR “body size” [Text Word]) AND (“organ transplant*” [Text Word] OR “transplant*” [Text Word] OR “heart transplant*” [Text Word] OR “liver transplant*” [Text Word] OR “lung transplant*” [Text Word] OR “kidney transplant*” [Text Word]) OR (“Kidney Transplantation” [Mesh] OR “Lung Transplantation” [Mesh] OR “Heart Transplantation” [Mesh] OR “Liver Transplantation” [Mesh] OR “Organ Transplantation” [Mesh:noexp] OR “Transplantation” [Mesh:noexp])).
Data collection and analysis
Selection of studies
The literature search will be performed by SB. The results will be transferred to a reference manager (EndNote X5, Thomson Reuters). Although duplicates should be excluded by merging the search results in the reference manager library, a visual inspection will be performed to check for any that remain. The study selection process covers two stages: stage 1 with title and abstract screening and stage 2 with full-text reading of potentially relevant studies. In both stages, the total number of studies will be divided into three equal work packages, i.e. one for each of three researchers (SB, NI, GD). Each researcher will independently evaluate the studies in the allocated work package against the inclusion and exclusion criteria (see Table 1). This deviates from The Cochrane Collaboration recommendations, which specify that at least two people should independently select studies and then verify all results . As the literature search of this systematic review has been pilot-tested several times, with the final version retrieving more than 13,000 hits, the proposed procedure was chosen for feasibility reasons. However, to monitor quality in stages 1 and 2, the three researchers will cross-check a random sample of 5% of one another’s inclusion and exclusion decisions. Where a question arises concerning eligibility, the decision will be discussed between the three researchers, with consensus required for inclusion of a study in the next stage of the process. In cases of disagreement, a fourth researcher (SDG) will be involved for further discussion until consensus is reached. The study selection process will be pilot-tested and evaluated in 50 studies for stage 1 and in 6 studies for stage 2. An Excel spreadsheet will be used to document the reasons for inclusion and exclusion. The selection process will be depicted using a PRISMA flow chart.
Data extraction and management
Studies meeting the inclusion criteria in stage 2 will be eligible for data extraction. The final set of studies will again be divided between three researchers (SB, NI, GD), who will then independently extract the data. An Excel spreadsheet has been developed to systematically collect the variables listed in Table 2. The three researchers will check one another’s data extraction in a randomly selected sample of 5% of the studies. The data extraction procedure will be pilot-tested and evaluated in 12 studies. In cases where two or more articles examine the same dataset, all will be used for data extraction.
For quality appraisal, we will use a 19-item instrument specifically adapted for this systematic review. The quality assessment instrument is provided in an additional file (see Additional file 1). Our instrument was primarily derived from the 27-item checklist compiled by Downs and Black  and modified in a three-step process: (1) As the current systematic review will not focus on the effectiveness of treatments, the 11 questions concerning interventions, follow-up, representativeness of participants, blinding and randomization, more precisely, the questions originally numbered 8, 9, 12–16, 19, 23, 24 and 27, were removed. (2) The sequence of the remaining 16 questions was re-arranged to better facilitate rating. (3) Three questions from a quality assessment instrument used for another systematic review project (De Geest S, Dobbels F, De Simone P, 2011: Search manual B-SERIOUS systematic literature review, personal communication) were added, which were numbered 2, 18 and 19 in our final instrument. The results of the quality appraisal will be displayed with the Cochrane Risk of Bias summary figure provided by Cochrane Review Manager 5.2 . The quality assessment of the studies will be performed independently by three researchers (SB, NI, GD). The three reviewers will randomly check one another’s quality assessments in a random sample of 5% of the appraised studies.
Data analysis and presentation
For all aims, findings will be presented both in a narrative synthesis, as well as in tables and figures. Meta-analysis techniques will be used where relationships (i.e. risk factors and outcomes associated with weight gain, overweight or obesity, respectively) were investigated in five studies or more by calculating effect sizes to analyse the strength and direction of the relationships. If multiple studies examine the same sample for the same outcome, the sample will only be included once in any meta-analysis. Effect sizes will be presented as standardized mean differences (d index) for outcomes analyzing changes from pre- to post-transplant. Outcomes will be expressed as odds ratios for meta-analyses of risk factors and comorbidities. All effect sizes will be reported with standard errors and corresponding 95% confidence intervals. Because we expect sample heterogeneity among the primary studies, estimated effects will be pooled using a random effects model. Heterogeneity between the included studies will be assessed using both the Cochran Q test, with a p value <0.1 indicating significant heterogeneity, and I2 statistics, with values of 25%, 50% and 75% indicating moderate low, moderate and high heterogeneity, respectively . Moderator analysis will be conducted using standard meta-regression (for continuous moderators) and ANOVA (for dichotomous moderators). Analyses will be conducted using Comprehensive Meta-Analysis software (Biostat, Inc., Englewood, NJ, USA). Study quality assessments will be analysed as moderators to investigate the influence of study quality on outcomes. Further, moderator analyses will be conducted on patient and study characteristics (e.g. type of transplant, sample mean age, race/ethnicity, gender, type of immunosuppression, publication date, geographical location) and comorbidities.
To the best of our knowledge, this systematic literature review will condense and compare, for the first time, the current state of evidence on weight gain, overweight and obesity, their risk factors and correlates, as well as their associated impacts on outcomes within and across all four solid organ transplant populations. The results should be valuable for both clinical practice and research. Although all solid organ transplant recipients seem to be susceptible to gain weight, the organ groups may differ in view of risk factors and consequences. An overview of the existing evidence will help healthcare workers to adapt and integrate relevant findings into their daily practice, to provide targeted patient education and to support patient self-management. Additionally, the results will add crucial evidence to expand our theoretical model. As a subsequent step, the identification of risk factors and correlates associated with post-transplant weight gain is potentially a key element for the development of effective interventions to prevent weight gain following solid organ transplantation. Finally, this systematic review will identify gaps in the literature, which might be addressed in future research.
Body mass index
Cumulative Index to Nursing and Allied Health Literature
Excerpta Medica DataBase
Medical Subject Headings
Participants Interventions/Exposure, Comparisons, Outcomes/Topics, Design
International Prospective Register of Systematic Reviews
Randomized controlled trial
World Health Organization.
World Health Organization: Obesity: preventing and managing the global epidemic. Report of a WHO consultation.World Health Organ Tech Rep Ser 2000, 894:i-xii. 1–253
World Health Organization: Obesity. Situation and trends. Geneva: World Health Organization; 2012.
Lim SS, Vos T, Flaxman AD, Danaei G, Shibuya K, Adair-Rohani H, et al.: A comparative risk assessment of burden of disease and injury attributable to 67 risk factors and risk factor clusters in 21 regions, 1990–2010: a systematic analysis for the Global Burden of Disease Study 2010.Lancet 2012, 380:2224–60. 10.1016/S0140-6736(12)61766-8
World Health Organization: Obesity and overweight. . Accessed 08 Oct 2014 http://www.who.int/mediacentre/factsheets/fs311/en/index.html
Sharma AM: Obesity and cardiovascular risk.Growth Horm IGF Res 2003,13(A):S10–7.
Donohoe CL, Pidgeon GP, Lysaght J, Reynolds JV: Obesity and gastrointestinal cancer.Br J Surg 2010, 97:628–42. 10.1002/bjs.7079
Flegal KM, Kit BK, Orpana H, Graubard BI: Association of all-cause mortality with overweight and obesity using standard body mass index categories: a systematic review and meta-analysis.JAMA 2013, 309:71–82. 10.1001/jama.2012.113905
Whitlock G, Lewington S, Sherliker P, Clarke R, Emberson J, Halsey J, et al.: Body-mass index and cause-specific mortality in 900 000 adults: collaborative analyses of 57 prospective studies.Lancet 2009, 373:1083–96. 10.1016/S0140-6736(09)60318-4
Watt KD: Reducing the load: the evolution and management of obesity and nonalcoholic steatohepatitis before liver transplantation.Liver Transpl 2012,18(Suppl 2):S52–8.
Grundy SM, Brewer HB Jr, Cleeman JI, Smith SC Jr, Lenfant C: Definition of metabolic syndrome: report of the National Heart, Lung, and Blood Institute/American Heart Association conference on scientific issues related to definition.Circulation 2004, 109:433–8. 10.1161/01.CIR.0000111245.75752.C6
Mottillo S, Filion KB, Genest J, Joseph L, Pilote L, Poirier P, et al.: The metabolic syndrome and cardiovascular risk a systematic review and meta-analysis.J Am Coll Cardiol 2010, 56:1113–32. 10.1016/j.jacc.2010.05.034
Watt KD, Charlton MR: Metabolic syndrome and liver transplantation: a review and guide to management.J Hepatol 2010, 53:199–206. 10.1016/j.jhep.2010.01.040
Thomsen M, Nordestgaard BG: Myocardial infarction and ischemic heart disease in overweight and obesity with and without metabolic syndrome.JAMA 2014,174(1):15–22.
Hall KD, Heymsfield SB, Kemnitz JW, Klein S, Schoeller DA, Speakman JR: Energy balance and its components: implications for body weight regulation.Am J Clin Nutr 2012, 95:989–94. 10.3945/ajcn.112.036350
Hill JO, Wyatt HR, Peters JC: Energy balance and obesity.Circulation 2012, 126:126–32. 10.1161/CIRCULATIONAHA.111.087213
National Institutes of Health: Strategic plan for NIH obesity research. NIH Publication No. 11–5493. Bethesda: U.S. Department of Health and Human Services; 2011.
Butland B, Jebb S, Kopelman P, McPherson K, Thomas S, Mardell J, et al.: Foresight. Tackling obesities: future choices – project report. 2nd ed. London: Government Office for Science; 2007.
National Institute for Health and Care Excellence (NICE): Obesity: the prevention, identification, assessment and management of overweight and obesity in adults and children. London: National Institute for Health and Care Excellence (NICE); 2006.
World Health Organization: 2008–2013 Action plan for the global strategy for the prevention and control of noncommunicable diseases. Geneva: World Health Organization (WHO); 2008.
Hill JO: Understanding and addressing the epidemic of obesity: an energy balance perspective.Endocr Rev 2006, 27:750–61. 10.1210/er.2006-0032
Hill JO, Thompson H, Wyatt H: Weight maintenance: what’s missing?J Am Diet Assoc 2005, 105:S63–6.
Leonard J, Heimbach JK, Malinchoc M, Watt K, Charlton M: The impact of obesity on long-term outcomes in liver transplant recipients-results of the NIDDK liver transplant database.Am J Transplant 2008, 8:667–72. 10.1111/j.1600-6143.2007.02100.x
Kim WR, Stock PG, Smith JM, Heimbach JK, Skeans MA, Edwards EB, et al.: OPTN/SRTR 2011 annual data report: liver.Am J Transplant 2013,13(Suppl 1):73–102.
Friedman AN, Miskulin DC, Rosenberg IH, Levey AS: Demographics and trends in overweight and obesity in patients at time of kidney transplantation.Am J Kidney Dis 2003, 41:480–7. 10.1053/ajkd.2003.50059
Weiss ES, Allen JG, Russell SD, Shah AS, Conte JV: Impact of recipient body mass index on organ allocation and mortality in orthotopic heart transplantation.J Heart Lung Transplant 2009, 28:1150–7. 10.1016/j.healun.2009.06.009
Allen JG, Arnaoutakis GJ, Weiss ES, Merlo CA, Conte JV, Shah AS: The impact of recipient body mass index on survival after lung transplantation.J Heart Lung Transplant 2010, 29:1026–33. 10.1016/j.healun.2010.05.005
Wawrzynowicz-Syczewska M, Karpinska E, Jurczyk K, Laurans L, Boron-Kaczmarska A: Risk factors and dynamics of weight gain in patients after liver transplantation.Ann Transplant 2009, 14:45–50.
Williams JJ, Lund LH, LaManca J, Kunavarapu C, Cohen DJ, Heshka S, et al.: Excessive weight gain in cardiac transplant recipients.J Heart Lung Transplant 2006, 25:36–41. 10.1016/j.healun.2005.06.016
Clunk JM, Lin CY, Curtis JJ: Variables affecting weight gain in renal transplant recipients.Am J Kidney Dis 2001, 38:349–53. 10.1053/ajkd.2001.26100
Anastacio LR, Garcia Ferreira L, Costa Liboredo J, de Sena RH, Soares Lima A, Garcia Vilela E, et al.: Overweight, obesity and weight gain up to three years after liver transplantation.Nutr Hosp 2012, 27:1351–6.
Everhart JE, Lombardero M, Lake JR, Wiesner RH, Zetterman RK, Hoofnagle JH: Weight change and obesity after liver transplantation: incidence and risk factors.Liver Transpl Surg 1998, 4:285–96. 10.1002/lt.500040402
Richards J, Gunson B, Johnson J, Neuberger J: Weight gain and obesity after liver transplantation.Transpl Int 2005, 18:461–6. 10.1111/j.1432-2277.2004.00067.x
Huscher D, Thiele K, Gromnica-Ihle E, Hein G, Demary W, Dreher R, et al.: Dose-related patterns of glucocorticoid-induced side effects.Ann Rheum Dis 2009, 68:1119–24. 10.1136/ard.2008.092163
Aberg F, Jula A, Hockerstedt K, Isoniemi H: Cardiovascular risk profile of patients with acute liver failure after liver transplantation when compared with the general population.Transplantation 2010, 89:61–8. 10.1097/TP.0b013e3181bcd682
van den Ham EC, Kooman JP, Christiaans MH, Nieman FH, van Hooff JP: Weight changes after renal transplantation: a comparison between patients on 5-mg maintenance steroid therapy and those on steroid-free immunosuppressive therapy.Transpl Int 2003, 16:300–6. 10.1111/j.1432-2277.2003.tb00304.x
Dolgos S, Hartmann A, Jenssen T, Isaksen GA, Pfeffer P, Bollerslev J: Determinants of short-term changes in body composition following renal transplantation.Scand J Urol Nephrol 2009, 43:76–83. 10.1080/00365590802273226
Lodhi SA, Lamb KE, Meier-Kriesche HU: Solid organ allograft survival improvement in the United States: the long-term does not mirror the dramatic short-term success.Am J Transplant 2011, 11:1226–35. 10.1111/j.1600-6143.2011.03539.x
Watt KD, Pedersen RA, Kremers WK, Heimbach JK, Charlton MR: Evolution of causes and risk factors for mortality post-liver transplant: results of the NIDDK long-term follow-up study.Am J Transplant 2010, 10:1420–7. 10.1111/j.1600-6143.2010.03126.x
Lentine KL, Brennan DC, Schnitzler MA: Incidence and predictors of myocardial infarction after kidney transplantation.J Am Soc Nephrol 2005, 16:496–506. 10.1681/ASN.2004070580
Christie JD, Edwards LB, Kucheryavaya AY, Benden C, Dipchand AI, Dobbels F, et al.: The Registry of the International Society for Heart and Lung Transplantation: 29th adult lung and heart-lung transplant report-2012.J Heart Lung Transplant 2012, 31:1073–86. 10.1016/j.healun.2012.08.004
Madhwal S, Atreja A, Albeldawdi M, Lopez R, Post A, Costa MA: Is liver transplantation a risk factor for cardiovascular disease? A meta-analysis of observational studies.Liver Transpl 2012, 18:1140–6. 10.1002/lt.23508
Anastacio LR, Ferreira LG, Ribeiro Hde S, Liboredo JC, Lima AS, Correia MI: Metabolic syndrome after liver transplantation: prevalence and predictive factors.Nutrition 2011, 27:931–7. 10.1016/j.nut.2010.12.017
Miller LW: Cardiovascular toxicities of immunosuppressive agents.Am J Transplant 2002, 2:807–18. 10.1034/j.1600-6143.2002.20902.x
Marcen R: Immunosuppressive drugs in kidney transplantation: impact on patient survival, and incidence of cardiovascular disease, malignancy and infection.Drugs 2009, 69:2227–43. 10.2165/11319260-000000000-00000
Nicoletto BB, Fonseca NK, Manfro RC, Goncalves LF, Leitao CB, Souza GC: Effects of obesity on kidney transplantation outcomes: a systematic review and meta-analysis.Transplantation 2014, 98:167–76. 10.1097/TP.0000000000000028
Saab S, Lalezari D, Pruthi P, Alper T, Tong MJ: The impact of obesity on patient survival in liver transplant recipients: a meta-analysis.Liver Int 2013. doi: 10.1111/liv.12431
Higgins JPT, Green S: Cochrane handbook for systematic reviews of interventions version 5.1.0. The Cochrane Collaboration; 2011. . Accessed 08 Oct 2014 http://www.cochrane-handbook.org
Downs SH, Black N: The feasibility of creating a checklist for the assessment of the methodological quality both of randomised and non-randomised studies of health care interventions.J Epidemiol Community Health 1998, 52:377–84. 10.1136/jech.52.6.377
Review Manager (RevMan) [Computer program]: Version 5.2. 2014. . Accessed 08 Oct 2014 http://tech.cochrane.org/revman
Higgins JP, Thompson SG, Deeks JJ, Altman DG: Measuring inconsistency in meta-analyses.BMJ (Clinical Research Ed) 2003, 327:557–60. 10.1136/bmj.327.7414.557
This systematic review is funded by the 2014 International Transplant Nurses Society research grant. We thank Ms. Heidrun Janka, Librarian at the University of Basel, for her support to develop the search strategy.
The authors declare that they have no competing interests.
SB is the principal investigator and project lead. She prepared the manuscript of the study protocol, performed the literature search and participated in study selection process stages 1 and 2, data extraction, quality appraisal and preparation of the study manuscript. NI and GD participated in study selection process stages 1 and 2, data extraction and quality appraisal. TR participated in the preparation of the codebook and the data analysis. As the project supervisor, SDG contributed to the study concept. All authors contributed to the manuscript’s development and read and approved the final protocol.
Electronic supplementary material
Additional file 1: Quality assessment instrument. The 19-item quality assessment instrument was primarily derived from the 27-item checklist by Downs and Black . The questions were re-arranged to better facilitate rating and questions from another systematic review project (De Geest S, Dobbels F, De Simone P, et al. 2011) were added to suit the needs of our review. (DOCX 51 KB)
About this article
Cite this article
Beckmann, S., Ivanović, N., Drent, G. et al. Weight gain, overweight and obesity in solid organ transplantation—a study protocol for a systematic literature review. Syst Rev 4, 2 (2015). https://0-doi-org.brum.beds.ac.uk/10.1186/2046-4053-4-2
- Weight gain
- Risk factors
- Systematic review