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What was the target age group for the clinical guidelines developed by ASPEN?
How many studies were retrieved for the systematic review conducted by ASPEN?
What was used to assess the diagnostic accuracy of the test method against a 'gold standard' reference?
What is the recommended method for the assessment of fat mass in patients with a variety of disease states?
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What is the current status of the validity of DXA for lean mass assessment in any clinical population?
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Why can't recommendations be made to support the use of US in the clinical setting?
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Why can't recommendations be made to support the use of BIA in the clinical setting?
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What is human body composition?
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What is the primary reason for not recommending DXA for lean mass assessment?
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What measure of fat mass was assessed by DXA in the studies?
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What was the range of correlation coefficients for the correlation between DXA-derived abdominal adipose tissue and CT-derived VAT?
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What was the summary correlation between DXA-derived total body fat and CT-derived VAT?
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What was the measure of heterogeneity between studies (I2) in the assessment of correlation between DXA-derived total body fat and CT-derived VAT?
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How many studies used MRI to validate DXA measures for regional adiposity and total body fat?
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What was the strength of the summary correlation between DXA-derived trunk fat and CT-derived VAT?
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How many studies with heterogeneous patient populations were used to examine the correlation between CT-derived VAT and DXA-derived abdominal adipose tissue?
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What was the range of correlation coefficients for the correlation between DXA-derived total body fat and CT-derived VAT?
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What was the GRADE recommendation for the use of DXA for fat mass assessment?
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What is the main reason why DXA is not widely used in the inpatient setting?
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What is the primary application of DXA in the outpatient setting?
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What is the correlation between CT-derived or MRI-derived VAT and DXA-derived total FM?
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What is the limitation of using DXA in select patient populations?
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What is the advantage of using whole body DXA for body composition assessment?
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What is the potential application of DXA in patients with cancer?
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What is the current status of the validity of DXA for body composition assessment?
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What is the benefit of using DXA for body composition assessment?
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What is the reason for the large heterogeneity between studies examining the correlations between CT-derived or MRI-derived VAT and DXA-derived total FM?
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What is the potential use of whole body DXA data in patients with cancer?
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In which patient populations is further research critically needed for CT imaging?
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What is a limitation of using US to assess body composition?
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What is an advantage of using US to assess SMM?
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What was a previous concern about using US to assess body composition?
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What is a characteristic of US that makes it promising for use in the clinical setting?
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Which of the following is a current limitation of using US in the clinical setting?
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What is a potential application of US in the clinical setting?
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What is a limitation of comparing results across studies using US?
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What is a characteristic of US that makes it suitable for use in healthy, nonminority, free-living populations?
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What is a benefit of using US to assess visceral adiposity?
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What is the primary reason for recommending a strong recommendation despite weak published evidence?
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What was the total number of studies retrieved from Medline for DXA, US, and BIA?
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What was the primary reason for eliminating studies from the initial search criteria?
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What was the primary reason for excluding 6 studies from the review?
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What percentage of patients have obesity at the time of evaluation?
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What is a characteristic of BIA devices that makes them ideal for follow-up studies?
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What is the primary limitation of assessing simple body weight?
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What is a limitation of BIA equations/algorithms?
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What is the primary application of body composition assessment in oncology populations?
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What is measured by BIA to estimate total body water and body composition?
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What is the primary limitation of current bedside nutrition assessment techniques?
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What is estimated by MF-BIA devices in kilograms or as a percentage of total body weight?
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What is the primary goal of evaluating the validity of body composition assessment techniques?
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What is a common characteristic of the patient populations studied in the included BIA studies?
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How many studies were included in the evidence tables for each question?
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Why was it not possible to compare studies using different BIA devices?
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What is the primary method used to develop practical recommendations for each question?
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What is a limitation of conflating data from studies using the same BIA device?
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What is a characteristic of SF-BIA devices?
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What is the main issue in human body composition research?
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What is the purpose of the 5-level organization model used in body composition research?
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How many studies used a combination of MF-BIA and SF-BIA devices?
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What does the term 'lean soft tissue' refer to in body composition research?
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Which of the following body composition techniques is used to assess skeletal muscle mass?
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What is the primary purpose of the GRADE approach in body composition research?
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What is the main difference between the current guideline and previous ASPEN guidelines?
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What is the purpose of the McInnes et al. recommendations in the context of body composition research?
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What is the benefit of using the GRADE methodology in body composition research?
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What is the focus of the task force in the current guideline?
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What is the purpose of the literature search in the current guideline?
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What is the main limitation of BIA validation studies in clinical settings?
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What is the emerging area of research using BIA?
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Why are BIA validation studies scarce in hospitalized patients?
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What is the primary goal of the task force in evaluating body composition assessment methods?
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What is the significance of the PRISMA recommendations in the context of this review?
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What is the current status of BIA validation studies in clinical populations?
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What is the reason for cautious interpretation of BIA results in individual patients?
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What is the future direction of research in BIA?
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What is the significance of phase angle in BIA research?
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What is the limitation of the task force's original approach?
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What is the primary reason for examining the interplay between lean and fat mass compartments in diet and physical activity interventions?
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What type of statistical modeling is required to link changes in lean and/or fat mass with serum biomarkers of disease?
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What is the limitation of the task force's review of body composition assessment in clinical populations?
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What type of coefficients would have been ideal to assess agreement between body composition methodologies?
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What is the importance of evaluating the validity of body composition assessment techniques in various clinical populations?
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What is the potential limitation of using data from studies that were not necessarily driven by validity?
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What is the implication of the task force's review of body composition assessment in clinical populations?
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What is the importance of evaluating the correlation between body composition assessments and serum biomarkers of disease?
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What is the primary issue with the terminology used in body composition studies?
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Why is it important to differentiate between superficial and deep subcutaneous adipose tissue?
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What is a limitation of using the term 'intraabdominal fat' in body composition studies?
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Why is it essential to establish cut-points for categorizing body composition characteristics?
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What is a challenge in working with body composition data?
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Why is it important to include 'healthy controls' in body composition studies?
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What is a limitation of body composition studies in terms of study design?
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Why is it essential to consider potential sources of relevant comparative data in the public domain?
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What is a limitation of using body composition data in patient care?
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Why is it important to develop a unified body composition vernacular?
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What is the main limitation of using ultrasound to evaluate body composition in patients with critical illness?
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Why is it difficult to directly compare or interpret US, DXA, and CT data?
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What is the main reason why recommendations cannot be made regarding the validity of using BIA in clinical populations?
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What is the main difference between BIA and other body composition techniques?
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What is the purpose of using a superior comparator method in the evaluation of BIA?
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What is the main advantage of using US over other body composition techniques in patients with critical illness?
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What is the limitation of measuring a single muscle group using US?
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What is the importance of investigating both upper and lower body muscle groups when evaluating longitudinal changes in body composition?
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What is the limitation of using BIA devices from different manufacturers?
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What is the purpose of establishing measurement protocols for US muscle evaluation?
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Study Notes
Introduction to Body Composition
- Human body composition is the study of the distribution of lean mass (LM) and adipose tissue, and their impact on health.
- The field is still emerging, but hindered by issues of nomenclature, with different terms used to describe the same compartments.
Body Composition Compartment
- The compartment being assessed/estimated can be referred to by technique (e.g., molecular, tissue, organ, or whole body levels).
- Examples of body composition compartments:
- Fat-free mass (includes bone, lean tissue, and bone mineral content)
- Lean soft tissue (sum of all lean tissues, including protein, water, carbohydrates, and soft tissue minerals)
- Skeletal muscle mass (primary component of lean tissue)
- Fat mass (lipid content, forms 80% of adipose tissue compartment)
- Adipose tissue (formed by connective tissues, fibroblasts, and capillaries)
Methods of Body Composition Assessment
- Dual-energy X-ray absorptiometry (DXA): uses x-ray technology to measure body composition.
- Bioelectrical impedance analysis (BIA): uses electrical signals to measure body composition.
- Ultrasound (US): uses high-frequency sound waves to capture live images and soft tissue structures.
- Computed tomography (CT): uses x-rays and computer technology to produce detailed images of the body.
- Magnetic resonance imaging (MRI): uses strong magnetic fields and radio waves to produce detailed images of the body.
American Society for Parenteral and Enteral Nutrition (ASPEN) Guidelines
- Conducted a systematic review to evaluate the best available evidence for the validity of body composition methods (DXA, US, and BIA) in clinical populations.
- Targeted adults >18 years with potentially inflammatory conditions or pathological end points associated with specific diseases.
- Retrieved 7375 studies, with 15 DXA, 7 US, and 23 BIA studies providing applicable data.
- Used the GRADE approach to evaluate the diagnostic accuracy of the test methods against a "gold standard" reference.
Recommendations
- Based on limited evidence, DXA is recommended for the assessment of fat mass in patients with various disease states.
- No recommendations can be made to support the use of US or BIA in the clinical setting due to limited data.
- The validity of DXA for lean mass assessment in any patient population remains unknown.
Future Directions
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Research is needed to evaluate the validity of DXA for lean mass assessment in various patient populations.
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Further studies are required to address the limitations of body composition assessment in clinical populations.
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The use of DXA, US, and BIA in different patient populations and disease states requires further exploration.### Advantages and Limitations of Ultrasound (US) for Skeletal Muscle Assessment
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US is a highly portable technique that can accurately measure visceral adipose tissue (VAT) when completed by experienced, trained technicians.
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US can quantify muscle quantity and "quality" through parameters like muscle thickness, cross-sectional area, and echogenicity.
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The major setback for US's universal use is the lack of standardized measurement protocols.
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There is no evidence to guide the alteration of nutrition provision based on US findings.
Limitations of Bioelectrical Impedance Analysis (BIA) for Body Composition Assessment
- BIA is a practical, portable, noninvasive tool that poses minimal risks and low costs.
- BIA devices can measure total body or segmental impedance, which can be used to estimate total body water and body composition.
- The proprietary nature of manufacturer-specific BIA regression models limits the comparison of studies using different BIA devices.
- BIA precision and accuracy are highly influenced by fever, certain medications, and fluid and electrolyte disturbances.
Current State of Body Composition Assessment in Clinical Populations
- The diagnostic accuracy of body composition assessment methods in nonhealthy populations is limited.
- There is a lack of standardized body composition terminology across studies.
- Cut-points are needed to categorize characteristics of interest in body composition.
- There is a need for more studies with sufficient sample size and statistical power.
- The inclusion of "healthy controls" is critical for making adequate comparisons across techniques.
Future Directions for Body Composition Assessment
- There is a need for more research on the use of US in clinical populations.
- BIA demonstrates good correlations with superior reference methods in several outpatient populations, but more validation studies are needed in hospitalized patients.
- An emerging area of research is the use of BIA to estimate phase angle, a surrogate of lean mass quality.
- There is a need for more studies on the use of body composition assessment methods in minority populations.
- Collaboration with investigators who have published in diverse, healthy populations is necessary.
- Sophisticated statistical modeling is required to examine clinically relevant outcomes and link changes in lean and/or fat mass with serum biomarkers of disease.
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Description
Evaluating the validity of body composition methods such as DXA, US, and BIA in clinical populations with inflammatory conditions.