Abstract
Background and Objectives
Intentional weight loss, by reducing insulin resistance, results in both better glycemic control and decreased need for anti-diabetic medications. However, not everyone who is successful with weight loss is able to reduce anti-diabetic medication use. In this retrospective cohort study, we assessed the predictive accuracy of baseline triglyceride (TGL)/HDL ratio, a marker of insulin resistance, to screen patients for success in reducing anti-diabetic medication use with weight loss.
Methods
Case records of 121 overweight and obese attendees at two outpatient weight management centers were analyzed. The weight loss intervention consisted of a calorie-restricted diet (~1000Kcal/day deficit), a behavior modification plan, and a plan for increasing physical activity.
Results
Mean period of follow-up was 12.5 ± 3.5 months. By study exit, mean weight loss and mean HbA1c% reduction were 15.4 ± 5.5 kgs and 0.5 ± 0.2% respectively. 81 (67%) in the study cohort achieved at least 1 dose reduction of any anti-diabetic medication. Tests for predictive accuracy of baseline TGL/HDL ratio ≤ 3 to determine success with dose reductions of anti-diabetic medications showed a sensitivity, specificity, positive predictive value, negative predictive value, area under the curve, likelihood ratio (LR) + and LR-of 81, 83, 90, 70, 78, 4.8 and 0.2, respectively. Reproducibility of TGL/HDL ratio was acceptable.
Citation: Palamaner Subash Shantha G, Kumar AA, Kahan S, Irukulla PK, Cheskin LJ (2013) Triglyceride/HDL Ratio as a Screening Tool for Predicting Success at Reducing Anti-Diabetic Medications Following Weight Loss. PLoS ONE 8(7): e69285. https://doi.org/10.1371/journal.pone.0069285
Editor: T. Mark Doherty, Glaxo Smith Kline, Denmark
Received: March 4, 2013; Accepted: June 6, 2013; Published: July 15, 2013
Copyright: © 2013 Palamaner Subash Shantha et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: The authors have no support or funding to report.
Competing interests: We have the following interests. Lawrence Jay Cheskin serves as a consultant and stockholder for Medifast, Inc. and Vivus, Inc. There are no patents, products in development or marketed products to declare. This does not alter our adherence to all the PLOS ONE policies on sharing data and materials, as detailed online in the guide for authors.
Introduction
In the last decade, the prevalence of obesity [body mass index (BMI; calculated as weight in kilograms divided by height in meters-squared) ≥ 30], among adult Americans was 35%, and is expected to increase in years to come [1]. Type 2 diabetes mellitus (DM) is an important problem among the obese. Overweight (BMI 25–29.9), obese (BMI 30–39.9), and extremely obese (BMI > 40) American adults had 1.59, 3.44 and 7.37 times higher odds, respectively, of diagnosed DM [2]. Obesity and DM in unison create enormous health care costs, of which the direct and indirect costs of pharmacotherapy plays a major role [3].
Intentional weight loss, by decreasing insulin resistance, is associated with better glycemic control [4,5] and consequently a decrease in the need for anti-diabetic medications [6]. However, it is well known that not everyone who loses weight is successful in reducing anti-diabetic medications [6]. Hence, a clinically applicable screening tool that can predict success with dose reductions of anti-diabetic medications would be useful, and could help motivate patients, as well as assist practitioners in patient counseling, and individualizing the intensity of weight loss intervention for a given obese patient attempting weight loss. Since insulin resistance is the central pathophysiology behind obesity-associated diabetes, we hypothesized that a marker of insulin resistance, measured at the onset of weight loss efforts, might serve as a screening tool to predict success with dose reductions of anti-diabetic medications accompanying successful weight loss. Tryglyceride (TGL)/HDL ratio is a known marker of insulin resistance [7]. To test this hypothesis, we studied overweight and obese patients from 2 University-based weight management programs, analyzing the relationship between triglyceride/HDL ratio and success in reducing anti-diabetic medications.
Materials and Methods
Study setting and design
This retrospective cohort study was conducted in two, University based, specialty, outpatient weight management clinics, the Johns Hopkins Weight Management Center in Baltimore, MD, and the George Washington Weight Management program in Washington, DC. Institutional review board approval was obtained from Johns Hopkins University institutional review board for conducting the study. Informed consent was not obtained from the participants, as the data was analyzed anonymously per institutional review board guidelines. Institutional review board waived the need for written informed consent from the participants.
Case records of patients with BMI > 25 kg/m2 at the time of enrollment into the two weight management programs during the period March 2008 to January 2012 were assessed for eligibility. The study cohort consisted of patients with a diagnosis of DM at the time of enrollment who reported taking anti-diabetic medications. Patients were excluded if they did not have a diagnosis of DM at the time of enrollment into the programs.
Baseline data collection
Demographic data (age, gender, race/ethnicity), cardiovascular risk factors (smoking, diabetes, hypertension), medication history (anti-diabetic medications, anti-hypertensive medications, and lipid-lowering drugs), clinical parameters (height, weight, systolic blood pressure (SBP) and diastolic blood pressure (DBP), and laboratory parameters (fasting glucose, HbA1c, total cholesterol, low-density lipoprotein cholesterol (LDL), high-density lipoprotein cholesterol (HDL), triglycerides) were collected from the study cohort. BMI was calculated as per standard guidelines [8]. DM was identified by physician diagnosis.
Patient follow-up and weight management intervention details
The weight loss intervention protocols followed at the two participating clinics were similar, and consisted of team-based, comprehensive evaluation and treatment for weight loss. The study participants had physician visits for follow-up twice a month on average. The baseline visit consisted of a physician-conducted medical history and physical examination, blood tests (as described above), and detailed dietary, behavioral, and exercise evaluations. Treatment was individualized, but typically consisted of an approximately 1000 kcal/day energy-deficit diet, often utilizing meal replacements, a behavior modification plan, and a plan for increasing physical activity utilizing both aerobic exercise and strength training. These interventions with diet, physical activity and behavior modification were similar in both participating institutions. Depending on treatment response, the intervention was tailored to address individual patient needs. The decision to alter the dose of or discontinue anti-diabetic medications was based on the clinical judgment of the treating physicians. Factors considered in deciding on dose reductions included magnitude of weight loss, glycemic control, hypoglycemic symptoms, and the patient’s compliance with the weight management protocol.
Triglyceride/HDL ratio cutoffs tested as screening tool
Triglyceride/HDL ratios of all study cohort participants at the time of their enrollment into the weight management programs were calculated. Cutoffs for triglyceride/HDL ratio of ≤ 2, ≤ 2.5, ≤ 3, ≤ 3.5, and ≤ 4.0 were evaluated to determine which cut-off value yielded optimal results as a screening tool. Using these baseline triglyceride/HDL cutoffs, each member of the study cohort was categorized, within each cutoff category, as successful or unsuccessful in achieving at least one dose reduction of any anti-diabetic medication by study exit. Patients exited the study if they achieved at least 1 dose reduction of any of their anti-diabetic medications, or at study conclusion in January 2012. One dose reduction was defined as any recorded decrease in dose of anti-diabetic medication, which included lowering the dose or completely stopping that particular medication.
Testing reproducibility of the triglyceride/HDL ratio
Three of the authors were involved in this experiment. One of them was an internist with 5 years’ post medical school experience; one was a MD with 3 years’ post medical school experience and third was a diabetes educator with 1 year post bachelors degree experience. All three authors received a brief 20 minutes training regarding calculation of triglyceride/HDL ratio. A computer generated random sample (n = 60) from the study cohort was selected. First the internist calculated baseline triglyceride/HDL ratio for this random study cohort patients, blinded with regard to patient and medication history. To test intra-observer correlation, the internist recalculated baseline triglyceride/HDL ratio, for the same random sample of study cohort participants after 1 week, blinded with regard to earlier triglyceride/HDL ratio results, patient and medication history. Correlation was calculated comparing the present and previous findings of the internist. Then, the MD calculated baseline triglyceride/HDL ratio for the same random sample used by the internist, blinded with regard to patient, medication details and triglyceride/HDL ratios. Correlation was calculated comparing the triglyceride/HDL ratios of the internist with that of the MD. Similarly, the diabetes educator calculated triglyceride/HDL ratio for the same random sample and correlation was calculated comparing her findings with that of the internist.
Statistical analysis
Data was expressed in number (%) for categorical variables, and as mean ± standard deviation for continuous variables. The baseline characteristics of study cohort participants who successfully dose reduced anti-diabetic medications were compared with the study cohort participants who were not successful with even 1 dose reduction of any anti-diabetic medications, using Student’s t test and chi-squared tests, as appropriate. Similarly, these 2 groups were compared with regard to magnitude of weight loss and HbA1C% reduction by study exit.
Multiple linear regression analysis and multiple logistic regression analysis were performed with magnitude of weight loss (kg) and dose reductions of anti-diabetic medications (coded as a dichotomous variable) as dependent variables. Age, gender, hypertension diagnosis, smoking, lipid lowering medication use, duration of diabetes, baseline BMI and TGL/HDL ratio were independent variables. In addition, logistic regression analysis assessing association between dose reductions of anti-diabetic medications and TGL/HDL ratio was adjusted for magnitude of weight loss.
To assess if triglyceride/HDL ratio is an effective screening tool to predict success with dose reductions of anti-diabetic medications, sensitivity, specificity, positive predictive value, negative predictive value, likelihood ratio of positive test, likelihood ratio of negative test and area under the receiver operating characteristics curve (ROC) were calculated, using standard methods, for the cut-off points for triglyceride/HDL ratios [9]. Also, TGL/HDL ratio was coded as continuous variable and AUC was computed. Kappa statistics was used to assess intra- and inter-observer agreement in interpreting triglyceride/HDL ratios [9]. A P-value of <0.05 was considered statistically significant. Statistical analyses were performed using Stata 11.0 statistical software [10].
Results
In total, 179 patient records (107 from Johns Hopkins and 72 from George Washington) were identified and reviewed. Of these, 58 (32%) were excluded (excluded cohort) because they did not have a diagnosis of diabetes at the time of enrollment into the programs. The remaining 121 (68%) with a diagnosis of diabetes formed the study cohort. All study cohort patients were taking one or more anti-diabetic medications at the time of enrollment. Demographic characteristics and medication details of the study cohort and excluded cohort are shown in Table 1. Follow-up details of the study cohort by study exit are detailed in Table 2.
Variables | Study cohort | Successful# | Not successful* | P-value |
---|---|---|---|---|
(n = 121) | (n = 81) | (n = 40) | ||
Age (yrs) | 51.8 ± 8.9 | 52.7 ± 9.1 | 53.7 ± 9.3 | 0.133 |
Males –n (%) | 67 (55) | 45 (56) | 22 (55) | 0.668 |
Caucasians –n (%) | 90 (74) | 63 (78) | 27 (68) | 0.042 |
African Americans –n (%) | 31 (26) | 18 (22) | 13 (32) | 0.044 |
Current smoking –n (%) | 24 (20) | 16 (20) | 8 (20) | 0.996 |
Duration of diabetes (yrs) | 7.5 ± 2.5 | 8.0 ± 2.0 | 7,5 ± 2.0 | 0.371 |
Mean baseline weight (Kgs) | 126.5 ± 18.2 | 127.1 ± 16.4 | 126.9 ± 19.3 | 0.417 |
Mean BMI (kg/m2) | 36.1 ± 6.2 | 36.1 ± 5.5 | 35.6 ± 4.7 | 0.226 |
BMI: 25-30 –n (%) | 30 (25) | 23 (28) | 7 (18) | 0.047 |
BMI: 31-40 –n (%) | 64 (53) | 51 (63) | 13 (33) | 0.021 |
BMI ≥ 41 – n (%) | 27 (22) | 7 (9) | 20 (50) | 0.017 |
HbA1C % | 8.2 ± 1.6 | 8.1 ± 2.3 | 8.0 ± 1.7 | 0.179 |
Mean TC (mmol/l) | 5.2 ± 1.3 | 5.2 ± 1.1 | 5.1 ± 1.7 | 0.113 |
Mean LDL – C (mmol/l) | 4.2 ± 1.3 | 4.0 ± 1.4 | 4.1 ± 1.2 | 0.091 |
Mean HDL – C (mmol/l) | 1.2 ± 0.4 | 1.1 ± 0.3 | 1.1 ± 0.4 | 0.216 |
Mean TGL (mmol/l) | 1.7 ± 0.3 | 2.0 ± 0.5 | 1.9 ± 0.6 | 0.166 |
Mean TGL/HDL ratio | 2.9 ± 1.2 | 3.1 ± 0.8 | 2.8 ± 1.1 | 0.051 |
HTN diagnosis –n (%) | 102 (84) | 69 (85) | 33 (83) | 0.067 |
MS –n (%) | 68 (56) | 45 (56) | 23 (58) | 0.116 |
Lipid lowering drugs –n (%) | 91 (75) | 64 (79) | 27 (68) | 0.055 |
Statins | 91 (75) | 64 (79) | 27 (68) | 0.055 |
Atorvastatin | 52 (43) | 27 (33) | 25 (63) | 0.172 |
Pravastatin | 24 (20) | 13 (16) | 11 (28) | 0.133 |
Rosuvastatin | 15 (12) | 8 (10) | 7 (18) | 0.226 |
Fenofibrate | 7 (6) | 4 (5) | 3 (8) | 0.417 |
Anti – HTN drugs –n (%) | 102 (84) | 69 (85) | 33 (83) | 0.067 |
Metformin-n (dose/day) | 71 (1.7g) | 51 (1.7g) | 20 (1.7g) | 0.044 |
Sulphonylureas-n (%) | 59 (49) | 40 (49) | 19 (48) | 0.133 |
Glyburide-n (dose/day) | 24 (10mg) | 16 (10mg) | 8 (10mg) | 0.091 |
Glipiside-n (dose/day) | 21 (10mg) | 12 (10mg) | 9 (10mg) | 0.046 |
Glymipride-n (dose/day) | 14 (2-4 mg) | 9 (2-4 mg) | 5 (2-4 mg) | 0.117 |
Sitagliptin-n (dose/day) | 19 (100 mg) | 11 (100 mg) | 8 (100 mg) | 0.061 |
Insulin-n (dose/day) | 59 (60 U) | 45 (65 U) | 14 (60 U) | 0.155 |
Study cohort | Successful# | Not successful* | P value | |
---|---|---|---|---|
Follow-up (months) | 12.5 ± 3.5 | 13.0 ± 2.5 | 12.5 ± 2.5 | 0.511 |
Baseline weight (Kgs) | 126.5 ± 18.2 | 127.1 ± 16.4 | 126.9 ± 19.3 | 0.417 |
Final weight (Kgs) | 110.3 ± 5.9 | 108 ± 11.2 | 117 ± 5.7 | 0.031 |
Weight loss (Kgs) | 15.4 ± 5.5 | 16.9 ± 4.7 | 9.2 ± 3.1 | 0.029 |
Baseline HbA1C% | 8.2 ± 1.6 | 8.1 ± 2.3 | 8.0 ± 1.7 | 0.179 |
Final HbA1C% | 7.7 ± 0.3 | 7.4 ± 0.6 | 7.9 ± 0.2 | 0.039 |
Change in HbA1C% | 0.5 ± 0.2 | 0.7 ± 0.2 | 0.2 ± 0.1 | 0.035 |
By study exit, 81 (67%) in the study cohort achieved at least 1 dose reduction of any anti-diabetic medication. The remaining 40 (33%) in the study cohort failed to achieve even 1 dose reduction of their anti-diabetic medication; their weight loss and HbA1c% reduction was significantly less than those in the study cohort who did successfully dose-reduce anti-diabetic medications (Table 2).
Baseline BMI and TGL/HDL ratio had a strong and independent association with magnitude of weight loss and dose reductions of anti-diabetic medications (Table 3).
Variables | Magnitude of weight loss (Kgs)# | Dose reductions* | ||
---|---|---|---|---|
ß (95% C.I) | P value | OR (95% C.I) | P value | |
Age | 1.57 (-0.11 – 3.11) | 0.136 | 1.01 (0.77 – 2.32) | 0.216 |
Gender | 0.91 (-0.62 – 2.17) | 0.133 | 1.15 (0.67 – 2.37) | 0.210 |
Hypertension | 2.45 (-0.12 – 3.16) | 0.133 | 0.96 (0.42 – 1.92) | 0.132 |
Smoking | 1.45 (-1.50 – 3.63) | 0.511 | 1.07 (0.66 – 2.11) | 0.286 |
Lipid lowering medication use | 0.97 (-1.10 – 2.36) | 0.162 | 1.13 (0.71 – 1.96) | 0.149 |
Baseline BMI | 1.53 (0.58 – 2.27) | 0.033 | 1.47 (1.14 – 2.35) | 0.031 |
TGL/HDL ratio | 5.28 (1.51 – 8.13) | 0.014 | 1.31 (1.03 – 2.41) | 0.022 |
Duration of diabetes (yrs) | 1.10 (-2.74 – 3.71) | 0.159 | 1.14 (0.68 – 2.66) | 0.291 |
Magnitude of weight loss (kgs) | - | - | 1.18 (1.09 – 1.96) | 0.031 |
Tests for TGL/HDL ratios as a screening tool to predict success with dose reductions of anti-diabetic medications is shown in Table 4. When TGL/HDL ratio was coded as a continuous variable AUC was 82. Of the selected cut-off values, TGL/HDL ratio ≤ 3 showed optimal results with a sensitivity, specificity, positive predictive value, negative predictive value, AUC, LR + and LR-of 81, 83, 90, 70, 78, 4.8 and 0.2 respectively (Table 4). ROC curves can be viewed in Figure S1 and Figure S2. Further, kappa statistics for intra-observer agreement was 0.99 and Inter-observer agreement between the internist and the MD was 0.99 and between the internist and the diabetes educator was 0.99.
Discussion
Our study of overweight and obese adults has identified TGL/HDL ratio as a potentially effective screening tool to predict success with dose reductions of anti-diabetic medications in patients who successfully lose weight.
We found, not surprisingly, that magnitude of weight loss was an important factor determining success with dose reductions of anti-diabetic medications (Table 2). Mechanistically, weight loss is accompanied by decreasing insulin resistance and hence better glycemic control [11]. This could explain the strong and independent association of TGL/HDL ratio, a marker of insulin resistance [7], with magnitude of weight loss, and thus with the higher probability of dose reductions of anti-diabetic medications that was observed (Table 3). This reasoning comports with our rationale for the use of TGL/HDL ratio as a screening tool to predict success with dose reductions of anti-diabetic medications. Prior studies have also shown TGL/HDL ratio to positively correlate with adiposity, and its decrease proportional to magnitude of weight loss [12,13].
Further, 75% of our patients were using lipid lowering medications at baseline (Table 1). However, the observed independent association of TGL/HDL ratio with dose reductions of anti-diabetic medications even after adjusting for lipid lowering medication use (Table 3) highlights the potential use of TGL/HDL ratio as a screening tool to predict success with dose reductions of anti-diabetic medications irrespective of lipid lowering medication use.
We note that when a screening tool is assessed for its predictive accuracy, the prevalence of the event of interest should be taken into consideration [14]. When the prevalence of the event of interest (dose reductions of anti-diabetic medications) is high (67% in our study), values of sensitivity, specificity, positive predictive value and negative predictive value may be less useful for clinical application, since all of the above-mentioned indicators of test accuracy vary with prevalence. In this context, the indicators of test accuracy which do not significantly vary with prevalence are the most clinically relevant. LR+ and LR-do not vary with prevalence of the disease [14]. An LR+ >1 and an LR− <1 makes a diagnostic test clinically meaningful, while a LR+ >10 and LR− <0.1 indicates very high accuracy [14]. In our study, among all arbitrary TGL/HDL ratio cut-offs assessed, TGL/HDL ratio ≤ 3, with its LR+ of 4.8 and LR-was 0.2, had the highest predictive accuracy. Area under the ROC curve of 78% also conveys the same meaning. Combined with its good reproducibility, TGL/HDL ratio may well be a clinically useful screening tool for this purpose. Interestingly, TGL/HDL ratio has been found in other studies to be an effective tool for predicting gestational diabetes [15], cardiovascular risk in patients with familial hypercholestrolemia [16], atherogenic apolipoprotein B levels [17] and as a surrogate marker in the mechanistic pathway through which pioglitazone possibly delays coronary atheroma progression in diabetic patients [18].
Limitations
We observed significantly greater magnitudes of weight loss (15.4 kgs by 15 months of follow-up) compared to typical randomized, controlled weight loss trials (RCTs) (weight loss: 4–6 kgs within 12-15 months of follow-up, SBP/DBP: 3-4/2-3 mmHg) [19,20]. It is thus possible that confounding due to unknown factors may have played a role. Or, surveillance bias is possible, due to the intensity of weight loss intervention being individualized, and the decision to dose reduce being subjective and at the discretion of the treating physicians. Also, small sample size limited us from analyzing our research question with individual anti-diabetic medications and individual BMI classes. Further, convenience sampling may have led to selection bias. Retrospective cohort design limited us to what was recorded in patient charts; for example, we did not have date on waist/hip ratio, which might also have relevance as a predictor.
Conclusions
In conclusion, TGL/HDL ratio was found to show promise as a clinically applicable screening tool. It showed moderately high accuracy in predicting success in reducing use of anti-diabetic medications among overweight and obese diabetics attempting weight loss. Further, it is easy to calculate and has good reproducibility. Before advocating widespread use, this tool should be prospectively validated in future RCTs or clinical settings, and evaluated in systematic reviews using data that is available from completed RCT’s [19,20].
Supporting Information
Figure S1. ROC curve for TGL/HDL ratio ≤ 3 as a screening tool to predict success with dose reductions of anti-diabetic medications.
https://doi.org/10.1371/journal.pone.0069285.s001
(DOC)
Figure S2. ROC curve when TGL/HDL ratio was coded as continuous variable.
https://doi.org/10.1371/journal.pone.0069285.s002
(DOC)
Acknowledgments
We thank Mr. Rohit Joshua Samson and Mr. Nelson David Boddu for their help with the chart review.
Author Contributions
Conceived and designed the experiments: GPSS AAK SK PKI LJC. Performed the experiments: GPSS AAK SK PKI LJC. Analyzed the data: GPSS AAK PKI LJC. Wrote the manuscript: GPSS AAK SK PKI LJC. Authors involved in screening tool analysis: GPSS AAK PKI. Physicians involved in the care of study patients: SK LJC.
References
- 1. Flegal KM, Carroll MD, Kit BK, Ogden CL (2012) Prevalence of obesity and trends in the distribution of body mass index among US adults, 1999-2010. JAMA 307(5): 491-497. doi:https://doi.org/10.1001/jama.2012.39. PubMed: 22253363.
- 2. Mokdad AH, Ford ES, Bowman BA, Dietz WH, Vinicor F et al. (2003) Prevalence of obesity, diabetes, and obesity-related health risk factors, 2001. JAMA 289(1): 76–79. doi:https://doi.org/10.1001/jama.289.1.76. PubMed: 12503980.
- 3. Colditz GA (1999) Economic costs of obesity and inactivity. Med Sci Sports Exerc 31(suppl): S663–S667. doi:https://doi.org/10.1097/00005768-199911001-00026. PubMed: 10593542.
- 4. Sunyer XP, Blackburn G, Brancati FL, Bray GA, Bright R et al. (2007) Look AHEAD Research Group. Reduction in weight and cardiovascular disease risk factors in individuals with type 2 diabetes: one-year results of the look AHEAD trial. Diabetes Care 30(6): 1374–1383. doi:https://doi.org/10.2337/dc07-0048. PubMed: 17363746.
- 5. Shantha GP, Kumar AA, Kahan S, Cheskin LJ (2012) Association between glycosylated hemoglobin and intentional weight loss in overweight and obese patients with type 2 diabetes mellitus: a retrospective cohort study. Diabetes Educ 38(3): 417-426. doi:https://doi.org/10.1177/0145721712443293. PubMed: 22508341.
- 6. Kumar AA, Shantha GP, Kahan S, Samson RJ, Boddu ND et al. (2012) Intentional weight loss and dose reductions of anti-diabetic medications: a retrospective cohort study. PLOS ONE 7(2): e32395. doi:https://doi.org/10.1371/journal.pone.0032395. PubMed: 22384240.
- 7. Chávez AG, Mendía LES, Argueta SE (2011) Elevated triglycerides/HDL-cholesterol ratio associated with insulin resistance. Cir Cir 79(2): 126-131. PubMed: 21631973.
- 8.
Jeffrey SF, Eleftheria MF (2005) Obesity. In: DL KasperE. BraunwaldAS FauciSL HauserDL Longo. Harrison’s Principles of Internal Medicine. New York: McGraw Hill Inc. pp. 422-423.
- 9.
Greenberg RS, Daniels SR, Dana Flanders W, Sanders FH, Robert RB et al. (2005) Diagnostic testing. In: RS Greenberg. Medical Epidemiology. New York: McGraw-Hill Inc. pp. 112-117.
- 10.
StataCorp (2009) Stata Statistical Software: Release 11. College Station, TX: StataCorp LP.
- 11. Rondanelli M, Opizzi A, Perna S, Faliva M, Solerte SB et al. (2012) Improvement in insulin resistance and favourable changes in plasma inflammatory adipokines after weight loss associated with two months’ consumption of a combination of bioactive food ingredients in overweight subjects. Endocrine.
- 12. Hatmi ZN, Mazdeh MM, Nazari SSH, Hajighasemi E, Nozari B et al. (2011) Relationship between the pattern of coronary artery disease risk factors and lipid ratios with five groups of body mass index in 28566 healthy adults. Acta Med Iran 49(11): 730-736. PubMed: 22131243.
- 13. Tovar JR, Oller I, Tomas A, Llavero C, Arroyo A et al. (2012) Midterm impact of sleeve gastrectomy, calibrated with a 50-Fr bougie, on weight loss, glucose homeostasis, lipid profiles, and comorbidities in morbidly obese patients. Am Surg 78(9): 969-974. PubMed: 22964206.
- 14.
Greenberg RS, Daniels SR, Dana Flanders W, Sanders FH, Robert RB et al. (2005) Diagnostic testing. In: RS Greenberg. Medical Epidemiology. New York: McGraw-Hill. pp. 227-233.
- 15. Weiss ICS, Réa RR, Picheth CMF, rego FG, Fde OP et al. (2012) The plasma logarithm of the triglyceride/HDL-cholesterol ratio is a predictor of low risk gestational diabetes in early pregnancy. Clin Chim Acta Pii: S0009-S8981(12)00574-8.
- 16. Soška V, Jarkovský J, Ravčuková B, Tichý L, Fajkusová L et al. (2012) The logarithm of the triglyceride/HDL-cholesterol ratio is related to the history of cardiovascular disease in patients with familial hypercholesterolemia. Clin Biochem 45(1-2): 96-100. doi:https://doi.org/10.1016/j.clinbiochem.2011.11.001. PubMed: 22119890.
- 17. Grundy SM, Vega GL, Tomassini JE, Tershakovec AM (2011) Comparisons of apolipoprotein B levels estimated by immunoassay, nuclear magnetic resonance, vertical auto profile, and non-high-density lipoprotein cholesterol in subjects with hypertriglyceridemia (SAFARI Trial). Am J Cardiol 108(1): 40-46. doi:https://doi.org/10.1016/j.amjcard.2011.03.003. PubMed: 21565322.
- 18. Nicholls SJ, Tuzcu EM, Wolski K, Bayturan O, Lavoie A et al. (2011) Lowering the triglyceride/high-density lipoprotein cholesterol ratio is associated with the beneficial impact of pioglitazone on progression of coronary atherosclerosis in diabetic patients: insights from the PERISCOPE (Pioglitazone Effect on Regression of Intravascular Sonographic Coronary Obstruction Prospective Evaluation) study. J Am Coll Cardiol 57(2): 153-159. doi:https://doi.org/10.1016/j.jacc.2010.06.055. PubMed: 21211686.
- 19. Appel LJ, Clark JM, Yeh HC, Wang NY, Coughlin JW et al. (2011) Comparative effectiveness of weight-loss interventions in clinical practice. N Engl J Med 365(21): 1959-1968. doi:https://doi.org/10.1056/NEJMoa1108660. PubMed: 22085317.
- 20. the Trials of Hypertension Prevention Collaborative Research Group (1997) Effects of weight loss and sodium reduction intervention on blood pressure and hypertension incidence in overweight people with high-normal blood pressure. The Trials of Hypertension Prevention, phase II. Arch Intern Med; 157(6): 657-667. doi:https://doi.org/10.1001/archinte.1997.00440270105009. PubMed: 9080920.