Management of dyslipidaemia in HIV infected children: rationale for treatment algorithm

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Management of dyslipidaemia in HIV infected children: rationale for treatment algorithm Authors: Julie Lanigan, Lisa Cooke and Clare Stradling Date of Preparation: September 2010 Date reviewed: October 2013 Next review date: October 2014 Background The introduction of highly active antiretroviral therapy (HAART) for treatment of paediatric HIV infection has markedly improved survival. However, both HIV and HAART are associated with metabolic complications and increased risk of cardiovascular disease (CVD). 1, 2 Lipid profiles in some infected children are similar to those with familial hyperlipidemia who usually develop premature atherosclerotic disease in adulthood. 3. Observational studies have demonstrated a clear correlation between lipoprotein disorders and the onset and severity of atherosclerosis in children, adolescents, and young adults. 4-6 Over the same time period a steep rise in obesity prevalence has led to an increase in children with dyslipidemia. HIV is recognised as a disease that is associated with moderately increased CVD risk ref. HIV and obesity can therefore be considered concomitant epidemics that increase CVD risk in children. Justification Evidence from observational studies suggest that Identification and treatment of dyslipidaemia in HIV infected children could reduce CVD risk. In the UK, screening recommendations for paediatric hyperlipidaemia are available for children with familial hyperlipidaemia only 7. Recent guidelines from the American National Heart Lung and Blood Institute recommend the use of single cut-offs to identify children with abnormal lipid and lipoprotein concentrations (Table 1) 8.

Table 1 Cut Offs for Total and LDL Cholesterol Concentration in Children and Adolescents Category Acceptable (mmol/l) Borderline High (mmol/l) Elevated (mmol/l) TC <4.4 4.4-5.2 >5.2 LDL-C <2.8 2.8 3.3 >3.3 TG 0-9 years <0.8 0.8 1.1 >1.1 TG 10-19 years <1.0 1.0 1.5 >1.5 HDL-C Non-HDL-C >1.2 <3.1 1.0 1.2 3.1-3.7 <1.0 >3.8 Adapted from NHLIB guidelines for children and adolescents (2011) Recommendations Lipid screening should be routinely carried out in HIV infected children in the UK to identify children at increased risk of premature CVD. In the absence of guidelines from the UK it is recommended that cut offs identified from the US NHANES study are used. A suggested pathway for screening, based on NHLBI guidelines ref (NHLBI 2011), is described in the attached algorithm (Fig 1). It is recommended that children undergo annual dietetic review (Appendix I for use by dietians),and are referred for advice on diet and lifestyle for lipid modification (Appendix 2 for use by dietitians). Pharmacologic intervention could be considered in children 10 years either with severe dyslipidaemia or borderline to raised lipids and additional risk factors (Appendix 3). Dietary Advice Within appropriate age- and gender-based requirements for growth and nutrition, in normal children and in children with hypercholesterolemia intake of total fat can be safely limited to 30% of total calories, saturated fat intake limited to 7% to 10% of calories. The remaining 20% of fat intake should comprise a combination of monounsaturated and polyunsaturated fats. Intake of trans fats should be limited as much as possible (AAP, 2011).

Figure 1 Algorithm for management of HIV associated dyslipidaemia in children aged more than 2 years

Appendix 1 Name: Age: Hospital No DOB: Dietetic Annual Assessment Form Date: Current Treatment: Ht (cm) Wt (kg) BMI MUAC(cm ) Waist (cm) Hip (cm) Calf (cm) Thigh (cm) Skinfold (mm) Triceps Biceps Subscapular Suprailiac 1 2 3 Mean Lipids (mmol/l) (1 = latest; 2 = previous) TC 1 Date Result Blood Results Date Result Hb TC 2 Ref: <4.4 >4.4 refer to Figure 1 HDL 1 HDL 2 Ref: > 1.0 <1.0 refer to Figure 1 LDL 1 LDL 2 Vit D Calcium Alk Phosphate PTH CD4 No. (%) Viral load Goals and Action

Ref: <2.8 >2.8 refer to Figure 1 TG 1 TG 2 Ref: <0.8 <9 y >0.8 refer to Figure 1 Ref: <1.0 >9 y >1.0 refer to Figure 1

Diet history Diet Summary Meat/ Fish/Pulses: Milk/dairy: Fruit/vegetables: Butter/margarine/oil: Drinks: Checklist: Snacks Nuts Crisps Cakes Sweets Choc Biscuits Sweet drinks Out of home e.g. friends/relatives/school: Weekends/holidays: Exercise and physical activity: Omega 3: Nutritional supplements:

Appendix 2 Dietary and lifestyle recommendations for targeting lipid abnormalities. Reducing LDL and non-hdl cholesterol levels Restrict proportion of total calories to: 25% to 30% from fat <7% from saturated fat Replace saturated with unsaturated fats where possible Avoid trans fats. Trans fatty acids are found mainly in processed foods including pies, pastries and meat products. Diets high in fat, and particularly those high in saturated and/or trans fats, are considered a risk factor for the development of atherosclerosis 9 Consideration use of foods enriched with plant sterol/stanol esters. Increased consumption of soluble dietary fibre (present in fruits, vegetables and pulses (peas, bean and lentils). Reducing triglyceride levels - Restrict proportion of total calories to: 25% to 30% from fat <7% from saturated fat Preferred use of mono and polyunsaturated fats Avoide of trans fats Increased consumption of soluble dietary fibre Decrease sugar intake, particularly sugar sweetened drinks Include foods high in n-3 (omega 3) fatty acids. Long chain n-3 fatty acids, in particular docosahexaenoic and eicosapentanoic acids found in high concentrations in fish have been shown to reduce triglyceride concentrations in many studies. Fish oils have repeatedly been shown to reduce plasma TG in a dose-dependent manner 10. Increasing HDL-C Increase soluble fibre intake (fruits, vegetables, pulses (peas/beans/lentils)) Assess and advise on appropriate exercise and physical activity levels For age specific guidance see link below http://www.dh.gov.uk/en/publicationsandstatistics/publications/publicationspolicyandguidanc e/dh_127931 For further information see table 9.8 NLHBI 2011 http://www.nhlbi.nih.gov/guidelines/cvd_ped/

Appendix 3 Recommendations Regarding Drug Therapy for Children and Adolescents. 1. Measure and average values from the 2 most recent lipid profiles. 2. Consider changing to a more lipid friendly antiretroviral therapy if above cut offs. 3. Consider medical management under the following circumstances: - Clinical CVD. - LDL-C >4.90 mmol/l (non-hdl-c>5.30 mmol/l) - LDL-C 4.15-4.89 mmol/l (non-hdl-c 4.50-5.29 mmol/l) and either positive family history of early CVD, or 1 CVD risk factors - LDL-C 3.35-4.14 mmol/l (non-hdl-c 3.75-4.49 mmol/l) and 2 risk factors (NB if triglycerides >2.25 mmol/l, may use non-hdl-c cut offs) Risk factors include: Hypertension requiring drug therapy (BP>99 th percentile + 5mm Hg) Passive smoke exposure or current smoker BMI >95 th percentile Diabetes (Type I or II). HIV, CKD, nephrotic syndrome, postorthotopic heart transplant, Kawasaki disease The choice of statin is a matter of preference. Start with the lowest dose, monitor for adverse effects, and titrate the dose upwards if therapeutic targets are not achieved. Therapeutic target: Minimal: LDL-C <3.35 mmol/l (non-hdl-c <3.75 mmol/l) Ideal: LDL-C <2.85 mmol/l (non-hdl-c <3.25 mmol/l) If LDL-C remains > 3.35 mmol/l after a sufficient trial of a statin, and TG < 2.25 mmol/l, consideration may be given to adding a bile acid sequestrant or cholesterol absorption inhibitor. In high LDL-C patients, if non-hdl-c remains > 3.75 mmol/l after effective LDL-C treatment then target therapy towards reducing triglycerides, by adding a fibrate or nicotinic acid. This should be done in consultation with a lipid specialist. Abbreviations: CVD, cardiovascular disease; HDL-C, high density lipoprotein cholesterol; LDL-C, low density lipoprotein cholesterol; RF/RC, risk factor/risk condition

Reference List (1) Rhoads MP, Lanigan J, Smith CJ, Lyall EG. Effect of specific ART drugs on lipid changes and the need for lipid management in children with HIV. J Acquir Immune Defic Syndr 2011 August 15;57(5):404-12. (2) Tassiopoulos K, Williams PL, Seage GR, III, Crain M, Oleske J, Farley J. Association of hypercholesterolemia incidence with antiretroviral treatment, including protease inhibitors, among perinatally HIV-infected children. J Acquir Immune Defic Syndr 2008 April 15;47(5):607-14. (3) McComsey GA, Leonard E. Metabolic complications of HIV therapy in children. AIDS 2004 September 3;18(13):1753-68. (4) Berenson GS, Srinivasan SR, Nicklas TA. Atherosclerosis: a nutritional disease of childhood. Am J Cardiol 1998 November 26;82(10B):22T-9T. (5) McGill HC, Jr., McMahan CA, Herderick EE et al. Effects of coronary heart disease risk factors on atherosclerosis of selected regions of the aorta and right coronary artery. PDAY Research Group. Pathobiological Determinants of Atherosclerosis in Youth. Arterioscler Thromb Vasc Biol 2000 March;20(3):836-45. (6) McGill HC, Jr., McMahan CA, Zieske AW et al. Associations of coronary heart disease risk factors with the intermediate lesion of atherosclerosis in youth. The Pathobiological Determinants of Atherosclerosis in Youth (PDAY) Research Group. Arterioscler Thromb Vasc Biol 2000 August;20(8):1998-2004. (7) NICE. Quality Standard 41 Familial Hypercholesterolaemia. 2013. Ref Type: Online Source (8) NHLBI. Expert Panel on Integrated Guidelines for Cardiovascular Health and Risk Reduction in Children and Adolescents. 2013. 17-10-2013. Ref Type: Online Source (9) Hall WL. Dietary saturated and unsaturated fats as determinants of blood pressure and vascular function. Nutr Res Rev 2009 June;22(1):18-38. (10) von Schacky C. A review of omega-3 ethyl esters for cardiovascular prevention and treatment of increased blood triglyceride levels. Vasc Health Risk Manag 2006;2(3):251-62.