ETÁRIA evaluation of nutritional status in patients with cystic fibrosis according to age group Lenycia de cassya

ABSTRACT Objective: To evaluate the nutritional profile of the population assisted at a reference center for cystic fibrosis treatment. Methods: Cross-sectional study including patients with cystic fibrosis assisted at a pediatric reference center in São Paulo, Brazil, in 2014. All patients attending regular visits who agreed to participate in the study were included. A questionnaire on dietary habits (24-hour diet recall) and socioeconomic characteristics was applied. Anthropometric data (compared with the reference from the World Health Organization, 2006 and 2007) and pulmonary function data were collected from medical records. Patients were stratified into age groups for statistical analysis. Results: A total of 101 patients were included in the study (59.4% male, 86.4% Caucasian), with median age of 10 years old. Most patients (n=77; 75%) were classified as eutrophic, but lower values of body mass index (BMI) Z scores were observed in schoolchildren and adolescents. The proportion of underweight patients was 10% (n=2) among preschoolers and 35% (n=6) of the school age group. Dietary intake was adequate, and the use of only two supplements (medium chain triglycerides and complete powdered supplement) was associated with adequacy of macronutrient intake. The socioeconomic characteristics did not show any statistical association with the nutritional state or nutritional consumption. Lung function was not significantly different between neither adolescents nor individuals with worse nutritional status in this sample. Conclusions: Most of the patients presented adequate nutritional status and adequate consumption of calories and macronutrients, indicating appropriate nutritional management. New studies focusing on preschool children should be performed to assess if it is possible to reduce the nutritional risk of patients with cystic fibrosis at older ages.

atients was 10% (n=2) among preschoolers and 35% (n=6) of the sc ool age group.Dietary intake was adequate, and the use of only two supplements (medium chain triglycerides and complete powdered supplement) was associated with adequacy of macronutrient intake.The socioeconomic characteristics did not show any statistical association with the nutritional state or nutritional consumption.Lung function was not significantly different between neither adolescents nor individuals with worse nutritional status in thi

sample.Conclu
ions: Most of the patients presented adequate nutritional status and adequate consumption of calories and macronutrients, indicating appropriate nutritional management.New studies focusing on preschool children should be performed to assess if it is possible to reduce the nutritional risk of patients with cystic fibrosis at older ages.

Resultados: Dos 101 pacientes incluídos no estudo, 59,4% eram masculinos, sendo a maioria caucasiana (86,4%), com mediana de idade de 10 anos.A maioria dos pacientes (n=77, 75%) foi classificada como eutrófica, mas valores menores de escore Z de índice de massa corpórea (IMC) foram observados em escolares e adolescentes.A proporção de pacientes com peso abaixo do esperado foi de 10% (n=2) na faixa etária pré-escolar e de 35% (n=6) em escolares.O consumo alimentar mostrou-se adequado, e somente dois suplementos (triglicérides de cadeia média e suplemento em pó completo) tiveram utilização ligada à adequação da ingesta de macronutrientes.Características


INTRODUCTION

Cystic fibrosis is an autosomal recessive inherited disorder which leads to changes in the transportation of ions and water in cells of the respiratory gastrointestinal, hepatobiliary, reproductive systems and sweat glands. 1,2

the dig
stive system, for most patients, cystic fibrosis is manifested as exocrine pancreatic insufficiency, changes in intestinal motility and excessive presence of mucus in the enterocytes.All of these factors cause the poor digestion of fats, proteins and carbohydrates, and consequently, poor absorption.The clinical manifestation consists of chronic diarrhea, with voluminous, fatty, pale stool, with a characteristic smell, which, if not treated properly, leads to protein-energy malnutrition. 35][6][7] Many studies have observed the close correlation between nutritional profile and respiratory conditions, and a better nutritional status can favor the patient's prognosis. 8,9herefore, the objective of this study was to assess the utritional profile of the population assisted at a reference center for the treatment of cystic fibrosis.


METHOD

This is a cross-sectional study including all patients with cystic fibrosis (diagnosed by two chloride sweat tests, with values indicating the disease) 10 assisted at the outpatient clinic of Instituto da Criança (ICr), at Hospital das Clínicas in the Medical School of Universidade de São Paulo (FMUSP), from January to August, 2014.

ICr is a tertiary, public, pediatric, uni ersity hospital located in the West zone of São Paulo, caring for children and adolescents aged between 0 and 19 years, especially by the Unified Health System (SUS).Care is provided by multidisciplinary teams, and the interval between appointments ranges according to the severity of the patient's condition, but, in general, every two or three months.

After the explanation about the research, the parents or tutors manifested accepting to participate in it by signing an informed consent form.The investigation was approved by the Ethics Committee of the institution (protocol from the Research Ethics Committee of Instituto de Medicina Tropical de São Paulo -CPE-IMT=000266).The only exclusion/loss criteria of the study were patients who did not accept being part of it, or those who missed schedu ed appointments in the collection period.

A questionnaire was applied by the nutritionist to the parents (tutors) and patients (adolescents), including socioeconomic characteristics (income, number of people in the household) and dietary intake (24-hour diet recall, use of dietary supplements).In the analysis of the diet recall on the day prior to the appointment, only the cases with a routine dietary intake were included; those patients with an extraordinary day or acute pulmonary exacerbation were excluded (according to criteria from the medical appointment).The choice to collect a single diet recall was an attempt to minimize seasonal differences, by increasing data collection, and flaws in threeday dietary records.Family income (obtained in Reais) was transformed in categories of more or less than one minimum wage per capita.

Anthropometric data (weight, height), pulmonary function and radiological clinical score were collected from the medical charts.When the charts did not have the described data, patients were excluded from the corresponding analysis.Anthropometry was carried out in the m dical appointment in a standardized manner (weight in a n electronic scale, without clothes, or only underwear, height was measured by a stadiometer, or wooden ruler for infants).Pulmonary function data (spirometry) were obtained from the Brazilian Record of Cystic Fibrosis (patients aged ≥6 years, best result of the year), and expressed in Z score of the forced expiratory volume of the first second (FEV1), using the reference equation by Stanojevic et al. 11 The general clinical status of the patient was measured by the Shwachman-Kulczycki score, annually, on the month of birthday of the patient. 12atients were classified in age groups; infants were those aged less than 2 years; preschoolers, aged between 2 and 5 years (incomplete), students, aged between 5 and 10 years (incomplete), and adolescents, aged more than 10 years.

Patients were classified for nutritional status according to the programs Who Anthro and WHO AnthroPlus, of the World Health Organization (WHO, Geneve, Switzerland, 2006 and 2007), 13 obtaining the Z score data of weight for age, height for age, weight for height and body mass index (BMI) for age.For the classification of eutrophy in infants, weight for height values were used, and, in other age groups.BMI values for age were used; those considered adequate were the ones that obtained indexes between -1 and +1 of the Z score.Z scores lower than -1 were classified as below expected, and higher than +1, above expected.The range between scores from -1 to -2, even though considered as "eutrophic" by the WHO 13 , and in the "low weight surveillance", by the Brazilian Society of Pediatrics, 14 was classified in this study as below expected, due to the close relationship between the worse nutritional status with the decreased pulmonary function in cystic fibrosis. 8,9he data about the intake of calories and macronutrients were calculated by the program NutWin (Universidade Federal Rev Paul Pediatr. 2019;37(1):58-64 de São Paulo -Unifesp, São Paulo, Brazil), 15 software that has a data base of home measurements for estimating the referred data.The analysis of the adaptation of dietary intake was carried out based on value established for each patient, by the Institute of Medicine, 16 using the nutritional recommendations of healthy children, with an increase of 20% in the necessary calories (as a minimum basic parameter in cystic fibrosis), and recommended distribution for cystic fibrosis: 40% of the calories of carbohydrates; 15% of the calories of proteins; and 35% of the calories of lipids. 1,17The analysis considered the percentages of adaptation of the real intake in relation to the recommendations (100% of adequacy indicates the consumption was equal to the recommendations).The dietary supplements used were examined in the analyses of adaptation of macronutrients according to their nutritional characteristics (for example, the supple

nts medi
m-chain triglycerides (MCT) was only considered for the adaptation of calories and lipids), and the indicated age group.

The obtained data were tabulated in Excel, version 2010 (Microsoft, Washington, the United States), and analyzed by descriptive statistics (median, 25 and 75 percentiles), with software Statistical Package for the Social Sciences (SPSS) version 19 (IBM, New York, the United States) and Stata version 11 (Statacorp, Texas, the United States).Nonparametric tests were used (Kruskal-Wallis for variables that did not have normal distribution.The analyses of associations between the categorical variables were carried out using the χ 2 and the Fisher tests.For the analyses of c ntinuous variables, with normal distribution, t-test and ANOVA were used.Significance level of 0.05 was considered for rejecting the null hypothesis.


RE ULTS

Data of 101 patients were collected from an approximate total of 138 being followed-up.The losses were a result of missed appointments (n=4), not accepting to participate in the study (n=1), appointments that were not scheduled in the collection period (n=8), not being cared for in the reference center (n=8), or being hospitalized (n=6).Demographic and respiratory function data collected from charts proved that the losses were not statistically different between the analyzed patients (data not shown).

Of the included patients, 59.4% were male (n=60), and most were Caucasian (86.4%), and median age for inclusion was 10 years (p 25 = 4.1; p 75 = 3.7).Median age at diagnosis was 8 months.

Most patients included in the study were classified as eutrophic, but lower values were observed in the age groups of students and adolescents (Table 1).
oncerning dietary intake, the consumption reported was considered adequate for most patients, even with excessive carbohydrates as a source of calories for most of them (Table 2).Regarding the use of supplements, there were no differences between the types of supplements in the different age groups, even if some supplements are indicated only for specific ages.There was higher frequency of use of supplements in general among students and adolescents.In the evaluation of the association between the consumption of supplements and the adaptation in the intake of macronutrients (categorized a alysis to verify if it reaches the recommendation or not, using the χ 2 test), the use of MCT was associated with the intake of lipids (p=0.010), and the use of complete powdered supplement, to the adequate intake of proteins (p=0.003) and lipids (p=0.010).

By analyzing the categories of classification of the nutritional status, according to age groups, the observation was that whereas no infant presented weight deficit (Z W/H <-1), in the age group of preschooler , about 10% of the patients presented a nutritional profile below expected (Z BMI <-1), and that proportion increased significantly

mong studen
s (35.3%) and adolescents (33.3%); Figure 1).The nutritional status categories were not related to worse values of nutritional adequacy to the recommendations of calories and macronutrients, or the consumption of nutritional supplements.

The pulmonary function data, available only for students and adolescents, show FEV1 values that are lower among adolescents (Figure 2), however, with no significant difference from the statistical point of vi w (p=0.199).By classifying the pulmonary function values according to the categories of nutritional diagnosis, reduced values are visualized in individuals with weight below expected, but, once again, without statistically significant differences (p=0.072).

Family income did not show any association with nutritional status, nor with the adequacy of energy and macronutrient consumption.


DISCUSSION

This study showed that nutritional status of most patients of the analyzed center are eutrophic, with adequate dietary intake.The prevalence of below expected nutritional status, however, increased progressively with age, especially among the age groups of preschoolers and students.This indicates that the approaches addressed for the preschooler age group can be expressive to preserve the nutritional health of patients with cystic fibrosis.

The importance of nutrition in the health of patients with cystic fibrosis is well established in the literature, [17][18][19] and several studies point adolescence as the most problematic age group in  nutritional terms, with significant association to worse clinical and functional outcomes. 20This study, however, illustrates the relevance of na earlier action, focusing on preschoolers, phase that is knowingly difficult regarding diet. 21t is likely that families of preschoolers with cystic fibrosis face difficulties to support adequate nutritional support, and to maintain the diet for the treatment of pulmonary disease, aiming at guaranteeing ideal growth.At this stage, the infection and inflammation of the airways may occur in a little symptomatic way, resulting in structural damage. 22ome of the major challenges for the families are the inadequate dietary behaviors in this phase of childhood, which may lead to unwanted outcomes in goals of weight and height. 22n the other hand, sometimes the parent's anxiety and poorly  measured expectations lead to increasing diet refusal in the referred age group. 21ome examples of behavioral strategies are pointed out to increase the energy intake, and to improve growth at this age group: to present new foods 10-12 times, even if the child refuses them at first; to limit the time of meals from 15 to 30 minutes; to increase the calories of meals progressively; to take small meals in snack times; to compliment appropriate dietary behaviors; to prevent distractions in meals; to diversify the presentation of presentations; to avoid snacks; and to encourage the effective participation of the parents. 18,23revious studies of nutrition in cystic fibrosis carried out in Brazil showed different results, possibly due to the variable availability of therapeutic and nutritional resources in the different Brazilian regions.In a cross-sectional study carried out in the Northeast, for instance, Pinto et al., in 2009, described worse nutritional status in patients with more unfavorable socioeconomic situation. 24In ICr, in a study carried out 12 years ago, the authors observed a higher proportion of patients with weight below expected through analysis of Z score in all of the anthropometric parameters and inadequate nutritional offers. 9This change in the nu ritional profile of patients with cystic fibrosis is also observed in other countries 25 and, is probably a result of factors such as earlier diagnosis, more strict control and more access to medicines and nutritional supplements.

Despite the diversity of options of available nutritional sup lements for the study patients, the only nutritional supplements whose used was associated with the adequacy of consumption of macronutrients were MCT and complete powdered supplement, both being most frequently used in childhood.

This investigation has several limitations.The choice of a cross-sectional study design does not allow temporal or causal explanations in the complications involving nutritional status, so it is possible to estimate only higher prevalence rates of nutritional status deficit at more advanced ages.Besides, the analysis of dietary intake based only on a diet recall may mask flaws, even when excluding extraordinary days.The genotype and profile of colonization of the respiratory tract were not assessed, despite being known factors that affect the nutritional status.Another limiting factor is the sample number, because, by stratifying subjects by age group, some age groups had a reduced number of participants, which may justify some analyses without statistical significance (such as pulmonary function and nutritional status data).

The performance of anthropometric measurements that do not discriminate body composition may hide the diagnosis of lean mass deficit, with consequent pulmonary damage.Therefore, the presence of weight above expected in 12.9% of the sample may not be followed by the improvement in pulmonary function.A study from the reference center of cystic fibrosis in Greece showed similar prevalence to that found in our study, of patients with overweight and obesity, 26 and another recent American study showed that the excess adiposity may reduce pulmonary function, even in patients considered eutrophic. 27t is possible that the recommendations for a hypercaloric fatrich diet cause unwanted effects in some patients, so the recommendations and nutritional treatment should be individual. 28o sum up, the data presented in this study reveal that the work of a multidisciplinary team prior to the decline in nutritional status, and the availability of medicines and nutritional supplements are essential and bring results.On the other hand, it was possible to see the importance of a different approach for patients in the preschooler age group, who are going through a moment that is apparently sensitive and has an impact on nutritional outcomes.Add

ional strategies, incl
ding activities for the parents and children a