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The effect of the Dietary Approaches to Stop Hypertension (DASH) diet on body composition, complete blood count, prothrombin time, inflammation and liver function in haemophilic adolescents

Published online by Cambridge University Press:  06 December 2021

Atena Mahdavi
Affiliation:
Food Security Research Center, Department of Community Nutrition, School of Nutrition and Food Science, Isfahan University of Medical Sciences, Isfahan, Iran
Hamed Mohammadi
Affiliation:
Department of Clinical Nutrition, School of Nutritional Sciences and Dietetics, Tehran University of Medical Sciences, Tehran, Iran
Mohammad Bagherniya
Affiliation:
Food Security Research Center, Department of Community Nutrition, School of Nutrition and Food Science, Isfahan University of Medical Sciences, Isfahan, Iran
Sahar Foshati
Affiliation:
Food Security Research Center, Department of Clinical Nutrition, School of Nutrition and Food Science, Isfahan University of Medical Sciences, Isfahan, Iran
Cain C. T. Clark
Affiliation:
Centre for Intelligent Healthcare, Coventry University, Coventry, UK
Alireza Moafi
Affiliation:
Pediatric Hematology and Oncology, Isfahan University of Medical Sciences, Isfahan, Iran
Mahshid Elyasi
Affiliation:
Food Security Research Center, Department of Community Nutrition, School of Nutrition and Food Science, Isfahan University of Medical Sciences, Isfahan, Iran
Mohammad Hossein Rouhani*
Affiliation:
Food Security Research Center, Department of Community Nutrition, School of Nutrition and Food Science, Isfahan University of Medical Sciences, Isfahan, Iran
*
*Corresponding author: Dr M. H. Rouhani, fax +98 31 36682509, email [email protected]
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Abstract

There is no dietary strategy that has yet been specifically advocated for haemophilia. Therefore, we sought to assess the effect of the Dietary Approaches to Stop Hypertension (DASH) diet in adolescents with haemophilia. In this parallel trial, forty male adolescents with haemophilia were dichotomised into the DASH group or control group for 10 weeks. The serum high sensitivity C-reactive protein, IL-6, complete blood count (CBC), serum glutamic oxaloacetic transaminase, serum glutamic pyruvic transaminase, partial thromboplastin time (PTT), waist circumference (WC), percentage of body fat, fat-free mass and liver steatosis were measured at the beginning and end of the study. Serum vitamin C was measured as a biomarker of compliance with the DASH diet. The DASH diet was designed to include high amounts of whole grains, fruits, vegetables and low-fat dairy products, as well as low amounts of saturated fats, cholesterol, refined grains, sweets and red meat. Serum vitamin C in the DASH group was significantly increased compared with the control (P = 0·001). There was a significant reduction in WC (P = 0·005), fat mass (P = 0·006), hepatic fibrosis (P = 0·02) and PTT (P = 0·008) in the DASH group, compared with the control. However, there were no significant differences regarding other selected outcomes between groups. Patients in the DASH group had significantly greater increase in the levels of erythrocyte, Hb and haematocrit, as compared with the control. Adherence to the DASH diet in children with haemophilia yielded significant beneficial effects on body composition, CBC, inflammation and liver function.

Type
Research Article
Copyright
© The Author(s), 2021. Published by Cambridge University Press on behalf of The Nutrition Society

Haemophilia is a hereditary haemorrhagic disorder caused by a deficient or defective clotting factor VIII (type A haemophilia) or clotting factor IX (type B haemophilia)(Reference Franchini and Mannucci1). The inheritance pattern of this disorder is X-linked recessive; therefore, haemophilia is exclusively transmitted through female carriers and affects only males(Reference Zimmerman and Valentino2). Recent evidence has shown that more than 1 125 000 men suffer from haemophilia around the world(Reference Iorio, Stonebraker and Chambost3). The World Federation of Hemophilia has announced that Iran is among the top ten countries with the highest prevalence of haemophilia, globally(Reference Dorgalaleh, Dadashizadeh and Bamedi4).

When a male patient manifests unusual haemorrhagic episodes, with an elevated partial thromboplastin time (PTT) but normal prothrombin time and platelet count, the diagnosis of haemophilia is suspected(Reference Zimmerman and Valentino2). The extent of coagulation factor VIII or IX deficiency determines the probability and severity of internal and external bleeding(Reference Franchini and Mannucci1). Depending on age, the predominant sites of haemorrhage are also varied; for instance, haemophilic newborns and toddlers are usually affected by head bleeding, while haemophilic adolescents typically experience intra-articular bleeding, known as haemarthrosis(Reference Kulkarni and Soucie5). Therefore, management of the disease becomes increasingly important in these subjects.

Prolonged haemorrhage, as evidenced by an elevated PTT, is a major concern in haemophilic patients(Reference Zimmerman and Valentino2). Due to recurrent bleeding and haemolysis, mild anaemia is also a common complication in subjects with haemophilia(Reference Buchanan, Holtkamp and Johnson6). Moreover, recent evidence has suggested that haemophilic individuals have chronic low-grade inflammation, originating from increased levels of lipopolysaccharide in their blood circulation(Reference Knowles, Eichler and Pilch7). Furthermore, haemarthrosis and subsequent synovitis and arthropathy make haemophilia sufferers less physically active in comparison with others(Reference Mulder, Cassis and Seuser8). Therefore, overweight, obesity and non-alcoholic fatty liver disease (NAFLD) are prevalent co-morbidities in this population(Reference Wong, Majumdar and Adams9). Unfortunately, no dietary approach has yet been designed or advocated to specifically manage the aforementioned problems in patients with haemophilia.

The Dietary Approaches to Stop Hypertension (DASH) diet is a well-known eating pattern, with multiple, documented, beneficial effects on weight management, body composition, liver function, inflammatory biomarkers and some other aspects of human health(Reference Chiavaroli, Viguiliouk and Nishi10Reference Azadi-Yazdi, Karimi-Zarchi and Salehi-Abargouei12). Adherence to this multifunctional diet creates a unique balance between the consumption of plant-based foods, including whole grains, fruits, vegetables, legumes and nuts, and animal-based foods, including poultry, fish and dairy products. In addition, it limits the intake of salt, red meat, fatty foods and sugar-sweetened beverages and foods(Reference Akhlaghi13). To the best of our knowledge, no study has yet been conducted to evaluate the efficacy of the DASH diet in haemophilic children and adolescents. Therefore, we sought to conduct a randomised controlled trial to assess the effect of the DASH diet on haematological parameters, inflammatory biomarkers, anthropometric indices, body composition and liver function in adolescents with haemophilia.

Method

Participants

The present parallel randomised clinical trial was conducted from March to June 2020. A total of forty adolescents with haemophilia were recruited from Omid Hospital, Isfahan, Iran. Volunteers were eligible if they: (1) were male, (2) were aged between 10 and 18 years old, (3) had clotting factor (VII, VIII and IX) deficiency, (4) had not used antioxidant supplements within the preceding 3 months and (5) were not on a specific diet. Also, incidence of a new chronic disease during the study has been considered as a premature withdrawal. The sample size was calculated by n 2((Z1-α/2 + Z1-β )2× S2)/Δ2, where α = 0·05 (type one error) and β = 20 % (type two error). BMI was considered as the main variable. A previous study showed that the standard deviation of BMI in haemophilic patients was 2·08 kg/m2(Reference Abdelrazik, Reda and El-Ziny14), and the minimal detectable difference of BMI was 1·34 kg/m2. Accordingly, forty haemophilia adolescents were recruited for the current clinical trial. An introductory session was set up to clarify plans and details regarding the study. Written consent was completed by parents and adolescents, and the study was ethically approved by The Research Council and Ethical Committee of Isfahan University of Medical Sciences, Isfahan, Iran, and Food Security Research Center, Isfahan University of Medical Sciences, Isfahan, Iran (Code: IR.MUI.RESEARCH.REC.1399.098). This randomised clinical trial was registered at IRCT.ir (IRCT20130903014551N6).

Study procedure and dietary intervention

In this current study, participants were randomly dichotomised into the DASH group (n 20) or control group (n 20) for 10 weeks. Each subject received a code and randomisation was run using select random number in SPSS 20. As is was a dietary intervention, patients and their parents could not be blinded. In DASH group, energy requirements of each participant were calculated individually based on the Harris–Benedict equation(Reference Kien and Ugrasbul15). The DASH diet was determined based on the previously modified DASH diet for adolescents(Reference Couch, Saelens and Levin16), where the macronutrient composition was as follows: 50–55 % of total energy from carbohydrates, 16–18 % of total energy from protein and 27–30 % of energy from fat. The DASH diet was designed to include high amounts of whole grains, fruits, vegetables and low-fat dairy products, as well as low amounts of saturated fats, cholesterol, refined grains, legumes, nuts, sweets and red meat. A sample of 1-d menu is demonstrated in Table 1. Also, the consumption of red meat and Na was limited. In this way, limiting red meat was applied by reducing the amount of red meat per serving in the diet and replacing red meat with white meat and poultry. It is recommended to consume a maximum of 180 g of meat/d with emphasis on the consumption of fish and white meat. Following recommendations were used to limit Na intake: (1) avoid using of table salt, (2) cooking low-salt food, (3) limit using Na-rich foods such as pickles and processed foods and (4) use of low-salt cheese and breads. A maximum Na intake of 2300 mg/d was allowed. All adolescents and their parents attended the meetings to learn daily food menus. Adolescents in the control group received nutritional recommendations based on healthy eating behaviours, including chewing food completely, using low-volume frequent meals, using healthy snacks, drinking adequate water, avoiding deep frying, limiting added fat and sugar. Serum vitamin C was defined as a biochemical indicator of compliance with DASH diet(Reference Saneei, Hashemipour and Kelishadi17). Accordingly, compliance with the DASH diet was assessed by measuring serum vitamin C at baseline and after 10 weeks of intervention. Serum vitamin C was measured using biochemical colorimetric analysis. All patients and their parents participated in meetings programmed at baseline and 2, 4, 6 and 8 weeks. Parents were required to complete a 1-d food record in the 1st, 5th and 10th week of the study. So, three, 1-d food records (two weekdays and one weekend day) were completed by each participant, and a researcher investigated the completeness of food diaries with parents. All collected food records were analysed using the United States Department of Agriculture (USDA) database.

Table 1. A sample menu of the prescribed diet to the Dietary Approaches to Stop Hypertension group (6276 kJ (1500 kcal), 55 % from carbohydrate, 17 % from protein, 28 % from fats)

Measurement of biochemical variables

Blood samples were drawn after 12 h of fasting, in the early morning, from the antecubital vein, and all of the related concentrations were prepared on the day of blood sampling. Samples were centrifuged at 3000 × g for 10 min to separate the serum. High sensitivity C-reactive protein (hs-CRP) was measured using the Inm.turbid method by Audit kit (Delta treatment), and IL-6 was measured using the commercially available ELISA kits (Siemens) by CLIA. Complete blood counts were conducted using an automated procedure (Mindray apparatus). Serum glutamic oxaloacetic transaminase and serum glutamic pyruvic transaminase were measured by the enzymatic system with a Pars Azmon kit (Pars Azmon). PTT tests were performed using the turbidometry method by IL kits (Instrument Lab). In the present study, serum vitamin C was measured using vials previously treated with meta-phosphoric acid based on a biochemical colorimetric analysis.

Measurement of anthropometric variables and body composition

Weight was measured to the nearest 100 g, with participants minimally clothed and unshod, while height was measured using a standard stadiometer according to standard protocols. BMI was calculated as weight in kg divided by the square of height in metres. Waist circumference (WC) was measured at the narrowest level, over light clothing, using a non-stretchable tape measure, without any pressure to the body surface. Weight, height and BMI percentiles were calculated based on Centers for Disease Control and Prevention growth charts for children and adolescents, aged 2–19 years(Reference Kuczmarski18). Body fat and fat-free mass (FFM) were measured using bioelectrical impedance analysis (Bodyvis A_1c), which is highly correlated with dual X-ray absorptiometry (r 0·88)(Reference Sun, French and Martin19). All measurements were conducted at baseline and at the end of the trial.

Measurement of fibrosis and steatosis

Liver fat was measured using FibroScan and accepted as the reference standard. All biopsy specimens were investigated by a circulatory expert who specialised in liver diseases. The probe transducer tip was located on the skin between the ribs and the level of the right lobe of the liver. The depth was between 25 and 65 mm under the skin exterior(Reference Sandrin, Fourquet and Hasquenoph20). Stages were recognised according to the NASH Clinical Research Network scoring system(Reference Kleiner, Brunt and Van Natta21).

Statistical analysis

The analyses were performed on the basis of an intention-to-treat (ITT) approach. Missing values were treated according to linear regression method. To evaluate the distribution of variables, we used the Kolmogorov–Smirnov test, which demonstrated that body fat, serum glutamic pyruvic transaminase and CRP were not normally distributed. Therefore, log transformation was applied. Quantitative variables were analysed between two groups utilising an independent Student’s t test, while an ANCOVA was conducted to set confounding variables, especially baseline values. Data were presented as means and standard deviations, unless otherwise stated. All statistical analyses were performed using SPSS (version 20) statistical software.

Results

Among the forty subjects with haemophilia who enrolled in the study, three patients in the DASH diet group (due to medical conditions and personal reasons) and four patients in the control group (due to medical conditions and low adherence to intervention) were excluded from follow-up data collection (Fig. 1). During the study process, two subjects had low adherence and they did not want to continue participation. Therefore, they excluded according to their tendency and researchers had no role in excluding these subjects. Nevertheless, baseline measurements were performed for these patients and we run ITT analysis according to the baseline measurements.

Fig. 1 CONSORT flow diagram of intervention.

We excluded two subjects from the control group because they stated that they did not start being on the prescribed diet. Therefore, we did not follow them because they had no compliance with prescribed diet. At the end of the study, we included baseline data of all subjects randomly assigned to the DASH or control groups using an ITT method.

The analyses were performed according to ITT approach; therefore, all forty participants were enrolled in the final analyses. There were no side effects following the DASH diet among the participants.

Table 2 indicates baseline characteristics of study participants in each group. There were no significant differences between the groups in terms of age, BMI percentile and WC. However, at baseline, individuals in the DASH diet group had higher weight and height percentiles, compared with those in the control group.

Table 2. Baseline characteristic of study subjects*

(Mean values and standard deviations)

DASH, Dietary Approaches to Stop Hypertension; WC; waist circumference.

* Variables are expressed as mean values and standard deviations.

P-values resulted from independent t tests for quantitative and χ 2 for qualitative variables between the two groups.

Dietary intake of the study participants as a sum of the three 1-d food records is presented in Table 3. Based on food diaries, the mean intakes of energy, carbohydrate, protein, fat, vitamin A, vitamin E, vitamin C, vitamin K, vitamin B1, vitamin B2, Se, Zn, Fe and dietary fibre during the trial were not significantly different between groups. As expected, dietary intakes of Na were significantly lower (1172·35 v. 1580·94 mg/d, P = 0·002), while Ca intakes were higher (754·26 v. 545·28 mg/d, P = 0·017), in the DASH v. control group. Individuals in the DASH group had higher intakes of K (1987·52 v. 1624·36 mg/d, P = 0·040) as compared with those in the control group.

Table 3. Dietary intake of the study participants as a sum of the three 1-d food records*

(Mean values and standard deviations)

DASH, Dietary Approaches to Stop Hypertension.

* Variables are expressed as mean values and standard deviations.

Obtained from ANCOVA adjusted for energy intake.

Presents serum vitamin C levels at baseline and at the end of trial in each group. At the end of the trial, serum vitamin C levels were significantly increased in the DASH diet group (0·28 mg/dl) and control group (0·10 mg/dl) compared with baseline values. Between group comparison indicated a significant increase in serum vitamin C levels in the DASH group compared with the control group (P = 0·001), suggesting a relatively good compliance of the participants to the DASH diet.

Table 4 details the effect of the DASH diet on anthropometric indices, inflammation and liver histology and enzymes. Within group comparison showed a significant reduction in WC (-2·25 cm), FAT (-0·52 kg) and PTT (-8·48), and a significant rise in FFM (1·25 kg), in the DASH diet group. Also, a significant increase was seen regarding FAT (0·88 kg), CRP (2·22 mg/l) and hepatic fibrosis (0·15 kPa) in the control group. Compared with the control group, adherence to the DASH diet led to significant reductions in WC (P = 0·005), FAT (P = 0·006), hepatic fibrosis (P = 0·02) and PTT (P = 0·008). There were no significant differences regarding other selected outcomes between groups. To attenuate the difference in baseline values, the effect of baseline measurements was adjusted.

Table 4. The effects of Dietary Approach to Stop Hypertension (DASH) diet on anthropometric indices, inflammation and liver histology and enzymes*

(Mean values and standard deviations)

WC, waist circumference; FFM, fat-free mass; CRP, C-reactive protein; SGOT, serum glutamic oxaloacetic transaminase; SGPT, serum glutamic pyruvic transaminase; PTT, partial thromboplastin time.

* Variables are expressed as mean values and standard deviations.

It shows the comparison baseline and final values in each group obtained from paired t test.

It shows the comparison final values between DASH and control groups obtained from independent t test comparing endpoint measurements.

§ It shows the comparison final values between two groups after adjusting for baseline measurements obtained from ANCOVA, adjusted for baseline value.

The effects of DASH diet on complete blood count profile are presented in Table 5. Within group analysis showed that leucocyte, erythrocyte, Hb, haematocrit (HCT) and mean corpuscular Hb were significantly increased after using DASH diet. Patients in the DASH group had significantly greater increase in the levels of erythrocyte (P = 0·02), Hb (P = 0·005) and HCT (P = 0·006), compared with the control group. To attenuate the difference in baseline values, the effect of baseline measurements was adjusted.

Table 5. The effects of Dietary Approach to Stop Hypertension (DASH) diet on complete blood count*

HCT, haematocrit; MCV, mean corpuscular volume; MCH, mean corpuscular Hb; MCHC, mean corpuscular Hb concentration.

* Variables are expressed as mean values and standard deviations.

It shows the comparison baseline and final values in each group obtained from paired t test.

It shows the comparison final values between DASH and control groups obtained from independent t-test comparing endpoint measurements.

§ It shows the comparison final values between two groups after adjusting for baseline measurements obtained from ANCOVA, adjusted for baseline value.

Discussion

In the current study, adherence to the DASH diet, for 10 weeks, among haemophilic adolescents resulted in a significant reduction in WC, fat mass, fibrosis and PTT, in comparison with the control group. In addition, erythrocyte, Hb and HCT significantly increased, while steatosis and CRP levels were marginally reduced, in response to following the DASH diet, compared with the control group. However, changes in weight, BMI, FFM, IL-6, serum glutamic oxaloacetic transaminase, serum glutamic pyruvic transaminase, mean corpuscular volume, mean corpuscular Hb and mean corpuscular Hb concentration were not significantly different between the two groups. To the best of our knowledge, this is the first study investigating the effects of the DASH diet on body composition, complete blood count, inflammatory markers and liver function in haemophilic adolescents. It has previously been demonstrated that overweight and obesity are major issues when concomitant to haemophilia and are associated with several metabolic abnormalities(Reference Wong, Majumdar and Adams9). With regard to the difficulties of these patients to be physically active(Reference Philpott, Houghton and Luke22,Reference Broderick, Herbert and Latimer23) , following a healthy diet and decreasing energy intake are suggested as key factors in the prevention or reduction of overweight and obesity among these patients(Reference Wong, Majumdar and Adams9). However, currently, no dietary recommendation has been specifically advocated for these patients. Therefore, our findings, which indicated the beneficial effects of the DASH diet on several health aspects of haemophilia, might be useful in clinical settings to prevent and treat health complications of these patients.

The results of our study showed that serum vitamin C level significantly increased following the DASH diet, compared with the control diet. In addition, intake of soluble fibre and Ca was significantly higher, and Na intake was notably lower, in the DASH group v. the control group. Currently, serum vitamin C level and dietary records represent the best tools to assess the compliance of study participants to the DASH diet(Reference Saneei, Hashemipour and Kelishadi17). Concordant with our results, in a previous study conducted on children with the metabolic syndrome, serum vitamin C significantly increased following the DASH diet, compared with the control group(Reference Saneei, Hashemipour and Kelishadi17). Indeed, it has been suggested that the consumption of vitamin C may be associated with lower blood pressure, by enhancing nitric oxide synthase activity(Reference d’Uscio, Milstien and Richardson24,Reference Ward, Hodgson and Croft25) . Therefore, one of the possible explanations for the anti-hypertension effects of the DASH diet might be due to the high fruits and vegetable content of this diet. Indeed, the focus of the DASH diet is on vegetables, fruits and low-fat dairy foods(Reference Appleby, Davey and Key26); thus, a significant increase in the soluble fibre and Ca intake is predictable among intervention participants, as compared with controls.

In the present study, WC and fat mass were significantly decreased in response to adherence to the DASH diet in comparison with the control diet. However, the differences between weight, BMI and FFM did not significantly differ between groups. It has previously suggested that overweight and obesity, which are highly prevalent among haemophilia patients, are associated with annual joint bleeding rate and influence the joint health of these patients(Reference Carpenter, Chrisco and Johnson27Reference Wilding, Zourikian and Di Minno29). It has also been widely demonstrated that overweight and obesity contribute to the reduction in motion of joints, acceleration of loss of joint mobility and increasing chronic pain(Reference Wilding, Zourikian and Di Minno29). Given that obesity in haemophilia patients is associated with an increasing prevalence of anxiety and depression and several other negative health consequences(Reference Wilding, Zourikian and Di Minno29), prevention and treatment of obesity are necessary in these patients. However, generally, weight reduction during childhood is not recommended and the aim of the diet therapy should be the maintenance of weight among children and adolescents. Therefore, our results, which indicate that adherence to the DASH diet, for 10 weeks, can maintain BMI and FFM, in addition to facilitating reductions in WC and fat mass, in adolescents with haemophilia, suggest that the DASH diet is a practical and safe dietary approach to help prevent obesity and its related complications among children and adolescents with haemophilia. Indeed, the results of a systematic review and meta-analysis showed that, in comparison with the control diet, adherence to the DASH diet elicited a significant reduction in weight, BMI and WC among adults(Reference Soltani, Shirani and Chitsazi30). Moreover, the results of a cohort study showed that, after 3-year follow-up, the DASH diet had an inverse association with central and general obesity among adolescents(Reference Farhadnejad, Asghari and Mirmiran31). In another previous study, it was reported that, after 6 weeks adherence to the DASH diet, weight, BMI and WC did not significantly change compared with usual dietary habits among children with the metabolic syndrome(Reference Saneei, Hashemipour and Kelishadi17). In Saneei et al., WC was significantly reduced in the DASH diet group compared with baseline; however, although the mean change of WC was higher in the DASH diet compared with control diet, it was not statistically significant(Reference Saneei, Hashemipour and Kelishadi17). Thus, discordance in findings of some previous work and our study, in terms of WC, might be attributable to the difference in compliance and longer treatment time of our study (10 weeks v. 6 weeks). Overall, the favourable effects of the DASH diet on WC and body composition in our sample might be due to the fact that the DASH diet is rich in fruits and vegetables, legumes and low-fat dairy products, as well as healthy vegetable oils, which provide a low-energy dietary pattern and simultaneously provide suitable amounts of nutrients for the growth and development of children and adolescents.

In our study, fibrosis and steatosis were markedly decreased in the DASH diet group compared with the controls. Although NAFLD is often associated with adulthood, recent studies have shown that the risk of developing NAFLD in adolescents has doubled in the past 20 years(Reference Welsh, Karpen and Vos32). Recent studies have presented NAFLD as one of the two most important complications of obesity in children and adolescents(Reference Faienza, Chiarito and Molina-Molina33). Also, it should be noted that children with haemophilia have limited physical activity due to the risk of bleeding, which increases the risk of NAFLD. In a previous randomised controlled trial study, in comparison with controls, following the DASH diet for 8 weeks among adult NAFLD patients resulted in improvements in several metabolic factors, such as weight, BMI, TAG, markers of insulin metabolism, inflammatory and stress oxidative markers of these patients(Reference Razavi Zade, Telkabadi and Bahmani11). Similarly, observational studies have reported that the consumption of the DASH diet has an inverse correlation with risk of NAFLD(Reference Hekmatdoost, Shamsipour and Meibodi34,Reference Xiao, Lin and Li35) . As mentioned above, haemophilia patients have several hindrances to being physically active and they are at high risk for obesity and related metabolic diseases. One the most important undesirable outcomes of being physically inactive and gaining weight, particularly enhancing visceral fat and central obesity, in both adolescents and adults is insulin resistance, which has a bilateral association with fatty liver(Reference Chiyanika, Chan and Hui36,Reference Bagherniya, Nobili and Blesso37) . The beneficial effects of the DASH diet on the metabolic status of patients with haemophilia might be explained by the low amounts of simple sugar and higher fibre, Mg and calcium of this dietary pattern, which may reduce markers of insulin metabolism, TAG and VLDL-cholesterol levels(Reference Lomba, Milagro and Garcia-Diaz38). It has recently been shown that the consumption of sugar-sweetened soda has a direct correlation with increased risk of NAFLD, since they possess high amounts of fructose and energy content which both have a substantial role in the aetiology of fatty liver(Reference Wijarnpreecha, Thongprayoon and Edmonds39,Reference Schulze, Manson and Ludwig40) . Animal studies have shown that high Ca and Mg diets, as exists in the DASH eating pattern, have a salient role in stimulating microsomal TAG transfer protein in the liver(Reference Cho, Kang and Choi41), suppression of endothelial injury, reduction in the peroxidation of lipids and enhancing the antioxidant capacity in both serum and tissues(Reference King, Miller and Blue42).

The findings of the present study demonstrated that the consumption of the DASH diet yielded, albeit marginal, significantly reduced serum CRP levels compared with the control group. In accordance with our results, it has been shown that following the DASH diet significantly reduced hs-CRP among adolescents with the metabolic syndrome(Reference Saneei, Hashemipour and Kelishadi17), adult NAFLD patients(Reference Razavi Zade, Telkabadi and Bahmani11) and polycystic ovary syndrome(Reference Asemi and Esmaillzadeh43) patients compared with control groups.

However, adhering to the DASH diet for 4 weeks did not lead to reductions in hs-CRP in women with gestational diabetes, while it significantly increased plasma total antioxidant capacity and total glutathione(Reference Asemi, Samimi and Tabassi44). Several potential mechanisms have been posited regarding the anti-inflammatory effects of DASH diet, including high amounts of antioxidants, such as vitamin C, and high amounts of Ca, Mg and fibre present within this diet(Reference Pikilidou, Lasaridis and Sarafidis45Reference Lopes, Martin and Nashar47). It has previously been shown that Mg inhibits nuclear factor kappa-light-chain-enhancer of activated B cells and has a role in the down-regulation of the inflammatory response(Reference Sargeant, Miller and Shaw48,Reference Almoznino-Sarafian, Berman and Mor49) .

One the most valuable findings of our study is that PTT significantly decreased after the consumption of the DASH diet compared with the control diet. A prolongation in the PTT is occurrent in patients with haemophilia, even in some cases with severe haemophilia the PTT is 2–3 times longer than the normal range(Reference Zimmerman and Valentino50). However, to our knowledge, there is no study that has assessed the relationship between healthy dietary patterns and PTT; thus, more preclinical and clinical trials are needed to clarify our results and its underlying mechanisms. The DASH diet is rich in vegetables that are full of vitamin K. As a result, following this diet increases vitamin K intake(Reference Booth51). In addition, DASH diet is a rich source of dietary fibre which can lead to more vitamin K production by altering gut microbiota(Reference Yang, Liang and Balakrishnan52). These suggested mechanisms should be investigated by additional studies. Similarly, our results indicated that adherence to the DASH diet significantly increased erythrocyte, Hb and HCT compared with the control group, which might due to the high antioxidant levels of the DASH diet, which are necessary in haematopoiesis(Reference Wambi, Sanzari and Wan53).

The average age of the subjects in our study was 13–14 years. According to the WHO height-for-age percentile(54), the rate of height growth is about 6–7 cm/year (0·11–0·12 cm/week) in this age. The duration of the present study was 10 weeks. Therefore, the subjects had a maximum height growth of 1·1–1·3 cm. It should be kept in mind that the impaired growth is prevalent among children with chronic disease such as haemophilia(Reference Hilgartner, Donfield and Willoughby55). Therefore, it is unlikely that our findings on body composition were affected by the height growth of the subjects.

Strengths and limitations

The strengths of our study included that we utilised serum levels of vitamin C as a valid biomarker of diet compliance, and we applied the ITT approach for the analysis data, which permitted all of the study participants who participated in our study into data analysis. Evidence determined that the concentration of Na and K in a 24-h urine sample can be considered as a biomarker of compliance with the DASH diet. Although, collecting 24-h urine samples is difficult, especially for children and adolescents. Additionally, day to day variation of 24-h urinary Na is high, and multiple samplings are required to attenuate day to day variation(Reference Cho, Kang and Choi41). Since it was not suitable for adolescents, we utilised vitamin C because it does not have these limitations. Moreover, to the authors’ knowledge, this is the first study investigating the effects of the DASH diet, as one of the most well-known healthy dietary patterns, on liver fibrosis and steatosis using a FibroScan, inflammatory factors, anthropometry and body composition, as well as complete blood count among haemophilic adolescents. Nevertheless, as a main limitation of our study, blinding was not applicable due to the nature of our intervention. Dietary intakes were not assessed before the intervention, and all the nutritional assessments were performed during the study. Also, dietary intake has been investigated during the study using three 1-d food records. Due to the difficulty of obtaining food records from children with specific disease conditions, we could not convince participants to increase the number of food records. However, due to the fact that the compliance with the intervention has been evaluated by biomarkers (serum vitamin C), these limitations had no serious unfavourable effect on the validity of the study.

Conclusion

Our findings showed that the DASH diet, which was primarily designed to control cardiovascular risk factors in healthy or unhealthy adults, has several beneficial effects on various health aspects of adolescents with haemophilia. Indeed, adherence to the DASH diet significantly reduced WC and fat mass, in addition to eliciting beneficial effects on CRP, liver fibrosis and steatosis, as well as RBS, Hb and HCT, in haemophilic adolescents. However, more, well-designed and well-conducted, studies are needed to confirm the results of the present study.

Acknowledgements

None.

This research did not receive any specific grant from funding agencies in the public, commercial or not-for-profit sectors.

M. H. R, A. M and H. M conceptualized the study and contributed in methodology. M. B, A. M and A. M contributed in resources of the study. M. H. R, S. F and C. C. T. C  curated data. A. M, H. M and M. H. R analyzed data. Investigation was performed by M. E, A. M, A. M, and H. M. M. B, S. F were supervisor. M. H. R was Project administrator. M. E, M. H. R, A. M, S. F and C. C. T. C wrote original draft. M. B and A. M edited and reviewed the manuscript.

There are no conflicts of interest.

References

Franchini, M & Mannucci, PM (2012) Past, present and future of hemophilia: a narrative review. Orphanet J Rare Dis 7, 18.CrossRefGoogle ScholarPubMed
Zimmerman, B & Valentino, LA (2013) Hemophilia: in review. Pediatr Rev 34, 289294.CrossRefGoogle Scholar
Iorio, A, Stonebraker, JS, Chambost, H, et al. (2019) Establishing the prevalence and prevalence at birth of hemophilia in males: a meta-analytic approach using national registries. Ann Intern Med 171, 540546.CrossRefGoogle ScholarPubMed
Dorgalaleh, A, Dadashizadeh, G & Bamedi, T (2016) Hemophilia in Iran. Hematology 21, 300310.CrossRefGoogle ScholarPubMed
Kulkarni, R & Soucie, JM (2011) Pediatric hemophilia: a review. Semin Thromb Hemost 37, 737744.CrossRefGoogle ScholarPubMed
Buchanan, GR, Holtkamp, CA & Johnson, A (1990) Reduced serum haptoglobin values in hemophiliacs receiving monoclonally purified factor VIII concentrates. Am J Hematol 33, 234237.CrossRefGoogle ScholarPubMed
Knowles, LM, Eichler, H & Pilch, J (2019) Low-grade inflammation in hemophilia. Blood 134, Suppl. 1, 1115.CrossRefGoogle Scholar
Mulder, K, Cassis, F, Seuser, D, et al. (2004) Risks and benefits of sports and fitness activities for people with haemophilia. Haemophilia 10, 161163.CrossRefGoogle ScholarPubMed
Wong, TE, Majumdar, S, Adams, E, et al. (2011) Overweight and obesity in hemophilia: a systematic review of the literature. Am J Prev Med 41, S369S375.CrossRefGoogle ScholarPubMed
Chiavaroli, L, Viguiliouk, E, Nishi, SK, et al. (2019) DASH dietary pattern and cardiometabolic outcomes: an umbrella review of systematic reviews and meta-analyses. Nutrients 11, 338.CrossRefGoogle ScholarPubMed
Razavi Zade, M, Telkabadi, MH, Bahmani, F, et al. (2016) The effects of DASH diet on weight loss and metabolic status in adults with non-alcoholic fatty liver disease: a randomized clinical trial. Liver Int 36, 563571.CrossRefGoogle ScholarPubMed
Azadi-Yazdi, M, Karimi-Zarchi, M, Salehi-Abargouei, A, et al. (2017) Effects of Dietary Approach to Stop Hypertension diet on androgens, antioxidant status and body composition in overweight and obese women with polycystic ovary syndrome: a randomised controlled trial. J Hum Nutr Diet 30, 275283.CrossRefGoogle ScholarPubMed
Akhlaghi, M (2020) Dietary approaches to stop hypertension (DASH): potential mechanisms of action against risk factors of the metabolic syndrome. Nutr Res Rev 33, 118.CrossRefGoogle ScholarPubMed
Abdelrazik, N, Reda, M, El-Ziny, M, et al. (2007) Evaluation of bone mineral density in children with hemophilia: Mansoura University children hospital (MUCH) experience, Mansoura, Egypt. Hematology 12, 431437.CrossRefGoogle ScholarPubMed
Kien, CL & Ugrasbul, F (2004) Prediction of daily energy expenditure during a feeding trial using measurements of resting energy expenditure, fat-free mass, or Harris-Benedict equations. Am J Clin Nutr 80, 876880.CrossRefGoogle ScholarPubMed
Couch, SC, Saelens, BE, Levin, L, et al. (2008) The efficacy of a clinic-based behavioral nutrition intervention emphasizing a DASH-type diet for adolescents with elevated blood pressure. J Pediatr 152, 494501.CrossRefGoogle ScholarPubMed
Saneei, P, Hashemipour, M, Kelishadi, R, et al. (2013) Effects of recommendations to follow the dietary approaches to stop hypertension (DASH) diet v. usual dietary advice on childhood metabolic syndrome: a randomised cross-over clinical trial. Br J Nutr 110, 22502259.CrossRefGoogle ScholarPubMed
Kuczmarski, RJ (2000) CDC Growth Charts. United States: US Department of Health and Human Services, Centers for Disease Control and Prevention.Google ScholarPubMed
Sun, G, French, CR, Martin, GR, et al. (2005) Comparison of multifrequency bioelectrical impedance analysis with dual-energy X-ray absorptiometry for assessment of percentage body fat in a large, healthy population. Am J Clin Nutr 81, 7478.CrossRefGoogle Scholar
Sandrin, L, Fourquet, B, Hasquenoph, J-M, et al. (2003) Transient elastography: a new noninvasive method for assessment of hepatic fibrosis. Ultrasound Med Biol 29, 17051713.CrossRefGoogle ScholarPubMed
Kleiner, DE, Brunt, EM, Van Natta, M, et al. (2005) Design and validation of a histological scoring system for nonalcoholic fatty liver disease. Hepatology 41, 13131321.CrossRefGoogle ScholarPubMed
Philpott, J, Houghton, K & Luke, A (2010) Physical activity recommendations for children with specific chronic health conditions: juvenile idiopathic arthritis, hemophilia, asthma and cystic fibrosis. Paediatr Child Health 15, 213218.CrossRefGoogle ScholarPubMed
Broderick, CR, Herbert, RD, Latimer, J, et al. (2012) Association between physical activity and risk of bleeding in children with hemophilia. JAMA 308, 14521459.CrossRefGoogle ScholarPubMed
d’Uscio, LV, Milstien, S, Richardson, D, et al. (2003) Long-term vitamin C treatment increases vascular tetrahydrobiopterin levels and nitric oxide synthase activity. Circ Res 92, 8895.CrossRefGoogle ScholarPubMed
Ward, NC, Hodgson, JM, Croft, KD, et al. (2005) The combination of vitamin C and grape-seed polyphenols increases blood pressure: a randomized, double-blind, placebo-controlled trial. J Hypertens 23, 427434.CrossRefGoogle ScholarPubMed
Appleby, PN, Davey, GK & Key, TJ (2002) Hypertension and blood pressure among meat eaters, fish eaters, vegetarians and vegans in EPIC–Oxford. Public Health Nutr 5, 645654.CrossRefGoogle ScholarPubMed
Carpenter, SL, Chrisco, M & Johnson, E (2006) The effect of overweight and obesity on joint damage in patients with moderate or severe hemophilia. Blood 108, 4064.CrossRefGoogle Scholar
Chang, C-Y, Li, T-Y, Cheng, S-N, et al. (2019) Obesity and overweight in patients with hemophilia: prevalence by age, clinical correlates, and impact on joint bleeding. J Chin Med Assoc 82, 289294.CrossRefGoogle ScholarPubMed
Wilding, J, Zourikian, N, Di Minno, M, et al. (2018) Obesity in the global haemophilia population: prevalence, implications and expert opinions for weight management. Obes Rev 19, 15691584.CrossRefGoogle ScholarPubMed
Soltani, S, Shirani, F, Chitsazi, MJ, et al. (2016) The effect of dietary approaches to stop hypertension (DASH) diet on weight and body composition in adults: a systematic review and meta-analysis of randomized controlled clinical trials. Obes Rev 17, 442454.CrossRefGoogle ScholarPubMed
Farhadnejad, H, Asghari, G, Mirmiran, P, et al. (2018) Dietary approach to stop hypertension diet and cardiovascular risk factors among 10- to 18-year-old individuals. Pediatr Obes 13, 185194.CrossRefGoogle ScholarPubMed
Welsh, JA, Karpen, S & Vos, MB (2013) Increasing prevalence of nonalcoholic fatty liver disease among United States adolescents, 1988–1994 to 2007–2010. J Pediatr 162, 496500.CrossRefGoogle ScholarPubMed
Faienza, MF, Chiarito, M, Molina-Molina, E, et al. (2020) Childhood obesity, cardiovascular and liver health: a growing epidemic with age. World J Pediatr, 16, 18.CrossRefGoogle ScholarPubMed
Hekmatdoost, A, Shamsipour, A, Meibodi, M, et al. (2016) Adherence to the dietary approaches to stop hypertension (DASH) and risk of nonalcoholic fatty liver disease. Int J Food Sci Nutr 67, 10241029.CrossRefGoogle Scholar
Xiao, ML, Lin, JS, Li, YH, et al. (2020) adherence to the dietary approaches to stop hypertension (DASH) diet is associated with lower presence of non-alcoholic fatty liver disease in middle-aged and elderly adults. Public Health Nutr 23, 674682.CrossRefGoogle Scholar
Chiyanika, C, Chan, DFY, Hui, SCN, et al. (2020) The relationship between pancreas steatosis and the risk of metabolic syndrome and insulin resistance in Chinese adolescents with concurrent obesity and non-alcoholic fatty liver disease. Pediatr Obes 15, e12653.CrossRefGoogle ScholarPubMed
Bagherniya, M, Nobili, V, Blesso, CN, et al. (2018) Medicinal plants and bioactive natural compounds in the treatment of non-alcoholic fatty liver disease: a clinical review. Pharmacol Res 130, 213240.CrossRefGoogle ScholarPubMed
Lomba, A, Milagro, FI, Garcia-Diaz, DF, et al. (2009) A high-sucrose isocaloric pair-fed model induces obesity and impairs NDUFB6 gene function in rat adipose tissue. J Nutrigenet Nutrigenomics 2, 267272.Google ScholarPubMed
Wijarnpreecha, K, Thongprayoon, C, Edmonds, P, et al. (2016) Associations of sugar-and artificially sweetened soda with nonalcoholic fatty liver disease: a systematic review and meta-analysis. QJM 109, 461466.CrossRefGoogle Scholar
Schulze, MB, Manson, JE, Ludwig, DS, et al. (2004) Sugar-sweetened beverages, weight gain, and incidence of type 2 diabetes in young and middle-aged women. JAMA 292, 927934.CrossRefGoogle Scholar
Cho, H-J, Kang, H-C, Choi, S-A, et al. (2005) The possible role of Ca2+ on the activation of microsomal triglyceride transfer protein in rat hepatocytes. Biol Pharm Bull 28, 14181423.CrossRefGoogle ScholarPubMed
King, JL, Miller, RJ, Blue, JP Jr, et al. (2009) Inadequate dietary magnesium intake increases atherosclerotic plaque development in rabbits. Nutr Res 29, 343349.CrossRefGoogle ScholarPubMed
Asemi, Z & Esmaillzadeh, A (2015) DASH diet, insulin resistance, and serum hs-CRP in polycystic ovary syndrome: a randomized controlled clinical trial. Horm Metab Res 47, 232238.Google ScholarPubMed
Asemi, Z, Samimi, M, Tabassi, Z, et al. (2013) A randomized controlled clinical trial investigating the effect of DASH diet on insulin resistance, inflammation, and oxidative stress in gestational diabetes. Nutrition 29, 619624.CrossRefGoogle ScholarPubMed
Pikilidou, MI, Lasaridis, A, Sarafidis, P, et al. (2009) Insulin sensitivity increase after calcium supplementation and change in intraplatelet calcium and sodium–hydrogen exchange in hypertensive patients with Type 2 diabetes 1. Diabetic Med 26, 211219.CrossRefGoogle Scholar
Chen, X, Touyz, RM, Park, JB, et al. (2001) Antioxidant effects of vitamins C and E are associated with altered activation of vascular NADPH oxidase and superoxide dismutase in stroke-prone SHR. Hypertension 38, 606611.CrossRefGoogle Scholar
Lopes, HF, Martin, KL, Nashar, K, et al. (2003) DASH diet lowers blood pressure and lipid-induced oxidative stress in obesity. Hypertension 41, 422430.CrossRefGoogle ScholarPubMed
Sargeant, HR, Miller, HM & Shaw, M-A (2011) Inflammatory response of porcine epithelial IPEC J2 cells to enterotoxigenic E. coli infection is modulated by zinc supplementation. Mol Immunol 48, 21132121.CrossRefGoogle ScholarPubMed
Almoznino-Sarafian, D, Berman, S, Mor, A, et al. (2007) Magnesium and C-reactive protein in heart failure: an anti-inflammatory effect of magnesium administration? Eur J Nutr 46, 230237.CrossRefGoogle ScholarPubMed
Zimmerman, B & Valentino, LA (2013) Hemophilia: in review. Pediatr Rev 34, 289294.CrossRefGoogle Scholar
Booth, SL (2012) Vitamin K: food composition and dietary intakes. Food Nutr Res 56, 5505.CrossRefGoogle ScholarPubMed
Yang, Q, Liang, Q, Balakrishnan, B, et al. (2020) Role of dietary nutrients in the modulation of gut microbiota: a narrative review. Nutrients 12, 381.CrossRefGoogle ScholarPubMed
Wambi, C, Sanzari, J, Wan, XS, et al. (2008) Dietary antioxidants protect hematopoietic cells and improve animal survival after total-body irradiation. Radiat Res 169, 384396.CrossRefGoogle ScholarPubMed
Hilgartner, MW, Donfield, SM, Willoughby, A, et al. (1993) Hemophilia growth and development study. Design, methods, and entry data. Am J Pediatr Hematol Oncol 15, 208218.CrossRefGoogle ScholarPubMed
Figure 0

Table 1. A sample menu of the prescribed diet to the Dietary Approaches to Stop Hypertension group (6276 kJ (1500 kcal), 55 % from carbohydrate, 17 % from protein, 28 % from fats)

Figure 1

Fig. 1 CONSORT flow diagram of intervention.

Figure 2

Table 2. Baseline characteristic of study subjects*(Mean values and standard deviations)

Figure 3

Table 3. Dietary intake of the study participants as a sum of the three 1-d food records*(Mean values and standard deviations)

Figure 4

Table 4. The effects of Dietary Approach to Stop Hypertension (DASH) diet on anthropometric indices, inflammation and liver histology and enzymes*(Mean values and standard deviations)

Figure 5

Table 5. The effects of Dietary Approach to Stop Hypertension (DASH) diet on complete blood count*