Research article

Prevalence of goiter among children aged 8–10 in Binh Dinh province, Vietnam in 2016–2017

  • Received: 13 February 2019 Accepted: 17 May 2019 Published: 23 May 2019
  • Objective: The study was conducted to estimate the goiter prevalence, and the median urine iodine concentrations among schoolchildren aged 8–10 in Binh Dinh province, Vietnam. Methods: A school-based cross-sectional survey was carried out from May 2016 to May 2017. A multistage, proportional-to-population-size sampling method with 30 clusters was used. The children were examined by palpation for the presence or absence of goiter based on the criteria of the World Health Organization (WHO), the United Nations Children’s Fund (UNICEF), International Council for the Control of Iodine Deficiency (ICCIDD); urinary iodine was determined in microplates by a modification of the Sandell-Kolthoff reaction. The Chi-square test was used to compare prevalences, and the Chi-square test for trend was employed to assess the trend of goiter prevalence and urine iodine levels by age and economic-social areas. Results: 1800 pupils from 8 to 10 years old including 900 males and 900 females were examined and 300 among them were tested for the urinary iodine concentration (UIC). The prevalence of goiter among schoolchildren was 6.6%. The prevalence of goiter tended to increase in areas with disadvantaged conditions, among which the urban areas occupied the lowest prevalence (5%) while the mountainous areas and Midland took the highest (8.8%) (the p-value of 0.0193). The median UIC of the study group was 159.9 µg/L; the 25th and 75th percentile value was 103 µg/L and 230.2 µg/L, respectively. Conclusion: According to the WHO/UNICEF/ICCIDD classification, the goiter prevalence indicated that some regions of Binh Dinh province appeared to be slightly affected by iodine deficiency. These have characterized an important public health challenge, highlighting the need to eliminate iodine deficiency disorders in these areas.

    Citation: Truong Quang Dat, Le Nguyen Huong Giang, Pham Van Bao, Nguyen Thi Hong Tuyen. Prevalence of goiter among children aged 8–10 in Binh Dinh province, Vietnam in 2016–2017[J]. AIMS Public Health, 2019, 6(2): 184-194. doi: 10.3934/publichealth.2019.2.184

    Related Papers:

    [1] Truong Quang Dat, Le Nguyen Huong Giang, Nguyen Thi Tuong Loan, Vo Van Toan . The prevalence of malnutrition based on anthropometry among primary schoolchildren in Binh Dinh province, Vietnam in 2016. AIMS Public Health, 2018, 5(3): 203-216. doi: 10.3934/publichealth.2018.3.203
    [2] Tran Thi Hai, Saptawati Bardosono, Luh Ade Ari Wiradnyani, Le Thi Hop, Hoang T. Duc Ngan, Huynh Nam Phuong . The optimal mid-upper-arm circumference cutoffs to screen severe acute malnutrition in Vietnamese children. AIMS Public Health, 2020, 7(1): 188-196. doi: 10.3934/publichealth.2020016
    [3] Nguyen Thanh Ha, Do Thi Hanh Trang, Le Thi Thu Ha . Is obesity associated with decreased health-related quality of life in school-age children?—Results from a survey in Vietnam. AIMS Public Health, 2018, 5(4): 338-351. doi: 10.3934/publichealth.2018.4.338
    [4] Talal Alharazi, Omar AA Bamaga, Nazeh Al-Abd, Jerold C Alcantara . Intestinal parasitic infection: prevalence, knowledge, attitude, and practices among schoolchildren in an urban area of Taiz city, Yemen. AIMS Public Health, 2020, 7(4): 769-777. doi: 10.3934/publichealth.2020059
    [5] Duong Minh Duc, Le Thi Vui, Hoang Ngoc Son, Hoang Van Minh . Smoking Initiation and Cessation among Youths in Vietnam: A Longitudinal Study Using the Chi Linh Demographic—Epidemiological Surveillance System (CHILILAB DESS). AIMS Public Health, 2017, 4(1): 1-18. doi: 10.3934/publichealth.2017.1.1
    [6] Hoang Van Minh, Vu Quynh Mai, Tran Tuan Anh, Nguyen Thuy Duyen, Le Danh Tuyen, Truong Tuyet Mai, Huynh Nam Phuong, Thahira Shireen Mustafa, Friday Nwaigwe, Do Hong Phuong . The cost of implementing Vietnam’s national plan of action for nutrition for 2017–2020. AIMS Public Health, 2019, 6(3): 276-290. doi: 10.3934/publichealth.2019.3.276
    [7] Nguyen Tuan Hung, Vu Thu Trang, Trinh Van Tung, Nguyen Xuan Long, Ha Thi Thu, Tran Song Giang, Tran Hoang Thi Diem Ngoc, Vu Thi Thanh Mai, Nguyen Kim Oanh, Nguyen Thi Phuong, Nguyen Hang Nguyet Van, Nguyen Hanh Dung, Pham Tien Nam . COVID-19-related music-video-watching among the Vietnamese population: lessons on health education. AIMS Public Health, 2021, 8(3): 428-438. doi: 10.3934/publichealth.2021033
    [8] Nguyen Thi Hong Tuyen, Truong Quang Dat, Huynh Thi Hong Nhung . Prevalence of depressive symptoms and its related factors among students at Tra Vinh University, Vietnam in 2018. AIMS Public Health, 2019, 6(3): 307-319. doi: 10.3934/publichealth.2019.3.307
    [9] Erivelton Fernandes França, Michel Monteiro Macedo, Fernando Francisco Pazello Mafra, Gabrielle Mitico Miyake, Romildo Torres da Silva, Tania Regina de França, Thyago Ribeiro dos Santos, João Pedro da Silva Junior, Victor Keihan Rodrigues Matsudo, Nelson Morini Junior, Eduardo Natali Della Valentina, Fábio Dupart Nascimento, Rodrigo Álvaro Brandão Lopes Martins . Back pain in elementary schoolchildren is related to screen habits. AIMS Public Health, 2020, 7(3): 562-573. doi: 10.3934/publichealth.2020045
    [10] Le Thi Thanh Huong, Tran Thi Tuyet Hanh, Luu Quoc Toan, Do Thi Hanh Trang, Nguyen Thuy Quynh, Nguyen Quynh Anh, Tran Khanh Long, Stanley Fenwick, Nguyen Thanh Ha, Bruce H Alexander . Training need assessment for a master training program in Environmental Health program in Vietnam. AIMS Public Health, 2020, 7(1): 197-212. doi: 10.3934/publichealth.2020017
  • Objective: The study was conducted to estimate the goiter prevalence, and the median urine iodine concentrations among schoolchildren aged 8–10 in Binh Dinh province, Vietnam. Methods: A school-based cross-sectional survey was carried out from May 2016 to May 2017. A multistage, proportional-to-population-size sampling method with 30 clusters was used. The children were examined by palpation for the presence or absence of goiter based on the criteria of the World Health Organization (WHO), the United Nations Children’s Fund (UNICEF), International Council for the Control of Iodine Deficiency (ICCIDD); urinary iodine was determined in microplates by a modification of the Sandell-Kolthoff reaction. The Chi-square test was used to compare prevalences, and the Chi-square test for trend was employed to assess the trend of goiter prevalence and urine iodine levels by age and economic-social areas. Results: 1800 pupils from 8 to 10 years old including 900 males and 900 females were examined and 300 among them were tested for the urinary iodine concentration (UIC). The prevalence of goiter among schoolchildren was 6.6%. The prevalence of goiter tended to increase in areas with disadvantaged conditions, among which the urban areas occupied the lowest prevalence (5%) while the mountainous areas and Midland took the highest (8.8%) (the p-value of 0.0193). The median UIC of the study group was 159.9 µg/L; the 25th and 75th percentile value was 103 µg/L and 230.2 µg/L, respectively. Conclusion: According to the WHO/UNICEF/ICCIDD classification, the goiter prevalence indicated that some regions of Binh Dinh province appeared to be slightly affected by iodine deficiency. These have characterized an important public health challenge, highlighting the need to eliminate iodine deficiency disorders in these areas.


    Iodine is one of the vital micronutrient components of the thyroid hormones (thyroxin and triiodothyronine), necessary for normal growth, development, and metabolism during the fetus period, infancy and throughout life [1]. When iodine requirements are not met, thyroid hormone synthesis is impaired, resulting in hypothyroidism and a series of functional and developmental abnormalities grouped under the heading of “Iodine Deficiency Disorders (IDDs)”. Depending on stages of life, the deficiency of iodine has different effects. Iodine deficiency in the fetal stage often causes brain damage such as cretinism, edema and many other harms affecting intellectual, physical, and psychological development. In children and adolescents, the most common manifestation is goiter [2].

    Iodine deficiency is a major public health problem for populations throughout the world, particularly for pregnant women and infant children [3]. Globally from 1993–2003, the total goiter prevalence in the general population is estimated to be 15.8%, varying from 4.7% in America to 15.4% in South-East-Asia and 37.3% in Eastern Mediterranean [4].

    In 1993, WHO and UNICEF recommended universal salt iodization as the main strategy to achieve elimination of IDDs [5]. This strategy has been implementing in most countries where iodine deficiency is a public health problem. Globally, it is estimated that 75% of households in the world consumed adequately iodized salt [6]. An assessment of global data in 2012 concluded that the number of iodine-deficient countries decreased from 54 to 32 and the number of countries with adequate iodine intake increased from 67 to 105 between 2003 and 2011 as a result of salt iodization [7].

    In 1994, the National Iodine Deficiency Disorders Control program was designated as a national priority program in Vietnam, with special funds and oversight [8]. The 2005/2006 national survey indicated that the program enabled Vietnam to achieve the goal of universal salt iodization and eliminate IDDs within a decade in Vietnam. The household coverage of adequately iodized salt increased from 24.9% in 1994 to 93% in 2005/2006, reaching the international goal of over 90%. As a result, the median UIC in children of this age group increased from 14 µg/L in 1998 to 130 µg/L in 2005/2006. The prevalence of goiter among school-age children fell from 12.9% in 1998 to 3.5% in 2005/2006; the global and national targets were to achieve a total goiter prevalence of less than 5% [9]. As the targets had been met, the Government of Vietnam downgraded the National Iodine Deficiency Disorders Control program to be a routine one. As a result of these programmatic changes, there was a dramatic decline in iodized salt coverage and urinary iodine levels to the extent that IDDs had reemerged as a public health problem [10].

    Located in the central coast of Vietnam, Binh Dinh has the population of 1,510,350 people in which there are about 122,800 primary schoolchildren all over the province. Binh Dinh's economic development is slow, and the province receives annual subsidies from the national budget [11]. Iodine Deficiency Disorders in Binh Dinh were eliminated in 2005, but the maintaining of this achievement is limited and unsustainable. A survey carried out in 2011 showed that Binh Dinh province had achieved two basic results, namely 92% of households were estimated to consume adequately iodized salt and the prevalence of goiter among children was 3.91%, but the median UIC was low at 93.1 µg/L [12]. Since then, there have not appeared any studies in the whole province for IDDs. We believed that the identification of some indicators of IDDs in Binh Dinh is necessary to know whether iodine deficiency is returning as mentioned in some recent reports. Thus, the present study was designed to identify the goiter prevalence and urinary iodine levels among 8–10-year-old schoolchildren in Binh Dinh Province in 2016–2017.

    This was a cross-sectional study based on schools. It was conducted in three socio-economic areas of Binh Dinh province including: (1) urban, (2) coastal plain, and (3) mountainous area and Midland in which the last is the most disadvantageous socio-economic region according to the socio-economic classification of the administrative units directly under the province. The last has the highest percentage of poor households and the lowest per capita incomes [11]. The study was carried out on 8-10-year-old children from May 2016 to May 2017. Participants with thyroid cancer and other thyroid diseases such as infectious thyroiditis, lymphadenopathy were excluded from the study.

    Sample sizes were calculated using the following formula: n=Z21α/2p(1p)d2; Where: n is the smallest sample size to be achieved; p is the expected prevalence; d is the absolute error; Z1α/2 is Z statistic for a confidence level of 95%.

    Sample size for investigating urinary iodine levels: p is the expected prevalence of the mean urine iodine level below 100 µg/L (prevalence of children at the mean urine iodine level below 100 µg/L was 75% [12]; d was the absolute error: 5%. The final sample size was 300 after rounding up.

    Sample size for investigating the goiter prevalence: p is the expected prevalence: 5% (a goiter prevalence of 5% or more in schoolchildren is an indication of iodine deficiency in a population) [13]; d is the absolute error: 2.5%. The sample size was adjusted to taking account of the stratification into two genders and three age groups. The final sample size was 1800 after rounding up.

    In this study, a total of 1800 children (with 900 males and 900 females) ranging from 8 to 10 years old was surveyed to determine the goiter prevalence and 300 students were tested to determine median urinary iodine levels in all socio-economic regions of Binh Dinh province. Sample sizes were met for analysis.

    Sampling method: Multi stage sampling was employed. Stage 1: There are 159 commune-level administrative units (communes, wards, townships) under Binh Dinh Povince as clusters in a sample frame [11]. Thirty clusters were selected using the Probability Proportionate to Size method. One primary school among each cluster was chosen at random. Stage 2: Based on the number of pupils aged 8 to 10 in each class, each cluster of 30 boys and 30 girls (20 students per each age group) was chosen to examine goiter, and then 10 students in every 60 students selected were randomly chosen to collect urine samples to test urinary iodine concentration.

    Two specialist doctors (for the physical examination) and four nurses were recruited to collect the data.

    Variable in goiter was classified using the following categories: grade 0, grade 1 and grade 2. A physical examination was performed at school to identify the presence and absence of goiter in accordance with the criteria of the WHO/UNICEF/ICCIDD [13]. Enlargement of the thyroid gland was assessed by clinical examination, and the goiter was graded as follows: Grade 0: Thyroid gland is neither palpable nor visible/no goiter. Grade 1: A mass in the neck that is consistent with an enlarged thyroid that is palpable but not visible when the neck is in normal position. The mass moves upwards with deglutition/goiter palpable but not visible. Grade 2: A swelling in the neck that is visible when the neck is in normal position and is consistent with enlarged thyroid when the neck is palpated/goiter visible and palpable.

    Take urine samples (each sample of 10 mL) to quantify the UIC. The total number of samples was 300. After being collected, urine samples are kept in a closed test tube and refrigerated in an insulated foam container. They were then transported to the laboratory of Nutrition Center of Ho Chi Minh City, which is the leading nutrition center authorized by the Ministry of Health of Vietnam to quantify urinary iodine concentrations in the program of iodine deficiency prevention in Vietnam. Urinary iodine concentrations were determined in micro plates by a modification of the Sandell-Kolthoff reaction. The laboratory clearly defined internal quality control procedures in place, and was opened to external audit. The level of the UIC was classified according to the guidelines of the WHO/UNICEF/ICCIDD [13]. The level of the median UIC lower than 20 µg/L, between 20 µg/L and 49 µg/L, between 50 µg/L, and 99 µg/L indicates the status of iodine deficiency corresponding to a severe, moderate and mild level. The level of the median UIC between 100 µg/L and 199 µg/L shows adequate iodine nutrition; between 200 µg/L and 299 µg/L means the iodine intake is more than necessary, and more than 300 µg/L means excess iodine intake.

    After cleaning, data were entered into Epi Data 3.1 software and transferred to Stata 10.0 software for data analysis. Absolute values and percentages were used to describe categorical variables. The median, the 25th and 75th percentile values were employed to describe the UIC. The Chi-square test for trend [14] was used to assess the trend of the prevalence of goiter by age and socio-economic areas. Then the Chi-square test was utilized to compare the prevalence in groups. The nonparametric tests (Kruskal-Wallis and Mann-Whitney) to compare the median urine iodine distribution were employed. A p-value < 0.05 was considered significant.

    The study was approved by Binh Dinh Department of Science and Technology. The research was allowed by Education and Training Committee Division in the selected districts and city, and the primary schools at the research sites. All schoolchildren voluntarily participated. The data collected were kept confidential. Students with goiter were advised on treatment. The study results were to be disseminated to relevant stakeholders in order to inform policies and interventions to improve the iodine deficiency status of schoolchildren and paved the way for future studies.

    The data set included the records of 1,800 children (with 900 males and 900 females) aged 8 to 10, among which the Kinh was 93.2% and other ethnic minority groups were 6.8%. Gender distribution for each age group was similar. The size of the samples varied from 840 for the coastal plain area, 540 for the urban area to 420 for the mountainous area and Midland. Similarly, sample sizes by age group from 8 to 10 were 600 for each age group.

    As shown in Table 1, children with no goiter, grade 1 and 2 of goiter were 93.4%, 6.3% (95% CI: 5.5–7.8%) and 0.3%, respectively. There was a significant difference between the prevalence of goiter 1 (95% CI: 5.2–7.4%) and goiter 2 (95% CI: 0.1–0.6%).

    Table 1.  The total prevalence of goiter among 8–10-year-old children in Binh Dinh, Vietnam.
    Goiter forms n = 1800 % 95% CI
    No goiter 1681 93.4 92.2–94.5
    Goiter 119 6.6 5.5–7.8
    Grade 1 of goiter 113 6.3 5.27.4
    Grade 2 of goiter 6 0.3 0.10.6

     | Show Table
    DownLoad: CSV

    Table 2 showed the goiter prevalence according to gender, age groups, ethnic, socio-economic areas. The goiter prevalence among female students was 8.7%, which roughly doubled—the prevalence among male students (p = 0.0004). The goiter prevalence varied across ages, in which the prevalence among 9-year-old pupils was 9.2%, which was two times higher than that of 8-year-old students (p < 0.05), however, there was no evidence of a trend in the prevalence across age groups (p = 0.0633). The goiter prevalence had a tendency to increase; the lowest was in the urban areas (5%), and the highest was in the mountainous areas and Midland (8.8%) with a p-value of 0.0193. Nevertheless, the distribution of goiter through socio-economic regions of Binh Dinh province was not different (p > 0.05). The prevalence of goiter among the Kinh (6.3%) was lower than that among other ethnic groups (11.5%) with a p-value of 0.025.

    Urinary iodine concentration among schoolchildren was presented in Table 3. There were 300 urine samples of students tested, and the median UIC was 159.9 µg/L; the 25th percentile value was 103 µg/L and the 75th percentile value was 230.2 µg/L.

    The percentage of urine iodine levels among schoolchildren by socio-economic areas was shown in Table 4. The percentage of the median UIC at the recommended level by the WHO/UNICEF/ICCIDD (100–199 µg/L) in the mountainous area and Midland, the coastal plain area and the urban was 41.1%, 38.6% and 47.1%, respectively but the levels were not associated with socio-economic areas (p = 0.4916).

    Table 2.  The goiter prevalence among 8 to 10-year-old children in Binh Dinh, Vietnam according to sex, age, socio-economic areas and ethnic groups.
    Variables Categories Total Goiter
    p
    n % 95% CI
    Genders Males 900 41 4.6 3.2–5.9 0.0004
    Females 900 78 8.7 6.8–10.5
    Age 8 years old 600 24 4.0 2.4–5.6 0.0633
    9 years old 600 55 9.2 6.9–11.5
    10 years old 600 40 6.7 4.8–8.7
    Socio-economic areas The mountainous area and Midland 420 37 8.8 6.1–11.5 0.0193
    The coastal plain area 840 55 6.5 4.9–8.2
    The urban area 540 27 5.0 3.2–6.8
    Ethnic groups The Kinh 1,678 105 6.3 5.1–7.4 0.0250
    Others 122 14 11.5 5.8–17.1

    Note: For gender and ethnic, the p is the probability value obtained in the Chi-square test for comparisons of the goiter prevalence between two genders, and between the Kinh and ethnic groups. For ages, socio-economic areas, the p is the probability value obtained in the nonparametric test for trends of the goiter prevalence across schoolchildren ages, and three areas.

     | Show Table
    DownLoad: CSV
    Table 3.  The urine iodine concentration among 8–10-year-old children in Binh Dinh, Vietnam according to sex, age, socio-economic areas and ethnic.
    Variables Categories n Urine iodine concentration (µg/L)
    p
    25th percentile 75th percentile Median
    Genders Males 148 106.2 244.9 168.5 0.260
    Females 152 99.2 227.3 153.5
    Age 8 years old 97 113.1 232.9 156.5 0.788
    9 years old 102 101.2 224.6 159.4
    10 years old 101 98.6 246.4 164.9
    Socio-economic areas The mountainous area and Midland 70 113.1 221.8 159.5 0.338
    The coastal plains area 140 95.8 222.4 157.7
    The urban area 90 110.9 251.6 165.2
    Ethnic groups The Kinh 277 107.1 239.6 163.7 0.008
    Others 23 93.1 203.3 107.0
    Total 300 103.0 230.2 159.9

    Note: The p is the probability value obtained in the nonparametric test for differences of the median UIC between genders, among age, between ethnic groups and among socio-economic areas.

     | Show Table
    DownLoad: CSV

    Table 5 showed the goiter prevalence by the median UIC. The goiter prevalence corresponding to the median urinary iodine level under 100 µg/L (iodine deficiency), from 100 to 199 µg/L, and more was 11.3%, 9.7% and 6.7%, respectively but the p-value > 0.05. The data set also showed that there was no evidence of a tendency for the goiter prevalence to go up when urinary iodine levels went down (p = 0.2796).

    Table 4.  The percentage of urinary iodine levels by socio-economic areas among 8–10-year-old children in Binh Dinh, Vietnam.
    Urinary iodine levels Median UIC Total The urban area (nu = 90) The coastal plains area (nc = 140) The mountainous area and midland (nm = 70) p

    No (%) No (%) No (%) No (%)
    < 100 µg/L 75.7 µg/L 71(23.7) 18(20.0) 39(27.9) 14(20.0) 0.8912
    100–199 µg/L 150.9 µg/L 124(41.3) 37(41.1) 54(38.6) 33(47.1) 0.4916
    ≥ 200 µg/L 279.2 µg/L 105(35.0) 35(38.9) 47(33.6) 23(32.9) 0.4053

    Note: The p is the probability value obtained in the nonparametric test for trends of urine iodine levels across the socio-economic areas.

     | Show Table
    DownLoad: CSV
    Table 5.  The percentage of goiter by urinary iodine levels among 8–10-year-old children in Binh Dinh, Vietnam.
    Urinary iodine levels Total Median UIC Goiter
    p
    n % 95% CI
    < 100 µg/L 71 75.7 µg/L 8 11.3 3.9–18.6 0.2796
    100–199 µg/L 124 150.9 µg/L 12 9.7 4.5–14.9
    ≥ 200 µg/L 115 279.2 µg/L 7 6.7 1.7–10.6

    Note: The p is the probability value obtained in the nonparametric test for trends of goiter prevalence across of urine iodine levels.

     | Show Table
    DownLoad: CSV

    The three most important indicators of impact used in IDDs surveillance are the goiter prevalence, the median UIC, and thyroid function tests [13]. Urinary iodine is the most useful indicator because it is reflective of the current intake of iodine in the diet [15]. To evaluate the severity of IDDs in a region, the most widely accepted marker is the goiter prevalence in schoolchildren. They are the preferred group as it is usually easily accessible. On the basis of the goiter prevalence, the WHO/UNICEF/ICCIDD recommended the criteria for understanding the severity of IDDs as a public health problem in a region. In the study, we observed only the goiter prevalence and the UIC among children aged 8–10.

    The present study showed that the overall prevalence of goiter among children from 8 to 10 years old in the study area was 6.6% (95% CI: 5.5–7.8%) in which grade 1 was 6.3% and grade 2 was 0.3%, and it was slightly higher than the cut-off point of the WHO/UNICEF/ICCIDD classification (5%) [13]. However, the prevalence of goiter (6.6%) can be seen as a warning sign for the trend of increasing the goiter prevalence in the study population. This prevalence was in agreement with results reported from a study in Binh Duong, Vietnam in which the general prevalence of goiter was 6.8% [16]. The prevalence of goiter in Binh Dinh is lower than that of the whole country as reported by the National Endocrinology Hospital (9.8%) [17] but higher than those in Binh Dinh over the previous years (3.91%) [12], in Nam Giang district, Quang Nam province, Vietnam (3.2%) [18]. This prevalence in the current study is much lower than those in the studies done in some countries. For example, the goiter prevalence was found to be 62.1% in northeast Ethiopia [19], 77% in Khoramabad, Iran [20], while the prevalence in Shendi, northern Sudan and Belgaum city, India was 14.6% [21] and 16.7% [22], respectively. The reason for the above-mentioned difference may be due to the fact that our study was undertaken after the universal salt iodization launched in Binh Dinh, Vietnam in 1993 [12].

    The prevalence of goiter among male students (4.6%) was much lower than that among female students (8.7%). This finding is almost consistent with earlier reports [22][25]. This may be due to differences in the developmental stages between males and females. That is, females start puberty earlier than males and require more iodine so girls could be more sensitive to iodine deficiency than boys. In contrast, some studies did not document this difference between boys and girls [18],[26],[27].

    In this study, the goiter prevalence ranged from 4% among 8-year-old students to 9.2% among 9-year-old ones. The prevalence of goiter is significantly higher among participants aged 9 than participants aged 8 but the data did not show a trend of the goiter prevalence across age groups. Some studies noted that there is no association between age and goiter [16],[18].

    This study also revealed that the goiter prevalence in the urban areas was 5%, but the prevalence tended to go up in the mountainous areas and Midland (8.8%). The high prevalence of goiter in the areas reflects the limited intake of iodine in children in this area. There are several reasons for the highest prevalence of goiter in the mountainous areas and Midland. Soil in these two areas having a limited amount of iodine is the first reason [11],[13],[28]. Another one is that the access to iodized salt of the population in these regions may be inadequate because the place is far from the center of the province, so the transportation, the sale network of iodized salt are very difficult [11],[12]. The proportion of the Kinh (6.3%) suffering from goiter is only about half in comparison with that of other ethnic minority groups (11.5%). This difference can be partly explained by the fact that other ethnic minority groups live in remote and mountainous areas as mentioned above. A recent study on nutrition of children from 6 to 10 years old in Binh Dinh province in 2016 also noted that the malnutrition status among children in the mountainous areas and Midland was the highest among the three social-economic regions of the province [29]. It is possible that this condition is accompanied by a lack of micronutrient deficiency, including iodine.

    The median UIC is used as a valuable indicator for the assessment of IDDs in a region. In children, the median UIC of between 100 µg/L and 299 µg/L and not more than 20% of samples below 50 µg/L defines a population which has no iodine deficiency [13]. In the current study, the median UIC is 159.9 µg/L and only 6.7% of samples below 50 µg/L. Therefore, the studied region is not biochemically iodine deficient at present. The median UIC is also much higher than 93.1 µg/L which was the result of the 2011 survey in Binh Dinh [12]. Authors of other studies from Vietnam or other countries indicated different median urinary iodine levels, which pointed to either a deficiency or no deficiency for certain populations, in their areas. Studies in India, Nepal, and Cambodia showed that median UIC was 96 µg/L [25], 93.5 µg/L [30], and 63 µg/L [31], respectively, all of which were below the recommended levels [13]. A study in China documented a 173.3 µg/L median urinary iodine level [32] while a study in Saudi Arabia reported 421 µg/L [33]. Some studies also showed adverse effects of excessive iodine intake [13],[34],[35]. This finding highlights the importance of monitoring the iodine concentration in local food salt and other sources, and not only the median UIC and the prevalence of goiter among schoolchildren.

    The median UIC was recorded with no difference between males and females, among age groups and socio-economic regions in the study. This result is consistent with the one in a study in Binh Duong province, Vietnam in which there was no difference in the median UIC by to age and gender [16]. However, the median UIC is significantly higher among the Kinh (163.7 µg/L) than that among other ethnic groups (107 µg/L) but the urine samples in the ethnic groups were relatively small. This difference is in-line with the difference mentioned in the goiter prevalence between the Kinh and other ethnic groups.

    In our study, the total goiter prevalence was 6.6%; it was slightly higher than the recommended level by the WHO/UNICEF/ICCIDD, but with the data set recorded in the study, we did not have evidence of the relationship between urinary iodine levels and the goiter prevalence (p = 0.2796). It is reported that thyroid size may not return to normal for months or years after the correction of iodine deficiency [13]. Some studies in different countries also did not find the association between urinary iodine levels and the goiter prevalence [25],[36].

    Study limitations: The study has some limitations. Firstly, the determination of goiter based only on palpation (without using ultrasonography) may not be objective and depends on the skill of the physicians. Secondly, the proportion of households with iodized salt was not provided in this study. Thirdly, there are certainly some other factors related to the goiter prevalence and urinary iodine levels in Binh Dinh but not yet clarified in this study.

    It is quite clear that the population is not biochemically iodine deficient at present, and the overall prevalence of goiter is found to be around the recommended level by the WHO/UNICEF/ICCIDD. However, the goiter prevalence in mountainous areas and Midland was a warning sign of the public health problem. These have characterized an important public health challenge, highlighting the need to eliminate IDDs in these areas.


    Acknowledgments



    The research team sincerely thanks Binh Dinh Province People's Committee, the teachers and pupils at the research sites for their assistance in the implementation of this work.
    Financial support and sponsorship: Binh Dinh Province People's Committee.

    Conflict of interest



    All authors declare no conflicts of interest in this paper.

    [1] Gunnarsdottir I, Dahl L (2012) Iodine intake in human nutrition: a systematic literature review. Food Nutr Res 56.
    [2] World Health Organization (2004) Iodine status worldwide: WHO Global Database on iodine deficiency. World Health Organization, Switzerland.
    [3] World Health Organization, Micronutrient deficiencies. Available from: https://www.who.int/nutrition/topics/idd/en/.
    [4] Andersson M, Takkouche B, Egli I, et al. (2005) Current global iodine status and progress over the last decade towards the elimination of iodine deficiency. Bull World Health Organ 83: 518–525.
    [5] UNICEF–WHO Joint Committee on Health Policy (1994) World Summit for Children-Mid Decade Goal: Iodine Deficiency Disorders. Geneva, United Nations Children's Fund, World Health Organization; (JCHPSS/94/2.7).
    [6] United Nations Children's Fund (2013) State of the World's Children 2014: Every Child Counts. UNICEF. Available from: http://data.unicef.org/nutrition/iodine.html.
    [7] Andersson M, Karumbunathan V, Zimmermann MB (2012) Global iodine status in 2011 and trends over the past decade. J Nutr 142: 744–750. doi: 10.3945/jn.111.149393
    [8] Prime Minister of Viet Nam (1994) Decision No. 481/TTg of the Prime Minister dated September 1994 on organizing and calling upon all people to buy and use iodized salt.
    [9] Hospital of Endocrinology (2012) Report on Iodine Deficiency Disorder Preventative Activities in Viet Nam.
    [10] Codling K, Quang NV, Phong L, et al (2015) The Rise and Fall of Universal Salt Iodization in Vietnam: Lessons Learned for Designing Sustainable Food Fortification Programs with a Public Health Impact. Food Nutr Bull 36: 441–454. doi: 10.1177/0379572115616039
    [11] Binh Dinh Statistics Office (2016) Binh Dinh Statistical Yearbook 2015, Statistical publishing house 2016.
    [12] Binh Dinh Center for Prevention of Malaria and Endocrine Diseases (2016) Report on the program to prevent iodine deficiency disorders in 2011–2015.
    [13] WHO/UNICEF/ICCIDD (2007) Assessment of iodine deficiency disorders and monitoring their elimination. A Guide for Programme Managers 2007.
    [14] Cambell MJ, Swinsco TDV (2009) Statistics at square one,11th ed. UK: John Wiley & Sons Ltd, 86–95.
    [15] DeMaeyer EM, Lowenstein FW, Thilly CH (1979) The control of endemic goiter, World Health Organization.
    [16] Luc DL (2007) Survey of goiter among students in the last 3 grades of primary school in Dau Tieng district in Binh Duong province in 2005. Full report on scientific topics of the 3rd National Scientific Conference on Endocrinology and Metabolism, Medical Publishing House, Hanoi, 190–199.
    [17] Ta VB, Hoang KH (2007) Study on evaluating the rate of goiter and median urinary iodine in 8 to 10-year-old students in 7 ecological regions in Vietnam in 2005. Report on the full text of scientific projects of the 3rd National Scientific Conference on Endocrinology and Metabolism. Medical Publishing House, 165–175.
    [18] Hoang S (2009) Situation and some factors related to simple goiter prevalence of pupils aged from 8 to 12 in Nam Giang District, Quang Nam Province. Hue Univ J Sci 55: 149–156.
    [19] Tigabu EK, Bekele B, Dachew BA (2017) Prevalence of goiter and associated factors among schoolchildren in northeast Ethiopia. Epidemiol Health 39: e2017055. doi: 10.4178/epih.e2017055
    [20] Mardani M, Gholaami F, Rezapour P, et al. (2015) The Prevalence of Endemic Goiter and Its Relationship to Urine Iodine in Primary School Age Children in Khoramabad. J Health Sci Surveill Sys 3: 71–75.
    [21] Ahmed FBM, Ahmed IEBM (2015) Goiter Incidence Among Basic Schools Children in Shendi Area-Northern Sudan. Sci J Clin Med 4: 117–120. doi: 10.11648/j.sjcm.20150406.11
    [22] Kamath R, Bhat V, Rao RS, et al. (2009) Prevalence of goitre among school children in Belgaum district. Indian J Pediatr 76: 825–828. doi: 10.1007/s12098-009-0101-6
    [23] Nguyen TH, Nguyen TD (2002) Endemic goiter status in one district of Bac Bo Delta. Vietnam J Physiol 6: 17–22.
    [24] Zein AZ, Al-Haithamy S, Obadi Q, et al. (2009) The epidemiology of iodine deficiency disorders in Yemen. Public Health Nutr 3: 245–252.
    [25] Chandra AK, Bhattacharjee A, Malik T, et al. (2008) Goiter prevalence and iodine nutritional status of school Children in a Sub-Himalyan Tarai region of Eastern Uttar Pradesh. India Pediatr 45: 469–474.
    [26] Sharma U, Sharma JP, Sharma A, et al. (2015) Prevalence of goitre among school going children in urban area of Dehradun. Int J Res Med Sci 3: 198–200.
    [27] Gupta RK, Langer B, Raina KS, et al. (2016) Goiter prevalence in school-going children: A cross-sectional study in two border districts of sub-Himalayan Jammu and Kashmir. J Family Med Prim Care 5: 825–828. doi: 10.4103/2249-4863.201150
    [28] Delange F (1994) The disorders induced by iodine deficiency. Thyroid 4: 107–128. doi: 10.1089/thy.1994.4.107
    [29] Truong QD, Le NHG, Nguyen TTL, et al. (2018) The prevalence of malnutrition based on anthropometry among primary schoolchildren in Binh Dinh province, Vietnam in 2016. AIMS Public Health 5: 203–216. doi: 10.3934/publichealth.2018.3.203
    [30] Jimba M, Aitken IW, Joshi AB, et al. (2006) A challenge for monitoring iodine deficiency disorders in rural Nepal. Trop Doct 37:106–107.
    [31] Laillou A, Sophonneary P, Kuong K, et al. (2016) Low Urinary Iodine Concentration among Mothers and Children in Cambodia. Nutrients 8: 172. doi: 10.3390/nu8040172
    [32] Zou Y, Luo X, Ding G, et al. (2014) An assessment of iodine nutritional status and thyroid hormone levels in children aged 8–10 year living in Zhejiang province, China: a cross-sectional study. Eur J Pediatr 173: 929–934. doi: 10.1007/s00431-014-2273-y
    [33] Alsanosy RM, Gaffar AM, Khalafalla HE, et al. (2012) Current iodine nutrition status and progress toward elimination of iodine deficiency disorders in Jazan, Saudi Arabia. BMC Public Health 12: 1006. doi: 10.1186/1471-2458-12-1006
    [34] Leung AM, Braverman LE (2014) Consequences of excess iodine. Nat Rev Endocrinol 10: 136–142. doi: 10.1038/nrendo.2013.251
    [35] Katagiri R, Yuan XY, Kobayashi S, et al. (2017) Effect of excess iodine intake on thyroid diseases in different populations: A systematic review and meta-analyses including observational studies. PLoS One 12: e0173722. doi: 10.1371/journal.pone.0173722
    [36] Manjunath B, Suman G, Hemanth T, et al. (2016) Prevalence and factors associated with goiter among 6–12-year-old children in a Rural area of Karnataka in South India. Biol Trace Elem Res 69: 22–26.
  • This article has been cited by:

    1. Peng Ning, Qian Ren, Di Teng, Zexin Zhang, Xuemei lv, Shuyou Meng, Xiaoguang Shi, Zhe Lou, Changhao Wu, Puxu Yang, Wenqian Zhang, Lingli Zhou, Yingying Luo, Zeding Zhuoma, Lihui Yang, Weiping Teng, Current Iodine Nutrition Status and Prevalence of Thyroid Disorders in Tibetan Adults in an Oxygen-Deficient Plateau, Tibet, China: A Population-Based Study, 2020, 30, 1050-7256, 759, 10.1089/thy.2019.0669
  • Reader Comments
  • © 2019 the Author(s), licensee AIMS Press. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0)
通讯作者: 陈斌, bchen63@163.com
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索

Metrics

Article views(5943) PDF downloads(1503) Cited by(1)

Figures and Tables

Tables(5)

/

DownLoad:  Full-Size Img  PowerPoint
Return
Return

Catalog