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International Journal of Environmental Research and Public Health logoLink to International Journal of Environmental Research and Public Health
. 2018 Mar 12;15(3):500. doi: 10.3390/ijerph15030500

Hair as a Biomarker of Long Term Mercury Exposure in Brazilian Amazon: A Systematic Review

Nathália Santos Serrão de Castro 1,*, Marcelo de Oliveira Lima 2
PMCID: PMC5877045  PMID: 29534534

Abstract

Many studies have assessed mercury (Hg) exposure in the Amazonian population. This article performs a literature search of the studies that used hair as a biomarker of Hg exposure in the Brazilian Amazonian population. The search covered the period from 1996 to 2016 and included articles which matched the following criteria: (1) articles related to Hg exposure into Brazilian Amazon; (2) articles that used hair as a biomarker of Hg exposure; (3) articles that used analytical tools to measure the Hg content on hair and (4) articles that presented arithmetic mean and/or minimum and maximum values of Hg. 36 studies were selected. The findings show that most of the studies were performed along margins of important rivers, such as Negro, Tapajós and Madeira. All the population presented mean levels of Hg on hair above 6 µg g−1 and general population, adults, not determined and men presented levels of Hg on hair above 10 µg g−1. The results show that most of the studies were performed by Brazilian institutions/researchers and the majority was performed in the State of Pará. The present study identified that Amazonian population has long-term been exposed to Hg. In terms of future perspectives, this study suggests the implementation of a strategic plan for environmental health surveillance in the region in order to promote health and benefit Amazonian population.

Keywords: mercury, methylmercury, Amazon, hair Amazonia

1. Background

The health effects of methylmercury (MeHg) exposure have been investigated since the accident that occurred in Minamata Bay, Japan. The clinical features of MeHg poisoning were classified as acute or chronic, based on the symptoms observed in patients living around the bay in the vicinity of the pollution source (a factory) and in patients living on the coast of the Shiranui Sea; both populations had consumed contaminated fish for almost 20 years [1].

Clinical studies of Japanese patients affected by dietary MeHg poisoning showed that mercury (Hg) had long-term effects on health. The patients from Goshoura Island, an area close to Minamata Bay, who had mean levels of total hair Hg of 37 µg g−1 in 1960 (n = 16) and 2.4 µg g−1 in 2002 (n = 23) showed persistent sensory disorders caused by their past history of MeHg exposure [2,3]. Evaluation of data from a population-based study performed in 1971 at Goshoura showed an increased incidence of neurological signs, such as ataxia (12%), dysarthria (5.9%), and paresthesia of extremities (5.7%) [4]. A study performed at Niigata, a town located along the Agano River that was affected by MeHg poisoning in 1965, showed that even people with chronic exposure to levels of Hg of less than 20 µg g−1 (n = 24) presented neurologic signs associated with MeHg poisoning [5]. Recently, a population-based study in Minamata and neighboring areas identified the association between neurological sign and the development of psychiatric symptoms.

In spite of the findings observed after the Minamata disaster, there is no clear consensus yet about a dose-response relationship between Hg exposure and health effects given that the genetic characteristics of the populations vary, the modes and times of exposure are diverse, and that life-styles and behavior can influence on the toxic effects of Hg exposure [6,7]. However, vulnerable populations (i.e., pregnant women, human fetuses, neonates, and children) are under the potential risks of Hg effects [8,9,10,11].

Analysis of scalp hair has been a valuable method used to assess the Hg exposure of different populations because hair is easy to collect, store, and manipulate [12]. Hair Hg levels strongly correlate with an individual’s dietary intake of MeHg. Moreover, its chemical stability facilitates retrospective studies [13]. However, Hg can be incorporated into hair in other ways, such as the sorption of volatile species (i.e., elemental Hg), and its level can be affected by hair color and growth rates, which are considered to be pre-analytical sources of variation that may cause bias and misleading interpretations [14,15]. In spite of these limitations, the versatility provided by scalp hair for assessing Hg exposure, especially in remote areas, has been valuable to access the Hg exposure in different populations.

In Brazil, many studies had been performed in the Amazonian region and hair has been selected as a biomarker of Hg exposure. The present article performs a systematic review of publications that analyzed Hg on hair of different populations into Brazilian Amazon. The objective of this article is to provide an overview of long-term exposure to Hg into Brazilian Amazon, identify populations under risk of Hg effects and give future perspectives for environmental health surveillance for the region.

2. Methods

This systematic review was registered in PROSPERO (registration number CRD42017056584). The search was performed using the following electronic databases: Pubmed, EBSCO, VHL (Virtual Health Library) and Scielo. Both authors performed independently the virtual search for articles titles and abstract using the search strategy showed in the Table 1. The search covered the studies that were published in the period from 1996 to 2016. The present study followed the following inclusion criteria for articles: (1) articles related to Hg exposure into Brazilian Amazon; (2) articles that used hair as a biomarker of Hg exposure; (3) articles that used analytical tools to measure the Hg content on hair and (4) articles that presented arithmetic mean and/or minimum and maximum values of Hg. As exclusion criteria, the present study followed: (1) review articles of Hg exposure and (2) articles which methodology was not clear, such as sample size, locality and analytical tools. The potential studies were screened and duplicates were removed. Articles not excluded were read by the two authors who extracted in detail the geographic location where the study was performed, sample size and type, the age range and/or mean age of the populations, the first author of the study, the year of the publication, and the arithmetic mean of Hg observed.

Table 1.

Search strategies in electronic database.

Strategy Keywords
#1 Mercury and hair and Amazon
#2 Methylmercury and hair and Amazon
#3 Mercury and Brazil and Amazonia
#4 Mercury and Amazon

The present study classified the type of the studied populations as follows: general population (0 to >60 years old), adult population (>15 years old), children (<15 years old), women, men, indigenous and not determined (nd) when the study did not identify the type and/or the age range of the target population.

According to the type of each population, the data of the mean level of Hg was used in order to determine a weighted average in which the number of individuals studied contributed equally to a final average (Equation (1)).

WA=((X1×I1)+(X2×I2)+(Xn×In))/(ΣI1+I2+In) (1)

where: WA = weighted average; X = arithmetic mean of Hg (µg g−1); I = Number of Individuals.

A cartographic quali-quantitative analysis of the data was performed. The classification of the populations determined for this study were considered for a qualitative evaluation and a quantitative analysis based on the degree of exposure followed the following criteria: lower (less than 2 µg g−1), medium (between 2 and 6 µg g−1) and higher (above 6 µg g−1).

The ArcMap 10.1 software (ESRI, Redlands, CA, USA) was used for georeferencing for studied where the geographic coordinates were not available. The geographic location was matched with the Brazilian Institute of Geography and Statistics (IBGE). The quantitative analysis was evaluated by a “choropleth map” where the differences of Hg exposure according to different populations and regions were shaded: yellow representing populations with low exposure to Hg and red high exposure.

Among the major source of risk of bias of the present study we can cite here:

(1) The period of the study.

The present study searched for studies that were published from 1996 to 2016 (20 years). Thus, the concentration of Hg on hair among the populations can vary, and, thus, the general visualization provided by the cartographic quali-quantitative analysis could not represent the current status.

(2) The methodologies for Hg measurement were not an exclusion or inclusion criteria.

Once the present study considered valid all the methodologies that measured Hg on hair, the results can not reflect a “gold standard” for Hg exposure in Amazon. Instead, all the selected articles were peer reviewed, thus the data could be considered to give an overview of long term Hg exposure in Amazonian population.

3. Results

The database search identified 1283 articles, of which 973 were duplicated and, consequently, removed. The potential 310 articles were screened and 274 of them were removed given that did not attended to some inclusion/exclusion criteria: 169 used other matrices rather than hair, 42 which methodology was not clear, 27 were review articles, 27 were performed in other regions rather than Brazilian Amazon (7 in Peru, 6 in Bolivia, 4 in Ecuador, 3 in French Guiana, 1 in Venezuela, 1 in Suriname, 1 in Peru and Ecuador, 1 Faroe Island, 1 in Colombia, 1 in Africa and 1 in the Northwest of Brazil), 5 were published out of the period of investigation and 4 contained generalist subject about Hg exposure. The study selection is summarized in the flowchart described in Figure 1.

Figure 1.

Figure 1

Study selection flowchart.

In this context, the present study comprised 36 articles, comprising a total of 11,827 individuals (Table 2). According to the year of publication, the articles were published as follows: three in 1998 [16,17,18], two in 1999 [19,20], three in 2000 [21,22,23], two in 2001 [24,25], one in 2002 [26], two in 2003 [27,28], four in 2005 [29,30,31,32], three in 2006 [33,34,35], two in 2007 [36,37], one in 2008 [38], one in 2009 [39], two in 2010 [40,41], three in 2012 [42,43,44], one in 2013 [45], one in 2014 [46], three in 2015 [47,48,49] and two in 2016 [50,51]. Most of the studies (61%) were performed exclusively by Brazilians Institution [16,18,20,21,22,24,28,29,30,31,32,33,34,37,41,42,43,44,45,46,49,51] and others (36%) had been performed in collaboration with them [17,19,23,25,26,35,36,38,39,40,47,48,50]. Only one study (3%) was developed for a foreign country solely [27].

Table 2.

Characteristics of the included studies (n = 36).

Year Author Locality State n Type of Population According to the Author Population Specificity Type of the Population According to the Present Study Range Hg (µg g−1) Mean Hg (µg g−1)
1998 Barbosa A.C. [16] Fresco River PA 28 Kayapo women childbearing women I 0.8–13.7 8.11
Madeira River RO 98 non-indigenous women childbearing women W 2.6–94.7 14.08
Fresco River PA 54 Kayapo children nd I 2.0–20.4 7.30
Madeira River RO 71 non-indigenous children nd C 0.8–44.4 10.82
1998 Kehrig H.A. [17] Balbina Village AM 53 total of population studied nd G nd 6.54
16 children female C 1.3–22.0 7.7
12 children male C 2.5–11.4 5.3
12 adults female A 2.2–15.5 7.4
13 adults male A 1.2–12.2 5.5
1998 Barbosa A.C. [18] Madeira River RO 37 women nd W 2.0–37.2 14.3
37 children 0.5–15 months C 1.4–34.2 9.8
1999 Silva-Forsberg M.C. [19] total (all the populations studied) AM 154 total of population studied 0.2–66 y.o G 5.76–171.24 75.46
Acariquara, Rio Urubaxi 15 nd 0.3–56 y.o G 14.37–146.25 69.18
Tupuruquara, Rio Marie 57 nd 0.2–66 y.o G 10.44–171.24 97.44
Macuna, Rio Uneiuxi 17 nd 0.7–52 y.o G 22.17–129.19 76.75
Perseverança, Rio Negro 23 nd 0.2–65 y.o G 15.77–122.32 65.72
Ilha do Pinto. Rio Negro 12 nd 1.6–37 y.o G 19.02–100.95 69.58
Tapera. Rio Padauari 11 nd 2–59 y.o G 19.20–55.59 37.48
Tapereira. Rio Negro 10 nd 2–47 y.o G 24.94–110.51 69.10
Aldeia Maia. Rio Maia 7 nd 13–40 y.o G 5.76–63.02 28.02
Sitio Velho. Rio Marauia 2 nd 42–62 y.o A 13.93–62.57 38.25
1999 Guimaraes J.R.D. [20] Pracuuba Lake AP 15 fishermen and their family nd nd nd 16.7
Duas Bocas Lake 15 fishermen and their family nd nd nd 28
2000 Hacon S. [21] Alta Floresta MT 75 pregnant women 14–45 y.o W 0.051–8.2 1.12
2000 Santos E.C.O. [22] Brasília Legal PA 220 total of population studied 0–>65 y.o G 0.53–49.99 11.75
30 nd 0–5 y.o C 1.09–20.46 5.84
68 nd 6–10 y.o C 0.70–35.80 13.06
33 nd 11–15 y.o C 1.22–47.00 14.2
12 nd 16–20 y.o A 5.56–19.90 13.39
10 nd 21–25 y.o A 1.40–29.50 15.25
9 nd 26–30 y.o A 3.70–21.40 11.06
16 nd 31–35 y.o A 2.84–37.20 12.57
12 nd 36–40 y.o A 5.0–33.0 14.21
1 nd 41–45 y.o A nd 11.7
7 nd 46–50 y.o A 1.02–14.24 7.06
8 nd 51–55 y.o A 3.57–49.99 11.53
5 nd 56–60 y.o A 0.53–7.07 4.93
6 nd 61–65 y.o A 5.01–15.94 11.33
3 nd >65 y.o A 2.78–16.46 7.45
São Luiz do Tapajós 327 total of population studied 0–>65 y.o G 0.10–94.50 19.91
75 nd 0–5 y.o C 0.10–94.50 21.06
74 nd 6–10 y.o C 2.40–52.50 22.1
51 nd 11–15 y.o C 3.90–61.80 23.24
21 nd 16–20 y.o A 2.10–33.60 19.11
21 nd 21–25 y.o A 1.73–32.0 15.68
15 nd 26–30 y.o A 3.90–34.90 15.34
15 nd 31–35 y.o A 5.10–38.0 18.98
15 nd 36–40 y.o A 2.60–27.8 14.31
14 nd 41–45 y.o A 3.20–33.60 15.13
8 nd 46–50 y.o A 4.0–47.0 21.71
4 nd 51–55 y.o A 5.90–20.60 15.4
6 nd 56–60 y.o A 7.90–27.60 17.13
3 nd 61–65 y.o A 3.8–27.80 12.6
5 nd >65 y.o A 3.20–20.80 12.6
Santana de Ituqui 321 total of population studied 0–>65 y.o G 0.40–11.60 4.33
37 nd 0–5 y.o C 0.50–8.50 3.67
81 nd 6–10 y.o C 0.40–10.9 4.44
62 nd 11–15 y.o C 2.0–11.6 4.47
25 nd 16–20 y.o A 2.5–9.60 5
17 nd 21–25 y.o A 1.30–7.10 3.34
16 nd 26–30 y.o A 1.70–9.20 4.69
19 nd 31–35 y.o A 1.90–9.60 5.36
18 nd 36–40 y.o A 1.20–6.0 3.44
10 nd 41–45 y.o A 2.70–6.80 4.18
10 nd 46–50 y.o A 1.90–6.40 4.02
9 nd 51–55 y.o A 2.30–9.0 5.39
6 nd 56–60 y.o A 3.10–6.90 4.37
4 nd 61–65 y.o A 1.90–9.0 4.15
7 nd >65 y.o A 0.70–5.70 3.61
2000 Dolbec J. [23] Cametá PA 68 total of population studied 12–79 y.o G nd 10.8
2001 Barbosa A.C. [24] Negro River AM 73 children <15 y.o C 0.51–45.89 18.52
76 adults >15 y.o A 1.66–59.01 21.4
2001 Harada M. [25] Barreiras PA 76 fisherman and family 1–67, mean 28 y.o G 1.8–53.8 16.4
Rainhas 12 fisherman and family 7–53, mean 31 y.o G 3.1–34.5 14.1
São Luiz do Tapajós 44 fisherman and family 3–47, mean 21 y.o G 5.1–42.2 20.8
Special group from Barreiras, Rainha and São Luiz do Tapajós 50 eligible subjects examined clinically that presented high level of Hg (>20 ppm) from March 1994 to February 1998 3–65, mean 25 y.o G 5.1–42.7 23.6
2002 Crompton P. [26] Jacareacanga PA 205 total of population studied general population, except children under 2 y.o G 0.3–83.2 8.6
nd men nd M nd 11.0
nd women nd W nd 6.7
2003 Passos C.J. [27] Brasília Legal PA 26 adults women 23–62, mean 41 y.o W 4.0–20.0 10.0
2003 Santos E.C.O. [28] Guajará Mirim e Nova Mamoré RO 910 total of studied population (Pakaanova indigenous) 0–>45 y.o I 0.52–83.89 8.37
57 nd 0–2 y.o I 1.48–83.89 10.54
115 nd 3–5 y.o I 1.67–47.22 9.34
152 nd 6–10 y.o I 0.52–63.81 8.16
114 nd 11–15 y.o I 0.65–31.11 6.86
177 nd 16–25 y.o I 0.65–39.42 8.45
114 nd 26–35 y.o I 1.37–28.64 8.56
50 nd 36–45 y.o I 1.49–21.25 8.39
131 nd >45 y.o I 1.37–25.84 7.84
2005 Dorea J.G. [29] Teles Pires (Tapajós Basin) PA 47 Kayabi indigenous Kayabi community from Teles Pires I nd 12.8
249 Munduruku indigenous Munduruku community from Teles Pires I nd 3.4
2005 Santos E.C.O. [30] São Gabriel da Cachoeira AM 157 total of population studied 0–>40 y.o G 0.30–83.11 13.02
9 nd 0–5 y.o C 1.01–14.40 5.71
8 nd 6–10 y.o C 2.05–15.00 7.35
37 nd 11–20 y.o NC 0.94–22.81 7.346
45 nd 21–30 y.o A 0.30–59.16 11.67
33 nd 31–40 y.o A 1.03–60.00 16.56
26 nd >40 y.o A 2.41–83.11 22.88
Barcelos 242 total of population studied 0–>40 y.o G 0.07–52.04 9.671
17 nd 0–5 y.o C 0.83–25.89 7.46
25 nd 6–10 y.o C 0.76–27.46 6.85
44 nd 11–20 y.o NC 0.07–21.53 7.00
62 nd 21–30 y.o A 0.25–42.64 9.05
27 nd 31–40 y.o A 0.23–52.04 12.02
67 nd >40 y.o A 2.60–32.86 12.67
2005 Tavares L.M.B. [31] Riverine communities of Bocas de Conchas, Cuiabá Mirim, Estirão Cumprido and Porto Brandão located near of Barão de Melgaço MT 72 riverine children 3–7 y.o C 0.58–17.14 5.37
Barão de Melgaço 114 urban children 3–7 y.o C 0.38–7.57 2.08
2005 Klautau-Guimaraes M.N. [32] Teles Pires PA 65 total of population studied (Kayabi indigenous) 0–>61, mean 24.53 y.o I nd 14.75
33 Kayabi indigenous 0–20 y.o I nd 17.86
25 Kayabi indigenous 21–40 y.o I nd 11.97
5 Kayabi indigenous 41–60 y.o I nd 14.35
2 Kayabi indigenous >61 y.o I nd 15.17
117 total of population studied (Munduruku indigenous) 0–>61, mean 30.90 y.o I nd nd
34 Munduruku indigenous 0–20 y.o I nd 4.26
56 Munduruku indigenous 21–40 y.o I nd 3.65
20 Munduruku indigenous 41–60 y.o I nd 3.75
7 Munduruku indigenous >61 y.o I nd 3.72
2006 Alves M.F.A. [33] total (all the riverine populations studied) AM 105 total of adult studied population 18–50, mean 32 y.o A nd 35.4
Mariuá (Negro River) 3 adults nd A nd 24.9
Marará (Negro River) 17 adults nd A nd 27.3
Piloto (Negro River) 25 adults nd A nd 33.2
Ponta da Terra (Cuiuni River) 12 adults nd A nd 38.2
São Luiz (Negro River) 21 adults nd A nd 41.4
Cumaru (Negro River) 16 adults nd A nd 43.7
Baturité (Negro River) 11 adults nd A nd 33
Manaus 105 total of studied population 18–50, mean 28 y.o A nd 1.0
2006 Bastos W.R. [34] total (all the populations studied) RO 713 total of population studied nd nd 5.99–150 15.22
Calama 34 nd nd nd 0.50–22.48 9.02
Boa Vitoria 3 nd nd nd 10.86–17.05 13.82
Cujubim 12 nd nd nd 1.55–14.67 6.30
Firmesa 4 nd nd nd 9.40–14.80 11.21
Itacoa 6 nd nd nd 5.28–16.00 11.97
Nazaré 64 nd nd nd 0.63–22.60 10.65
Papagaios 13 nd nd nd 4.76–27.22 13.72
Santa Rosa 19 nd nd nd 7.68–20.78 13.99
São Carlos 15 nd nd nd 1.84–22.83 9.51
Terra Caida 7 nd nd nd 5.01–14.61 9.61
Sto Antônio do Pau Queimado 14 nd nd nd 5.87–26.86 14.69
Puruzinho AM 28 nd nd nd 4.57–28.27 14.83
Livramento 15 nd nd nd 18.96–63.54 36.89
Valparaiso 21 nd nd nd 2.98–82.38 18.93
Auxiliadora 34 nd nd nd 1.12–22.78 9.34
Curralinho 5 nd nd nd 10.70–34.49 19.69
Nazaré do Retiro 15 nd nd nd 9.69–24.77 17.90
Novos Prazeres 20 nd nd nd 2.77–24.28 11.90
São Pedro 14 nd nd nd 6.61–28.00 15.77
Barreiras do Manicoré 9 nd nd nd 1.45–23.04 10.82
Cachoeirinha 14 nd nd nd 1.54–37.22 14.74
São Lazaro 6 nd nd nd 2.50–23.37 9.48
Maraca II 6 nd nd nd 8.57–15.69 11.37
Vista Nova 4 nd nd nd 21.40–28.54 25.69
Vista Alegre 17 nd nd nd 7.28–26.28 16.02
Bom Suspiro 12 nd nd nd 6.43–30.06 16.29
Carara 39 nd nd nd 4.18–34.71 18.13
Miriti 16 nd nd nd 6.70–50.37 22.34
São Sebastiao (Lago Lucio) 17 nd nd nd 6.61–18.52 12.84
Boca do Carapanatuba 18 nd nd nd 3.43–19.22 10.45
São Sebastiao do Tapuru 18 nd nd nd 20.43–150.00 62.76
Moanenses 13 nd nd nd 3.26–20.49 12.73
Três Casas 9 nd nd nd 5.62–70.70 33.07
Boa Ventura 7 nd nd nd 4.73–35.79 16.55
Auara Grande 19 nd nd nd 6.21–24.98 15.97
Fazenda Tabocal 2 nd nd nd 0.50–1.50 1.00
Remanso 12 nd nd nd 8.36–29.02 18.16
Arapapa 7 nd nd nd 10.43–21.33 16.56
Axinim 13 nd nd nd 3.27–23.02 8.65
Espirito Santo 18 nd nd nd 3.51–21.28 12.47
Santa Maria 7 nd nd nd 6.70–16.84 9.28
Caicara 23 nd nd nd 1.94–17.98 10.04
Paquique 6 nd nd nd 7.49–11.57 9.23
Uricurituba 46 nd nd nd 0.36–19.12 9.09
Santa Rosa II 12 nd nd nd 5.81–16.89 11.65
2006 Fillion M. [35] Tapajós (São Luiz do Tapajós, Nova Canaã, Santo Antônio, Mussum, Vista Alegre, Açaituba) PA 251 adults 15–89, mean 35.2 y.o A 0.21–77.2 17.8
2007 Passos C.J. [36] Tapajós (São Luiz do Tapajós, Nova Canaã, Santo Antônio, Ipaupixuna, Novo Paraiso, Teca, Timbó, Açaituba, Campo Alegre, Sumauma, Vista Alegre, Mussum, Santa Cruz) PA 449 adults 15–89, mean 38.6 y.o A 0.2–58.3 16.8
2007 Pinheiro M.C.N. [37] Panacauera PA 8 children 0–1 y.o C 0.39–4.66 1.11
13 children 2–6 y.o C 0.65–5.16 2.27
15 children 7–12 y.o C 0.86–9.46 2.99
Barreiras (Tapajós Basin) 17 children 0–1 y.o C 1.80–15.70 5.35
45 children 2–6 y.o C 1.43–23.60 6.21
22 children 7–12 y.o C 1.63–14.50 6.72
São Luiz do Tapajós 11 children 0–1 y.o C 1.99–30.30 5.97
23 children 2–6 y.o C 2.76–53.80 13.22
14 children 7–12 y.o C 1.34–38.80 10.83
2008 Passos C.J.S. [38] Tapajós (São Luiz do Tapajós, Nova Canaã, Santo Antônio, Vista Alegre, Mussum, Açaituba) PA 256 adults 15–89, mean 35.3 y.o A 0.2–58.3 17.9
2009 Fillion M. [39] Tapajós (São Luiz do Tapajós, Nova Canaã, Santo Antônio, Mussum, Vista Alegre, Açaituba, Santa Cruz, Sumauma, Campo Alegre, Ipaupixuna, Novo Paraiso, Curi-Teca, Curi-Timbó) PA 456 adults 15–>65 y.o A 0.2–77.7 17.8
2010 Grotto D. [40] Tapajós PA 108 total of population studied mean 41.1 y.o nd 1–57.8 13.7
54 men nd M nd 11.5
54 women nd W nd 8.8
2010 Bortoli M.C. [41] Novo Airão AM 55 women mean 32.3 y.o W 0.04–18.67 5.67
2012 Barcelos G.R.M. [42] Tapajós PA 144 adults 15–83, mean 43 y.o A 1–43.3 10.4
2012 Dutra M.D.S. [43] Itaituba PA 90 children population from urban area, samples collected in 2004 C nd 1.01
47 children population from urban area, samples collected in 2006 C nd 1.18
90 children population from urban area, samples collected in 2010 C nd 1.18
2012 Farias L.A. [44] Manaus AM 201 children 2–7 y.o C 0.02–34.4 1.93
2013 Khoury E.D.T. [45] Barreiras PA 78 general population 13–53 y.o G nd 8.66
São Luiz do Tapajós 30 general population 13–53 y.o G nd 9.19
Furo do Maracujá 49 general population 13–53 y.o G nd 0.73
2014 Rocha A.V. [46] Demarcação—Machado River RO 10 children 3–9 y.o C nd 3.57
Gleba do Rio Preto 10 children 3–9 y.o C nd 6.24
2015 Faial K. [47] Itaituba PA 6 male 0–2 y.o C 4.14–9.79 6.85
6 male 3–5 y.o C 16.01–23.80 19.57
10 male 6–10 y.o C 12.59–24.93 18.58
6 male 11–15 y.o C 5.83–15.57 13.08
7 male 16–20 y.o A 17.82–24.16 20.87
4 male 21–25 y.o A 9.42–20.09 15.52
nd male 26–30 y.o A nd nd
3 male 31–35 y.o A 8.55–10.83 9.69
5 male 36–40 y.o A 10.92–20.03 15.29
1 male 41–45 y.o A 14.81–14.81 14.81
1 male 46–50 y.o A 2.07–2.07 2.07
1 male 51–55 y.o A 13.89–13.89 13.89
3 male 56–60 y.o A 14.00–14.16 14.08
5 male >60 y.o A 12.04–21.47 14.57
4 female 0–2 y.o C 8.25–12.89 10.38
7 female 3–5 y.o C 12.20–19.29 15.83
7 female 6–10 y.o C 11.46–23.21 15.84
8 female 11–15 y.o C 8.41–21.71 13.12
5 female 16–20 y.o A 13.52–22.01 16.74
14 female 21–25 y.o A 6.33–17.66 11.22
7 female 26–30 y.o A 4.84–10.6 7.16
8 female 31–35 y.o A 4.95–20.78 13.52
3 female 36–40 y.o A 7.30–15.73 11.09
3 female 41–45 y.o A 14.69–23.02 18.62
3 female 46–50 y.o A 7.31–14.98 10.27
4 female 51–55 y.o A 15.52–18.52 17.02
1 female 56–60 y.o A 14.29–14.29 14.29
9 female >60 y.o A 14.60–27.02 20.39
2015 Castilhos Z. [48] São Chico PA 172 nd nd nd 0.14–35.90 3.44
Creporizinho 146 nd nd nd 0.23–10.49 2.25
2015 Hoshino A. [49] Lago do Puruzinho AM 58 general population 1–47, mean 17.3 y.o G nd 12.78
2016 Rocha A.V. [50] Porto Velho RO 200 women 18–48, mean 26.60 y.o W nd 0.60
2016 Carvalho L.V.B. [51] Belmont RO 42 nd mean 11.3 y.o nd nd 2.71
Cunia 52 nd mean 11.3 y.o nd nd 7.18
11.827

Legend. NC: not included for map classification, nd: not determined; G: general population; C: children; A: adults; W: women; M: men; I: Indigenous, >older than. y.o: year(s) old.

There was a predominance of studies that were performed in the State of Pará (47%) [22,23,25,26,27,29,35,36,37,38,39,40,42,43,45,47,48]. Some studies had been performed in the State of Amazonas (22%) [17,19,24,30,33,41,44,49], Rondônia (14%) [18,28,46,50,51], Mato Grosso (8%) [21,31,32] and Amapá (3%) [20]. Two studies were performed using samples from populations from two different States: Pará and Rondônia (3%) [16] and Rondônia and Amazonas (3%) [34].

The results shows that general population presented the highest mean level of Hg exposure (29.59 µg g−1, ranging from 0.73 to 97.44 µg g−1), followed by adult population (21.08 µg g−1, ranging from 1.00 to 43.70 µg g−1), not determined (14.60 µg g−1, ranging from 1.00 to 62.76 µg g−1), men population (11.25 µg g−1, ranging from 11.00 to 11.50 µg g−1), children population (7.95 µg g−1, ranging from 1.11 to 22.00 µg g−1), women population (7.66 µg g−1, ranging from 0.60 to 14.30 µg g−1) and Indigenous population (6.95 µg g−1, ranging from 4.90 to 8.37 µg g−1) (Figure 2).

Figure 2.

Figure 2

Mean level (µg g−1) of Hg exposure in populations of Brazilian Amazon according to the present study.

The analysis of the georeferencing data is presented as a map which shows a geospatial distribution of the populations and their respective degree of Hg exposure. The results show that most of the studies were performed along the margins of the Amazonian rivers and that most of these populations are highly exposed (Figure 3).

Figure 3.

Figure 3

The georeferencing results showing a geospatial distribution of the Brazilian Amazonian populations and their respective degree of Hg exposure on hair.

4. Discussion

The theme of Hg exposure in Amazonian population is an intriguing form of environmental contamination for some reasons: (1) the mean level of Hg exposure in Amazonian population usually exceed the normal limit preconized by WHO [24,30,33,52,53,54]; (2) there is a dichotomy in the clinical findings in different Amazonian populations, where some studies associate Hg exposure with the development of clinical symptoms [35,55,56,57] while others do not [45,58,59,60,61] and (3) even “non-exposed” populations are at risk of Hg effects [58].

The present study performed a systematic review of Hg exposure in Brazilian Amazon population. The results show that the majority of the studies were performed by Brazilian Institutions and researchers, reflecting the low international insertion despite that Hg is a global problem [62]. The high number of studies that were performed in the State of Pará is in agreement with the high prevalence of gold miners in the region (legal and illegal miners), especially in the Tapajós Basin [26,63].

The analysis shows that most of the studies were performed along the margins of important rivers, such as Negro, Tapajós and Madeira Rivers. The results show that all the populations presented mean levels above 6 µg g−1 of Hg on hair and that general population, adults, not determined and men presented mean levels above 10 µg g−1 of Hg on hair. Thus, the findings support the idea that Amazonian population present (along the period of time covered by this study) mean levels of Hg above the normal limit preconized by WHO (1–2 µg g−1 and levels above 10 µg g−1 for daily fish consumers) [64]. Although, affirm that this population is under risk of Hg effect is premature. Discussions about this issue should be evaluated based on other studies.

As future perspectives, the present study suggests an implementation of a strategic plan for the region in order to promote health and benefit the population. As strategies, we propose:

  • (1)

    Increase the technical capacity for Hg determination in the region;

  • (2)

    Implement an environmental health surveillance program that considerers the Amazonian life style, behavior and ecosystem dynamics;

  • (3)

    A follow up program to monitor the Hg content and health of individuals that presents high levels of Hg on biological matrices.

5. Conclusions

The Hg exposure in the Amazonian population is a fact. The high level of Hg on hair revealed by this study shows that this population has been long-term exposed to this metal.

The data reveals that the studies focused on population that lives along the margins of the rivers and, of utmost importance, populations under risk of Hg exposure from gold mining activities, especially from Tapajós Basin located in the State of Pará.

Author Contributions

Nathália Santos Serrão de Castro and Marcelo de Oliveira Lima were responsible for: (1) Design, analysis and interpretation of data; (2) Article writing and critical review of the intellectual content; (3) Final approval of the version to be published; (4) All aspects of the work, ensuring the accuracy and integrity of any part of the work.

Conflicts of Interest

The authors declare no conflict of interest.

Disclaimer

The opinions or assertions contained herein are the private views of the author(s) and are not to be construed as official or to reflect the views of the Evandro Chagas Institute or the Metropolitan College of Amazon.

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