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. Author manuscript; available in PMC: 2012 Feb 5.
Published in final edited form as: Heart. 2011 Sep 13;98(3):185–194. doi: 10.1136/heartjnl-2011-300599

Effect of rural-to-urban within-country migration on cardiovascular risk factors in low and middle income countries: A systematic review

Adrián V Hernández 1,2, Vinay Pasupuleti 3, Abhishek Deshpande 4, Antonio Bernabé-Ortiz 5, J Jaime Miranda 5
PMCID: PMC3272377  EMSID: UKMS40462  PMID: 21917659

Abstract

Context

Limited information is available of effects of rural-to-urban within-country migration on cardiovascular (CV) risk factors in low and middle income countries (LMIC).

Objective

We performed a systematic review of studies evaluating these effects and having rural and/or urban control groups.

Study Selection

Two teams of investigators searched observational studies in MEDLINE, Web of Science and Scopus until December 2010. Studies evaluating international migration were excluded.

Data Extraction

Three investigators extracted the information stratified by gender. We captured information on 17 known CV risk factors.

Results

Eighteen studies (n=58,536) were included. Studies were highly heterogeneous with respect to study design, migrant sampling frame, migrant urban exposure, and reported CV risk factors. In migrants, commonly reported CV risk factors –systolic and diastolic blood pressure, body mass index, obesity, total cholesterol, and LDL– were usually higher or more frequent than the rural group, and usually lower or less frequent than the urban group. This gradient was usually present in both genders. Anthropometric (waist-to-hip ratio, hip/waist circumference, triceps skinfolds) and metabolic (fasting glucose/insulin, insulin resistance) risk factors usually followed the same gradient, but conclusions are weak due to information paucity. Hypertension, HDL, fibrinogen and C-reactive protein did not follow any pattern.

Conclusions

In LMIC, most but not all CV risk factors have a gradient of higher or more frequent in migrants than in the rural groups but lower or less frequent than the urban groups. Such gradients may or may not be associated to differential CV events and long-term evaluations remain necessary.

Keywords: emigration and immigration, cardiovascular system, risk factors, income, meta-analysis as topic

INTRODUCTION

Non-communicable diseases (NCDs) kill people mostly in low- and middle-income countries (LMIC).[1] The Grand Challenges report highlights the need to study the impact of poverty and urbanization on NCDs.[2] Urbanization is occurring at a fast rate in LMIC, which may be associated with less physical activity, poorer nutritional habits, and rapidly growing prevalence of cardiovascular (CV) risk factors, CV disease (CVD) and other NCDs.[3] Rural-to-urban migration is one of the key larger drivers of urbanization in LMIC. Thus, the evaluation of the impact of rural to urban migration on CV risk factors is relevant due to its huge public health consequences.

The effect of international migration to developed countries on CV risk factors and CVD has been systematically studied.[4] As a result of the unique pattern and rate at which migration is occurring within LMIC, international migration results cannot be inferred to these settings. In LMIC, differences in design and patient characteristics make it difficult to reach a definitive conclusion on the effects on CV risk factors [5-9]. Also, it is not known whether the effect of rural to urban migration is uniform across CV risk factors and across LMIC. Finally, the effect on emerging CV risk factors such as fibrinogen, HOMA insulin resistance, or C-reactive protein could also be evaluated in the most recent studies.

We conducted a systematic review of observational studies evaluating the effect of rural-to-urban within-country migration on CV risk factors in LMIC. We hypothesized that migrants would have a worse CV risk profile than rural individuals and better CV risk profile than urban individuals.

METHODS

Study selection

A comprehensive literature search using PubMed-Medline, The Web of Science, and Scopus until December 31, 2010 was conducted. The following keywords were used: migration, emigration, immigration, residential mobility, transient and migrants, rural population, urban population, cardiovascular risk factors and cardiovascular disease. The search strategy of PubMed is available in the Appendix (Web only). We searched observational studies published in any language, performed in LMIC as defined by the World Bank.[10] We excluded studies of international migration or those from high income countries. A formal protocol was developed for this project.

Rural to urban migration was defined as the individual’s self-report or objective information of birth in a rural setting and, at the time of the study, self-report or objective ascertainment of urban residence. Three types of control groups were possible: a) a rural comparison group, where migrants originated from the same area, b) an urban comparison group, where migrants share the same urban environment and c) both a rural and an urban comparison group. This strategy excluded studies focusing only on differences between rural and urban settings. Sampling frames for migrants were classified as: i) random sample of migrants from urban population, ii) cohort of people born in a rural area who moved to an urban area and were traced, iii) rural individuals selected and their family members followed up in urban area (sib-pair); and iv) population level survey where migration was based on a retrospective question (“were you born here?”).

A list of retrieved articles was reviewed independently by 2 groups of investigators based in USA and Peru in order to choose potentially relevant articles, and disagreements were discussed and resolved. When multiple articles for a single study had been published, we used the most relevant publication and supplemented it, if necessary, with data from the other publications.

Data extraction

Data extraction was performed independently by 3 investigators (AVH, VP, AD). Disagreement was resolved by consensus. Using a standardized data extraction form, we collected information on lead author, year of study or publication year, study design, sample size, sampling frames for migrants, length of urban exposure, age of migration, average age, percentage of male participants, and 17 CV risk factors for migrants and control groups.

Outcomes

CV risk factors we collected were systolic blood pressure (SBP), diastolic blood pressure (DBP), hypertension; total cholesterol (TC), low density lipoprotein (LDL) cholesterol, high density lipoprotein (HDL) cholesterol; body mass index (BMI), obesity; triceps skinfolds thickness, waist circumference, hip circumference, waist-to-hip ratio (WHR); fibrinogen, C-reactive protein (CRP); fasting glucose, fasting insulin, and homeostasis model assessment (HOMA) scores, a validated measure of insulin resistance. Extracted information was stratified by gender. In the case of repeated measures, extracted information corresponded to the longest follow-up.

Study quality assessment

The order of quality of studies was considered as follows: 1) prospective cohort study, 2) retrospective cohort study, 3) case-control study, and 4) cross-sectional study. Also, we systematically assessed other key points of study quality proposed by the MOOSE collaboration.[11] These key points were: 1. clear identification of study population, 2. clear definition of outcome and outcome assessment, 3. independent assessment of outcome parameters (i.e. ascertainment of outcomes done by researchers other than the ones involved in the study), 4. selective loss during follow-up, and 5. important confounders and/or prognostic factors identified. Each point was rated as Yes/No. If the description was unclear, we considered that this as ‘no’.

Statistical analysis

Our systematic review followed the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) statement.[12] Differences between migrants and either rural or urban control groups are shown as absolute differences (i.e. migrant minus control) and its 95% Confidence Intervals (CI) for both continuous and categorical CV risk factors. Non-normally distributed risk factors were described in some studies as geometric means, and we extracted them as published.

A high degree of heterogeneity among studies was expected and therefore we did not combine all studies in a formal meta-analysis. Taking into account the sources of heterogeneity, three subgroup meta-analyses were pre-specified: 1. studies with similar characteristics including cross sectional design, random sampling frame, and >5 years of urban exposure; 2. cross-sectional studies; and 3. studies published after 1990. Subgroup meta-analyses were stratified by gender, as differences were expected between genders.

DerSimonian and Laird random effects models were used for meta-analyses.[13] For dichotomous CV risk factors, we used the Mantel-Haenzel (M-H) method to calculate pooled odds ratios (OR) and 95% CIs. For continuous CV risk factors, we used the Inverse Variance method to calculate Mean Differences (MD) and 95% CIs. Statistical heterogeneity was evaluated with the Cochran Chi-square (χ2) and the I2 statistics. Funnel plots were used to evaluate publication bias for the meta-analyses. All analyses were stratified by gender. We used Review Manager (RevMan 5.0, Oxford, UK; The Cochrane Collaboration, 2008).

RESULTS

Study Characteristics

A total of 394 citations were identified and screened, of which 80 were retrieved for detailed assessment. Of these, 62 did not fit our criteria (Figure 1). Thus, 18 studies were chosen in the qualitative synthesis,[5-9,14-26] including 58,536 individuals (Table 1). Studies included mostly adults, with very few individuals <15 years-old.

Figure 1.

Figure 1

Search strategy profile of the systematic review.

Table 1.

Characteristics of studies included in the systematic review.

Study,
Publication
year
Years
conducted,
Country
Total
sample
Mean age or age
groups / % of
young individuals
%
Male
Migrant
population
Rural
population
Urban
population
Urban
exposure
Study
design
Sampling
frame
Reported CV
risk factors
Cruz-Coke14,
1964
1962-1963,
Chile
179 32.9
6% <20 years-old and
2% <10 years-old
47 A group of Chilean
Polynesian population
who migrated to
mainland Chile
Isolated Chilean
Polynesian population
living in its own
ecological niche
N/A Not
reported
Cross-
Sectional
Traced
cohort
DBP
Benyoussef15,
1974
1970,
Senegal
469 ≤30y: 234 (49%);
31-40y: 113 (24%);
>40y: 122 (26%)

22% <20 years-old
52 Random sample
drawn from a census
of native Serers, from
a particular tribe,
living in certain parts
of Dakar
A cluster-random
sample of native
Serers living in one of
65 villages in Niakhar
county
N/A Not
Reported
Cross-
Sectional
Random
Sample
BP, cholesterol,
weight,
hematocrit,
mental health
Nadim5, 1978 1976,
Iran
1428 40-49y: 815 (57%);
50-59y: 613 (43%)

0% <20 years-old
40 Cluster-random
sample from East
Azerbaijan living in
West Teheran, Iran
A cluster-random
sample of rural areas
of East Azerbaijan
A cluster-random
sample of non-
migrants from East
Azerbaijan, living in
West Teheran
Not
reported
Cross-
Sectional
Random
Sample
BP,
hypertension,
obesity
(ponderal
index)
Poulter16,
1984
1980,
Kenya
1171 ≤34y: 571 (49%);
35-54y: 385 (33%);
≥55y: 215 (18%)

0% <20 years-old
41 Random sample of
Luo Tribe members
originated from Siaya
District, Nyanza
Province, Kenya, and
now living in poor
urban slums of
Nairobi, Kenya drawn
from a census
A random sample of
individuals living in
Siaya District, Nyanza
Province, Kenya
N/A Not
Reported
Cross-
Sectional
Traced
cohort
BP, BMI, weight,
skinfolds
Poulter17,
1990
1981-1985,
Kenya
206 <20y: 260 (41%);
20-29y: 288 (45%);
≥30y: 89 (4%)

1% <15 years-old
60 All individuals who
had migrated from
ruralWestern Kenya
(Luo Tribe) to Nairobi
(poor slum
communities) on a
permanent basis was
identified and
followed-up in Nairobi,
Kenya
Local controls,
matched for age and
sex, were selected
from the same Luo
tribe villages
N/A 2y Prospective
Cohort
Traced
cohort
BP, weight,
pulse rate,
serum sodium,
and potassium,
urine sodium,
potassium, and
creatinine
He Migrant6,
1991
1989,
China
14505 32.7

0% <15 years-old
61 All Yi people who had
migrated to the county
seats (Butuo, Meigu
and Zhaojue) or
Xichang city 5 or more
years prior to the
survey
A cluster-random
sample of Liangshan
Yi people from remote
mountain districts of
Sichuan province,
Southwestern China
for at least 5 years
A cluster-random
sample of Han
people residing in
Xichang city or
Country seats
(Butuo, Meigu,
Zhaojue)
Median:
10y,
Mean:
14.9y
Cross-
Sectional
Random
Sample
BP, hypertension,
BMI, physical
activity
He People18,
1991
1986-1988,
China
6618 31.1

0% <10 years-old
53 Yi People and their
families employed at a
power plant, paper
mill, hospital, middle
school, and the
government agency,
in Puge county seat
A cluster-random
sample of Liangshan
Yi People living in
remote mountain
districts drawn from a
census
Han people and
their families
employed at a
power plant, a
paper mill, a
hospital, a middle
school, and the
government agency
in Puge county
seat.
Not
reported
Cross-
Sectional
Random
Sample
BP, BMI, heart
rate, nutrient
intake,
electrolyte
serum and
urine
concentrations
Yamauchi19,
2001
1994-1995,
Papua New
Guinea
56 20-30y: 18 (32%);
30-40y: 25 (45%);
>40y: 13 (23%)

0% <20 years-old
52 Volunteers from two
villages in Tari Basin,
comprising of almost
the entire adult
population
N/A Volunteers from
three settlements in
Port Moresby
selected to match
the age distribution
of their village
counterparts
Average:
15y
Cross-
Sectional
Traced
cohort
BMI, physical
activity
Lindgarde20,
2004
N/A,
Peru
210 35.5

% of young individuals
not available
0 Women of indigenous
Andean ascent
(Quechua) who had
been residing in
northern suburbs of
Lima, Peru
Convenience sample
of women residing in
small rural villages at
high altitude in the
Cuzco region
N/A 89% for
>20y
Cross-
Sectional
Random
Sample
BP, BMI, waist
circumference,
% body fat, body
fat mass,
glucose, insulin,
HOMA index,
leptin
Hollenberg21,
2005
1999,
Panama
458 38.3

0% < 18 years-old
43 Random sample
drawn from a census
of people of Kuna
origin (O positive
blood) and long term
residents (≥ 5 years)
of Abayala, Panama
city
Kuna Amerinds
residing in their
indigenous home in
the island of Ailigandi
(Caribbean island off
the coast of Panama)
N/A >5 y Cross-
Sectional
Random
Sample
BP, BMI, weight,
mental health
Ramirez-
Zea7,
2005
1969-2004,
Guatemala
1311 32.3

0% <18 years-old
45 People living in
Guatemala City and
who were participants
of a longitudinal
growth and
development study
(1969 and 1977) and
born in rural East
Guatemala
People residing in or
near their native
villages and who
were participants of a
longitudinal growth
and development
study (1969 and
1977) and born in
rural East Guatemala
N/A Not
Reported
Prospective
cohort
Traced
cohort
BP, BMI, waist
circumference,
plasma glucose,
total cholesterol,
triglycerides,
LDL, HDL,
skinfolds,
waist/hip ratio,
abdomen/hip
ratio, body fat,
physical activity
McCullough22,
2006
1999,
Panama
311 37.4

0% <18 years-old
39 A random sample of
Kuna families residing
in Vera Cruz, Panama
City drawn from a
census
Kuna Amerinds
residing in their
indigenous home in
the island of Ailigandi
(Caribbean island off
the coast of Panama)
N/A Average:
20y
Cross-
Sectional
Random
Sample
BP, BMI, weight,
cholesterol,
urinary
electrolytes (urea,
sodium,
potassium,
calcium,
magnesium)
Unwin23,
2006
N/A,
Tanzania
323 29.2

0% <15 years-old
48 Individuals living in
the rural district of
Morogoro, Tanzania,
who migrated to Dar
es Salaam for at least
6 months
For each migrant, an
age and sex matched
non-migrant was
identified in Morogoro,
Tanzania
N/A 6 mo Prospective
Cohort
Traced
cohort
BP, BMI, weight,
waist,
cholesterol,
triglycerides,
LDL, HDL,
HbA1c
Szklarska24,
2008
2006,
Poland
863 43

0% <16 years-old
43 Convenience sample
of people living in
Wroclaw, Poland who
migrated after the age
of 16y and recruited
during a health
screening program
N/A Convenience
sample of people
living in Wroclaw,
Poland, those who
were born in
Wroclaw or
migrated before 16
years of age
Not
Reported
Cross-
Sectional
Population
Survey
BP, BMI,
waist/hip ratio,
skinfolds,
cholesterol,
HDL, LDL,
triglycerides,
glucose
Khan25,
2009
2004,
Bangladesh
2807 30.7

12% <20 years-old and
0% <10 years-old
0 Women who had
moved from countryside
or town to urban
center, or who lived in
country-side town
when <12y-old
N/A Women who were
living in an urban
area when<12-old,
and did not move to
urban city
Not
reported
Cross-
Sectional
Population
Survey
Overweight,
Obesity
Ebrahim8,
2010
2005-2007,
India
6510 41.1

0% <17 years-old
58 Factory workers for 4
cities and their
coresident spouses
were recruited. They
were rural-urban
migrants using
employer records as a
sampling frame
Each migrant worker
and spouse invited
one nonmigrant full
sibling of the same
sex and closest to
them in age still
residing in their rural
place of origin
A 25% random
sample of
nonmigrants invited
to participate.
Nonmigrants were
also asked to invite
a sib who resided in
the same city but
did not work in the
factory
86% for
>10y
Cross-
Sectional
Sib-Cohort BMI, waist/hip
ratio, % body fat,
BP, cholesterol,
triglycerides,
blood glucose,
fasting insulin,
HOMA score, fat
intake, metabolic
equivalent tasks
(METs)
Lu26,
2010
1997-2000,
Indonesia
20122 29.7

0% <18 years-old
46 Identified from the
1997 and 2000 waves
of the Indonesia
Family Life Survey,
representing 83% of
the population
Identified from the
1997 and 2000 waves
of the Indonesia
Family Life Survey,
representing 83% of
the population
N/A Not
Reported
Retrospective
Cohort
Population
Survey
Hypertension,
mental health
Miranda9,
2010
2007,
Peru
989 48

0% <30 years-old
47 Stratified random
sample of individuals
born in Ayacucho but
now residing in urban
shanty town of Lima,
Peru, drawn from
updated census
Stratified random
sample of local
residents of San Jose
de Secce in Ayacucho
was drawn from an
updated census
Stratified random
sample of
individuals born and
permanently living
in urban shanty
town of Lima, Peru
Average:
32y
Cross-
Sectional
Random
Sample
BP,
hypertension,
BMI, skinfolds,
waist-to-hip ratio,
fasting glucose,
diabetes,
lipoprotein
profile,
hypercholesterol
emia C-reactive
protein,
fibrinogen

Fourteen studies were cross-sectional, one was a retrospective cohort,[26] and three were prospective cohorts.[7,17,23] Studies were heterogeneous with respect to several characteristics. These studies were reported between 1964 and 2010. Fifteen studies compared the migrant group to the rural control group, and nine studies reported the years of urban exposure for the migrant group (urban exposure ≥ 6 months, and mostly >5 years). Sampling frames for migrants were also heterogeneous: random sampling in eight studies, a traced cohort in six studies, a population survey in three studies, and a sib-pair strategy in one study.

All studies clearly identified the study population and defined the outcome and outcome assessment (Table 1w, Web only). None of studies independently assessed the outcomes, and four studies had a selective loss of patients during follow-up.[7,17,23,26] Six studies identified important confounders or prognostic factors[6,8,9,18,25,26] and adjusted the association between migration and the CV risk factors.

The most commonly reported CV risk factors were SBP (13 studies), DBP (13 studies), hypertension (11 studies), BMI (11 studies), obesity (four studies), TC (six studies), LDL (five studies) and HDL (four studies). Hypertension was defined as BP ≥140/90 in only six studies, all of them published after 1990. Other CV risk factors including WHR, waist and hip circumference, triceps skinfolds, fasting glucose and insulin, HOMA scores, fibrinogen and CRP, were reported by fewer studies.

Effect of rural-to-urban migration on commonly reported CV risk factors

In most of the studies, values or rates in migrants were higher than the rural group, and lower than the urban group. Nine out of 12 studies showed higher SBP levels in migrants vs. rural (range 0.9 to 11.9 mmHg, significant differences in seven), and five out of six studies shower lower SBP in migrants vs. urban (range −0.2 to −8.3 mmHg, significant differences in two) (Table 2). Ten out of 12 studies reported higher DBP in migrants vs. rural (range 1.5 to 13.9 mmHg, significant differences in nine), and three out of five studies showed lower DBP in migrants vs. urban (range −1.2 to −4.9 mmHg, significant differences in two) (Table 3). Eight out of nine studies showed higher hypertension rates for migrants vs. rural (range 2.3% to 25.3%, significant differences in five), and two out of four studies reported non-significant lower hypertension rates for migrants vs. urban (range −0.7% to −16.6%) (Table 2w, Web only).

Table 2.

Systolic Blood Pressure (SBP) in mmHg for the migrant, rural and urban groups

Study SBP Migrants
Mean (SD) [n]
SBP Rural
Mean (SD) [n]
SBP Urban
Mean (SD) [n]
Absolute
difference
M vs. R
(95% CI)
Absolute
difference
M vs. U
(95% CI)

Male Female All Male Female All Male Female All
Nadim5 134.9
(23.1)[278]
141.8
(24.9)[414]
138.1
(24.6)[692]
119.7
(20.2)[176]
127.9
(26.2)[203]
126.2
(23.7)[379]
137.3
(21.1)[117]
136.5
(23.1)[240]
138.4
(24.1)[357]
11.90
(8.89,14.91)
−0.30
(−3.40,2.80)
Poulter16 128.2
(15.2)[220]
119.5
(13.7)[90]
124.7
(14.7)[310]
122.1
(18.3)[264]
120.0
(18.3)[597]
121.4
(18.7)[861]
- - - 3.30
(1.24,5.36)
-
Poulter17 125.6
(10.9)[43]
113.7
(9.9)[20]
121.0
(13.3)[63]
117.0
(11.4)[82]
106.2
(9.2)[61]
112.2
(12.1)[143]
- - - 8.80
(4.96,12.64)
-
He Migrant6 113
(14)[1656]
106
(12.8)[919]
111.0
(13.6)[2575]
110.8
(12.3)[5023]
111.2
(12.6)[3218]
110.8
(12.5)[8241]
114.5
(14.6)[2173]
108.1
(15.3)[1516]
112.2
(15.2)[3689]
0.20
(−0.39,0.79)
−1.20
(−1.92,−0.48)
He People 107.3
(11.6)[316]
101.6
(13.0)[201]
105.7
(12.6)[517]
101.2
(9.7)[2522]
101.1
(9.4)[2436]
101.1
(9.5)[4958]
108.3
(12.1)[638]
102.1
(11.2)[505]
105.0
(12.4)[1143]
4.60
(3.48,5.72)
0.70
(−0.60,2.00)
Lindgarde20 - 96
(11)[105]
96
(11) [105]
- 97
(10) [105]
97
(10)[105]
- - - −1.00
(−3.84,1.84)
-
Hollenberg21 115[146] 100.5[179] 107.0
(17.7)[325]
104.4[51] 95.2[82] 98.7
(13.8)[133]
- - - 8.30
(5.27,11.33)
-
Ramirez-
Zea7
118.4
(11.6)[143]
113.0
(15.3)[202]
115.4
(13.7)[345]
116
(11)[424]
107
(12)[542]
111.3
(12.1)[966]
- - - 4.10
(2.47,5.73)
-
McCullough22 - - 102
(14.7)[178]
- - 98.2
(13.8)[133]
- - - 3.80
(0.61,6.99)
-
Unwin23 - - 116.2
(21.3)[153]
- - 118.9
(18.9)[170]
- - - −2.70
(−7.11,1.71)
-
Szklarska24 128.3
(15.6)[99]
115.2
(16.2)[178]
120.9
(17.8)[277]
- - - 128.6
(16.1)[268]
118.3
(16.8)[318]
123.1
(17.8)[586]
- −2.20
(−4.74,0.34)
Ebrahim8* 125.1
(17.1)[1127]
118.9
(16.0)[985]
122.7
(17.0)[2112]
122.9
(15.6)[1459]
118.9
(16.9)[652]
121.8
(16.2)[2111]
125.7
(17.7)[1201]
119.4
(16.8)[1086]
122.9
(17.8)[2287]
0.90
(−0.10,1.90)
−0.20
(−1.23,0.83)
Miranda9 123.5
(14.9) [280]
116.6
(16.9)[309]
119.9
(16.4)[589]
125.2
(17.4)[95]
117.1
(19.1)[106]
120.9
(18.7)[201]
132.2
(23.2)[92]
124.7
(22.2)[107]
128.2
(22.9)[199]
−1.00
(−3.90,1.90)
−8.30
(−11.75,−4.85)
*

adjusted for occupation, age, age group, and factory including a random effect of sibling pair.

Table 3.

Diastolic Blood Pressure (DBP) in mmHg for the migrant, rural and urban groups

Study DBP Migrants
Mean (SD) [n]
DBP Rural
Mean (SD) [n]
DBP Urban
Mean (SD) [n]
Absolute
difference
M vs. R
(95% CI)
Absolute
difference
M vs. U
(95% CI)

Male Female All Male Female All Male Female All
Cruz-Coke14 - - 86.8
(12.2)[50]
- - 84.2
(9.4)[129]
- - - 2.60
(−1.15,6.35)
-
Nadim5 83.5
(15.3)[278]
87.1
(16.3)[414]
86.0
(16.0)[692]
71.5
(14.2)[176]
73.6
(15.2)[203]
72.1
(13.7)[379]
85.5
(15.6)[117]
84.7
(16.0)[240]
84.7
(15.3)[357]
13.90
(12.08,15.72)
1.30
(−0.68,3.28)
Poulter16 70.8
(14.5)[220]
67.2
(11.4)[90]
70.1
(13.0)[310]
68.1
(11.4)[264]
66.8
(11.2)[597]
67.4
(11.3)[861]
- - - 2.70
(1.07,4.33)
-
Poulter17 66.3
(14.0)[43]
61.7
(9.3)[20]
65.7
(10.0)[63]
53.1
(12.2)[82]
54.9
(9.6)[61]
53.5
(11.7)[143]
- - - 12.20
(9.07,15.33)
-
He Migrant6 70.9
(11.6)[1656]
65.2
(10.1)[919]
68.7
(11.6)[2575]
66.3
(12)[5023]
65.8
(11.8)[3218]
66.1
(12.1)[8241]
72.6
(10.4)[2173]
67.7
(10.3)[1516]
70.4
(10.5)[3689]
2.60
(2.08,3.12)
−1.70
(−2.26,−1.14)
He People18 69.6
(10.1)[316]
63.2
(8.8)[201]
67.2
(10.1)[517]
63.0
(7.2)[2522]
62.5
(7.0)[2436]
62.6
(7.1)[4958]
69.2
(9.1)[638]
63.4
(7.6)[505]
66.6
(9.0)[1143]
4.60
(3.71,5.49)
0.60
(−0.42,1.62)
Lindgarde20 - 66
(6) [105]
66
(6) [105]
- 59
(9) [105]
59
(9) [105]
- - - 7.00
(4.93,9.07)
-
Hollenberg21 74.2[146] 64.9[179] 69.1
(13.7)[325]
61.7[51] 57.9[82] 59.4
(6.9)[133]
- - - 9.70
(7.80,11.60)
-
Ramirez-
Zea7
73.7
(10.5)[143]
71.5
(11.0)[202]
72.4
(10.4)[345]
72
(9)[424]
69
(9)[542]
70.9
(9.3)[966]
- - - 1.50
(0.26,2.74)
-
McCullough22 - - 64
(16) [178]
- - 58.4
(8.1)[133]
- - - 5.60
(2.88,8.32)
-
Unwin23 - - 70.3
(12.0)[153]
- - 73.2
(10.0)[170]
- - - −2.90
(−5.32,−0.48)
-
Szklarska24 82.2
(9.5)[99]
75.5
(10)[178]
78.8
(9.6)[277]
- - - 84.8
(11.2)[268]
77.6
(10.6)[318]
80.0
(12.1)[586]
- −1.20
(−2.70,0.30)
Miranda9 74
(9.2)[280]
69
(8.7)[309]
71.3
(9.3)[589]
76.1
(8.9)[95]
72.5
(9.2)[106]
74.2
(9.2)[201]
79.1
(11.8)[92]
73.7
(10.6)[107]
76.2
(11.5)[199]
−2.90
(−4.38,−1.42)
−4.90
(−6.67,−3.13)

Nine out of 10 studies reported higher BMI values in migrants vs. rural (range 0.2 to 3.8 kg/m2, significant differences in six), and all of the four studies showed significant lower BMI values in migrants vs. urban (range −0.3 to −1.3 kg/m2) (Table 4). Two studies showed higher obesity rates in migrants vs. rural (range 0.2% to 18.1%, one with significant differences), and two studies showed significant lower obesity rates in migrant vs. urban (range −3.9% to −13.1%) (Table 3w, web only).

Table 4.

Body mass index (BMI) in Kg/m2 for the migrant, rural, and urban groups

Study BMI Migrants
Mean (SD) [n]
BMI Rural
Mean (SD) [n]
BMI Urban
Mean (SD) [n]
Absolute
difference
M vs. R
(95% CI)
Absolute
difference
M vs. U
(95% CI)

Male Female All Male Female All Male Female All
Poulter16 20.5
(2.6)[220]
21.8
(3.0)[90]
20.8
(2.9)[310]
20.0
(2.9)[264]
20.1
(3.0)[597]
20.2
(3.0)[861]
- - - 0.60
(0.22,0.98)
-
He People18 20.2
(2.3)[316]
20.9
(2.6)[201]
20.3
(2.5)[517]
18.9
(2.3)[2522]
18.9
(2.5)[2436]
18.9
(2.4)[4958]
20.5
(2.3)[638]
20.6
(2.3)[505]
20.6
(2.4)[1143]
1.40
(1.17,1.63)
−0.30
(−0.56,−0.04)
Yamauchi19 26.4
(3.3)[14]
25.5
(3.1)[15]
25.9
(4.0)[29]
24.8
(1.6)[11]
23.2
(3)[9]
24.4
(2.2)[20]
- - - 1.50
(−0.25,3.25)
-
Lindgarde20 - 25.1
(4.7)[105]
25.1
(4.7)[105]
- 24.6
(3.9)[105]
24.6
(3.9)[105]
- - - 0.50
(−0.67,1.67)
-
Hollenberg21 22.6[146] 23.6[179] 23.1[325] 22.4[51] 22.5[82] 22.5[133] - - - 0.6** -
Ramirez-
Zea7
26.0
(4.0)[143]
27.0
(3.8)[202]
26.5
(3.8)[345]
24.3
(3.4)[424]
26.8
(4.9)[542]
25.4
(4.6)[966]
- - - 1.10
(0.61,1.59)
-
McCullough22 - - 23.4
(4)[178]
- - 22.6
(3.5)[133]
- - - 0.80
(−0.04,1.64)
-
Unwin23 - - 24.0
(1.6)[153]
- - 23.6
(1.0)[170]
- - - 0.40
(0.11,0.69)
-
Szklarska24 26.9
(3.1)[99]
24.4
(4.4)[178]
25.1
(4.1)[277]
- - - 27.2
(4.1)[268]
24.5
(4.8)[318]
25.9
(4.5)[586]
- −0.80
(−1.40,−0.20)
Ebrahim8* 24
(3.4)[1127]
25.2
(3.2)[985]
24.6
(3.4)[2112]
21.9
(3.9)[1459]
22.5
(3.9)[652]
22.0
(4.0)[2111]
24.3
(3.5)[1201]
25.9
(3.4)[1086]
25.0
(3.5)[2287]
2.60
(2.38,2.82)
−0.40
(−0.60,−0.20)
Miranda9 25.9
(3.5)[280]
28
(4.7)[309]
27
(4.3)[589]
22.9
(2.1)[95]
23.5
(3.2)[106]
23.2
(2.7)[201]
26.8
(4)[92]
29.5
(6.1)[107]
28.3
(5.4)[199]
3.80
(3.29,4.31)
−1.30
(−2.13,−0.47)
*

adjusted for occupation, age, age group, and factory including a random effect of sibling pair.

**

No standard errors available for groups.

All of the five studies showed higher TC levels in migrants vs. rural (range 4.0 to 35.1 mg/dL, significant differences in four); all of the three studies showed non-significant lower TC levels in migrants vs. urban (range −1.9 to −4.1 mg/dL) (Table 4w, Web only). Three out of four studies reported significantly higher LDL levels in migrants vs. rural (range 5.3 to 30.3 mg/dL); two out of three studies reported non-significant lower LDL levels in migrants vs. urban (range −1.0 to −3.9 mg/dL) (Table 5w, Web only). Finally, two out of three studies showed lower HDL levels in migrants vs. rural (range −0.1 to −1.8 mg/dL, one significant difference); one out of two studies showed lower HDL levels in migrants vs. urban (absolute difference 1.2 mg/dL) (Table 6w, Web only).

Effect of rural-to-urban migration on uncommonly reported CV risk factors

In two studies[8,9] WHR values in migrants were significantly higher than in the rural and urban (range 0.01 to 0.06, and −0.01, respectively). Three studies[7,9,20] showed larger waist circumference levels in migrants vs. rural (range 0.6 to 12.0 cm, significant differences in two); one study[9] showed shorter waist circumference levels in migrants vs. urban (difference −3.3 cm, 95% CI −1.4 to −5.2). In one study,[9] a significant larger hip circumference was shown in migrants vs. rural (difference 7.0 cm, 95% CI 6.1-8.0) and significant shorter hip circumference in migrants vs. urban (difference −4.5 cm, 95% CI −2.9 to −6.1). Two studies[9,16] showed larger triceps skinfolds thickness in migrants vs. rural (range 0.1 to 10.9 mm, one significant difference); one study reported significantly shorter triceps skinfolds thickness in migrants vs. urban (difference −8.9 mm, 95% CI −5.5 to −12.3).

Two out of three studies[7,9,20] reported higher mean or geometric mean glucose values in migrants vs. rural; two studies[9,24] reported lower mean or geometric mean glucose values in migrants vs. urban. Three studies[8,9,20] showed higher mean or geometric mean fasting insulin levels in migrants vs. rural; two of the studies[8,9] also showed lower fasting insulin levels in migrants vs. urban. The mean or geometric means of HOMA scores were significantly higher in migrants vs. rural in two studies;[9,20] in one study[9] the geometric mean of the HOMA score was significantly lower in migrants vs. urban. Geometric means of fibrinogen and CRP in migrants were significantly higher vs. rural, and similar to the values in urban.[9]

The observed gradient for most of commonly and uncommonly reported CV risk factors among migrants, rural and urban groups was found in both males and females separately.

Meta-analyses in subgroups of studies

Due to limited availability of CV risk factors, we only included SBP, DBP, and BMI in these meta-analyses. Substantial heterogeneity of effects among studies and no evidence of publication bias were seen in all three sets of meta-analyses.

Five studies[6,92,20-22] fulfilled our first pre-specified criteria of being cross-sectional studies, with a random sampling frame for migrants, and with at least 5 years of urban exposure for migrants. No differences were found between migrants and rural individuals in terms of SBP, DBP or BMI. A pattern of significantly lower SBP (MD −3.5 mmHg, 95% CI −5.6 to −1.4) and lower DBP (MD −3.0 mmHg, 95% CI −4.2 to −1.72) in migrants vs. urban was seen overall and for both males and females.

Fourteen studies were cross-sectional (Table 1) fulfilling our second pre-specified criteria, and thirteen studies were published after 1990 (Table 1) fulfilling our third criteria. Gradients were similar to the overall results for SBP, DBP and BMI on these subgroups.

DISCUSSION

Main findings

Studies conducted in LMIC evaluating the effect of within-country migration on CV risk factors showed substantial heterogeneity with respect to design, sample size, time of urban exposure, migrant sampling frame, and reported CV risk factors between migrants and rural or urban individuals. In general, when observing the absolute differences between migrants and comparison groups, a gradient for most of the commonly reported CV risk factors was noted: higher values or rates in migrants in comparison to rural individuals, and lower values or rates in migrants in comparison to urban individuals. This gradient was also seen in most of the studies when evaluating males and females separately. Nevertheless, against our hypothesis, some CV risk factors such as hypertension rates, HDL, fibrinogen and CRP levels did not follow any gradient.

What the current literature reports

The effect of international migration to developed countries on CV risk factors has been systematically studied by McKay et al.[4] These migrants are exposed not only to increased consumption of saturated fats and sugars and sedentary behavior but also to stressful life conditions. International migrants have poorer health and more disadvantaged CV risk factor profile than non-migrants, and this profile may worsen with increasing duration of stay in the urban environment.

Rural-to-urban within-country migration is a very common phenomenon in LMIC countries,[5] largely due to economic reasons. Its effects on CV risk factors have been poorly studied,[26] mostly for blood pressure/hypertension and BMI/obesity. Even less information is available for lipid profiles[27] or emerging and newer CV risk factors (e.g. CRP, fasting insulin, HOMA scores, fibrinogen).[9]

In the context of LMIC, urban-rural comparisons are of limited relevance in examining the effects of urban migration as the urbanization process in these countries is due to growth of existing urban populations, expansion of urban boundaries, and rural-to-urban migration.[28] Also particular genetic, cultural and life-style backgrounds of migrants and urban individuals further limit the value of urban-rural comparisons. However, several urban-rural comparisons of CV risk factors have been published in the literature. Comparisons of urban and rural areas in sub-Saharan Africa[29] and India[30] showed higher rates of hypertension, obesity and adverse lipid profiles for urban individuals; however, no differences between urban and rural areas for these risk factors have lately been found in China.[31]

What our study adds to current literature

We hypothesized that there would be a gradient with worse CV profile for the urban individuals than for migrants and worse for migrants than for rural individuals. This was the case for most of the CV risk factors; in most cases reported differences were significant. Some CV risk factors such as hypertension rates, HDL, fibrinogen and CRP levels did not follow any gradient. It seems implausible that these CV risk factors are not modified by migration given significant modifications of major risk factors, but recent reports, at least for blood pressure levels, suggest that the patterns of change following migration are very complex and do not necessarily follow the expected gradient.[23,32] An alternative explanation may include the scarcity of studies. Our chosen studies did not evaluate the effect of modified CV risk factors on CV events, and the gradients may or may not be associated to differential CV events across groups in the future. Thus, long-term longitudinal evaluations are necessary.

The gradient urban-migrant-rural for most of CV risk factors seems relevant in the context of studies with substantial heterogeneity. Recognizing the sources of heterogeneity, we secondarily analyzed three subgroups of studies. Cross-sectional and after 1990 subgroups of studies showed similar gradients between urban, migrant and rural as seen in all studies. The subgroup of cross-sectional studies with random sampling of migrants and at least 5 years of urban exposure for migrants showed lower SBP and DBP for migrants in comparison to urban individuals and non-significant differences between migrants and rural individuals. Although subgroup results should be taken with caution as heterogeneity of effects remained significant in all three subgroups of studies, they may highlight potential changes of gradient with longer urban exposure for migrants.

There was a notorious paucity of information on other important anthropometric risk factors (e.g. WHR, hip circumference, triceps skinfolds thickness) or metabolic and inflammation risk factors (e.g. glucose, fasting insulin, insulin resistance scores, fibrinogen, CRP). Our conclusions for these infrequently reported risk factors are weak at this moment and deserve further reevaluation in the future.

Only 6 studies[6,8,9,18,25,26] provided adjusted values of CV risk factors or adjusted estimates of the differences between migrants and controls. Adjusters included age, BMI, gender, socioeconomic status, education, occupation, marital status, physical activity, initial health status, and altitude. Most of these studies were published in 2009 and 2010, with the exception of the Yi Migrant[6] and Yi People[18] studies. Our main and secondary analyses were based on unadjusted values of CV risk factors, and therefore some bias may be present in our association measures between migration groups. Combination of adjusted metrics was not possible given the different sets of confounders adjusted for, the heterogeneity of studies, and the limited number of studies.

Limitations

First, we included studies that were heterogeneous with respect to several characteristics and therefore a meta-analysis of all studies was not possible. Pre-specified subgroups of more homogeneous studies also showed significant heterogeneity and subgroup results should be taken with caution. Second, we evaluated unadjusted differences between groups, as only unadjusted values were published by authors for most of the studies. Few recent studies provided adjusted values for a few of the CV risk factors we used in our analyses. Third, publication bias is always a concern in a systematic review; however we decreased it in our study by having no language restrictions, by using a comprehensive study search strategy in 4 literature engines, and by involving 2 groups of investigators with at least 2 researchers in each group. Fourth, we expect some differences on the effect of within-country migration on CV risk factors across different countries and continents. We could not explore this hypothesis given the few numbers of studies available. Finally, the scarcity of reporting of several metabolic and inflammatory risk factors did not allow reaching stronger conclusions of the effect of migration on them.

Conclusions

Studies investigating the effect of rural-to-urban within-country migration on CV risk factors in LMIC are highly heterogeneous. Most of CV risk factors in migrants follow a gradient: higher or more frequent than in the rural groups, and lower or less frequent than the urban groups. Furthermore, some CV risk factors, such as hypertension rates, HDL, fibrinogen and CPR levels did not follow a pattern. Such gradients may or may not be associated to differential CV events across groups and long-term longitudinal evaluations of such associations remain necessary.

Supplementary Material

SupplTables1-6

Acknowledgments

FUNDING STATEMENT The CRONICAS Center of Excellence in Chronic Diseases at UPCH is funded by the National Heart, Lung and Blood Institute (NHLBI), under contract No. HHSN268200900033C. The funders had no role in study design; data collection, analysis, or interpretation; in writing the report, or in the decision to submit the article for publication. The researchers are all independent from the funding source.

Footnotes

COMPETING INTERESTS None for all authors

AUTHOR CONTRIBUTIONS Conception and design: AVH, JJM

Analysis and interpretation of data: AVH, VP, AD, AB-O, JJM

Drafting of the article: AVH, JJM

Critical revision of the article for intellectual content: AVH, VP, AD, AB-O, JJM

Final approval of the article: AVH, VP, AD, AB-O, JJM

Statistical expertise: AVH

Collection and assembly of data: VP, AD, AVH

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Supplementary Materials

SupplTables1-6

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