Submit manuscript...
Journal of
eISSN: 2373-6453

Human Virology & Retrovirology

Research Article Volume 10 Issue 1

Estimation of Rubella virus antibodies among aborted women in Ibb City-Yemen 

Abdul Baset Abbas,1,2 Rasha Moharam,2 Latifa Al-Gmashi,2 Ebtesam Negad,2 Naba Al-Bana’a,2 Maha Alqadri,2 Nogoom Alosimey,2 Noha Alqadri,2 Firuz Ali,2 Kamal Hezam3

1Medical Laboratories Department, Faculty of Medicine and Health Sciences, Ibb University, Yemen
2Medical Laboratories Department, Faculty of Allied Medical Sciences, The National University, Yemen
3Department of Parasitology & Immunology, Faculty of Applied Science, Taiz University, Yemen

Correspondence: Abdul Baset Abbas, Faculty of Medicine and Health Sciences, Ibb University, Ibb City 70270, Yemen. Faculty of Allied Medical Sciences, The National University, Ibb branch, Yemen

Received: March 01, 2023 | Published: March 9, 2023

Citation: Abbas AB, Moharam R, Al-Gmashi L, et al. Estimation of Rubella virus antibodies among aborted women in Ibb City-Yemen. J Hum Virol Retrovirol. 2023;10(1):21-23. DOI: 10.15406/jhvrv.2023.10.00259

Download PDF

Abstract

German measles is a public health disease caused by rubella virus resulting in adverse consequences among pregnant women as congenital rubella syndrome (CRS) including abortions. Abortion is one of the most common health problems in the world. So, this study purposed to estimate prevalence of rubella virus antibodies among aborted women in Ibb city, Yemen. A cross-sectional investigation was accomplished from January 2022 to June 2022. 150 serum samples were collected from aborted women attending the obstetrics and gynecology department of various hospitals to analyze rubella virus IgG and IgM antibodies by Electro-Chemiluminescence Immunoassay (ECLIA). Demographical and clinical features were collected using a questionnaire. The data were analyzed using GraphPad software and P values ≤0.05 were considered statistically significant. With regards to the prevalence of rubella virus antibodies among aborted women, 149 cases (99.3%) of aborted women were rubella IgG antibodies positive. Rubella virus IgM antibodies were negative (100%) in all aborted women. The prevalence of rubella virus IgG antibodies in the age 26-30 was less than in other age groups. Moreover, the seroprevalence of rubella virus IgG was higher in rural aborted women (100%) compared to urban ones. Demographical and clinical features among aborted women were not statistically significant concerning rubella IgG positive results. In conclusion, the low rate of rubella IgM and a high proportion of rubella IgG for the most aborted women in this study suggest that rubella infection might indicate a previous infection.

Keywords: rubella, CRS, IgG, IgM, aborted women, Ibb, Yemen

Abbreviations

Ig, immunoglobulin; ECLIA, electro-chemiluminescence immunoassay; CRS, congenital rubella syndrome; RNA, ribonucleic acid

Introduction

German measles is a public health illness caused by rubella virus. It is an RNA virus that belongs to the Rubivirus genus and Matonavirida family.1–4 It is an infectious disease transmitted through respiratory droplets from person to person or through placenta from mother to her fetus.3–6

The average incubation period is 14 days and a range of 12–23 days. The first symptom is a maculopapular rash, which appears on the face and then extends to the body surface, lasting almost three days. Other symptoms include fever, reddened eyes, headache, post-auricular adenopathy, arthralgia, tiredness, cough and runny nose.7

Rubella virus infection during pregnancy can result in severe consequences such as abortion, stillbirth, and serious birth deficits, known as congenital rubella syndrome (CRS).3 CRS birth defects may include low birth weight, microcephaly, mental retardation, hearing impairment, bone alterations and developmental delay. Other CRS defects may include heart defects (persistent ductus arteriosus and pulmonary stenosis) and may cause eye defects (retinitis, cataracts, glaucoma, and microphthalmia).3,8,9 Hepatomegaly, jaundice thyroiditis, autism, and diabetes mellitus are considered as late symptoms of CRS.1,6,7

Annually, 100,000 newborns were born with CRS7. 90% of newborns with CRS were born to females infected by the rubella virus in the first trimester of pregnancy.1,10

Countries that have used vaccine since the 1960s, there succeeded in controlling CRS.3,7,11 According to the WHO Eastern Mediterranean Region report, the rubella virus vaccine was not part of the expanded programme of immunization in Yemen until 2015.12

In addition, there are no previous studies available to investigate the role of the rubella virus on abortion in Yemen. Most previous studies have focused on rubella antibodies among females at childbearing age, during pregnancy and schoolgirl, as well as cytomegalovirus antibodies.13–17 Accordingly, our study aimed to estimate rubella virus antibodies (IgG and IgM) seroprevalence among aborted women attending the obstetrics and gynecology department of various hospitals in Ibb city, Yemen.

Material and methods

This descriptive cross-sectional study was conducted between January and June 2022. The study participants included 150 aborted women (aged 18-40 years) were attended obstetrics and gynecology departments of different hospitals in Ibb city, Yemen.

Serum samples were separated from blood and then the sera were analyzed for rubella IgG and IgM using Electro-Chemiluminescence Immunoassay (ECLIA) technique on Cobas e411 analyzer depending on the company’s protocol (Roach Diagnostic GmbH, Mannheim, Germany). All serum samples were tested at the Zain Medical Laboratories (ZML).

A standardized questionnaire administered via face-to-face interview was used to get information on sociodemographic, residence and clinical features of the aborted women. The questionnaire was translated into Arabic, the mother tongue of Yemen.

The ethical clearance for this research was granted by the Medical Laboratories Department, Faculty of Allied Medical Sciences, The National University ethical committee after due process was followed. The Ethics Research Committee is aligned with the Declaration of Helsinki for the Protection of Human Subjects. Aborted women were informed about the study and consented before study enrolment. A consent to use the survey data was also obtained.

The data obtained from the results of the laboratory analysis and the questionnaires were analyzed using GraphPad prism version 5.01 (GraphPad Inc. USA). The results showed that percentages (%) and P values. The p value was used to estimate the correlation between the prevalence rates and the collected data. P values ≤0.05 were considered statistically significant.

Results

Briefly, the seroprevalence of rubella virus IgG antibodies among aborted women were 149 (99.33 %), whereas rubella virus IgM antibodies were negative in this study as revealed in Table 1. The results were revealed statistically significant (P-value <0.0001).

Serological results

IgG positive

IgM positive

 

No.

%

No.

%

P-value

Positive

149

99.33

0

0

<0.0001

Negative

1

0.67

150

100

Table 1 Estimation of rubella virus antibodies among aborted women, Ibb city-Yemen

The age range of the aborted women was 15 to 40 years, while the mean age ± SD was 26.6 ± 5.2 years; third (33.3%) were 26-30 of age as presented in Table 2. Concerning educational level, 57 (38 %) had a primary level of education (29 were illiterate, 45 were secondary and 19 university education). The majority of aborted women lived in the rural area of Ibb (80; 53.3%) while 70 (47.7%) lived in the urban areas. Regarding socioeconomic status, more than two-thirds 107 (71.33%) were middle (30 low and 13 high). More than three-quarters of the participants 116 (77.33 %) reported having an abortion during the first trimester compared with the second and third trimesters 28 (18.86 %) and 6 (4 %), respectively.

Variable

Participants

IgG positive

(No.)

(%)

No.

(%)

P value

Age

 

 

 

 

 

15-20

20

13.3

20

100

0.9845

21-25

49

32.7

49

100

 

26-30

50

33.3

49

98

 

31-35

25

16.7

25

100

 

36-40

6

4

6

100

 

Residence

 

 

 

 

 

Rural

80

53.3

80

100

0.9505

Urban

70

47.7

69

98.57

 

Education Level

 

 

 

 

 

Illiterate

29

19.3

29

100

 

Primary

57

38

57

100

 

Secondary

45

30

44

97.7

 

University

19

12.7

19

100

 

Socioeconomic status

 

 

 

 

Low

30

20

30

100

0.9993

Middle

107

71.33

106

99.06

 

High

13

8.67

 

100

 

Abortion time (trimester)

 

 

 

First

116

77.33

115

99.14

0.9995

Second

28

18.67

28

100

 

Third

6

4

8

100

 

Table 2 Sociodemographic characters and rubella virus antibodies prevalence among 150 aborted women in Ibb city, Yemen

The seroprevalence of rubella virus IgG antibodies among 150 aborted women were shown in Table 2. Regarding age, all groups showed 100 % IgG passivity except 26-30 years, which revealed 98 %. The rate of rubella IgG antibody prevalence was higher in rural areas than urban areas with percentages 100% and 98.57 %, respectively. It is noted that the prevalence of rubella virus IgG antibodies in all participants at all educational levels were high. Likewise, the prevalence of IgG according to socioeconomic status 99.14 % of aborted women in the first trimester were IgG positive while in the third and second once were 100% of rubella IgG positive. All variables were non-statistically significant.

Among the aborted women, 143 (95.33%) had a history of a previous abortion and 7 (4.67%) had no previous abortion. Out of 143 (95.33%) with an abortion history, rubella IgG antibody was positive in 142 (99.3%) as presented in Table 3. The majority of aborted women had a previous history of abortion, where 46 %, 36.67 %, 7.33 % or 5.33 % had one, two, three or four times, respectively. Most participants were rubella IgG antibodies positive. These results were significant (P value = 0.0001). Additionally, according to history of congenital defects such as heart defects and premature birth, the seroprevalence of rubella IgG was 100 % positive among all aborted women, but it was not statistically significant. As presented in Table 3, out of 59 aborted women with arthritis, rubella IgG was positive in 58 cases (96.3 %). Out of 36 and 4 aborted women with arthritis and lymphadenopathy, rubella IgG was positive in all cases (100 %). These differences were not statistically significant.

Symptoms

Participants

IgG Positive

No.

%

No.

%

P- value

Abortion history

 

 

 

 

 

With

143

95.33

142

99.3

0.9509

Without

7

4.67

7

100

 

Number of last abortion

 

 

 

None

7

4.67

7

100

0.0001

1

69

46

68

98.55

 

2

55

36.67

55

100

 

3

11

7.33

11

100

 

4

8

5.33

8

100

 

Congenital defects

 

 

 

 

 

Heart defect

4

2.67

4

100

0.9999

Premature birth

6

4

6

100

 

Symptoms

 

 

 

 

 

Skin rash

36

24.7

36

100

0.9983

Arthritis

59

30.6

58

98.3

Lymphadenopathy

4

2.67

4

100

Table 3 Seroprevalence of rubella IgG among aborted women according to symptoms associated with rubella infection

Discussion

The present study was conducted to investigate the seroprevalence of rubella virus antibodies (IgG and IgM) among aborted women attending the obstetrics and gynecology department of various hospitals in Ibb city; Yemen. We observed an overall seroprevalence of rubella virus IgG 99.33%, while seroprevalence of rubella virus IgM was negative in all aborted women. The high prevalence of rubella IgG among aborted women as well as the rubella vaccine in Yemen started in 201512 indicating previous exposure to viral infection and the high percentage of immunity due to viral infection. The prevalence of rubella IgM antibody observed in this study almost agreed with that described in Odisha, India.3 No past study has studied the association between abortion and rubella virus infection in Yemen and different countries. Reports from various countries showed the prevalence of rubella among schoolgirls, pregnant women and women at productive age (child bearing age).13–15,18–22 In the current study, there was no statistically significant difference between the rate of rubella virus antibodies and residence age, socioeconomic status, education levels, abortion time, congenital defects and symptoms. On the other hand, there was a significant between rubella IgG antibody and a previous number of abortions.

Conclusion

Overall, our study showed a high prevalence of rubella virus IgG among aborted women in Ibb city, Yemen. This outcome indicates that they had immunity against rubella virus. Furthermore, the results revealed that the prevalence of rubella IgG among women living in rural was more than urban. Other studies recommend using another technique like PCR to detect the risk of rubella virus infection among aborted women. Additional studies assessing the causal agents of abortion in Ibb city and new cities in Yemen, with suitable sampling and sample numbers are required.

Acknowledgments

We would like to express our deep gratitude to all colleagues in Faculty of Allied Medical Sciences, The National University, Ibb branch who participated in this study, for their faithfully cooperation. We also thank Dr. Soaad Al-Qadri the head of the gynecological and obstetrics department at AL-Thawrah hospital. We also thank Dr. Ghadeer Shokri, Ekhtear Al-Absi, Dr. Eman Al-Awzali, Dr. Lara Al-Awzali, Dr. Abdulmajeed Al-Hakeem and Dr. Ebrahim Al-Aaei who enriched us with all the information required in the field of research methodology. Finally, we would thank all laboratory staff of Zain medical laboratories especially, Dr. Ali Al-Rashidi for their help in the practical part of the research.

Funding

None.

Conflicts of interest

The authors have no conflict of interest to declare.

References

  1. Chimhuya S, Manangazira P, Mukaratirwa A, et al. Trends of rubella incidence during a 5-year period of case based surveillance in Zimbabwe. BMC Public Health. 2015;15:294.
  2. Lulandala L, Mirambo MM, Matovelo D, et al. Acute rubella virus infection among women with spontaneous abortion in Mwanza city, Tanzania. J Clin Diagn Res. 2017;11(3):25–27.
  3. Sahoo PK, Sabat J, Shubhadra S, et al. Burden of Rubella virus infection among females attending tertiary care hospitals of Odisha, India: a need for adult women vaccination. Human Vaccines & Immunotherapeutics. 2021;17(10):3757–3760.
  4. Woyessa AB, Ali MS, Korkpor TK, et al. Rubella transmission and the risk of congenital rubella syndrome in Liberia: a need to introduce rubella-containing vaccine in the routine immunization program. BMC Infectious Diseases. 2019;19(1):813.
  5. Vueba A, Faria C, Almendra R, et al. Seroepidemiology study of Cytomegalovirus and Rubella in pregnant women in Luanda, Angola: geospatial distribution and its association with socio-demographic and clinical-obstetric determinants. BMC Infectious Diseases. 2022;22(1):124.
  6. Al Dossary RA, Althuwaiqeb S, Alkharsah KR, et al. Susceptibility to Rubella Infection and Incidence of Congenital Rubella Infection: 6 Years Retrospective Study. Int J Gen Med. 2022;15:3605–3611.
  7. Hong H, Malfeld S, Smit S, et al. A retrospective 5-year review of rubella in South Africa prior to the introduction of a rubella-containing vaccine. Plos one. 2022;17(5):e0265870.
  8. Figueroa-Damián R, Ortiz-Ibarra F, Arredondo-García J, et al. The outcome of pregnancies complicated by rubella, 1990-1997. Salud Publica de Mexico. 1999;41(4):271–277.
  9. Bale Jr JF. Measles, mumps, rubella, and human parvovirus B19 infections and neurologic disease. Handbook of Clinical Neurology. 2014;121:1345–1353.
  10. Miller E, Cradock-Watson J, Pollock T. Consequences of confirmed maternal rubella at successive stages of pregnancy. Lancet. 1982;2(8320):781–784.
  11. Plotkin SA. Rubella eradication: not yet accomplished, but entirely feasible. J Infect Dis. 2021;224(4):S360–S366.
  12. Organization WH. Progress report on emergency preparedness and response: World Health Organization. Regional Office for the Eastern Mediterranean. 2015.
  13. Sallam T, Al-Jaufy A, Al-Shaibany K, et al. Prevalence of antibodies to measles and rubella in Sana’a, Yemen. Vaccine. 2006;24(37–39):6304–6308.
  14. Sallam TA, Raja'a YA, Benbrake MS, et al. Prevalence of rubella antibodies among schoolgirls in Sana'a, Republic of Yemen. Eastern Mediterranean Health J. 2003;9(1–2):148–151.
  15. Al-Madhagi A, Al-Moyed K, Almezgagi MM, et al. Prevalence of rubella IgG antibodies among productive-age‎ women in Al-Mahweet governorate, Yemen. Univ J of Pharmal Res. 2020;5(4):28–32.
  16. Al-Thobhani A, Abdullah Q, Alghalibi S, et al. Seroprevalence of Rubella Virus antibodies among pregnant women in Hodeidah city, Western Yemen. J Hum Virol Retrovirol. 2023;10(1):7–10.
  17. Abbas AB, Saba A-M, Al-Zafri J, et al. Seroprevalence of cytomegalovirus antibodies among aborted women in Ibb city-Yemen. J Hum Virol Retroviral. 2022;9(2):49–52.
  18. Eno AA, Makemgue LS, Tonye III DS, et al. Seroprevalence of rubella-specific IgM and IgG antibodies among pregnant women in a Catholic Hospital in Yaoundé, Cameroon. Int J Biological Chem Sci. 2018;12(3):1123–1130.
  19. Hossain A. Seroepidemiology of rubella in Saudi Arabia. J Tropical Pediatr. 1989;35(4):169–170.
  20. Alsibiani SA. Rubella immunity among pregnant women in Jeddah, Western region of Saudi Arabia. Obstetrics and Gynecology International. 2014;2014.
  21. Pandolfi E, Gesualdo F, Rizzo C, et al. Global seroprevalence of rubella among pregnant and childbearing age women: a meta-analysis. Eur J Public Health. 2017;27(3):530–537.
  22. Olajide OM, Aminu M, Randawa AJ, et al. Seroprevalence of rubella-specific IgM and IgG antibodies among pregnant women seen in a tertiary hospital in Nigeria. Int J Women's Health. 2015;7:75–83.
Creative Commons Attribution License

©2023 Abbas, et al. This is an open access article distributed under the terms of the, which permits unrestricted use, distribution, and build upon your work non-commercially.