- Research article
- Open Access
- Open Peer Review
Finger joint laxity, number of previous pregnancies and pregnancy induced back pain in a cohort study
© Lindgren and Kristiansson; licensee BioMed Central Ltd. 2014
- Received: 30 May 2013
- Accepted: 29 January 2014
- Published: 6 February 2014
General joint hypermobility is estimated to affect about 10% of the population and is a prerequisite of heritable connective tissue disorders where fragile connective tissue is a prominent feature. Pregnancy induced back pain is common whereas about 10% of women still have disabling pain several years after childbirth. The pathogenesis of the pain condition is uncertain, although several risk factors are suggested including general joint hypermobility. In the present study, the possible association of peripheral joint mobility in early pregnancy on the incidence of back pain with onset during pregnancy and persisting after childbirth was explored.
A cohort of 200 pregnant women recruited from antenatal health care clinics was assessed by questionnaire and clinical examination, including measurement of passive abduction of the left fourth finger, throughout pregnancy and at 13 weeks postpartum. Comparisons were made between women with and without back pain. Statistical tests used were χ2-test, t-test, Spearman correlation and multiple logistic regression.
In the cohort, the mean passive abduction angle of the left fourth finger increased from 40.1° in early pregnancy to 41.8° at the postpartum appointment. At the postpartum appointment, women in the back pain group had a significantly larger mean passive abduction angle of the left fourth finger of 4.4°, twice as many previous pregnancies and deliveries, and more than twice as frequent back pain in previous pregnancy, as compared with women with no persistent back pain. A similar pattern was displayed in late pregnancy. In a multiple regression analysis, the passive abduction angle of the left fourth finger in early pregnancy and the number of previous pregnancies were positively, significantly and independently associated to the incidence of back pain in late pregnancy and postpartum.
Finger joint laxity as a reflection of constitutional weakness of connective tissue and number of previous pregnancies were associated with the development of back pain induced in pregnancy and persisting after childbirth. These factors may provide a foundation for development of targeted prevention strategies, but this have to be confirmed in future research including measurement of general joint laxity.
- Finger joint laxity
- Back pain
General joint hypermobility is estimated to affect about 10% of the population and is a prerequisite of heritable connective tissue disorders where fragile connective tissue is a prominent feature [1–4]. The cause of the higher prevalence of general joint hypermobility among women is uncertain however suggested to be related to sex-specific adaptations of the connective tissue . Throughout pregnancy, with dramatic hormonal changes, an increased mobility of peripheral joints with partial reversion after delivery has been reported [6–8].
One in three women in the world experience back pain induced during pregnancy with the number of previous deliveries as a strong determinant . Other known determinants of pregnancy induced back pain include early menarche, hormone contraceptive use before first pregnancy, physically demanding work and emotional distress [10–12]. In addition, hormonal and reproductive factors have been associated with risk of chronic low back pain .
In most women, the back pain disappears soon after delivery [14, 15]. However, in about 8% of women disabling pregnancy-induced back pain continues several years after delivery, even up until old age [15, 16], that entails severe changes of everyday life activities . Characteristics of women with slow regression of back pain include early onset, longer periods of pain and higher intensity of pain during pregnancy, and work dissatisfaction, disbelief in improvement and emotional distress, and heavy work situation regardless of pregnancy [14, 18–21].
The connective tissue of the low back and pelvis are fundamental to transmitting body forces between the axial skeleton and the lower extremities. Results from several studies indicate that pregnancy affects the connective tissue in general and in the pelvic region particularly [22, 23]. Thus, hormonal influence on particularly fragile connective tissue could be an important factor in the development of pregnancy-induced back pain persisting after childbirth. In a previous study self-reported joint hypermobility was a determinant of back pain persistent after childbirth .
In the present study, using previously studied data, we hypothesized that peripheral joint laxity, as a proxy of general joint hypermobility, measured in early pregnancy was associated with pregnancy-induced back pain in late pregnancy and three months postpartum.
All pregnant women living in two districts of the city of Sundsvall, Sweden, were identified through check-ups at the antenatal care units in the metropolitan area, at the offices of practicing gynecologists and at the outpatient clinic at the local hospital. All Caucasian and Swedish speaking women attending during early pregnancy in 1991 were sampled for this study. Two hundred and twenty-seven pregnant women fulfilled the sampling criteria, of whom 222 attended the antenatal care units serving the two districts. These 222 women were invited to participate in the study. Twenty-two declined participation, which left 200 (88.1%) women as the final study population. All women were apparently healthy, and none had ongoing medication. During the follow-up period, 10 women left the study because of spontaneous abortion, two women declined further participation, and one woman moved from the area.
The methods for this back pain study have been described in detail previously . Briefly, data were collected at three appointments during pregnancy, on average at 11 (range 6 to 19), 24 (range 21 to 27) and 36 (range 34 to 38) completed gestational weeks, and at a fourth appointment 13 (range 4 to 29) weeks postpartum. Early pregnancy was defined as gestational week 11. At each appointment, the women completed a questionnaire and underwent a general clinical examination including measurement of the passive abduction angle of the left fourth finger. For all women, the duration of pregnancy was confirmed by ultrasonography in estimated gestational week 19 and was registered as completed weeks of gestation.
The questionnaire included an instrument for measuring ongoing pain, its location, intensity, and consequences in terms of disability. In addition, there were questions about previous obstetric history, previous back pain problems and current smoking habits. The questionnaire was completed in privacy with no time limit and was checked for completeness.
Women who reported pain were instructed to indicate the location of the pain on a pain drawing. More than one location could be indicated. The back locations were coded as cervical spine, thoracic spine, lumbar spine, and sacral spine. In the present study, women who reported any of these four back pain locations were pooled into a group labeled “back pain” and women who reported neither of these back pain locations were pooled into a group labeled “no back pain”, at each study visit. The women were also asked to estimate the date of onset of pain for each pain location. Only one onset time was registered at each appointment. If several back pain locations were indicated, the time of onset of the lowest back pain location was registered.
The intensity of pain at the moment and the worst pain during the past week, was described on two visual analogue scales (VAS): 0 mm indicating no pain and 100 mm indicating intolerable pain .
Twelve disability ratings measuring the ability to perform activities of daily living were recorded on VAS scales, where 0 mm indicated no restriction on the activity and 100 mm indicated inability to do the activity. The mean score of the 12 ratings was used as the disability rating index (DRI) .
At study inclusion weight and height were measured. Height was measured barefoot with a wall-mounted tape measure to the nearest centimeter. Weight was measured with indoor clothing on a balance lever scale with digital presentation of kilograms to one decimal point. Body mass index was calculated as weight (kg)/height2 (m2).
No systematic pain treatment was given, but women with severe pain were offered sick listing or physiotherapy, which included sacroiliac belt and pool training.
Ethics and consent
Permission for this study was obtained from the Research and Ethics Committee of the University of Umeå and all women gave their informed consent. The procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation and with the Helsinki Declaration of 1975, as revised in 1983.
Descriptive data were given as frequencies, percentages, means and standard deviations (SD). Spearman correlation was used to test association of inter-individual abduction angles at different time intervals. Differences between the dependent intra-individual abduction angles at different time intervals were tested with paired t-test. Comparison between groups regarding continuous data was performed using t-test and comparisons of categorical data with χ2. Only two-tailed tests were used and a p-value <0.05 was considered statistically significant. No account was taken of multiple comparisons.
Characteristics in early pregnancy of the women included in the study
Mean (S.D.) or proportion (%)
Body mass index (kg/m2)
No cigarette smoking (%)
Pregnant for the first time (%)
Number of previous pregnancies
Number of previous deliveries
Time since previous delivery (yr)
Previous back pain, not during pregnancy (%)
Back pain in previous pregnancy (%)
Abduction angle of the left fourth finger (°) throughout pregnancy and post-partum
24 to 62
28 to 64
24 to 59
13 w pp
26 to 58
Change from g.w. 11 to 24
Change from g.w. 24 to 36
Change from g.w. 36 to 13 w pp
Change from g.w. 11 to 13 w pp
The point prevalence rate of women reporting back pain with onset during the present pregnancy increased from 19% in gestational week 11, to 47% and 49% in gestational weeks 24 and 36, respectively, with a clear decline to 9% (16 women) at the postpartum appointment. At this particular time point, 14 of these 16 women reported pain located in the sacral back region and 2 reported pain in the lumbar region. The mean pain intensity at the postpartum appointment among those 16 women, 38.1 mm (SD 31.3), was significantly higher (p < 0.0001) than the mean pain intensity of 12.4 mm (SD 23.4) reported by the 154 women without back pain at this time. Another significant difference (p = 0.04) was shown for the disability rating index, 13.3 (SD 17.5) and 3.4 (SD 9.0), respectively, for the pain and no-pain groups postpartum.
Factors measured in early pregnancy by women with and without persistent back pain post partum
Back pain group
No back pain group
Mean (SD) or n (%)
Mean (S.D.) or n (%)
AA in early pregnancy (°)
AA pp – AA early pregnancy (°)
Body mass index (kg/m2)
Cigarette smoking (%)
No. of previous pregnancies
No. of previous deliveries
Time since previous delivery (yr)
Previous back pain, not in pregnancy (%)
Back pain in previous pregnancy (%)
Association between factors in early pregnancy and back pain induced in pregnancy persistent post partum
AA in early pregnancy (°)
Body mass index (kg/m2)
Cigarette smoking (%)
No. of previous pregnancies
Previous back pain (%)
To find determinants for reported back pain with onset during the present pregnancy and persisting postpartum a multiple logistic regression analysis was performed, with all factors measured in early pregnancy included as independent variables, Table 4. The abduction angle of the left fourth finger in early pregnancy and the number of previous pregnancies were both positively, significantly and independently associated with the incidence of back pain. The concordance of the model was 83%.
Mean back pain incidence estimates based on the passive abduction angle of the left fourth finger in early pregnancy and the number of previous pregnancies was computed using the logistic regression technique and illustrated in Figure 2. Women with the greatest passive abduction angle of the left fourth finger and the highest number of previous pregnancies showed the highest back pain incidence, and vice versa. When the most extreme observed combinations of passive abduction angle of the left fourth finger and number of previous pregnancies were used, the highest incidence of back pain was estimated to 94% and the lowest to 0.8%.
The ability of the passive abduction angle of the left fourth finger measurement in early pregnancy to predict the risk of development of back pain with onset during pregnancy persisting 3 months postpartum was calculated using the receiver operating characteristic curve. At the optimal cut-off angle of approximately 40°, the sensitivity and specificity were 0.42 and 0.63, respectively. In a logistic regression analysis with back pain as the dependent variable and the finger angle as the independent variable the area under the curve was 0.66 and the odds of an event of back pain postpartum increased by a factor of 2.1 (C.I. 1.1-4.4) for each 10° increase of the angle (p = 0.03).
The number of previous pregnancies and the fourth finger joint laxity in early pregnancy, but not the change of joint laxity throughout pregnancy or previous back pain, were positively and independently associated to the incidence of pregnancy-induced back pain reported in late pregnancy and three months after delivery. The association of finger joint laxity might be as a reflection of general joint laxity in pregnancy and postpartum, which could be used in future preventive care. On the individual level, the ability of the finger laxity measured in early pregnancy to predict back pain incidence was moderate.
The association between peripheral joint laxity measured in early pregnancy and back pain induced in pregnancy and persisting after delivery, has not been presented before to the best of our knowledge. However, in an epidemiological study the women reporting a diagnosis of perceived joint hypermobility had a 1.5 times greater risk of having low back pain persistent 6 months after childbirth, which is in accordance with our results . In contrast to our findings, a similar previous study displayed an inverse association between joint mobility in early pregnancy and reported back pain in pregnancy, although restricted to women pregnant for the first time . In that study, the same method of finger joint mobility measurement was used but without taking into account whether the back pain started before or during the present pregnancy, which might explain the divergent results. The association between pregnancy induced back pain and number of previous pregnancies and deliveries has been established previously .
The association of finger joint laxity on development of back pain in pregnancy might be as a reflection of general joint laxity in pregnancy and postpartum, which in turn reflects a constitutional weakness of connective tissue [2, 29]. The concept that the degree of joint laxity of any one individual is generalized throughout the body and that the majority of the stiffness of the metacarpophalangeal joints of the hand is a result of the capsule ligament complex and not the muscle-tendon units supports this view , as well as reported high correlations between finger joint laxity and general joint mobility measures [27, 31, 32]. In parallel, a constitutional connective tissue weakness in the pelvic region is suggested as a cause in women presenting with genitourinary prolapse and urinary incontinence [33, 34].
Strengths of the present study were the high participation rate, the low drop-out rate, inclusion of only Caucasian women, assessment of only the left hand and one person measured the finger joint laxity at all time periods. In addition, possible confounding factors were controlled for in the multiple regression analyses.
There were several limitations of this study. Information of the validity of the used angle measurement device was limited although reassuring . Stability in repeated angle measurements of the device was ascertained by intra-individual coefficient of variance between 0.07 and 0.08 in the present study. In previous studies of finger joint mobility two papers have presented reliability as coefficients of variance. In these studies lower coefficients of variance (1.5% and 3.6%) were presented with tests repeated within the same day as compared to several months in the present study [35, 36]. Also, the wide dispersion of the time since delivery might have distorted the data, since recovery might be expected 29 weeks after delivery but not necessarily after 4 weeks. In addition, the number of women with persistent back pain after delivery was small and there was no information of socio-economic data. All these limitations probably reduced the sensitivity of the study to show only the strongest associations, and suggest that the chance of a false positive in detecting the shown associations is small.
Our finding of an association between peripheral joint laxity and pregnancy-induced back pain needs to be confirmed in future research, including measurement of general joint laxity measurement with high reliability, such as Beighton score .
Finger joint laxity as a reflection of constitutional weakness of connective tissue and number of previous pregnancies were associated with the development of back pain induced in pregnancy and persisting after childbirth. These factors may provide a foundation for the development of targeted prevention strategies for women in early pregnancy at risk of developing disabling back pain after childbirth.
This work was supported by Uppsala University, Medical Faculty and the Emil Andersson Foundation for Medical Research, Sweden.
- Larsson LG, Baum J, Mudholkar GS, Srivastava DK: Hypermobility: prevalence and features in a Swedish population. Br J Rheumatol. 1993, 32 (2): 116-119. 10.1093/rheumatology/32.2.116.View ArticlePubMedGoogle Scholar
- Grahame R: Joint hypermobility and genetic collagen disorders: are they related?. Arch Dis Child. 1999, 80 (2): 188-191. 10.1136/adc.80.2.188.View ArticlePubMedPubMed CentralGoogle Scholar
- Remvig L, Jensen DV, Ward RC: Epidemiology of general joint hypermobility and basis for the proposed criteria for benign joint hypermobility syndrome: review of the literature. J Rheumatol. 2007, 34 (4): 804-809.PubMedGoogle Scholar
- De Paepe A, Malfait F: The Ehlers-Danlos syndrome, a disorder with many faces. Clin Genet. 2012, 82 (1): 1-11. 10.1111/j.1399-0004.2012.01858.x.View ArticlePubMedGoogle Scholar
- Miller BF, Hansen M, Olesen JL, Schwarz P, Babraj JA, Smith K, Rennie MJ, Kjaer M: Tendon collagen synthesis at rest and after exercise in women. J Appl Physiol. 2007, 102 (2): 541-546.View ArticlePubMedGoogle Scholar
- Garras DN, Carothers JT, Olson SA: Single-leg-stance (flamingo) radiographs to assess pelvic instability: how much motion is normal?. J Bone Joint Surg Am. 2008, 90 (10): 2114-2118. 10.2106/JBJS.G.00277.View ArticlePubMedGoogle Scholar
- Calguneri M, Bird HA, Wright V: Changes in joint laxity occurring during pregnancy. Ann Rheum Dis. 1982, 41 (2): 126-128. 10.1136/ard.41.2.126.View ArticlePubMedPubMed CentralGoogle Scholar
- Schauberger CW, Rooney BL, Goldsmith L, Shenton D, Silva PD, Schaper A: Peripheral joint laxity increases in pregnancy but does not correlate with serum relaxin levels. Am J Obstet Gynecol. 1996, 174 (2): 667-671. 10.1016/S0002-9378(96)70447-7.View ArticlePubMedGoogle Scholar
- Bjelland E, Eskild E, Johansen R, Eberhard-Gran M: Pelvic Girdle Pain in Pregnancy: The Impact of Parity. 2010, Oslo: Norwegian Institute of Public HealthGoogle Scholar
- Bjelland EK, Kristiansson P, Nordeng H, Vangen S, Eberhard-Gran M: Hormonal contraception and pelvic girdle pain during pregnancy: a population study of 91 721 pregnancies in the Norwegian Mother and Child Cohort. Hum Reprod. 2013, 28 (11): 3134-3140. 10.1093/humrep/det301.View ArticlePubMedPubMed CentralGoogle Scholar
- Kumle M, Weiderpass E, Alsaker E, Lund E: Use of hormonal contraceptives and occurrence of pregnancy-related pelvic pain: a prospective cohort study in Norway. BMC Pregn Childbirth. 2004, 4 (1): 11-10.1186/1471-2393-4-11.View ArticleGoogle Scholar
- Bjelland EK, Eberhard-Gran M, Nielsen CS, Eskild A: Age at menarche and pelvic girdle syndrome in pregnancy: a population study of 74 973 women. Bjog. 2011, 118 (13): 1646-1652. 10.1111/j.1471-0528.2011.03099.x.View ArticlePubMedGoogle Scholar
- Wijnhoven HA, de Vet HC, Smit HA, Picavet HS: Hormonal and reproductive factors are associated with chronic low back pain and chronic upper extremity pain in women--the MORGEN study. Spine (Phila Pa 1976). 2006, 31 (13): 1496-1502. 10.1097/01.brs.0000220706.96724.76.View ArticleGoogle Scholar
- Kristiansson P, Svardsudd K, von Schoultz B: Back pain during pregnancy: a prospective study. Spine (Phila Pa 1976). 1996, 21 (6): 702-709. 10.1097/00007632-199603150-00008.View ArticleGoogle Scholar
- Albert H, Godskesen M, Westergaard J: Prognosis in four syndromes of pregnancy-related pelvic pain. Acta Obstet Gynecol Scand. 2001, 80 (6): 505-510. 10.1080/j.1600-0412.2001.080006505.x.View ArticlePubMedGoogle Scholar
- Svensson HO, Andersson GB, Johansson S, Wilhelmsson C, Vedin A: A retrospective study of low-back pain in 38- to 64-year-old women. Frequency of occurrence and impact on medical services. Spine (Phila Pa 1976). 1988, 13 (5): 548-552. 10.1097/00007632-198805000-00019.View ArticleGoogle Scholar
- Elden H, Lundgren I, Robertson E: Life’s pregnant puase of pain: Pregnant women’s experiences of pelvic girdle pain related to life: A Swedish interview study. Sex Reprod Health. 2013, 4 (1): 29-34. 10.1016/j.srhc.2012.11.003.View ArticleGoogle Scholar
- Ostgaard HC, Andersson GB: Postpartum low-back pain. Spine (Phila Pa 1976). 1992, 17 (1): 53-55. 10.1097/00007632-199201000-00008.View ArticleGoogle Scholar
- Gutke A, Ostgaard HC, Oberg B: Predicting persistent pregnancy-related low back pain. Spine (Phila Pa 1976). 2008, 33 (12): E386-E393. 10.1097/BRS.0b013e31817331a4.View ArticleGoogle Scholar
- To WW, Wong MW: Factors associated with back pain symptoms in pregnancy and the persistence of pain 2 years after pregnancy. Acta Obstet Gynecol Scand. 2003, 82 (12): 1086-1091. 10.1046/j.1600-0412.2003.00235.x.View ArticlePubMedGoogle Scholar
- Olsson CB, Nilsson-Wikmar L, Grooten WJ: Determinants for lumbopelvic pain 6 months postpartum. Disabil Rehabil. 2012, 34 (5): 416-422. 10.3109/09638288.2011.607212.View ArticlePubMedGoogle Scholar
- Putschar WG: The structure of the human symphysis pubis with special consideration of parturition and its sequelae. Am J Phys Anthrop. 1976, 45: 589-594. 10.1002/ajpa.1330450324.View ArticlePubMedGoogle Scholar
- Marnach ML, Ramin KD, Ramsey PS, Song SW, Stensland JJ, An KN: Characterization of the relationship between joint laxity and maternal hormones in pregnancy. Obstet Gynecol. 2003, 101 (2): 331-335. 10.1016/S0029-7844(02)02447-X.PubMedGoogle Scholar
- Mogren IM: BMI, pain and hyper-mobility are determinants of long-term outcome for women with low back pain and pelvic pain during pregnancy. Eur Spine J. 2006, 15 (7): 1093-1102. 10.1007/s00586-005-0004-9.View ArticlePubMedPubMed CentralGoogle Scholar
- Carlsson AM: Assessment of chronic pain. I. Aspects of the reliability and validity of the visual analogue scale. Pain. 1983, 16 (1): 87-101. 10.1016/0304-3959(83)90088-X.View ArticlePubMedGoogle Scholar
- Salen BA, Spangfort EV, Nygren AL, Nordemar R: The Disability Rating Index: an instrument for the assessment of disability in clinical settings. J Clin Epidemiol. 1994, 47 (12): 1423-1435. 10.1016/0895-4356(94)90086-8.View ArticlePubMedGoogle Scholar
- Ostgaard HC, Andersson GB, Schultz AB, Miller JA: Influence of some biomechanical factors on low-back pain in pregnancy. Spine (Phila Pa 1976). 1993, 18 (1): 61-65. 10.1097/00007632-199301000-00010.View ArticleGoogle Scholar
- Ostgaard HC: Back pain and pregnancy. 1991, Goteborg, Sweden: Goteborg UniversityGoogle Scholar
- Simmonds JV, Keer RJ: Hypermobility and the hypermobility syndrome. Man Ther. 2007, 12 (4): 298-309. 10.1016/j.math.2007.05.001.View ArticlePubMedGoogle Scholar
- Kuo PH, Deshpande AD: Muscle-tendon units provide limited contributions to the passive stiffness of the index finger metacarpophalangeal joint. J Biomech. 2012, 45 (15): 2531-2538. 10.1016/j.jbiomech.2012.07.034.View ArticlePubMedGoogle Scholar
- LeResche L, Sherman JJ, Huggins K, Saunders K, Mancl LA, Lentz G, Dworkin SF: Musculoskeletal orofacial pain and other signs and symptoms of temporomandibular disorders during pregnancy: a prospective study. J Orofac Pain. 2005, 19 (3): 193-201.PubMedGoogle Scholar
- Bird HA, Brodie DA, Wright V: Quantification of joint laxity. Rheumatol Rehabil. 1979, 18 (3): 161-166. 10.1093/rheumatology/18.3.161.View ArticlePubMedGoogle Scholar
- Norton PA, Baker JE, Sharp HC, Warenski JC: Genitourinary prolapse and joint hypermobility in women. Obstet Gynecol. 1995, 85 (2): 225-228. 10.1016/0029-7844(94)00386-R.View ArticlePubMedGoogle Scholar
- Soderberg MW, Falconer C, Bystrom B, Malmstrom A, Ekman G: Young women with genital prolapse have a low collagen concentration. Acta Obstet Gynecol Scand. 2004, 83 (12): 1193-1198. 10.1080/j.0001-6349.2004.00438.x.View ArticlePubMedGoogle Scholar
- Jobbins B, Bird H, Wrigth V: A joint hyperextensometer for the quantification of joint laxity. Eng Med. 1979, 8: 103-104. 10.1243/EMED_JOUR_1979_008_024_02.View ArticleGoogle Scholar
- Sweetman BJ, Anderson JA, Dalton ER: The relationships between little-finger mobility, lumbar mobility, straight-leg raising, and low-back pain. Rheumatol Rehabil. 1974, 13 (4): 161-166. 10.1093/rheumatology/13.4.161.View ArticlePubMedGoogle Scholar
- Juul-Kristensen B, Rogind H, Jensen DV, Remvig L: Inter-examiner reproducibility of tests and criteria for generalized joint hypermobility and benign joint hypermobility syndrome. Rheumatology (Oxford). 2007, 46 (12): 1835-1841. 10.1093/rheumatology/kem290.View ArticleGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2393/14/61/prepub
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