Postmenopausal weight change and incidence of fracture: post hoc findings from Women’s Health Initiative Observational Study and Clinical TrialsBMJ 2015; 350 doi: http://dx.doi.org/10.1136/bmj.h25 (Published 27 January 2015) Cite this as: BMJ 2015;350:h25
- Carolyn J Crandall, professor of medicine1,
- Vedat O Yildiz, statistical analyst2,
- Jean Wactawski-Wende, professor3,
- Karen C Johnson, professor4,
- Zhao Chen, professor5,
- Scott B Going, professor6,
- Nicole C Wright, assistant professor7,
- Jane A Cauley, professor of epidemiology and vice chair for research8
- 1David Geffen School of Medicine at University of California, Los Angeles, Division of General Internal Medicine and Health Services Research, UCLA Medicine/GIM, 911 Broxton Avenue, 1st floor, Los Angeles, CA, 90024, USA
- 2Center for Biostatistics, Ohio State University, 2012 Kenny Road, Columbus, Ohio, USA
- 3Department of Social and Preventive Medicine, University at Buffalo, State University of New York, 65 Farber Hall, 3435 Main Street, Buffalo, NY 14214-3000 State University of NY at Buffalo, Buffalo, NY, USA
- 4Department of Preventive Medicine, University of Tennessee Health Science Center, 66 N. Pauline, Suite 633, Memphis, TN 38163, USA
- 5Division of Epidemiology and Biostatistics, University of Arizona, Tucson, Arizona, USA
- 6Department of Nutritional Sciences, University of Arizona, Tucson, Arizona, USA
- 7Department of Epidemiology, University of Alabama at Birmingham, RPHB 523C, Birmingham, AL, 35294, USA
- 8Department of Epidemiology, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA
- Correspondence to: C J Crandall
- Accepted 5 December 2014
Objectives To determine associations between postmenopausal change in body weight and incidence of fracture and associations between voluntary and involuntary weight loss and risk of fracture.
Design Post hoc analysis of data from the Women’s Health Initiative Observational Study and Clinical Trials.
Setting 40 clinical centers in the United States.
Participants 120 566 postmenopausal women, aged 50-79 at baseline (1993-98), followed through 2013 (mean fracture follow-up duration 11 years from baseline).
Exposures Annualized percentage change in measured body weight from baseline to year 3, classified as stable (<5% change), weight loss (≥5%), or weight gain (≥5%). Self assessment of whether weight loss was intentional or unintentional. Cox proportional hazards regression models were adjusted for age, race/ethnicity, baseline body mass index (BMI), smoking, alcohol intake, level of physical activity, energy expenditure, calcium and vitamin D intake, physical function score, oophorectomy, hysterectomy, previous fracture, comorbidity score, and drug use.
Main outcomes Incident self reported fractures of the upper limbs, lower limbs, and central body; hip fractures confirmed by medical records.
Results Mean participant age was 63.3. Mean annualized percent weight change was 0.30% (95% confidence interval 0.28 to 0.32). Overall, 79 279 (65.6%) had stable weight; 18 266 (15.2%) lost weight; and 23 021 (19.0%) gained weight. Compared with stable weight, weight loss was associated with a 65% higher incidence rates of fracture in hip (adjusted hazard ratio 1.65, 95% confidence interval 1.49 to 1.82), upper limb (1.09, 1.03 to 1.16), and central body (1.30, 1.20 to 1.39); weight gain was associated with higher incidence rates of fracture in upper limb (1.10, 1.05 to 1.18) and lower limb (1.18, 1.12 to 1.25). Compared with stable weight, unintentional weight loss was associated with a 33% higher incidence rates of hip fracture (1.33, 1.19 to 1.47) and increased incidence rates of vertebral fracture (1.16, 1.06 to 1.26); intentional weight loss was associated with increased incidence rates of lower limb fracture (1.11, 1.05 to 1.17) and decreased incidence of hip fracture (0.85, 0.76 to 0.95).
Conclusions Weight gain, weight loss, and intentional weight loss are associated with increased incidence of fracture, but associations differ by fracture location. Clinicians should be aware of fracture patterns after weight gain and weight loss.
The influence of body weight on the risk of fracture is complex. Low body weight is considered a risk factor for osteoporotic fracture.1 There is, however, increasing recognition that a high proportion of postmenopausal women with low trauma fractures are obese.2 Moreover, beyond low body weight per se, change in body weight can have an important influence on risk of fracture. For example, longitudinal studies of postmenopausal white women in the United States have found that weight loss increases the risk of subsequent hip and other frailty fractures.3 4 5 6 Similar studies of postmenopausal non-white women are lacking, yet differences in body weight distributions7 and absolute risk of fracture8 across racial groups are striking.
There is also a paucity of information on whether the influence of weight change on subsequent risk of fracture varies by anatomical site. In longitudinal studies of white women aged ≥65, weight loss measured in various ways (over four years or since maximum weight or since age 50) was associated with an increased risk of hip fracture,4 5 6 whereas weight gain since age 25 was associated with a higher risk of ankle fracture.9 No longitudinal studies, however, have focused specifically on how weight change can differentially influence upper limb, lower limb, hip, and central body fractures among postmenopausal white or non-white women in the US. Also, few studies have considered the reason for underlying weight loss in the analysis of associations between weight loss and fractures. This distinction might be important because serious illness could be an underlying cause of both involuntary weight loss and osteoporosis. In one study, associations between weight loss and increased risk of frailty fracture were significant only among women reporting involuntary, but not voluntary weight loss,3 whereas in another study, voluntary and involuntary weight loss among overweight women were each associated with similar (2.5-fold) increases in risk of hip fracture.4 Neither of those two studies adjusted for baseline weight or body mass index (BMI).
We investigated associations between change in body weight (baseline to third annual visit) and subsequent incidence of fracture classified by anatomical region (for example, upper limb, lower limb, central body) among postmenopausal women and to what extent self reported voluntary and involuntary weight loss are associated with increased incidence of fracture. We hypothesized that associations between weight loss and increased fracture incidence would be more pronounced for hip fractures than for limb fractures because of the potential loss in soft tissue padding around the hip that could counteract traumatic forces. We also hypothesized that even voluntary weight loss would be associated with an increased incidence of hip fracture. We further postulated that weight gain would increase the incidence of limb fractures, as the upper and lower extremities have little overlying soft tissue to absorb the increased impact resulting from weight gain and because of poor neuromuscular conditioning.
Women’s Health Initiative Study
We used data from the Women’s Health Initiative Observational Study and the Women’s Health Initiative Clinical Trials. At 40 clinical centers nationwide between 1993 and 1998, the Women’s Health Initiative study enrolled postmenopausal women aged 50-79 at baseline who were free from serious cardiac, pulmonary, renal, and hepatic conditions and had at least three years’ life expectancy.10 11 12 The three placebo controlled Women’s Health Initiative clinical trials tested several interventions among postmenopausal women: a low fat eating pattern, menopausal hormone therapy, and calcium and vitamin D supplementation.12 The Women’s Health Initiative Observational Study examined the predictors and natural course of important causes of morbidity and mortality in postmenopausal women.11 Recruitment details are available at https://cleo.whi.org/about/SitePages/About%20WHI.aspx. The combined studies enrolled 161 808 participants (93 676 in the observational study and 68 132 in the clinical trial). Our analytic sample consisted of 120 566 participants from the two studies for whom information was available regarding weight change (from baseline to year three) and at least one year of follow-up (after the year three visit) regarding incident fractures (fig 1⇓). Follow-up data were available for 31 March 1995 through 17 September 2013.
Participants were asked to complete baseline self assessment questionnaires. Weight and height were measured at baseline and at the third annual follow-up visit with standardized protocols. BMI was calculated as body weight in kilograms (kg) divided by the square of height in meters. Waist:hip ratio was calculated as the ratio of waist circumference (cm) to hip circumference (cm).
Our study outcome was incidence of fracture. Each year, participants were asked to report fracture events since the previous annual visit: “Has a doctor told you for the first time that you have a new broken, crushed, or fractured bone? Which bone did you break?” Questionnaire response choices included: hip, upper leg (not hip), pelvis, knee (patella), lower leg or ankle, foot (not toe), spine or back (vertebra), lower arm or wrist, hand (not finger), elbow, and upper arm or shoulder. We grouped each fracture into one of the following (mutually exclusive) categories: upper limb fracture (elbow, hand except fingers, lower arm/wrist, upper arm/humerus or shoulder), lower limb (foot except toes, knee/patella, upper leg except hip, lower leg/ankle), central body (hip, pelvis, and spine). All hip fractures were centrally adjudicated. Because our goal was to examine incidence of fracture subsequent to a change in weight between baseline and year three, we excluded fractures that were reported before the third annual follow-up visit.
The main predictor of this study was change in body weight between baseline and year three (plus/minus 90 days), operationalized in two ways. First, based on percentage change in body weight (for instance, ((weightvisit 3−weightbaseline)/weightbaseline)×100), we classified each participant’s change in body weight into one of three categories: weight loss (decrease of 5% or more since the baseline examination), stable weight (change of less than 5% from baseline weight), and weight gain (increase of 5% or more since the baseline examination). We excluded data from participants who did not undergo measurement of body weight within 90 days of the year three visit. From the two Women’s Health Initiative groups, we had information from 120 566 participants regarding weight change (from baseline to year three) and at least one year of follow-up (after the year three visit) regarding incident fractures. After exclusion of data from participants for whom we lacked data regarding covariates (10%), the sample size for analysis was 108 709.
Second, we examined unintentional and intentional weight loss as separate predictors of incident fracture. At the year three follow-up visit, participants were asked two yes/no questions: “In the past two years, did you lose five or more pounds [about ≥2.2 kg] not on purpose at any time?” (unintentional weight loss) and “In the past two years, did you lose five or more pounds on purpose at any time?” (intentional weight loss). We had responses from 81 652 participants regarding unintentional weight loss and 81 587 participants regarding intentional weight loss.
On baseline self assessment questionnaires, participants were asked whether they had experienced previous fracture (response choices were hip, spine/back/vertebra, upper arm/humerus, lower arm/wrist, hand other than finger, lower leg/ankle, foot other than toe, or other). For this study, we collapsed responses to this question into a binary (yes/no) variable.
From the baseline self report questionnaires we gathered information on age, race/ethnicity, smoking, alcohol intake (non-drinker, past drinker, <1 drink/month, <1 drink/ week, 1-<7 drinks/week, >7 drinks/week, where one drink corresponded to 12 ounces (240 ml) of beer, 6 ounces (170 ml) of wine, or 1.5 ounces (43 ml) of liquor), general health status (“in general, would you say your health is excellent, very good, good, fair, poor?”), number of falls to the ground during the past 12 months (none, once, twice, three times or more), oophorectomy or hysterectomy, recreational physical activity (total MET (metabolic equivalent) hours a week), energy expenditure from walking (MET hours a week), Rand 36-item health survey (SF-36) quality of life physical functioning score (range 0-100), comorbidity (modified Charlson index score13), previous diagnosis of cancer, average protein intake from foods and beverages (g/day),14 dietary14 and supplemental calcium intake (mg/day), and dietary14 and supplemental vitamin D intake (IU/day).
Information regarding current use of menopausal hormone therapy, daily oral corticosteroid use, baseline use of drugs for osteoporosis (bisphosphonates, selective estrogen receptor modulators, calcitonin, parathyroid hormone, denosumab), and use of oral or injectable drugs for the treatment of diabetes (thiazolidinediones, dipeptidyl peptidase-4 inhibitors, meglitinides, glucagon-like peptide-1 agonists, insulin injection, amylin analog, sulfonylureas, biguanides, and alpha-glucosidase inhibitors) was assessed at baseline by clinic staff who examined labels of drug containers.
We used Cox proportional hazards regression15 to determine the association between weight change between baseline and the third annual follow-up visit and time to first fracture after the third annual follow-up visit, using individual regression models for each anatomical fracture location: central body (hip, pelvis, spine), lower extremity (upper leg except hip, knee/patella, lower leg/ankle, foot except toe), and upper extremity (upper arm/humerus, shoulder, lower arm/wrist, hand except finger, elbow). Fractures during the first three years of follow-up were excluded from this analysis. Among women who experienced fracture, duration of follow-up was defined as time to first fracture. Among women who did not experience fracture during follow-up, duration of follow-up was defined as time until last follow-up visit, or death, whichever came first. The main predictors (in separate regression models) were category of (measured) weight change (stable, weight loss, weight gain); self reported intentional weight loss of ≥2.2 kg in the two years preceding the year three follow-up visit (yes v no [reference]); and self reported unintentional weight loss (yes v no [reference]) of ≥2.2 kg in the two years before the year three follow-up visit.
Covariates included baseline height, baseline weight, age, race, smoking (current, never, past), alcohol intake, general health status, number of falls in the 12 months before baseline, oophorectomy, hysterectomy, recreational physical activity (MET hours/week), physical function score, comorbidity (Charlson index) score, baseline dietary and supplemental vitamin D intake, baseline dietary and supplemental calcium intake, use of menopausal hormone therapy at baseline, daily use of oral corticosteroids at baseline, use of oral or injectable diabetes drugs at baseline, study cohort (participation in the Women’s Health Initiative Observational Study), previous fracture, and previous diagnosis of cancer (yes/no). To explore the influence of protein intake and walking on the associations of weight loss with risk of fracture, we added dietary protein intake (g/day) and energy expenditure from walking in kcal/week/kg (MET hours a week). Continuous predictors were handled as if linear, with the exception of vitamin D and calcium intake, which were categorized (<200, 200-<400, 400-<600, and ≥600 IU/day for vitamin D and <800, 800-<1200, or ≥1200 mg/day for calcium).
We tested the assumption that the hazard ratio of the primary predictor remained constant over time by introducing a cross product term for Δ weight*log(time) into the statistical model. The proportionality assumption was not violated.
We made the a priori decision to determine whether race/ethnicity, age category, and number of falls in the past 12 months (none, once, twice, three or more times) modified the associations between change in weight and incidence of fracture by including interaction terms in regression models. Race/ethnicity categories for interaction testing were white, black, Hispanic, Asian/Pacific Islander, and other. Age categories for interaction testing were <50-59, 60-69, and ≥70. We also examined whether associations between change in weight and fracture incidence varied by physical activity level (continuous, or binary above v below median), physical function level (continuous, or binary above v below median), and waist:hip ratio (≥0.9 v <0.916).
We also examined the results stratified by category of baseline BMI (<24.9, 25.0-29.9, >29.9) because previous studies suggest that associations between weight change and incident fracture could vary according to baseline BMI.5 6
Because participants in the Women’s Health Initiative Dietary Modification Trial could have had weight change patterns that were different from those of the remainder of the analytic sample, we performed a sensitivity analysis in which we restricted the analytic sample to participants in that trial (samples sizes of 34 050 for lower limb fracture, 34 089 for upper limb fracture, 34 657 for central body fracture, and 34 851 for hip fracture analyses). In another sensitivity analysis, we excluded data from participants who reported the use of drugs for osteoporosis at baseline. In the final sensitivity analysis, we used the following alternative categories of weight change: stable weight (<5% change, reference), weight gain 5%-<10%, weight gain ≥10%, weight loss 5%-<10%, and weight loss ≥10%.
Statistical analyses were performed with SAS 9.3 (SAS Institute, Cary, NC).
The mean age of our study population was 63.3 (median 63, interquartile range 58-69) (table 1)⇓. Sixteen percent of participants were non-white (table 2⇓). At baseline, fewer than 10% of participants were current smokers (table 2)⇓ and about 30% had fallen at least once in the past 12 months (table 3)⇓. Among the weight change groups, the mean duration of follow-up for incident fractures ranged from 11.5-12.0 years from baseline.
Figure 2⇓ shows the distribution of annualized weight change. Mean annualized percentage change in measured body weight was 0.30%/year overall (−3.6 %/year in the weight loss group n=18 266, 0.09%/year in the stable weight group n=79 279, and 4.1%/year in the weight gain group n=23 021). Mean weight change (from baseline to year three) was −10.0 kg (SD 15.0 kg) in the weight loss group and 8.7 kg (SD 13.4 kg) in the weight gain group. Of the participants who responded to questions regarding unintentional (n=62 185) and intentional (n=62 142) weight loss (2.2 kg in the past two years), 27 530 (44%) reported intentional weight loss, and 14 653 (24%) of participants reported unintentional weight loss.
Characteristics of the analytic sample were similar to those of excluded participants except that, compared with the excluded participants, the participants in the analytic sample were more likely to be participants in the clinical trial (47% v 26%) and were more likely to be white (84% v 78%) (data not shown).
Adjusted associations between annualized percentage weight change and incidence of fracture
Associations between category of weight change (≥5% weight loss, ≥5% weight gain, stable weight) and incidence of fracture were adjusted for baseline age, race, baseline height, baseline weight, smoking, alcohol intake, total energy expended a week, baseline vitamin D intake, baseline calcium intake, physical function score, general health status, oophorectomy, hysterectomy, Charlson index score, use of menopausal hormone therapy, daily oral corticosteroid use, use of oral or injectable treatment for diabetes, study assignment (Women’s Health Initiative Observational Study, Women’s Health Initiative Clinical Trials), history of previous fracture, and previous diagnosis of cancer (table 4⇓). Compared with women who had stable weight between baseline and the third annual visit, women who lost weight had a 9% higher incidence of upper limb fracture (adjusted hazard ratio 1.09, 95% confidence interval 1.03 to 1.16), a 30% higher incidence of central body fracture (1.30, 1.22 to 1.39), and 65% higher incidence of hip fracture (1.65, 1.49 to 1.82). Compared with women who had stable weight, women who gained weight had a 10% higher incidence of upper limb fracture (1.10, 1.04 to 1.17) and an 18% higher incidence of lower limb fracture (1.18, 1.12 to 1.25). The addition of a covariate representing the number of falls in past 12 months did not notably alter the hazard ratios for the associations between weight change and fracture incidence. Similarly, further adjustment for weekly energy expenditure from walking, weekly energy expenditure from recreational activity, use of antidepressant drugs, and total protein intake did not notably alter the hazard ratios for the associations between weight change and incidence of fracture (data not shown).
When we restricted the analytic sample to participants in the Women’s Health Initiative Dietary Modification Trial, results were similar to results in the overall analytic sample (data not shown).
Adjusted associations between intentional and unintentional weight loss and fracture incidence
We examined associations of self reported unintentional and intentional weight loss in the past two years with incidence of fracture (see table A in appendix). Compared with no unintentional weight loss, unintentional weight loss was associated with a 21% higher incidence of central body fracture (adjusted hazard ratio 1.21, 95% confidence interval 1.13 to 1.29), 33% higher incidence of hip fracture (1.33, 1.19 to 1.47), and 16% higher incidence of vertebral fracture (1.16, 1.06 to 1.26). Compared with stable weight, intentional weight loss was associated with increased incidence rates of lower limb fracture (1.11, 1.05 to 1.17) and decreased incidence of central body fracture (0.93, 0.88 to 0.99) and hip fractures (0.85, 0.76 to 0.95).
Interaction tests: associations between weight change and fracture incidence according to baseline BMI, frequency of falls, age, race/ethnicity, diabetes, physical activity, physical function, and waist:hip ratio
Associations of intentional and unintentional weight loss did not vary by age group, with one exception: associations between intentional weight loss and lower limb fracture were more pronounced in younger than in older women (P=0.008 for interaction). Among women aged 50-59, those with intentional weight loss had a 25% higher risk of lower limb fracture than women without intentional weight loss (see table B in appendix).
Associations between weight change and incidence of fracture did not significantly differ by baseline BMI category, number of falls in the past 12 months, race/ethnicity, presence or absence of diabetes mellitus at baseline, physical activity levels, and physical function levels (for upper limb, lower limb, and central body fractures all P>0.05 for interaction).
Among women who gained weight, associations between weight gain and fracture did not differ by waist:hip ratio (>0.9 v ≤0.9).
We performed a sensitivity analysis in which we added extra categories of weight change. We used the following categories: stable weight (<5% change, reference), weight gain 5%-<10%, weight gain ≥10%, weight loss 5%-<10%, and weight loss ≥10%. The pattern of results was similar to those of the primary analyses (table 5⇓).
For all analyses, results were similar when we excluded data from participants who reported the use of drugs for osteoporosis at baseline (data not shown).
In this large cohort of postmenopausal women, compared with women with stable weight over three years, women who had lost 5% or more of their body weight had about 65% higher incidence rates of hip fracture, 30% higher rates of central body fracture, and 9% higher rates of upper limb fracture over about 11 years of follow-up. Also, compared with women who had stable weight, women who had weight gain of 5% or more had 10% higher incidence rates of upper and 18% higher rates of lower limb fractures but no difference in central body fractures. These associations were not explained by baseline frequency of falls or diagnosis of cancer before the third year of follow-up. Compared with stable weight, unintentional weight loss was associated with an increased risk of hip and spine fractures, whereas intentional weight loss was associated with a decreased risk of hip fractures and increased risk of lower limb fractures.
Comparison with other studies
As far as we are aware, this study is the first longitudinal study to focus specifically on how weight change can differentially influence upper limb, lower limb, and central body fractures among postmenopausal women in the US. The associations that we found between weight loss and increased rates of hip fracture, however, agree with those of previous studies. In a previous study of white women aged ≥65, weight loss over four years of follow-up was associated with an increased risk of hip fracture.4 Similarly, self reported weight loss of ≥10% of body weight since age 50 among white women aged 67 and older5 and self reported weight loss of ≥10% from maximum weight among white women aged 50-746 were each associated with an increased risk of hip fracture. Our results were also consistent with those of a previous study in which weight gain since age 25 was associated with a higher risk of ankle fracture among white women aged ≥65.9 Finally, our results are consistent with results of studies from other countries—for example, Norwegian cohort studies that found associations between weight loss and an increased risk of distal forearm fractures17 and non-vertebral fractures18 in women.
Although our study focused on change in body weight and incidence of fracture, a previous Women’s Health Initiative study examined the differential effects of baseline weight on fractures at various anatomical locations.19 In that study, higher baseline BMI was associated with a decreased incidence of hip fractures and central body fractures, whereas the risk of upper extremity fracture was independent of baseline BMI. The authors of that study postulated that the greater soft tissue padding of the hip and central body could counteract the higher traumatic forces that accompany higher body weight. The results of our study possibly support that hypothesis, in that weight gain was not associated with an increased risk of hip fracture but was associated with an increased incidence of upper and lower limb fractures, anatomical sites that have less soft tissue padding.
Serious illness can be an underlying cause of both involuntary weight loss and osteoporosis. The associations that we found between weight loss and incidence of fracture persisted after adjustment for a diagnosis of cancer and other comorbidities. Also, in the current study, only unintentional, not intentional, weight loss was associated with an increased risk of hip fracture. Previous studies regarding voluntary weight loss and risk of fracture have focused on non-vertebral or overall frailty fractures rather than fractures according to specific anatomical regions.3 20 In one study, however, voluntary and involuntary weight loss among overweight women were each associated with similar (2.5-fold) increases in risk of hip fracture.4 Compared with the participants of the previous study, participants of the Women’s Health Initiative were younger at baseline and probably generally healthier.
Strengths and limitations
Strengths of our study include its long duration of follow-up, detailed information regarding risk factors for fracture, objective measurement of body weight (as opposed to self reported body weight), and large sample size including more than 18 000 non-white women (9539 black women) and nearly 40 000 younger postmenopausal women (aged 50-59 at baseline) who were not the focus of previous studies.3 4
Our study has potential limitations. Although we used adjudicated information regarding hip fractures, information regarding other fractures was self reported. The validity of self report of fractures varies by anatomical site in Women’s Health Initiative, being higher for hip (78%) and forearm/wrist (81%) fractures than for clinical spine fractures (51%).21 We did not have information regarding circumstances of the fracture (such as specific activities that immediately preceded fractures). To examine associations between weight change and subsequent incident fractures, we examined associations between change in weight from baseline to the third annual follow-up visit in relation to incident fractures subsequent to the third annual follow-up visit. Participants might, however, have experienced weight change during the fracture follow-up period. Finally, we did not adjust for multiple statistical comparisons, so the probability that at least one of the reported confidence intervals will exclude unity under an overall null hypothesis is greater than 0.05.
Conclusions and policy implications
In conclusion, our finding that weight gain (≥5% of body weight over three years) is associated with increased incidence rates of upper and lower limb fractures is a novel finding. We found that weight loss (≥5% of body weight over three years) is associated with a markedly increased rate of hip fracture, as well as increased rates of central body and upper limb fractures, compared with stable weight. These findings have clinical and research implications and challenge the traditional clinical paradigm of weight gain protecting against fractures. Clinicians should be aware that even intentional weight loss is associated with increased rates of lower limb fractures. Weight loss intervention trials should consider potential effects on the incidence of fracture.
What is already known on this topic
Low body weight is associated with increased risk of fracture
However, associations of weight loss and weight gain with subsequent fracture incidence, classified by anatomical region, in postmenopausal women are unclear.
How fracture patterns may differ after intentional and unintentional weight loss in postmenopausal women is also unknown
What this study adds
Weight gain, weight loss, and even intentional weight loss are associated with increased fracture incidence, but associations differ by anatomical fracture location.
Our findings challenge the traditional clinical model of weight gain being protective against fractures
Clinicians should be aware of fracture patterns both after weight gain and weight loss
Cite this as: BMJ 2015;350:h25
We thank the women who generously participated in the Women’s Health Initiative and the Women’s Health Initiative investigators and staff for their dedicated efforts.
Program office: (National Heart, Lung, and Blood Institute, Bethesda, Maryland) Jacques Rossouw, Shari Ludlam, Dale Burwen, Joan McGowan, Leslie Ford, Nancy Geller.
Clinical coordinating center: (Fred Hutchinson Cancer Research Center, Seattle, WA) Garnet Anderson, Ross Prentice, Andrea LaCroix, Charles Kooperberg, Barbara Cochrane, Julie Hunt, Marian Neuhouser, Lesley Tinker, Susan Heckbert, Alex Reiner.
Regional centers: (Brigham and Women’s Hospital, Harvard Medical School, Boston, MA) JoAnn E Manson, Kathryn M Rexrode, Brian Walsh, J Michael Gaziano, Maria Bueche; (MedStar Health Research Institute/Howard University, Washington, DC) Barbara V Howard, Lucile Adams-Campbell, Lawrence Lessin, Cheryl Iglesia, Brian Walitt, Amy Park; (Ohio State University, Columbus, OH) Rebecca Jackson, Randall Harris, Electra Paskett, W Jerry Mysiw, Michael Blumenfeld; (Stanford Prevention Research Center, Stanford, CA) Marcia L Stefanick, Mark A Hlatky, Manisha Desai, Jean Tang, Stacy T Sims; (University of Arizona, Tucson/Phoenix, AZ) Cynthia A Thomson, Tamsen Bassford, Cheryl Ritenbaugh, Zhao Chen, Marcia Ko; (University at Buffalo, Buffalo, NY) Jean Wactawski-Wende, Maurizio Trevisan, Ellen Smit, Amy Millen, Michael LaMonte; (University of Florida, Gainesville/Jacksonville, FL) Marian Limacher, Michael Perri, Andrew Kaunitz, R Stan Williams, Yvonne Brinson; (University of Iowa, Iowa City/Davenport, IA) Robert Wallace, James Torner, Susan Johnson, Linda Snetselaar, Jennifer Robinson; (University of Pittsburgh, Pittsburgh, PA) Lewis Kuller, Jane Cauley, N Carole Milas; (University of Tennessee Health Science Center, Memphis, TN) Karen C Johnson, Suzanne Satterfield, Rongling Li, Stephanie Connelly, Fran Tylavsky; (Wake Forest University School of Medicine, Winston-Salem, NC) Sally Shumaker, Stephen Rapp, Claudine Legault, Mark Espeland, Laura Coker, Michelle Naughton.
Women’s Health Initiative Memory Study: (Wake Forest University School of Medicine, Winston-Salem, NC) Sally Shumaker, Stephen Rapp, Claudine Legault, Mark Espeland, Laura Coker, Michelle Naughton.
Former principal investigators and project officers: (Albert Einstein College of Medicine, Bronx, NY) Sylvia Wassertheil-Smoller; (Baylor College of Medicine, Houston, TX) Haleh Sangi-Haghpeykar, Aleksandar Rajkovic, Jennifer Hays, John Foreyt; (Brown University, Providence, RI) Charles B Eaton, Annlouise R Assaf; (Emory University, Atlanta, GA) Lawrence S Phillips, Nelson Watts, Sally McNagny, Dallas Hall; (Fred Hutchinson Cancer Research Center, Seattle, WA) Shirley A A Beresford, Maureen Henderson; (George Washington University, Washington, DC) Lisa Martin, Judith Hsia, Valery Miller; (Harbor-UCLA Research and Education Institute, Torrance, CA) Rowan Chlebowski; (Kaiser Permanente Center for Health Research, Portland, OR) Erin LeBlanc, Yvonne Michael, Evelyn Whitlock, Cheryl Ritenbaugh, Barbara Valanis; (Kaiser Permanente Division of Research, Oakland, CA) Bette Caan, Robert Hiatt; (National Cancer Institute, Bethesda, MD) Carolyn Clifford; (Medical College of Wisconsin, Milwaukee, WI) Jane Morley Kotchen; (National Heart, Lung, and Blood Institute, Bethesda, Maryland) Linda Pottern; (Northwestern University, Chicago/Evanston, IL) Linda Van Horn, Philip Greenland; (Rush University Medical Center, Chicago, IL) Lynda Powell, William Elliott, Henry Black; (State University of New York at Stony Brook, Stony Brook, NY) Dorothy Lane, Iris Granek; (University at Buffalo, Buffalo, NY) Maurizio Trevisan; (University of Alabama at Birmingham, Birmingham, AL) Cora E Lewis, Albert Oberman; (University of Arizona, Tucson/Phoenix, AZ) Tamsen Bassford, Cheryl Ritenbaugh, Tom Moon; (University of California at Davis, Sacramento, CA) John Robbins; (University of California at Irvine, CA) F Allan Hubbell, Frank Meyskens Jr; (University of California at Los Angeles, CA) Lauren Nathan, Howard Judd; (University of California at San Diego, LaJolla/Chula Vista, CA) Robert D Langer; (University of Cincinnati, Cincinnati, OH) Michael Thomas, Margery Gass, James Liu; (University of Hawaii, Honolulu, HI) J David Curb; (University of Massachusetts/Fallon Clinic, Worcester, MA) Judith Ockene; (University of Medicine and Dentistry of New Jersey, Newark, NJ) Norman Lasser; (University of Miami, Miami, FL) Mary Jo O’Sullivan, Marianna Baum; (University of Minnesota, Minneapolis, MN) Karen L Margolis, Richard Grimm; (University of Nevada, Reno, NV) Robert Brunner, Sandra Daugherty; (University of North Carolina, Chapel Hill, NC) Gerardo Heiss, Barbara Hulka, David Sheps; (University of Tennessee Health Science Center, Memphis, TN) Karen Johnson, William Applegate; (University of Texas Health Science Center, San Antonio, TX) Robert Brzyski, Robert Schenken; (University of Wisconsin, Madison, WI) Gloria E Sarto, Catherine Allen; (Wake Forest University School of Medicine, Winston-Salem, NC) Mara Vitolins, Denise Bonds, Electra Paskett, Greg Burke; (Wayne State University School of Medicine/Karmanos Cancer Institute, Detroit, MI) Michael S Simon, Susan Hendrix.
Contributors: CJC and JAC had the original idea and designed the study. JW-W and KCJ acquired data and obtained funding. All authors analyzed and interpreted the data. CJC drafted the manuscript and all authors critically revised it for important intellectual content. VOY carried out the statistical analysis. CJC supervised the study and is guarantor.
Funding: The WHI program is funded by the National Heart, Lung, and Blood Institute, National Institutes of Health, US Department of Health and Human Services through contracts HHSN268201100046C, HHSN268201100001C, HHSN268201100002C, HHSN268201100003C, HHSN268201100004C, and HHSN271201100004C. The funders had no role in the design and conduct of the study, the collection, analysis, and interpretation of the data, or the preparation, review, or approval of the manuscript.
Competing interests: All authors have completed the ICMJE uniform disclosure form at www.icmje.org/coi_disclosure.pdf and declare: no support from any organization for the submitted work; no financial relationships with any organizations that might have an interest in the submitted work in the previous three years; no other relationships or activities that could appear to have influenced the submitted work.
Ethical approval: The Women’s Health Initiative was overseen by ethics committees at all 40 clinical centers, by the coordinating center, and by a data and safety monitoring board. Each institution obtained human subjects committee approval. Each participant provided written informed consent.
Role of sponsor: The Women’s Health Initiative (WHI) project office at the National Heart, Lung, and Blood Institute (NHLBI), which was the sponsor, had a role in the design and conduct of the study and in the collection and management of the data. The sponsor did not have a role in analysis and interpretation of the data, the preparation of the manuscript, or the decision to submit the manuscript for publication. Review and approval of the manuscript was carried out by committees composed of WHI investigators and NHLBI representatives.
Transparency declaration: The lead author affirms that this manuscript is an honest, accurate, and transparent account of the study being reported; that no important aspects of the study have been omitted; and that any discrepancies from the study as planned have been explained.
Data sharing: Women’s Health Initiative Study data are available via the BioLINCC website of the National Heart, Lung, and Blood Institute at https://biolincc.nhlbi.nih.gov/home/
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